Prospects for malaria control through manipulation of mosquito larval habitats and olfactory-mediated behavioural responses using plant-derived compounds
Parasites & Vectorsvolume 10, Article number: 184 (2017)
Malaria presents an overwhelming public health challenge, particularly in sub-Saharan Africa where vector favourable conditions and poverty prevail, potentiating the disease burden. Behavioural variability of malaria vectors poses a great challenge to existing vector control programmes with insecticide resistance already acquired to nearly all available chemical compounds. Thus, approaches incorporating plant-derived compounds to manipulate semiochemical-mediated behaviours through disruption of mosquito olfactory sensory system have considerably gained interests to interrupt malaria transmission cycle. The combination of push-pull methods and larval control have the potential to reduce malaria vector populations, thus minimising the risk of contracting malaria especially in resource-constrained communities where access to synthetic insecticides is a challenge. In this review, we have compiled information regarding the current status of knowledge on manipulation of larval ecology and chemical-mediated behaviour of adult mosquitoes with plant-derived compounds for controlling mosquito populations. Further, an update on the current advancements in technologies to improve longevity and efficiency of these compounds for field applications has been provided.
Ever since mosquitoes were discovered to transmit malaria parasites more than a century ago [1, 2], malaria remains a significant threat to human life, with major fatalities disproportionately inflicting children of less than 5 years and pregnant women . Significant decline in global disease burden has been reported by various surveillance studies between 2000 and 2015 following intensive deployment of key interventions: indoor residual spraying (IRS), long-lasting insecticide treated nets (LLINs) and artemisinin-based combination therapies (ACTs) [4, 5]. However, the epidemiological burden of malaria persists in sub-Saharan Africa due to inevitable drug and insecticide-induced resistance [6–8]. This is reflected by residual transmission to the vulnerable groups that accounted for 92% of global deaths reported from African region in 2016 . Residual transmission, which is characterised by shifts in vector feeding patterns, variation in species composition, insecticide-induced behavioural avoidance from IRS and LLINs, outdoor resting and increased outdoor parasite transmission, has emerged following the operational scale-up of these interventions [9–11]. It is postulated that the current tools could lead towards malaria elimination in various epidemiological settings by suppressing vectorial capacity . Yet, the inexhaustive protection implicated by these interventions coupled with reduced susceptibility of malaria vectors to insecticides increases exposure risk and requires pivotal approaches to reduce the annual entomological inoculation rates (EIRs) to less than 1 [10, 13].
Since the inception of integrated vector management (IVM) model by Major Williams C. Grogas in the early 20th century and its adoption by world health organization (WHO) in 2004, significant research has been conducted in search of novel strategies to disrupt disease transmission cycle [14, 15]. These include genetic modification (sterile insect technique (SIT) and paratransgenesis), the use of microbial larvicides, transmission blocking interventions, mosquito behavioral modification, and the recent CRISPR Cas-9 mediated disruption of mosquito reproduction. However, one of the intriguing questions is: why is the fight against malaria still beyond the horizon? To address this fundamental question, Ferguson et al. pointed out that mosquito ecology stands out as the greatest obstacle to malaria elimination and eradication . As many countries within the geographical malaria fringe strive to enter elimination phase, vector control, and the ultimate disruption of Plasmodium falciparum transmission cycle is faced with a multitude of challenges encompassing mosquito ecology, and a clear understanding is required to drive the envisioned goal to its realisation. According to Ferguson et al. the complexity of vector populations that evade control interventions , genetic variation of mosquito behaviour [17, 18], insecticide resistance [19, 20], and environmental changes  constitute the dynamic complex of mosquito ecology that favour propagation of parasite sporogonic stages. While major progress has been made to understand the ecology of malaria vectors, constraints in fully unravelling the interactions with other bio-factors within the ecosystem (such as competitors, predators, and preys in food web complexes) for amplification of malaria transmission risks present a great challenge towards malaria eradication . Russell et al. proposed that the effective control of malaria could also be improved by approaches aimed at manipulating the adult vector behaviours that lead to outdoor transmission through avoidance of IRS-targeted killing .
In essence, mosquitoes require and acquire vital resources from the immediate environment to complete their life-cycle, and in turn, facilitate transmission of P. falciparum parasites to humans. These resources include aquatic breeding sites, carbohydrate sugar sources, blood hosts, and resting places which influence the capacity of mosquitoes to transmit malaria parasites. Despite the high ownership of LLINs and intensive IRS in malaria hotspots, these interventions have failed to break the transmission cycle sufficiently and to linearly push EIR to levels required for local elimination, a scenario creating malaria transmission heterogeneities [12, 23]. Entomological surveillance studies indicate that emergence of behaviorally-resistant and aggressive vectors that evade targeted killing of IRS and LLINs has contributed to high rates of outdoor P. falciparum transmission in different epidemiological regions [24, 25]. Imperatively, interruption of malaria transmission would require integrative interventions that limit mosquitoes from acquiring these resources. Therefore, in addition to the first line interventions (IRS and LLINs), larviciding and the mosquito olfactory system appears to be the targetable Achilles heel  that could be explored to considerably improve control of vector populations and malaria vector annual inoculation rates. There is a close association between vector density and entomological inoculation rates which are paramount parameters of vectorial capacity and malaria epidemiology . Indeed, the vector-parasite-host interactions such as host seeking, blood feeding, parasite development and successful transmission to a natural mammalian host are fine-tuned by the mosquito larval ecology  in which olfactory system plays a primordial role . Given the above, the quality of environment which the juvenile aquatic stages encounter during their development fundamentally influences the success of resultant adult mosquitoes as vectors [28, 30]. Consequently, suboptimal larval conditions have been reported to negatively implicate vector life history traits such as adult female body size, blood meal acquisition frequency and volume, reproductive viability and cycles, and vector longevity which directly impact vectorial capacity and competence [28, 31, 32].
Functional ecology of malaria vectors
Communication within and between insect species and subsequent interaction with natural environment depend chiefly on volatile organic compounds referred to as semiochemicals, which are chemical messengers selectively detected by the olfactory system from a sophisticated chemical ecology [33, 34]. Canonically, the olfactory system in insects not only provides a core link that coordinately mediates various behavioural and physiological responses to their external environment but also a guide towards their control [35, 36]. In mosquitoes, semiochemical cues characterise the functional ecology for oviposition site selection, copulation, host seeking, host selection and sugar foraging [29, 37, 38] (Fig. 1). For many years of insect research, olfaction has been a top priority in understanding chemical ecology with an evolutionary generalisation of various aspects based on Drosophila model [35, 39]. Based on this model, stimulant and inhibitory odorant compounds from natural environment are received by olfactory receptor neurones (ORNs) upon binding onto soluble odorant binding proteins (OBPs) expressed within the sensilla lymph of insect olfactory architecture [40, 41]. On solubilization, the odour complex is transported to odorant receptors (ORs) for detection  and subsequently, generates an action potential to the brain for odour decoding and behavioural response . Over the last decade, several insect genome sequences including that of the malaria mosquito Anopheles gambiae  were annotated and released, tipping the comprehensive study of the olfactory system and design of robust control tools . Some OBPs and ORs have been identified and characterised, with An. gambiae is having 276 G-protein coupled receptors (GPCRs) and 33 candidate OBPs that constitute the sensory pathway . Comprehensive functional studies employing RNAi-mediated gene silencing, heterologous expression in an “empty neurone system” and electrophysiological assays have allowed elucidation of several volatile compounds that mosquitoes detect and respond to in varying degrees [47–49]. Several mosquito attractants and repellents have been extensively studied, in laboratory and semi-field settings, to unravel their roles in mediating distinct behavioural responses. For example, irrespective of the differential mosquito hosts’ attractiveness [50, 51], human skin emanations such as L-lactic acid and microbiota metabolites, exhaled breathe composition viz carbon dioxide (CO2), 1-Octen-3-ol and acetone constitute the principal mosquito attractants for host location and blood feeding [52, 53]. Binding of these chemical blends to the odorant receptors, AgGr22 on maxilla palp specific for CO2 and AgOR8 on antennal dendrites for 1-Octen-3-ol, stimulates chemosensation and flight-anemotactic behaviour for host seeking [29, 54]. On the other hand, geranyl acetate and citronellal from plant essential oils suppress sensitivity of specific receptors to host attractive cues mediating repellent effect against female An. gambiae vectors [48, 55].
Another important aspect of mosquito functional ecology with a great impact on vectorial capacity and malaria epidemiology is oviposition site selection, a critical factor in population dynamics. Evolutionarily, irrespective of the state of insecticide susceptibility, biting tendency and resting places, gravid female mosquitoes face the challenge of locating an appropriate oviposition site that guarantees progeny development and survival . Following mating and bloodmeal acquisition, physiological changes that influence egg development and subsequent behaviour of searching an oviposition site ensue . In addition to visual and tactile cues, the gravid females use to a larger extent olfactory signals to discriminatively select potential breeding sites [58–60]. A considerable number of field studies have reported the role of volatile organic semiochemicals emanating from aquatic habitats to attract or repel mosquitoes in a push-pull manner [61–65]. These semiochemicals interact with female chemoreceptors for cognition before egg laying process . For example, in the event of characterising odour coding in mosquitoes, Carey et al.  and Rinker et al.  demonstrated that perception of oviposition cues such as 3-methylindole, indole, 2-propylphenol, and 4-methylcyclohexanol by female chemoreceptors could be presumably responsible for inducing egg laying. Importantly, volatile organic compounds produced by habitat-associated bacteria such as fatty acids, aromatic amino acids (L-tyrosine, L-phenylalanine and L-tryptophan), and carbohydrates show attraction to Aedes aegypti and Culex pipiens [67, 68]. While efforts to identify the key compounds mediating attraction and selective behaviour in mosquitoes had been made decades ago for Aedes and Culex , those responsive to anophelines lagged behind . It was until recently when Lindh et al.  reported cedrol, a fermentation metabolite produced by fungi found on rhizomes of Cyperus rotundus grass, as a strong oviposition attractant for gravid An. gambiae (s.s.) mosquitoes that aroused interests to characterise anopheline oviposition ecology. In course, Wondwosen et al.  showed that volatiles from various rice cultivars strongly attracts gravid An. arabiensis females. In this study, using electrophysiology and chemical analyses, the authors demonstrated that headspace rice volatiles rich in β-caryophyllene, decanal, sulcatone (6-methyl-5-hepten-2-one) and limonene elicited antennal responses that on evaluation with BioGent (BG) sentinel traps stimulated long range oviposition site seeking behaviour. Elsewhere, Eneh et al.  reported that p-cresol, a strong oviposition attractant of Aedes and Culex from Bermuda grass (Cynodon dactylon) hay infusion, elicited avoidance response to gravid An. gambiae (s.s.). Cumulatively, these studies open avenues for the search of other compounds acting together to mediate the responses that could aid in developing not only general but also species-specific oviposition deterrents or attractive lethal ovitraps (ALOTs). Studies characterising the bio-physicochemical parameters of larval habitats show that habitat selection by female mosquitoes is species-specific and anopheline mosquitoes prefer shallow, temporary, less turbid, and open sunlit water bodies with adequate food resources and absence of predators [74–76]. However, in some extreme cases, these larvae have been reported to colonise polluted urban waters, a phenomenon depicting some form of adaptive divergence . Also, the observed proximity of anopheline larval habitats to human dwellings was suggested to be an evolutionary strategy of mosquitoes to conserve energy for host seeking . Therefore, interventions aimed at manipulating or disrupting the sensory signals in mosquitoes could lead to abrogation of olfactory-driven behaviours that contribute to malaria transmission [45, 79].
Indeed, approaches that target the behavioural attributes of adult mosquito vectors and their juvenile aquatic stages using chemical insecticides have been shown to substantially reduce mosquito populations [80–82]. However, the negative implications such as chemical pollution, loss of biodiversity, and the emergence of resistance associated with their application call for urgent interventions that safeguard environmental health as well as effectively reduce the risk of malaria transmission . Over time, a paradigm shift in vector control has been experienced as the application of natural products especially from plants continues to be appreciated [84–88]. Hence, prospecting for bioactive chemistries from natural sources forms a basis for developing eco-friendly insecticides with less impact on biodiversity [89, 90]. Various approaches ranging from basic evaluation to complex molecular and in silico ligand docking studies, in search of inexpensive, safe, and effective classes of compounds have been deployed as pathways for developing new mosquito control agents [91, 92]. Although this does not guarantee 100% resistance-resilience, we feel that motivation for studying plant-based insecticides vis-à-vis their synthetic counterparts originate from previous reports showing few or no cases of resistance development to natural compounds derived from plants. In nature, plants constitutively and inductively synthesise a myriad of bioactive allelochemicals such as alkaloids, terpenoids, flavonoids, coumarins, glycosides, steroids, tannins, protease inhibitors, phenolics and growth regulators to counteract environmental stress effects and herbivory attacks [93, 94]. These harmful compounds have the potential of controlling both medically and veterinary important disease-transmitting insect vectors owing to their chemistry and structural characteristics that alter the normal physiology of insects, thus reducing their fitness and performance .
This review mainly focuses on the manipulation of larval habitats and chemical-mediated behaviour of adult mosquitoes using plant-based chemicals for reduced risk of malaria transmission. On application, plant-derived compounds could alter the immediate chemical ecology of mosquitoes disrupting the olfactory-mediated location of vital resources required for completing their life-cycle and transmitting malaria parasites. Importantly, we demonstrate how these compounds could be incorporated into IVM programmes for mosquito control.
Push-pull technology for control of adult mosquitoes
The push-pull approach is not a new terminology in the context of pest management. The technique was first developed by Australian researchers, Pyke et al.  to manipulate the distribution of cotton pests of Helicoverpa spp. By then, scientific information on behavioural manipulation for controlling nuisance insects was rudimentary. A comprehensive review compiled by Foster & Harris  advanced and provided a clear understanding of behavioural manipulation for pest management that involves the use of stimuli to activate or inhibit a behaviour thereby changing its expression. From this knowledge, a push-pull approach for controlling mosquito vector populations by manipulating the vector behaviour and their relative spatiotemporal distribution for trapping and subsequent killing of the trapped insect vectors was conceptualised and adapted about 20 years later . This technology has been successfully applied for controlling populations of mosquitoes , tsetse flies , as well as stem borers and Striga weeds from maize plantations [100–102]. In this context, repellents and baits are integratively deployed for driving the mosquitoes away from their vertebrate hosts and luring them towards the trap. For instance, the combinatorial use of a trap baited with an attractant blend that simulated human sweat and a microencapsulated synthetic repellent (δ-undecalactone) in malaria endemic region of western Kenya reduced mosquito house entry by more than 50% and high numbers of outdoor flying mosquitoes captured . Although the use of repellents may deflect mosquitoes from repellent users to non-users , the dual deployment of repellents and attractive traps in push-pull systems would reduce vector densities and EIRs experienced by unprotected people in epidemiological settings by substantial fold . Under such conditions, mosquito olfactory system acts as the possible target to deprive acquisition of resources from the host and environment. Carey & Carlson  pointed out that utilisation of cheap, stable and less hazardous compounds that either stimulate or inhibit mosquito odorant receptors, gustatory receptors and ionotropic receptors could lead to the development of effective, eco-friendly vector control tools that overcome the challenges faced by the current mosquito control strategies. Thus, in an attempt to implement this robust system at remote settings, the design of low-tech and non-power dependent traps that deploy natural products is highly encouraged to reduce human-biting mosquito populations. Combined use of plant-derived compounds with repellent and luring characteristics has the potential of designing such novel push-pull systems. For example, nepetalactone from Nepeta cataria (catnip) essential oil  and linalool oxide  are potent plant-based compounds that could be utilised in the “push” and “pull” effects, respectively. Inspirations from this technique have observed considerable success in the small scale mass trapping of mosquitoes and are currently under field expansion trials in Kenya and Tanzania [103, 107]. To discuss how plant-derived compounds could be applicable in the push-pull approach, we have split it into plant-derived insect repellents and ‘attract and kill’ phenomenon using toxic sugar baits.
Plant-derived insect repellents
An insect repellent is presumably a compound that acts singly or in a cocktail of others to successfully deter a nuisance insect from locating the source of attractive host stimuli. Based on the induced insect behaviour, repellents can be broadly classified into; stimuli-irritants, odour masking and feeding deterrents . In this context of mosquitoes, by sensing or coming into contact with the compound, stimuli-irritants induce behavioural avoidance from the source of the chemical. Odour masking compounds reduce the abundance of host attractive cues while feeding deterrents interfere with bloodmeal and nectar sugar acquisition. To mediate repellent effect, the sensation of these aversive compounds to mosquito sensilla may activate specific insect ORs, block firing of neuron currents or disrupt behavioural responses [109–111]. It remains a hot debate within the malaria community on whether to repel or kill mosquitoes . Nevertheless, the aim of either topical or spatial application of repellents is to disrupt the mosquito olfactory signalling and subsequent host-seeking behaviour.
Before the advent of synthetic chemical repellents, man used and still uses plants with repellent characteristics to drive away mosquitoes with or without the knowledge of their efficacy, mode of action and their safety . As early as 1901, botanical derivatives such as essential oils of citronella (Cymbopogon spp), neem (Azadirachta indica) and lemon eucalyptus (Eucalyptus maculata) were used in ancient Greece, Egypt, China, India and even northern America to ward off biting insects and protect crops against destructive pests . These botanicals are effective even up-to-date, however, due to their high volatilization, their reliability dropped in 1953 for synthetic repellent DEET (N, N-diethyl-3-methylbenzamide) which was adopted as the gold standard mosquito repellent in the United States . DEET is effective against bites of most disease-transmitting vectors offering up to 99.9% personal protection for the long residual period. Although the mechanisms of action of DEET have been debatable for several years, initial studies hypothesised that DEET masks lactic acid on the human skin thus reducing attraction to biting mosquitoes . However, though controversy still exists, molecular and functional studies disputed this notion and showed that DEET selectively inhibits specific insect ORs by blocking electrophysiological signals of sensory neurones to attractive stimuli [109, 117, 118]. These findings were seconded by De Gennaro et al.  who showed that mosquitoes with non-functional OR complexes were only responsive to contact with DEET. Findings from Bohbot & Dickens  suggested that the structurally diverse repellent compounds including DEET, IR3535 (3-(N-acetyl-N-butyl) amino propionic acid ethyl ester), KBR 3023 or Picaridin (2-(2-hydroxyethyl)-1-methylpropylester) and MR08 (menthol propylene glycol carbonate) modulate the function of mosquito odorant receptors reducing vector-host contacts. Despite the excellent efficacy of DEET against mosquitoes, its use has been associated with various challenges. Its cost ineffectiveness and chronic human toxic effects  coupled with recent reports of resistance [121–123] compromise user reliability and human beings seem to have diverted preference to cheap, safe, eco-friendly and effective natural products of plant origin . A review by Maia & Moore highlighted some adverse side effects such as dermatitis sensation that resulted from the application of plant essential oils, thus in their view, plant-derived compounds may not be necessarily safer than synthetic insecticide DEET . However, the documented chronic side effects of DEET in children  surpass those implicated by plant derivatives.
Studies continue to report plants as potential sources of effective insecticides and interest on studies of plant-derived repellents renewed [86, 114, 124, 125]. For instance, pyrethroids used to impregnate LLINs were initially sourced from Chrysanthemum plant extracts (pyrethrum) in Kenya . With the close interactions of humans and nuisance mosquitoes that bay for blood, local communities in malaria endemic regions have devised cheap means of trying to drive these organisms out of their reach by using plants. In the African region, ethnobotanical knowledge has been immensely deployed to identify plants with repellent characteristics used by local communities to drive away mosquitoes from human dwellings as a preliminary source of mosquito control agents [127–131]. These surveillance studies show that bruising, burning or smouldering of the repellent plant parts, planting repellent plants around homesteads, and topical application of plant-derived oil formulations on the skin and garments are common local practices for keeping mosquitoes away from human hosts. A well-documented example was where Seyoum et al. reported that natives from western Kenya drove away An. gambiae (s.s.) mosquitoes from their huts via the direct burning of Lantana camara, Azadirachta indica, Lippia ukambensis, Tagetes minuta, and Ocimum americana . It has been suggested that the smoke produced by burning these plants masks human kairomones and convention currents used by mosquitoes for host seeking . Also, the smoke lowers relative humidity making mosquitoes vulnerable to desiccation and reducing sensory input as mosquito receptors respond well in the presence of moisture . Though this may appear primitive, this local method of reducing vector-human contacts forms the basis of today’s formulations against nuisance mosquitoes, and thus ethnobotanical knowledge has played a significant role in the search of natural products with repellent properties . Plant-derived compounds applied on human host skin surface, or space spraying interferes with mosquito host-seeking and blood feeding process . Given the fact that mosquitoes detect and respond to host volatiles, it is conceivable that reduction of the relative abundance of each chemical cue detected using repellents during sampling process would significantly minimise overall attraction.
The most plant-derived compounds reported to possess mosquito repellent effects include citral, geraniol, citronellal, citronellol, myrcene, α-pinene, β-pinene, p-menthane-3,8-diol (PMD), linalool, thymol, eugenol, carvacrol and caryophyllene [86, 124, 134] (Fig. 2). These natural compounds which potentiate excited-repellent effects are flavours and fragrances of plant essential oils mainly categorised as monoterpenes (acyclic and cyclic), sesquiterpenes and aliphatic compounds (alkanes, alkenes, ketones, aldehydes, acids and alcohols) . Among these constituents, terpenes (monoterpenes and sesquiterpenes) have been reported to be as effective as DEET in intoxicating insects when topically applied or sprayed in space .
In fact, the US Centers for Disease Control and Prevention (CDC) recommends the use of repellents against mosquito-borne diseases for travellers and military [135, 136]. For instance, potent plant-derived repellents such as p-methane-3,8-diol (PMD) (from Eucalyptus spp.) and citronella oil (from Cymbopogon spp.) are fully registered and recommended for topical use because of their protection efficacy of over 95% against mosquitoes [137, 138]. This report is supported by field studies, conducted in Ghana, where subjects wearing PMD- and citronella-treated garments were significantly protected from mosquito bites . Furthermore, topical application of PMD repellent on forearms by subjects in South Africa offered long-term 90–100% (for 5–6 h) protection against An. arabiensis mosquito bites which were equally effective as the commercial standard, DEET .
Laboratory evaluations by Deletre et al. [140, 141] highlighted strong repellency and electrophysiological responses from pure aldehydes of essential oil relative to the constituent monoterpenes against An. gambiae (s.s.), a potential observation that warranted consideration of these plant-derived compounds to replace pyrethroids in impregnation of bed nets and window curtains. The tested essential oils were derived from plants: Thymus vulgaris, Cymbopogon winterianus, Cuminum cyminum, and Cinnamomum zeylanicum. It was observed that the activity of the individual major constituents could not match with that of the parent oils suggesting coherent interactions of the individual compounds to potentiate bioactivity. It is worth noting at this point that strong electrophysiological response elicited by compounds does not necessarily correlate to their repellent characteristics. In the arms-in-cage assay, Omolo et al.  tested the repellent activity of essential oils extracted from selected Kenyan plants; Conyza newii, Plectranthus marrubioides, Lippia javanica, Lippia ukambensis, Tetradenia riparia, Iboza multiflora and Tarchonanthus camphoratus. Findings from this study showed that application of the essential oils on arms of volunteers strongly elicited repellent efficacy of 79–100% protection against An. gambiae (s.s.) mosquitoes are deterring host blood feeding. Major constituents of the essential oils eliciting repellent effects were identified as perillyl alcohol, cis-verbenol, cis-carveol, geraniol, citronellal, perillaldehyde, caryophyllene oxide and a sesquiterpene alcohol. They further tested the repellent activities of the most abundant compounds within synthetic blend formulations for different plant essential oils. Four formulations of C. newii - perillaldehyde, perillyl alcohol, 1,8-cineole, limonene [29:4:10:7]; T. riparia - fenchone, limonene, 1,8-cineole, [64:2:1.5]; T. camphoratus - camphene, α-pinene, α-fenchyl alcohol, 1,8-cineole, α-terpeneol, p-cymene [17:17:15:7:4:3]; and L. javanica - limonene oxide, cis-verbenol, verbenone, linalool, limonene, α-terpeneol [39:11:6:3:2.5:2] were found highly comparable to the activity of individual crude essential oil. In another study, Wanzala & Ogoma  evaluated the repellency efficacy of essential oil extracted from Tagetes minuta against An. arabiensis females. The essential oil rich in ocimene, tagetones, dihydrotagetone, ocimenones, piperitenones, 3,9-epoxy-p-metha-1,8(10)diene, β-caryophyllene, bicyclogermacrene, and AR-turmerone significantly deterred host seeking and biting by female mosquitoes relative to control subjects who applied vaseline petroleum jelly on their arms. This protective effect of plant-based repellents has been extended to planting repellent plants around homesteads and thermal expulsions that reduce the rates of mosquito entry into the houses [86, 132, 143, 144]. Repellent efficacy of plant-derived compounds has been summarised in Table 1.
Mechanisms of action of plant-derived insect repellents
Until today, the modes of action of most plant-derived repellent compounds are still unclear although neurotoxic effects involving gamma aminobutyric acid (GABA), octopamine synapses, inhibition of acetyl cholinesterases and regulation of ion channels have been characterised . Binding of thymol to GABA receptors blocks the GABA-gated chloride channels on postsynaptic neurone membranes resulting in CNS hyper-excitations, convulsions and death . Eugenol activates octopaminergic receptors reducing production levels of cyclic AMP (cAMP) . Also, eugenol has been reported to increase the intracellular levels of calcium ions, thus inducing toxicity by mimicking the action of octopamine . Other essential oil constituents inhibit acetyl cholinesterase (AchE) resulting in ataxia, either by irreversible inhibitory effect or reversible competition for the enzyme’s active site . Geraniol and linalool reversibly compete with hydrophobic functional groups of AchE’s active site. Also, linalool was shown to inhibit neuronal electrical activity by inducing a reduction in amplitude of action potential and subsequent decrease in post hyperpolarization phase and firing frequency of action potentials . Using Drosophila, Kwon et al.,  demonstrated that citronellal interacts with transient receptor potential channel (TRPA1) modulating the Ca2+-dependent activation of potassium channel, but in An. gambiae TRPA1 is directly activated by citronellal. Loss of Ca2+-activated K+ channel resulted in impaired citranellal-elicited avoidance and increased the frequency of action potential in olfactory receptor neurones. In another study, plant essential oils from Verbenaceae, Lamiaceae, Asteraceae and Rivularaceae families were reported to inhibit mosquito odorant degrading enzymes of cytochrome P450 family on a metabolic standpoint . Taken together, these compounds disrupt various insect cellular activities and biological processes conferring repellent or toxicity effect. The repellent efficacy of plant essential oils varies significantly according to the phytochemical profile of the plant extract and the target insect. On the other hand, toxicity is influenced by the chemical composition of the essential oil, which depends on the source, season and ecological settings, extraction method, time of extraction and plant part used for extraction .
Other plant compounds elicit oviposition deterrence effects to gravid female mosquitoes by rendering the site unfavourable for egg laying. For instance, dual choice experiments performed using essential oils of Ocimum kilimandscharicum, and Ocimum suave deterred gravid An. gambiae (s.s.) mosquitoes from laying eggs as shown by reduced egg count about controls . (E)-caryophyllene and α-humulene from the essential oil of Commiphora leptophloeos have shown oviposition deterrence to Aedes mosquitoes, suggesting their potential to deter anopheline mosquitoes as well .
Attract and kill phenomenon using attractive toxic sugar baits
Mosquitoes supplement nutritional requirements by foraging nectar sources to provide energy for flight, longevity and enhance fecundity [153, 154]. Hien et al.  showed that plant sugar sources differentially influence infection prevalence and intensity, and hence natural sugar sources present a great threat to control of malaria by enhancing the survival and fecundity of mosquito vectors as well as development of P. falciparum [156, 157]. This finding is supported by Nyasembe et al. who demonstrated that infection with P. falciparum stimulates urge of nectar sugar uptake by female mosquitoes . Indeed, studies utilising behavioural response assays performed in dual-response olfactometer and coupled gas chromatography electroantennogram detectors (GC-EADs) have shown that anopheline mosquitoes discriminatively prefer certain plant odours for foraging , providing a basis for developing mosquito odor-baited traps using plant-based lures . Extensive behavioural and chemical ecology studies have recently come up with attractive toxic sugar bait (ATSB) method that kills mosquitoes questing for essential sugar sources, oviposition sites and bloodmeal . This technique was first developed by Israel-based researchers  and has been currently adopted by various research groups working in Africa, Florida (USA) and Israel  for trapping mosquitoes. Most formulations of ATSB involve the use of fruit juices from guavas and mangoes as phytochemical lures, sugar solution as feeding stimulant, and an oral toxin of 1% boric acid that kills mosquitoes upon ingestion [106, 160]. The technique has been successfully deployed for mass trapping of mosquitoes during vector surveillance operations, and for studies aimed at reducing the proportion of endophagic female mosquitoes . Although this new technique is still in the early stages of development, upscaling of its potential to cover large field applications would prove it a powerful malaria vector management tool that complements the existing vector control strategies. For instance, in a field assessment study conducted in Mali, ATSB significantly reduced indoor feeding mosquito populations by 90% suggesting its great potential to control malaria vectors . Additionally, spraying of ATSB on plants was found to reduce the relative abundance of female and male anopheline mosquitoes (by about 90%) with a concomitant reduction in the completion of the gonotrophic cycle . Irrespective of the availability of high-favoured sugar-rich sources, Beier et al. demonstrated that ATSB methods reduced the densities of female anopheline mosquitoes in arid oases during a 47-day field trial study . In summary, these testimonial reports demonstrate the efficacious impact of ATSBs in reducing the prevalence of malaria-transmitting mosquito populations as well as reducing their reproduction cycles.
Larvicidal agents derived from plants
Mosquitoes spend a considerable amount of time in the water during the development of juvenile stages. Therefore, vector control interventions targeting the larval habitats could considerably suppress the populations of adult mosquitoes consequently contributing to reduced vectorial capacity and parasite transmission . According to WHO , larviciding complements the existing vector controls in regions where the sites are “few, fixed and findable” such as urban and rural settings, potentially protecting several households within a small radius. As a component of IVM and larval source management (LSM), the approach reduces the proportion of both indoor and outdoor feeding mosquitoes, hence lowering residual malaria transmission rates [81, 167, 168]. Historically, it is one of the reported successful strategies of mosquito control , but its operational implementation in the prevention of malaria in sub-Saharan Africa is limited possibly due to its labour intensiveness, robust technical difficulties, the variability of vector site preferences and demand for frequent applications . Despite these constraints, community-based participatory small scale field trial programmes using formulations of microbial larvicides, Bacillus thuringensis var. israelensis (Bti) and Bacillus sphaericus (Bs), in African countries such as Gambia, Kenya, Tanzania, Burkina Faso, Côte d’Ivoire, and Benin have shown revitalizing efforts to revive larviciding for malaria vector control [170–177]. Unfortunately, apart from the high cost of these larvicides, the emergence of resistance through larval midgut modifications pose a challenge to their sustainability , a scenario that imperatively calls for cost-effective and resistance-resilient chemistries.
Many plant extracts have been investigated for bioactivity against immature stages of mosquito vectors, several with promising efficacies. However, only a few have undergone chemical characterization to elucidate the bioactive ingredients, the core of phytochemistry research that promotes optimisation of plant compounds into vector control . The plant derivatives reported to have larvicidal activity include; N-containing alkaloids, limonoids, phytoecdysteroids, sesquiterpene lactones, flavonoids, essential oils, naphthoisoquinolines, tannins and saponins from Annonaceae, Asteraceae, Cyperaceae, Ebeneceae, Euphorbiaceae, Lamiaceae, Lauraceae, Leguminosae, Meliaceae, Cledophoraceae, Labiatae, Oocystaceae and Rutaceae families . A summary of plant-sourced larvicidal agents has been presented in Table 2. Most of these compounds exert direct toxicity on application to mosquito breeding water, while others cause growth inhibiting effects similar to those exhibited by insect growth regulators (IGRs), reducing survival and development of mosquitoes . For instance, pyridone alkaloids from Ricinus communis and sesquiterpene lactones from Tithonia diversifolia reduced the survival of An. gambiae (s.s.) larvae by 60–95% at LC50 0.18 mg/ml and LC50 0.33 mg/ml, respectively . Naphthoisoquinolines from Lantana viburnoides and Plumbago zeylanica have shown activity against An. gambiae (s.s.) and An. arabiensis larvae [180, 181]. Well-studied mosquito control agents from plants are insect growth regulatory compounds and essential oils.
Plant-derived insect growth regulators as potential agents for vector control
Limonoids (i.e. sesquiterpenoids and triterpenoids) and phytoecdysteroids (Fig. 3) are plant-based compounds derived from Azadirachta indica (neem), Melia azedarach, Vitex payos, Vitex schiliebenii, Melia volkesnii, Plumbago zeylanica, P. dawei, P. stenophylla, Hugonia castaneifolia, H. busseana, Dysoxylum malabaricum, D. beddomei, Turraea abyssinica and Turraea cornucopia. These compounds occur in a small portion of 5–10% of terrestrial plants and may show diverse structural characteristics which are associated with efficacy against insect juveniles by mimicking the endogenous developmental hormones . In previous studies conducted by Nathan et al. limonoids from neem and Melia azedarach elicited 95–100% mortality at 1 ppm against An. stephensi larvae [183, 184]. In another similar study, limonoids sourced from Turraea abyssinica and T. cornucopia inhibited larval development in An. gambiae (s.s.) at a range of LC50 202–265 ppm indicating the requirement for much higher concentration to achieve larval inhibition . Triterpenoids (salannin and volkensin) derived from Melia volkesnii caused larval mortality at 5.4 mg/l against An. arabiensis . Similarly, triterpenes from Dysoxylum malaricum and D. beddomei caused 90% larval mortality against An. stephensi . Moreover, phytoecydsteroids (20-hydroxyecdysone, γ-sitosterol, stigmasterol) sourced from Vitex payos, V. schiliebenii and Plumbago spp have been reported to exert pronounced toxicity (100% mortality) on developing An. gambiae (s.s.) larvae at relatively high doses and inducing developmental defects at sublethal doses [180, 188]. Recently, Muema et al. reported non-steroidal compounds, proanthocyanidins from green tea leaves, that produced similar IGR-related effects on developing malaria mosquito larvae suggesting their potential control mosquito populations at a low dose of 5 ppm . Additionally, Agerantum conyzoides, previously reported to possess anti-juvenile hormone precocenes and bioactivity against Culex, Aedes and An. stephensi was demonstrated to elicit toxicity and inhibit the precocious larval development of An. gambiae (s.s) and An. arabiensis by inducing abnormal larval-pupal intermediates and disrupted adult emergence .
Mechanism of action of plant-derived insect growth regulators
The phytoecdysteroids structurally resemble plant growth steroids (brassinosteroids), but they defend the plants against phytophagous insect attacks . On ingestion, these compounds produce detrimental effects on insect development causing the insect to die as a result of moulting failure . Structural resemblance of these compounds to endogenous insect developmental hormone 20-hydroxyecdysone (20-E) is believed to interfere with moulting process through competition for the same endogenous hormone receptors arresting larval development at larval-pupal intermediates and consequently death [188, 192]. Although the distinct mode of action of phytoecdysteroids and limonoids is ambiguous, these compounds are speculated to either antagonise or agonise insect ecdysteroid and juvenile hormone receptors leading to disruption of endocrine balance [182, 192]. In addition to interfering with the hormonal balance, neem derivatives target cholinergic nerve transmission, hence disrupting neuromuscular coordination . Further, Azadirachtin has been reported to exhibit anti-mitotic effect by disrupting tubulin polymerization  and cell cycle arrest by down-regulating cyclin B and D1, in addition to inducing pro-apoptotic signals . On exposure to these compounds, some juveniles exhibit demelanized cuticle, absence or reduced chitin content, extended larval phase, elongated abdominal region, abnormal behaviour changes (tonic immobility) and adults with deformed flight muscles that fail to thrive suggesting dysregulation of neuroendocrine system [195–197]. Besides causing growth regulatory defects, exposure to mosquitoes to these compounds at sublethal doses negatively impact fecundity, reproductive fitness and egg viability - suggesting the potential of these compounds in insect control .
Use of plant-derived essential oils in larval control
Manipulation of larval habitats with biodegradable plant-derived essential oils has replaced the use of kerosene for mosquito control . These complex blends form a thin emulsion layer over the surface of mosquito breeding water, hence preventing oxygen entry, reducing amounts of water-dissolved oxygen, and induces larval intoxication upon ingestion. Existing reports indicate that essential oils evoke larval toxicity and are potent against An. gambiae (s.s.), An. arabiensis and An. stephensi  (Table 2). Findings by Kweka et al. showed that δ-3-carene from Schinus terebinthifolia essential oil was responsible for larval mortality rates of 13.75–97.91% in An. gambiae (s.s.) . Thymol and carvacrol from Plecranthus amboinicus produced lethality at LC50 55.20 ppm and LC90 99.09 ppm against An. gambiae (s.s.) within 24 h of exposure . Babatunde et al. reported that Ocimum canum essential oil reduced survivorship of An. gambiae (s.s.) larvae at LC50 49.51 × 10−3 mg/ml and LC90 103 × 10-3 mg/ml . It has also been reported that essential oils of Plectaranthus glangulosus and Callestemon rigidus were active against An. gambiae (s.s.) at LC50 7.37 ppm and 99.61 ppm respectively . In addition, laboratory- and field-based studies performed using An. gambiae (s.s.) demonstrated that trans-cinnamaldehyde from Cinnamomum osmophloeum and kau-16-rene, β-elemol from Cryptomeria japonica leaf essential oils caused larval toxicity at LC50 11.91–63.63 μg/ml and LC50 5.55–134.84 μg/ml, respectively [199, 204]. Moreover, monoterpenes from Zanthoxylum armatum essential oil evoked lethality to An. stephensi at LC50 58 ppm , while thymol from Trychyspermum ammi caused larval mortality at LC50 80 mg/ml . Neem oil formulation killed late larval instars of An. gambiae (s.s.) at LC50 11 ppm and inhibited adult emergence at IC50 6 ppm .
It is important to note that the efficacy of different plant compounds depends on various parameters such as; extraction method, geographical location of the plant, plant part used, concentration, test mosquito species, solvents used, the photosensitivity of some phytochemicals and time of extraction .
Synergistic phenomena in malaria control
Incorporation of plant-based compounds to potentiate the effects of the existing vector control methods has been studied, and findings from these studies indicate the synergistic potential of botanical derivatives in reducing risks of malaria transmission. For instance, in a randomized trial study carried out in the Bolivian Amazon, a reduction of 80% in malaria episodes was reported among participants who used plant-based repellent (PMD) and slept under LLINs, thus indicating a synergistic potential of PMD to LLINs relative to placebo group which slept under LLINs only without using the repellent . Additionally, in a community-based clustered randomised trial, Deressa et al. reported that the combined use of LLINs and mosquito repellent (Buzz-Off® petroleum jelly, essential oil blend) significantly reduced malaria infection by 34–47% relative to the control groups which received LLINs alone . Kweka et al. showed that individual compounds and their blends of plant-derived menthol propylene glycol carbonate (MR08) and DEET offered a protective efficacy in the range of 92–100%, suggesting that these blends could be of additional value for personal protection in the absence of IRS and LLINs . Elsewhere, Stewart et al. found out that indoor application of ATSBs in combination with LLINs could be a promising strategy to control pyrethroid-resistant mosquitoes .
Regulatory issues, advancements and commercialization of plant-derived mosquito control compounds
The demand for relatively safe and effective plant-based mosquito control agents by consumers continues to increase relative to synthetic counterparts . However, despite the extensive research on the insecticidal potential of plant-based compounds, only a few have been successfully registered and approved for commercialization . Strict regulatory laws imposed on the marketing of these compounds in many developed countries have slowed down the full exploitation of many established effective plant-derived chemistries to control nuisance insects. The concerns on potential risks associated with plant-derived compounds to environment, humans and non-target organisms are variable and majority lack of experimental basis . In spite of these issues, EcoSMART Technologies Inc. (Atlanta, USA) has succeeded in introducing plant-based insecticidal compounds for agricultural and consumer utilisation . In developing countries rich in biodiversity, many promising plant-derived compounds remain untapped for control of harmful insects, although in some cases, whole plant parts or crude extracts have been reported to protect humans from mosquito bites effectively . Concerns raised on the variability of product chemistries during pre- and post-harvest processing, that may affect the activity of the end product, are subject to debate [87, 95]. Some compounds are effective when in a cocktail of other plant components, whereas others require being isolated and purified. Nevertheless, whether to use crude extracts, for instance, essential oil to drive away mosquitoes or a formulation of the major chemical components is subject to user preference . Stability of the isolated compounds under different environmental conditions must be considered because some compounds may change the chemical conformation of functional groups upon storage due to photosensitivity and other environmental factors . For instance, neem derivatives and pyrethrum compounds are highly sensitive to UV exposure leading to degradation that in turn reduces their efficacy .
Residual efficacy of plant-based repellents and ATSBs is also under consideration. While many repellent compounds offer high protection efficacy similar to DEET against malaria mosquito vectors, volatility minimises their longevity to mediate protection . Advancements in technologies such as encapsulation and microencapsulations, nanoemulsions and fixatives have been pursued to improve the longevity of potent repellent compounds [86, 212]. For instance, slow-release encapsulated citronella oil nanoemulsion has been used to increase the efficacy of citronella-treated fabrics for up to 30 days . The shelf life and efficacy of neem-based products have been enhanced through microencapsulation, microemulsions, inclusion complexes and granular formulations [214, 215]. Membrane-based ATSBs enhance the release of bio-lures and increasing their efficiency in field applications (unpublished information from Günter Müller, Hebrew University, Jerusalem, Israel). Although enhancement of longevity would mean prolonged protection against mosquitoes, potential issues regarding environmental toxicity may arise. Environmental impact of many plant compounds is generally considered low owing to their biodegradability and short half-lives of < 30 h . Neem derivatives have fewer impacts on pollinators, natural pest predators and vertebrate species, despite its efficacy in controlling more than 300 insect species [216, 217]. In contrast to synthetic insecticides, many plant-derived compounds exhibit no persistence, bioaccumulation and biomagnification . Thus, it would be more advantageous when persistence is reduced to minimise negative implications. Widespread application of plant-based compounds especially mosquito repellents creates wary on the selectivity of these compounds to target invertebrates . Though generally regarded safe, it is yet to be established if some of these repellents could have negative impacts on non-target arthropods.
Other drawbacks to the commercialization of plant-derived mosquito control agents involve sustainability of the botanical resource, industrial confidence in the products, up-scaling potential of plant resource products, standardisation of chemically complex extracts, slow action of other compounds and availability of competing products such as newer synthetics, fermentation and microbial products.
As the world’s human population continues to increase (world’s population growth rate currently approximated at 1.24% annually ), more land is needed to sustain developments, agriculture and settlements. These anthropogenic activities contribute to opening up of potential mosquito breeding sites and even speciation of malaria vectors [172, 219]. Also, the overwhelming development of vector resistance to the currently available synthetic insecticides, following persistent application, continues to challenge the effective control towards malaria transmission [8, 220]. It is therefore anticipated that the identification of bioactive plant compounds will continue for improved management of malaria-transmitting mosquito vectors. A handful of biologically active compounds identified from plants is yet to be exploited for controlling insect pests and vectors on a large scale. Therefore, ‘bench to field’ transition of laboratory tested bioactive compounds and subsequent incorporation into IVM could offset insecticide resistance, undoubtedly reducing malaria vector populations and risk of malaria transmission by greater magnitudes. Successful interventions to control malaria-transmitting mosquitoes using plant-derived compounds would require available, scalable and sustainable technologies for both local and large-scale manufacture. Nanotechnology is currently revolutionising the production of market pesticides. Production of plant-derived nanoparticles and nanoencapsulation compounds increases the longevity of essential oils through slow-release phenomenon conferring prolonged protection against mosquito bites . Furthermore, the silver nanoparticle larvicidal agents derived from plant extracts will find useful applications in larviciding . Advances in applied nanobiotechnology have revolutionised synthesis of plant-based silver nanoparticles that are currently being reported effective against even insecticide resistant disease-transmitting vectors, primarily targeting the immature stages at low dosages of 1–30 ppm . The membrane-based ‘attract and kill’ systems will also in future be revolutionising field-based applications of bio-lure compounds for mass trapping of mosquitoes (unpublished information from Günter Müller, Hebrew University, Jerusalem, Israel). It is therefore anticipated that more robust technologies for controlling malaria vectors using bio-products are underway. Plant-derived compounds could potentially be used for controlling mosquito vectors by manipulating their behaviour and possibly replace pyrethroids in impregnating bed nets as suggested by Deletre et al. .
Comprehensive understanding of the mechanistic role of mosquito olfaction, odour coding and larval ecology is crucial for developing new strategies for disrupting malaria transmission cycle. Integrated vector management programmes advocate for strategies that aim at improving the cost-effectiveness, efficacy, ecological soundness and sustainability of control interventions. In nature, economically feasible plant bioactive compounds are in abundance, many of which are unexploited for vector control. We state that the tools and compounds presented in this review, despite showing promising efficacy against outdoor mosquito populations under laboratory and small field trials, effectiveness under large-scale field trials and various epidemiological settings remain unexplored. The blends of secondary metabolites extracted from plants cannot be used alone, hence will require being integrated with the existing vector control methods so as to provide synergistic tools that can sustainably help to reduce and possibly eliminate malaria vector populations.
Attractive toxic sugar bait
Entomological inoculation rates
Gamma aminobutyric acid
Indoor residual spraying
Integrated vector management
Long-lasting insecticide treated nets
World Health Organization
Ross R. On some peculiar pigmented cells found in two mosquitos fed on malarial blood. Br Med J. 1897;2:1786.
Cox FEG. History of the discovery of the malaria parasites and their vectors. Parasit Vectors. 2010;3(1):5.
WHO. World malaria report. Geneva: World Health Organization; 2016. p. 1–186.
Bhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, et al. The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature. 2015;526:207–11.
Cibulskis RE, Alonso P, Aponte J, Aregawi M, Barrette A, Bergeron L, et al. Malaria: global progress 2000–2015 and future challenges. Infect Dis Poverty. 2016;5:61.
Mukonka VM, Chanda E, Haque U, Kamuliwo M, Mushinge G, Chileshe J, et al. High burden of malaria following scale-up of control interventions in Nchelenge District, Luapula Province. Zambia Malar J. 2014;13:153.
Nkumama IN, O’Meara WP, Osier FHA. Changes in malaria epidemiology in Africa and new challenges for elimination. Trends Parasitol. 2016;33:128–40.
Ranson H, Lissenden N. Insecticide resistance in African Anopheles mosquitoes: a worsening situation that needs urgent action to maintain malaria control. Trends Parasitol. 2016;32:187–96.
Russell TL, Govella NJ, Azizi S, Drakeley CJ, Kachur SP, Killeen GF. Increased proportions of outdoor feeding among residual malaria vector populations following increased use of insecticide-treated nets in rural Tanzania. Malar J. 2011;10:80.
Killeen GF. Characterizing, controlling and eliminating residual malaria transmission. Malar J. 2014;13:146.
Killeen GF, Govella NJ, Lwetoijera DW, Okumu FO. Most outdoor malaria transmission by behaviourally-resistant Anopheles arabiensis is mediated by mosquitoes that have previously been inside houses. Malar J. 2016;15:225.
Killeen GF, Seyoum A, Sikaala C, Zomboko AS, Gimnig JE, Govella NJ, et al. Eliminating malaria vectors. Parasit Vectors. 2013;6:172.
Griffin JT, Hollingsworth TD, Okell LC, Churcher TS, White M, Hinsley W, et al. Reducing Plasmodium falciparum malaria transmission in Africa: a model-based evaluation of intervention strategies. PLoS Med. 2010;7:e1000324.
Ramirez JL, Garver LS, Dimopoulos G. Challenges and approaches for mosquito targeted malaria control. Curr Mol Med. 2009;9:116–30.
Hammond A, Galizi R, Kyrou K, Simoni A, Siniscalchi C, Katsanos D, et al. A CRISPR-Cas9 gene drive system targeting female reproduction in the malaria mosquito vector Anopheles gambiae. Nat Biotech. 2016;34:78–83.
Ferguson HM, Dornhaus A, Beeche A, Borgemeister C, Gottlieb M, Mulla MS, et al. Ecology: a prerequisite for malaria elimination and eradication. PLoS Med. 2010;7(8), e1000303.
Neafsey DE, Waterhouse RM, Abai MR, Aganezov SS, Alekseyev MA, Allen JE, et al. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoes. Science. 2015;347:1258522.
Coluzzi M, Sabatini A, Petrarca V, Di Deco MA. Chromosomal differentiation and adaptation to human environments in the Anopheles gambiae complex. Trans R Soc Trop Med Hyg. 1979;73(5):483–97.
Ranson H, N’Guessan R, Lines J, Moiroux N, Nkuni Z, Corbel V. Pyrethroid resistance in African anopheline mosquitoes: what are the implications for malaria control? Trends Parasitol. 2011;27:91–8.
Yewhalaw D, Wassie F, Steurbaut W, Spanoghe P, Van Bortel W, Denis L, et al. Multiple insecticide resistance: an impediment to insecticide-based malaria vector control program. PLoS One. 2011;6:e16066.
Patz JA, Githeko AK, McCarty JP, Hussein S, Confalonieri U. Climate change and infectious diseases. Infect Dis. 2008;9:103–32.
Russell TL, Beebe NW, Cooper RD, Lobo NF, Burkot TR. Successful malaria elimination strategies require interventions that target changing vector behaviours. Malar J. 2013;12:56.
Zhou GF, Afrane YA, Vardo-Zalik AM, Atieli H, Zhong DB, Wamae P, et al. Changing patterns of malaria epidemiology between 2002 and 2010 in western Kenya: the fall and rise of malaria. PLoS One. 2011;6(5):e20318.
Gatton ML, Chitnis N, Churcher T, Donnelly MJ, Ghani AC, Godfray HCJ, et al. The importance of mosquito behavioural adaptations to malaria control in Africa. Evolution. 2013;67:1218–30.
Durnez L, Mao S, Denis L, Roelants P, Sochantha T, Coosemans M. Outdoor malaria transmission in forested villages of Cambodia. Malar J. 2013;12:329.
Killeen GF, Fillinger U, Kiche I, Gouagna LC, Knols BGJ. Eradication of Anopheles gambiae from Brazil: lessons for malaria control in Africa? Lancet Infect Dis. 2002;2:618–27.
Cohuet A, Harris C, Robert V, Fontenille D. Evolutionary forces on Anopheles: what makes a malaria vector? Trends Parasitol. 2010;26:130–6.
Moller-Jacobs LL, Murdock CC, Thomas MB. Capacity of mosquitoes to transmit malaria depends on larval environment. Parasit Vectors. 2014;7:593.
Takken W, Knols BGJ. Odor-mediated behavior of Afrotropical malaria mosquitoes. Annu Rev Entomol. 1999;44:131–57.
Okech BA, Gouagna LC, Yan G, Githure JI, Beier JC. Larval habitats of Anopheles gambiae s.s. (Diptera: Culicidae) influences vector competence to Plasmodium falciparum parasites. Malar J. 2007;6:50.
Vantaux A, Lefèvre T, Cohuet A, Dabiré KR, Roche B, Roux O. Larval nutritional stress affects vector life history traits and human malaria transmission. Sci Rep. 2016;6:36778.
Mwangangi JM, Mbogo CM, Muturi EJ, Nzovu JG, Kabiru EW, Githure JI, et al. Influence of biological and physicochemical characteristics of larval habitats on the body size of Anopheles gambiae mosquitoes (Diptera: Culicidae) along the Kenyan coast. J Vector Borne Dis. 2007;44:122–7.
Tumlinson JH. The importance of volatile organic compounds in ecosystem functioning. J Chem Ecol. 2014;40:212.
Logan JG, Birkett MA. Semiochemicals for biting fly control: their identification and exploitation. Pest Manag Sci. 2007;63:647–57.
Syed Z. Chemical ecology and olfaction in arthropod vectors of diseases. Curr Opin Insect Sci. 2015;10:83–9.
Masiga D, Obiero G, Macharia R, Mireji P, Christoffels A. Chemosensory receptors in tsetse flies provide link between chemical and behavioural ecology. Trends Parasitol. 2014;30:426–8.
Nyasembe VO, Torto B. Volatile phytochemicals as mosquito semiochemicals. Phytochem Lett. 2014;8:196–201.
Bohbot JD, Lu T, Zwiebel LJ. Molecular regulation of olfaction in mosquitoes. In: Takken W, Knols BGJ, editors. Olfaction in vector-host interactions. Wageningen: Wageningen Academic Publishers; 2010. p. 17–38.
Hansson BS, Stensmyr MC. Evolution of insect olfaction. Neuron. 2011;72:698–711.
Biessmann H, Andronopoulou E, Biessmann MR, Douris V, Dimitratos SD, Eliopoulos E, et al. The Anopheles gambiae odorant binding protein 1 (AgamOBP1) mediates indole recognition in the antennae of female mosquitoes. PLoS One. 2010;5(3), e9471.
Leal WS. Odorant reception in insects: roles of receptors, binding proteins, and degrading enzymes. Annu Rev Entomol. 2013;58:373–91.
Leal WS. Proteins that make sense. In: Blomquist GJ, Vogt RG, editors. Insect pheromone biochemistry and molecular biology. USA: Elsevier Academic Press; 2003. p. 447–67.
Wang G, Carey AF, Carlson JR, Zwiebel LJ. Molecular basis of odor coding in the malaria vector mosquito Anopheles gambiae. Proc Natl Acad Sci USA. 2010;107(9):4418–23.
Holt RA, Subramanian GM, Halpern A, Sutton GG, Charlab R, Nusskern DR, et al. The genome sequence of the malaria mosquito Anopheles gambiae. Science. 2002;298:129–49.
Carey AF, Carlson JR. Insect olfaction from model systems to disease control. Proc Natl Acad Sci USA. 2011;108:12987–95.
Hill CA, Fox AN, Pitts RJ, Kent LB, Tan PL, Chrystal MA, et al. G Protein-coupled receptors in Anopheles gambiae. Science. 2002;298(5591):176–8.
Dobritsa AA, van Naters W, van der G, Warr CG, Steinbrecht RA, Carlson JR. Integrating the molecular and cellular basis of odor coding in the Drosophila antenna. Neuron. 2003;37:827–41.
Carey AF, Wang G, Su C-Y, Zwiebel LJ, Carlson JR. Odorant reception in the malaria mosquito Anopheles gambiae. Nature. 2010;464:66–71.
McMeniman CJ, Corfas RA, Matthews BJ, Ritchie SA, Vosshall LB. Multimodal integration of carbon dioxide and other sensory cues drives mosquito attraction to humans. Cell. 2014;156:1060–71.
Verhulst NO, Andriessen R, Groenhagen U, Kiss GB, Schulz S, Takken W, et al. Differential attraction of malaria mosquitoes to volatile blends produced by human skin bacteria. PLoS One. 2010;5, e15829.
Mukabana WR, Takken W, Coe R, Knols BGJ. Host-specific cues cause differential attractiveness of Kenyan men to the African malaria vector Anopheles gambiae. Malar J. 2002;1:17.
Meijerink J, Braks MAH, Brack AA, Adam W, Dekker T, Posthumus MA, et al. Identification of olfactory stimulants for Anopheles gambiae from human sweat samples. J Chem Ecol. 2000;26:1367–82.
Qiu YT, Van Loon JJA, Takken W, Meijerink J, Smid HM. Olfactory coding in antennal neurons of the malaria mosquito, Anopheles gambiae. Chem Senses. 2006;31:845–63.
Dekker T, Geier M, Cardé RT. Carbon dioxide instantly sensitizes female yellow fever mosquitoes to human skin odours. J Exp Biol. 2005;208:2963–72.
Omolo MO, Okinyo D, Ndiege IO, Lwande W, Hassanali A. Repellency of essential oils of some Kenyan plants against Anopheles gambiae. Phytochemistry. 2004;65:2797–802.
Day JF. Mosquito oviposition behavior and vector control. Insects. 2016;7(4):65.
Fernandes L, Briegel H. Reproductive physiology of Anopheles gambiae and Anopheles atroparvus. J Vector Ecol. 2005;30(1):11–26.
Navarro-Silva MA, Marques FA, Duque L, Jonny E. Review of semiochemicals that mediate the oviposition of mosquitoes: a possible sustainable tool for the control and monitoring of Culicidae. Rev Bras Entomol. 2009;53:1–6.
Bentley MD, Day JF. Chemical ecology and behavioral aspects of mosquito oviposition. Annu Rev Entomol. 1989;34:401–21.
Afify A, Galizia CG. Chemosensory cues for mosquito oviposition site selection. J Med Entomol. 2015;52:120–30.
Herrera-Varela M, Lindh J, Lindsay SW, Fillinger U. Habitat discrimination by gravid Anopheles gambiae sensu lato - a push-pull system. Malar J. 2014;13:1.
Rejmánková E, Higashi R, Grieco J, Achee N, Roberts D. Volatile substances from larval habitats mediate species-specific oviposition in Anopheles mosquitoes. J Med Entomol. 2005;42:95–103.
Sumba LA, Guda TO, Deng AL, Hassanali A, Beier JC, Knols BGJ. Mediation of oviposition site selection in the African malaria mosquito Anopheles gambiae (Diptera: Culicidae) by semiochemicals of microbial origin. Int J Trop Insect Sci. 2004;24:260–5.
Blackwell A, Johnson SN. Electrophysiological investigation of larval water and potential oviposition chemo-attractants for Anopheles gambiae s.s. Ann Trop Med Parasitol. 2000;94:389–98.
Leroy PD, Sabri A, Verheggen FJ, Francis F, Thonart P, Haubruge E. The semiochemically mediated interactions between bacteria and insects. Chemoecology. 2011;21:113–22.
Rinker DC, Zhou X, Pitts RJ, Rokas A, Zwiebel LJ. Antennal transcriptome profiles of anopheline mosquitoes reveal human host olfactory specialization in Anopheles gambiae. BMC Genomics. 2013;14:749. http://www.who.int/malaria/publications/atoz/larviciding_position_statement/en/.
Ikeshoji T, Saito K, Yano A. Bacterial production of the ovipositional attractants for mosquitoes on fatty acid substrates. Appl Entomol Zool. 1975;10:239–42.
Schulz S, Dickschat JS. Bacterial volatiles: the smell of small organisms. Nat Prod Rep. 2007;24:814–42.
Ponnusamy L, Xu N, Böröczky K, Wesson DM, Ayyash LA, Schal C, et al. Oviposition responses of the mosquitoes Aedes aegypti and Aedes albopictus to experimental plant infusions in laboratory bioassays. J Chem Ecol. 2010;36:709–19.
Lindh JM, Kännaste A, Knols BGJ, Faye I, Borg-Karlson A-K. Oviposition responses of Anopheles gambiae s.s. (Diptera: Culicidae) and identification of volatiles from bacteria-containing solutions. J Med Entomol. 2008;45:1039–49.
Lindh JM, Okal MN, Herrera-Varela M, Borg-Karlson A-K, Torto B, Lindsay SW, et al. Discovery of an oviposition attractant for gravid malaria vectors of the Anopheles gambiae species complex. Malar J. 2015;14:119.
Wondwosen B, Birgersson G, Seyoum E, Tekie H, Torto B, Fillinger U, et al. Rice volatiles lure gravid malaria mosquitoes, Anopheles arabiensis. Sci Rep. 2016;6:37930.
Eneh LK, Okal MN, Borg-Karlson A-K, Fillinger U, Lindh JM. Gravid Anopheles gambiae sensu stricto avoid ovipositing in Bermuda grass hay infusion and its volatiles in two choice egg-count bioassays. Malar J. 2016;15:1.
Minakawa N, Sonye G, Mogi M, Yan G. Habitat characteristics of Anopheles gambiae s.s. larvae in a Kenyan highland. Med Vet Entomol. 2004;18(3):301–5.
Ndenga BA, Simbauni JA, Mbugi JP, Githeko AK. Physical, chemical and biological characteristics in habitats of high and low presence of anopheline larvae in western Kenya highlands. PLoS One. 2012;7, e47975.
Mereta ST, Yewhalaw D, Boets P, Ahmed A, Duchateau L, Speybroeck N, et al. Physico-chemical and biological characterization of anopheline mosquito larval habitats (Diptera: Culicidae): implications for malaria control. Parasit Vectors. 2013;6:320.
Mireji PO, Keating J, Hassanali A, Mbogo CM, Nyambaka H, Kahindi S, et al. Heavy metals in mosquito larval habitats in urban Kisumu and Malindi, Kenya, and their impact. Ecotoxicol Environ Saf. 2008;70:147–53.
Kweka EJ, Zhou G, Munga S, Lee M-C, Atieli HE, Nyindo M, et al. Anopheline larval habitats seasonality and species distribution: a prerequisite for effective targeted larval habitats control programmes. PLoS One. 2012;7, e52084.
Sparks JT, Bohbot JD, Dickens JC. Olfactory disruption: toward controlling important insect vectors of disease. Prog Mol Biol Transl Sci. 2015;130:81–108.
Sadasivaiah S, Tozan Y, Breman JG. Dichlorodiphenyltrichloroethane (DDT) for indoor residual spraying in Africa: how can it be used for malaria control? Am J Trop Med Hyg. 2007;77:249–63.
Walker K, Lynch M. Contributions of Anopheles larval control to malaria suppression in tropical Africa: review of achievements and potential. Med Vet Entomol. 2007;21:2–21.
Oxborough RM. Trends in US President’s Malaria Initiative-funded indoor residual spray coverage and insecticide choice in sub-Saharan Africa (2008–2015): urgent need for affordable, long-lasting insecticides. Malar J. 2016;15:1.
Khater HF. Ecosmart biorational insecticides: alternative insect control strategies. In: Perveen F, editor. Insectic Adv Integr Pest Manag. Rijeka: InTech; 2012.
Shaalan EAS, Canyon D, Younes MWF, Abdel-Wahab H, Mansour AH. A review of botanical phytochemicals with mosquitocidal potential. Environ Int. 2005;31:1149–66.
Hardin JA, Jackson FLC. Applications of natural products in the control of mosquito-transmitted diseases. African J Biotechnol. 2009;8(25):7373–8.
Maia MF, Moore SJ. Plant-based insect repellents: a review of their efficacy, development and testing. Malar J. 2011;10:S11.
Ghosh A, Chowdhury N, Chandra G. Plant extracts as potential mosquito larvicides. Indian J Med Res. 2012;135:581–98.
Innocent E, Hassanali A, Kisinza WNW, Mutalemwa PPP, Magesa S, Kayombo E. Anti-mosquito plants as an alternative or incremental method for malaria vector control among rural communities of Bagamoyo District, Tanzania. J Ethnobiol Ethnomed. 2014;10:1.
Isman MB. Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annu Rev Entomol. 2006;51:45–66.
Regnault-Roger C, Vincent C, Arnasson T. Essential oils in insect control: low-risk products in a high-stakes world. Annu Rev Entomol. 2012;57:405–24.
Affonso R d S, Guimarães AP, Oliveira AA, Slana GBC, França TCC. Applications of molecular modeling in the design of new insect repellents targeting the odorant binding protein of Anopheles gambiae. J Brazilian Chem Soc. 2013;24(3):473–82.
Gaddaguti V, Mounika SJ, Sowjanya K, Rao T, Chakravarthy MSRK, Allu R. GC-MS analysis and in silico molecular docking studies of mosquito repellent compounds from Hyptis suaveolens. Int J Bioassays. 2012;1:36–41.
Kliebenstein DJ. Secondary metabolites and plant/environment interactions: a view through Arabidopsis thaliana tinged glasses. Plant Cell Environ. 2004;27:675–84.
Tsao R, Romanchuk FE, Peterson CJ, Coats JR. Plant growth regulatory effect and insecticidal activity of the extracts of the Tree of Heaven (Ailanthus altissima L.). BMC Ecol. 2002;2:1.
George D, Finn R, Graham K, Sparagano O. Present and future potential of plant-derived products to control arthropods of veterinary and medical significance. Parasit Vectors. 2014;7:28.
Pyke B, Rice M, Sabine B, Zalucki MP. The push-pull strategy-behavioural control of Heliothis. Aust Cott Grow. 1987;9:7–9.
Foster SP, Harris MO. Behavioral manipulation methods for insect pest-management. Annu Rev Entomol. 1997;42:123–46.
Menger DJ, Otieno B, de Rijk M, Mukabana WR, van Loon JJA, Takken WA. A push-pull system to reduce house entry of malaria mosquitoes. Malar J. 2014;13:1.
Brightwell R, Dransfield RD, Kyorku C. Development of a low‐cost tsetse trap and odour baits for Glossina pallidipes and G. longipennis in Kenya. Med Vet Entomol. 1991;5:153–64.
Khan Z, Midega C, Pittchar J, Pickett J, Bruce T. Push-pull technology: a conservation agriculture approach for integrated management of insect pests, weeds and soil health in Africa: UK Government’s Foresight Food and Farming Futures project. Int J Agric Sustain. 2011;9:162–70.
Khan Z, Midega CAO, Hooper A, Pickett J. Push-pull: chemical ecology-based integrated pest management technology. J Chem Ecol. 2016;42:689–97.
Hassanali A, Herren H, Khan ZR, Pickett JA, Woodcock CM. Integrated pest management: the push-pull approach for controlling insect pests and weeds of cereals, and its potential for other agricultural systems including animal husbandry. Philos Trans R Soc Lond B Biol Sci. 2008;363:611–21.
Menger DJ, Omusula P, Holdinga M, Homan T, Carreira AS, Vandendaele P, et al. Field evaluation of a push-pull system to reduce malaria transmission. PLoS One. 2015;10:e0123415.
Maia MF, Onyango SP, Thele M, Simfukwe ET, Turner EL, Moore SJ. Do topical repellents divert mosquitoes within a community? Health equity implications of topical repellents as a mosquito bite prevention tool. PLoS One. 2013;8. e84875.
Birkett MA, Hassanali A, Hoglund S, Pettersson J, Pickett JA. Repellent activity of catmint, Nepeta cataria, and iridoid nepetalactone isomers against Afro-tropical mosquitoes, ixodid ticks and red poultry mites. Phytochemistry. 2011;72:109–14.
Nyasembe VO, Tchouassi DP, Mbogo CM, Sole CL, Pirk C, Torto B. Linalool oxide: generalist plant based lure for mosquito disease vectors. Parasit Vectors. 2015;8:581.
Wagman JM, Grieco JP, Bautista K, Polanco J, Briceño I, King R, et al. The field evaluation of a push-pull system to control malaria vectors in Northern Belize, Central America. Malar J. 2015;14:1.
Deletre E, Schatz B, Bourguet D, Chandre F, Williams L, Ratnadass A, et al. Prospects for repellent in pest control: current developments and future challenges. Chemoecology. 2016;26:127–42.
Ditzen M, Pellegrino M, Vosshall LB. Insect odorant receptors are molecular targets of the insect repellent DEET. Science. 2008;319:1838–42.
Bohbot JD, Dickens JC. Selectivity of odorant receptors in insects. Front Cell Neurosci. 2012;6:29.
Pask GM, Bobkov YV, Corey EA, Ache BW, Zwiebel LJ. Blockade of insect odorant receptor currents by amiloride derivatives. Chem Senses. 2013;38(3):221–9.
Killeen GF, Chitnis N, Moore SJ, Okumu FO. Target product profile choices for intra-domiciliary malaria vector control pesticide products: repel or kill. Malar J. 2011;10:207.
Karunamoorthi K, Girmay A, Hayleeyesus SF. Mosquito repellent activity of essential oil of Ethiopian ethnomedicinal plant against Afro-tropical malarial vector Anopheles arabiensis. J King Saud Univ Sci. 2014;26:305–10.
Moore SJ, Debboun M. History of insect repellents. In: Debboun M, Frances SP, Strickman D, editors. Insect repellents, principles, methods and uses. Boca Raton: CRC Press; 2007. p. 3–29.
Debboun M, Strickman D. Insect repellents and associated personal protection for a reduction in human disease. Med Vet Entomol. 2013;27:1–9.
Dogan EB, Ayres JW, Rossignol PA. Behavioural mode of action of deet: inhibition of lactic acid attraction. Med Vet Entomol. 1999;13:97–100.
Syed Z, Leal WS. Mosquitoes smell and avoid the insect repellent DEET. Proc Natl Acad Sci USA. 2008;105:13598–603.
Bohbot JD, Dickens JC. Insect repellents: modulators of mosquito odorant receptor activity. PLoS One. 2010;5, e12138.
DeGennaro M, McBride CS, Seeholzer L, Nakagawa T, Dennis EJ, Goldman C, et al. Orco mutant mosquitoes lose strong preference for humans and are not repelled by volatile DEET. Nature. 2013;498(7455):487–91.
Briassoulis G, Narlioglou M, Hatzis T. Toxic encephalopathy associated with use of DEET insect repellents: a case analysis of its toxicity in children. Hum Exp Toxicol. 2001;20:8–14.
Stanczyk NM, Brookfield JFY, Ignell R, Logan JG, Field LM. Behavioral insensitivity to DEET in Aedes aegypti is a genetically determined trait residing in changes in sensillum function. Proc Natl Acad Sci USA. 2010;107:8575–80.
Pellegrino M, Steinbach N, Stensmyr MC, Hansson BS, Vosshall LB. A natural polymorphism alters odour and DEET sensitivity in an insect odorant receptor. Nature. 2011;478:511–4.
Stanczyk NM, Brookfield JFY, Field LM, Logan JG. Aedes aegypti mosquitoes exhibit decreased repellency by DEET following previous exposure. PLoS One. 2013;8, e54438.
Paluch G, Bartholomay L, Coats J. Mosquito repellents: a review of chemical structure diversity and olfaction. Pest Manag Sci. 2010;66:925–35.
Odalo JO, Omolo MO, Malebo H, Angira J, Njeru PM, Ndiege IO, et al. Repellency of essential oils of some plants from the Kenyan coast against Anopheles gambiae. Acta Trop. 2005;95:210–8.
Lengeler C. Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database Syst Rev. 2004;2:CD000363.
Pålsson K, Jaenson TGT. Plant products used as mosquito repellents in Guinea Bissau, West Africa. Acta Trop. 1999;72:39–52.
Kweka EJ, Mosha F, Lowassa A, Mahande AM, Kitau J, Matowo J, et al. Ethnobotanical study of some of mosquito repellent plants in north-eastern Tanzania. Malar J. 2008;7:1.
Mavundza EJ, Maharaj R, Finnie JF, Kabera G, Van Staden J. An ethnobotanical survey of mosquito repellent plants in uMkhanyakude district, KwaZulu-Natal province, South Africa. J Ethnopharmacol. 2011;137:1516–20.
Karunamoorthi K. Plant-based insect repellents: is that a sustainable option to curb the malaria burden in Africa? Med Aromat Plants. 2012;2012(1):e106.
Pavela R, Benelli G. Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends Plant Sci. 2016;21:1000–7.
Seyoum A, Pålsson K, Kung’a S, Kabiru EW, Lwande W, Killeen GF, et al. Traditional use of mosquito-repellent plants in western Kenya and their evaluation in semi-field experimental huts against Anopheles gambiae: ethnobotanical studies and application by thermal expulsion and direct burning. Trans R Soc Trop Med Hyg. 2002;96:225–31.
Davis EE, Bowen MF. Sensory physiological basis for attraction in mosquitoes. J Am Mosq Control Assoc. 1994;10:316–25.
Wang Z, Song J, Chen J, Song Z, Shang S, Jiang Z, et al. QSAR study of mosquito repellents from terpenoid with a six-member-ring. Bioorg Med Chem Lett. 2008;18:2854–9.
CDC. Updated information regarding mosquito repellents. 2008. Available from: http://www.cdc.gov/ncidod/dvbid/westnile/repellentupdates.htm (Accessed 9 Aug 2016).
Novak RJ, Gerberg EJ. Natural-based repellent products: efficacy for military and general public uses. J Am Mosq Control Assoc. 2005;21:7–11.
Carroll SP, Loye J. PMD, a registered botanical mosquito repellent with DEET-like efficacy. J Am Mosq Control Assoc. 2006;22:507–14.
Nerio LS, Olivero-Verbel J, Stashenko E. Repellent activity of essential oils: a review. Bioresour Technol. 2010;101(1):372–8.
Govere J, Durrheim DN, Baker L, Hunt R, Coetzee M. Efficacy of three insect repellents against the malaria vector Anopheles arabiensis. Med Vet Entomol. 2000;14:441–4.
Deletre E, Martin T, Campagne P, Bourguet D, Cadin A, Menut C, et al. Repellent, irritant and toxic effects of 20 plant extracts on adults of the malaria vector Anopheles gambiae mosquito. PLoS One. 2013;8, e82103.
Deletre E, Chandre F, Williams L, Duménil C, Menut C, Martin T. Electrophysiological and behavioral characterization of bioactive compounds of the Thymus vulgaris, Cymbopogon winterianus, Cuminum cyminum and Cinnamomum zeylanicum essential oils against Anopheles gambiae and prospects for their use as bednet treatments. Parasit Vectors. 2015;8:316.
Wanzala W, Ogoma SB. Chemical composition and mosquito repellency of essential oil of Tagetes minuta from the southern slopes of mount Elgon in western Kenya. J Essent Oil Bear Plants. 2013;16:216–32.
Mng’ong’o FC, Sambali JJ, Sabas E, Rubanga J, Magoma J, Ntamatungiro AJ, et al. Repellent plants provide affordable natural screening to prevent mosquito house entry in tropical rural settings - results from a pilot efficacy study. PLoS One. 2011;6:e25927.
Seyoum A, Killeen GF, Kabiru EW, Knols BGJ, Hassanali A. Field efficacy of thermally expelled or live potted repellent plants against African malaria vectors in western Kenya. Trop Med Int Heal. 2003;8:1005–11.
Bloomquist JR. Chloride channels as tools for developing selective insecticides. Arch Insect Biochem Physiol. 2003;54:145–56.
Enan EE. Molecular and pharmacological analysis of an octopamine receptor from American cockroach and fruit fly in response to plant essential oils. Arch Insect Biochem Physiol. 2005;59:161–71.
Rattan RS. Mechanism of action of insecticidal secondary metabolites of plant origin. Crop Prot. 2010;29:913–20.
Kwon Y, Kim SH, Ronderos DS, Lee Y, Akitake B, Woodward OM, et al. Drosophila TRPA1 channel is required to avoid the naturally occurring insect repellent citronellal. Curr Biol. 2010;20:1672–8.
Jaramillo Ramirez GI, Logan JG, Loza-Reyes E, Stashenko E, Moores GD. Repellents inhibit P450 enzymes in Stegomyia (Aedes) aegypti. PLoS One. 2012;7, e48698.
Gerberg EJ, Novak RJ. Considerations on the use of botanically-derived repellent products. In: Debboun M, Frances S, Strickman D, editors. Insect repellents, principles, methods and uses. Boca Raton: CRC Press; 2007. p. 305–10.
Kweka EJ, Lyatuu EE, Mboya MA, Mwang’onde BJ, Mahande AM. Oviposition deterrence induced by Ocimum kilimandscharicum and Ocimum suave extracts to gravid Anopheles gambiae ss (Diptera: Culicidae) in laboratory. J Glob Infect Dis. 2010;2:242.
Da Silva RCS, Milet-Pinheiro P, da Silva PCB, da Silva AG, da Silva MV, Navarro DM, et al. (E)-Caryophyllene and α-Humulene: Aedes aegypti oviposition deterrents elucidated by gas chromatography-electrophysiological assay of Commiphora leptophloeos leaf oil. PLoS One. 2015;10:e0144586.
Manda H, Gouagna LC, Foster WA, Jackson RR, Beier JC, Githure JI, et al. Effect of discriminative plant-sugar feeding on the survival and fecundity of Anopheles gambiae. Malar J. 2007;6:113.
Briegel H. Physiological bases of mosquito ecology. J Vector Ecol. 2003;28:1–11.
Hien DF, Dabiré KR, Roche B, Diabaté A, Yerbanga RS, Cohuet A, et al. Plant-mediated effects on mosquito capacity to transmit human malaria. PLoS Pathog. 2016;12:e1005773.
Gu W, Müller G, Schlein Y, Novak RJ, Beier JC. Natural plant sugar sources of Anopheles mosquitoes strongly impact malaria transmission potential. PLoS One. 2011;6, e15996.
Nyasembe VO, Cheseto X, Kaplan F, Foster WA, Teal PEA, Tumlinson JH, et al. The invasive American weed Parthenium hysterophorus can negatively impact malaria control in Africa. PLoS One. 2015;10, e0137836.
Nyasembe VO, Teal PEA, Sawa P, Tumlinson JH, Borgemeister C, Torto B. Plasmodium falciparum infection increases Anopheles gambiae attraction to nectar sources and sugar uptake. Curr Biol. 2014;24:217–21.
Nyasembe VO, Teal PEA, Mukabana WR, Tumlinson JH, Torto B. Behavioural response of the malaria vector Anopheles gambiae to host plant volatiles and synthetic blends. Parasit Vectors. 2012;5:234.
Nyasembe VO, Tchouassi DP, Kirwa HK, Foster WA, Teal PEA, Borgemeister C, et al. Development and assessment of plant-based synthetic odor baits for surveillance and control of malaria vectors. PLoS One. 2014;9:e89818.
Müller GC, Schlein Y. Efficacy of toxic sugar baits against adult cistern-dwelling Anopheles claviger. Trans R Soc Trop Med Hyg. 2008;102:480–4.
Müller GC, Beier JC, Traore SF, Toure MB, Traore MM, Bah S, et al. Successful field trial of attractive toxic sugar bait (ATSB) plant-spraying methods against malaria vectors in the Anopheles gambiae complex in Mali, West Africa. Malar J. 2010;9:1.
Qualls WA, Müller GC, Traore SF, Traore MM, Arheart KL, Doumbia S, et al. Indoor use of attractive toxic sugar bait (ATSB) to effectively control malaria vectors in Mali, West Africa. Malar J. 2015;14:1–8.
Beier JC, Müller GC, Gu W, Arheart KL, Schlein Y. Attractive toxic sugar bait (ATSB) methods decimate populations of Anopheles malaria vectors in arid environments regardless of the local availability of favoured sugar-source blossoms. Malar J. 2012;11:1.
Fillinger U, Lindsay SW. Suppression of exposure to malaria vectors by an order of magnitude using microbial larvicides in rural Kenya. Trop Med Int Heal. 2006;11:1629–42.
WHO. The role of larviciding for malaria-control in sub-Saharan Africa. Glob Malar Progr. 2012;1–21.
Killeen GF, Fillinger U, Knols BGJ. Advantages of larval control for African malaria vectors: Low mobility and behavioural responsiveness of immature mosquito stages allow high effective coverage. Malar J. 2002;1:1–7.
Msellemu D, Namango HI, Mwakalinga VM, Ntamatungiro AJ, Mlacha Y, Mtema ZJ, et al. The epidemiology of residual Plasmodium falciparum malaria transmission and infection burden in an African city with high coverage of multiple vector control measures. Malar J. 2016;15:1.
Tusting LS, Thwing J, Sinclair D, Fillinger U, Gimnig J, Bonner KE, et al. Mosquito larval source management for controlling malaria. Cochrane Database Syst Rev. 2013;8:CD008923.
Majambere S, Lindsay SW, Green C, Kandeh B, Fillinger U. Microbial larvicides for malaria control in The Gambia. Malar J. 2007;6:1–14.
Geissbühler Y, Kannady K, Chaki PP, Emidi B, Govella NJ, Mayagaya V, et al. Microbial larvicide application by a large-scale, community-based program reduces malaria infection prevalence in urban Dar es Salaam, Tanzania. PLoS One. 2009;4:e5107.
Imbahale SS, Mweresa CK, Takken W, Mukabana WR. Development of environmental tools for anopheline larval control. Parasit Vectors. 2011;4:130.
Tchicaya ES, Koudou BG, Keiser J, Adja AM, Cissé G, Tanner M, et al. Effect of repeated application of microbial larvicides on malaria transmission in central Côte d’Ivoire. J Am Mosq Control Assoc. 2009;25:382–5.
Dambach P, Traore I, Becker N, Kaiser A, Sie A, Sauerborn R. EMIRA: Ecologic malaria reduction for Africa - innovative tools for integrated malaria control. Glob Health Action. 2014;7:25908.
Diabat S, Druetz T, Millogo T, Ly A, Fregonese F, Kouanda S, et al. Domestic larval control practices and malaria prevalence among under-five children in Burkina Faso. PLoS One. 2015;10:e0141784.
Afrane YA, Mweresa NG, Wanjala CL, Gilbreath III TM, Zhou G, Lee M-C, et al. Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya. Malar J. 2016;15:577.
Zhou G, Wiseman V, Atieli HE, Lee M-C, Githeko AK, Yan G. The impact of long-lasting microbial larvicides in reducing malaria transmission and clinical malaria incidence: study protocol for a cluster randomized controlled trial. Trials. 2016;17:423.
Tetreau G, Bayyareddy K, Jones CM, Stalinski R, Riaz MA, Paris M, et al. Larval midgut modifications associated with Bti resistance in the yellow fever mosquito using proteomic and transcriptomic approaches. BMC Genomics. 2012;13:1.
Wachira SW, Omar S, Jacob JW, Wahome M, Alborn HT, Spring DR, et al. Toxicity of six plant extracts and two pyridone alkaloids from Ricinus communis against the malaria vector Anopheles gambiae. Parasit Vectors. 2014;7:1–8.
Maniafu BM, Wilber L, Ndiege IO, Wanjala CC, Akenga TA. Larvicidal activity of extracts from three Plumbago spp against Anopheles gambiae. Mem Inst Oswaldo Cruz. 2009;104:813–7.
Pradeepa V, Sathish-Narayanan S, Kirubakaran SA, Senthil-Nathan S. Antimalarial efficacy of dynamic compound of plumbagin chemical constituent from Plumbago zeylanica Linn (Plumbaginaceae) against the malarial vector Anopheles stephensi Liston (Diptera: Culicidae). Parasitol Res. 2014;113:3105–9.
Dinan L, Savchenko T, Whiting P. On the distribution of phytoecdysteroids in plants. Cell Mol Life Sci. 2001;58:1121–32.
Nathan SS, Kalaivani K, Murugan K. Effects of neem limonoids on the malaria vector Anopheles stephensi Liston (Diptera: Culicidae). Acta Trop. 2005;96:47–55.
Nathan SS, Savitha G, George DK, Narmadha A, Suganya L, Chung PG. Efficacy of Melia azedarach L. extract on the malarial vector Anopheles stephensi Liston (Diptera: Culicidae). Bioresour Technol. 2006;97:1316–23.
Owino J, Hassanali A, Ndung’u M. Bio-assay guided fractionation of anti-mosquito limonoids from Turraea abyssinica and Turraea cornucopia. J Biofertilizers Biopestic. 2014;5:1.
Mwangi RW, Mukiama TK. Evaluation of Melia volkensii extract fractions as mosquito larvicides. J Am Mosq Control Assoc. 1988;4:442–7.
Nathan SS, Hisham A, Jayakumar G. Larvicidal and growth inhibition of the malaria vector Anopheles stephensi by triterpenes from Dysoxylum malabaricum and Dysoxylum beddomei. Fitoterapia. 2008;79:106–11.
Nyamoita MG. Toxicity of individual and blends of pure phytoecdysteroids isolated from Vitex schiliebenii and Vitex payos against Anopheles gambiae s.s. larvae. World J Org Chem. 2013;1:1–5.
Muema JM, Bargul JL, Nyanjom SG, Mutunga JM, Njeru SN. Potential of Camellia sinensis proanthocyanidins-rich fraction for controlling malaria mosquito populations through disruption of larval development. Parasit Vectors. 2016;9:512.
Muema JM, Njeru SN, Colombier C, Marubu RM. Methanolic extract of Agerantum conyzoides exhibited toxicity and growth disruption activities against Anopheles gambiae sensu stricto and Anopheles arabiensis larvae. BMC Complement Altern Med. 2016;16:475.
Dinan L, Hormann RE. Ecdysteroid agonists and antagonists. In: Gilbert LI, Iatrou K, Gill SS, editors. Comprehensive molecular insect science. Amsterdam: Elsevier; 2005. p. 197–242.
AJ M (L), Morgan ED, Nisbet AJ. Azadirachtin, a natural product in insect control. In: Gilbert LI, Iatrou K, Gill SS, editors. Comprehensive molecular insect science. Amsterdam: Elsevier; 2005. p. 35.
Salehzadeh A, Akhkha A, Cushley W, Adams RLP, Kusel JR, Strang RHC. The antimitotic effect of the neem terpenoid azadirachtin on cultured insect cells. Insect Biochem Mol Biol. 2003;33:681–9.
Priyadarsini RV, Murugan RS, Sripriya P, Karunagaran D, Nagini S. The neem limonoids azadirachtin and nimbolide induce cell cycle arrest and mitochondria-mediated apoptosis in human cervical cancer (HeLa) cells. Free Radic Res. 2010;44:624–34.
Nyamoita MG, Ester I, Zakaria MH, Wilber L, Bwire OJ, Ahmed H. Comparison of the effects of extracts from three Vitex plant species on Anopheles gambiae s.s. (Diptera: Culicidae) larvae. Acta Trop. 2013;127:199–203.
Ndung’u M, Torto B, Knols BGJ, Hassanali A. Laboratory evaluation of some eastern African Meliaceae as sources of larvicidal botanicals for Anopheles gambiae. Int J Trop Insect Sci. 2004;24:311–8.
Sharma P, Mohan L, Srivastava CN. Phytoextract-induced developmental deformities in malaria vector. Bioresour Technol. 2006;97:1599–604.
Okumu FO, Knols BGJ, Fillinger U. Larvicidal effects of a neem (Azadirachta indica) oil formulation on the malaria vector Anopheles gambiae. Malar J. 2007;6:63.
Mdoe FP, Cheng S-S, Lyaruu L, Nkwengulila G, Chang S-T, Kweka EJ. Larvicidal efficacy of Cryptomeria japonica leaf essential oils against Anopheles gambiae. Parasit Vectors. 2014;7:426.
Kweka EJ, Nyindo M, Mosha F, Silva AG. Insecticidal activity of the essential oil from fruits and seeds of Schinus terebinthifolia Raddi against African malaria vectors. Parasit Vectors. 2011;4:129.
Kweka EJ, Senthilkumar A, Venkatesalu V. Toxicity of essential oil from Indian borage on the larvae of the African malaria vector mosquito, Anopheles gambiae. Parasit Vectors. 2012;5:277.
Babatunde S, Adedayo R, Ajiboye E, Ojo S, Ajuwon I. Phytochemical composition and larvicidal activity of Ocimum canum (L.) essential oil against Anopheles gambiae (Diptera: Culicidae). European J Med Plants. 2016;11:1–7.
Pierre DYS, Nchiwan NE, Okechukwu EC, Lame Y. Larvicidal and pupicidal toxicities of Plectranthus glandulosus and Callistemon rigidus leaf essential oils against three mosquito species. J Mosq Res. 2014;4(2):5–14.
Mdoe FP, Cheng S-S, Msangi S, Nkwengulila G, Chang S-T, Kweka EJ. Activity of Cinnamomum osmophloeum leaf essential oil against Anopheles gambiae s.s. Parasit Vectors. 2014;7:209.
Tiwary M, Naik SN, Tewary DK, Mittal PK, Yadav S. Chemical composition and larvicidal activities of the essential oil of Zanthoxylum armatum DC (Rutaceae) against three mosquito vectors. J Vector Borne Dis. 2007;44:198.
Pandey SK, Upadhyay S, Tripathi AK. Insecticidal and repellent activities of thymol from the essential oil of Trachyspermum ammi (Linn) Sprague seeds against Anopheles stephensi. Parasitol Res. 2009;105:507–12.
Hill N, Lenglet A, Arnez AM, Carneiro I. Plant based insect repellent and insecticide treated bed nets to protect against malaria in areas of early evening biting vectors: double blind randomised placebo controlled clinical trial in the Bolivian Amazon. Br Med J. 2007;335:1023.
Deressa W, Yihdego YY, Kebede Z, Batisso E, Tekalegne A, Dagne GA. Effect of combining mosquito repellent and insecticide treated net on malaria prevalence in Southern Ethiopia: a cluster-randomised trial. Parasit Vectors. 2014;7:132.
Kweka EJ, Munga S, Mahande AM, Msangi S, Mazigo HD, Adrias AQ, et al. Protective efficacy of menthol propylene glycol carbonate compared to N, N-diethyl-methylbenzamide against mosquito bites in Northern Tanzania. Parasit Vectors. 2012;5:189.
Stewart ZP, Oxborough RM, Tungu PK, Kirby MJ, Rowland MW, Irish SR. Indoor application of attractive toxic sugar bait (ATSB) in combination with mosquito nets for control of pyrethroid-resistant mosquitoes. PLoS One. 2013;8:e84168.
Isman MB, Akhtar Y. Plant natural products as a source for developing environmentally acceptable insecticides. In: Ishaaya I, Nauen R, Horowitz AR, editors. Insecticides design using advanced technologies. Berlin: Springer; 2007. p. 235–48.
Maji TK, Baruah I, Dube S, Hussain MR. Microencapsulation of Zanthoxylum limonella oil (ZLO) in glutaraldehyde crosslinked gelatin for mosquito repellent application. Bioresour Technol. 2007;98:840–4.
Sakulku U, Nuchuchua O, Uawongyart N, Puttipipatkhachorn S, Soottitantawat A, Ruktanonchai U. Characterization and mosquito repellent activity of citronella oil nanoemulsion. Int J Pharm. 2009;372:105–11.
Saha S, Walia S, Parmar BS. Exploring the diversity of neem bioactives as eco-benign pesticides: a reappraisal. Toxicol Environ Chem. 2011;93:1508–46.
Jerobin J, Sureshkumar RS, Anjali CH, Mukherjee A, Chandrasekaran N. Biodegradable polymer based encapsulation of neem oil nanoemulsion for controlled release of Aza-A. Carbohydr Polym. 2012;90:1750–6.
Nisbet AJ. Azadirachtin from the neem tree Azadirachta indica: its action against insects. An da Soc Entomológica do Bras. 2000;29:615–32.
Abudulai M, Shepard BM, Mitchell PL. Effects of neem (Azadirachta indica A. Juss) on predators of Nezara viridula (L.)(Hemiptera: Heteroptera: Pentatomidae). J Agr Urban Entomol. 2004;21:9–13.
Melorose J, Perroy R, Careas S. World population prospects. United Nations. 2015;1:587–92.
Kamdem C, Fossog BT, Simard F, Etouna J, Ndo C, Kengne P, et al. Anthropogenic habitat disturbance and ecological divergence between incipient species of the malaria mosquito Anopheles gambiae. PLoS One. 2012;7, e39453.
Nkya TE, Akhouayri I, Kisinza W, David J-P. Impact of environment on mosquito response to pyrethroid insecticides: Facts, evidences and prospects. Insect Biochem Mol Biol. 2013;43:407–16.
Benelli G. Plant-mediated biosynthesis of nanoparticles as an emerging tool against mosquitoes of medical and veterinary importance: a review. Parasitol Res. 2016;115:23–34.
Benelli G. Plant-mediated synthesis of nanoparticles: a newer and safer tool against mosquito-borne diseases? Asian Pac J Trop Biomed. 2016;6:353–4.
We acknowledge the contributions of Sheila Ogoma and Luicer Ingasia towards this review.
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The datasets supporting the conclusion of this article are included within the article.
JMM, JLB reviewed the literature and formulated the review. JMM wrote the paper with assistance from JLB, SNN, JOO, and SSI. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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About this article
- Vector control
- Anopheline mosquitoes
- Plant-derived compounds
- Larval habitat manipulation
- Mosquito functional ecology
- Integrated vector management