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Invasive hematophagous arthropods and associated diseases in a changing world

Abstract

Biological invasions have increased significantly with the tremendous growth of international trade and transport. Hematophagous arthropods can be vectors of infectious and potentially lethal pathogens and parasites, thus constituting a growing threat to humans—especially when associated with biological invasions. Today, several major vector-borne diseases, currently described as emerging or re-emerging, are expanding in a world dominated by climate change, land-use change and intensive transportation of humans and goods. In this review, we retrace the historical trajectory of these invasions to better understand their ecological, physiological and genetic drivers and their impacts on ecosystems and human health. We also discuss arthropod management strategies to mitigate future risks by harnessing ecology, public health, economics and social-ethnological considerations. Trade and transport of goods and materials, including vertebrate introductions and worn tires, have historically been important introduction pathways for the most prominent invasive hematophagous arthropods, but sources and pathways are likely to diversify with future globalization. Burgeoning urbanization, climate change and the urban heat island effect are likely to interact to favor invasive hematophagous arthropods and the diseases they can vector. To mitigate future invasions of hematophagous arthropods and novel disease outbreaks, stronger preventative monitoring and transboundary surveillance measures are urgently required. Proactive approaches, such as the use of monitoring and increased engagement in citizen science, would reduce epidemiological and ecological risks and could save millions of lives and billions of dollars spent on arthropod control and disease management. Last, our capacities to manage invasive hematophagous arthropods in a sustainable way for worldwide ecosystems can be improved by promoting interactions among experts of the health sector, stakeholders in environmental issues and policymakers (e.g. the One Health approach) while considering wider social perceptions.

Graphical abstract

Background

Invasive hematophagous arthropods (those that establish and spread outside of their native range) can be major vectors of pathogens and parasites to animal and human populations. When they spread outside their historical range because of human activities, these blood-feeding arthropods, such as mosquitoes and ticks, can have ecological, economic and social impacts. The pathogens they bear include arthropod-borne viruses—also called arboviruses, belonging to the Flaviviridae, Togaviridae, Reoviridae and Bunyaviridae families—which are responsible for numerous widely distributed illnesses, such as dengue, yellow fever, chikungunya, Zika and West Nile viruses [1]. As such, they give rise to major ecological, economic and health problems worldwide [2,3,4] and require significant management and surveillance efforts (also see Box 1). In parallel, the world’s economic growth and intensification of international trade and travel exacerbate these threats by promoting the emergence of vector-borne diseases [5, 6]. As is the case for most invasive arthropods and plant species, ongoing climate and land-use changes, as well as other human pressures on the environment, may create new suitable niches for the proliferation of hematophagous arthropods, boost their performances, and thus facilitate their range shifts and establishment beyond their former geographical limits [7,8,9,10,11,12].

Socioeconomic factors are major drivers facilitating the transport and spread of alien species. For instance, using data collated by DAISIE (Delivering Alien Invasive Species Inventories for Europe, http://www.europe-aliens.org/), Pyšek et al. [13] showed that large industrialized countries in western Europe have harbored the highest numbers of alien populations. That is partly because these countries are historically more interconnected through colonialism and trade and therefore have accrued a larger number of alien invasive species. Moreover, a positive relationship has been observed between national gross domestic product (GDP) and the total number of alien species per country, indicating that economic growth could link to invasion rates [14]. In turn, relationships between economic measures—such as GDP, international trade or research effort—and the economic impact of biological invasions have been reported [15,16,17]. Often, invasive alien species have tremendous costs to national economies [18,19,20,21]; this is particularly true for invasive hematophagous arthropods, which are sources of extremely high healthcare costs [4]. Recent assessments estimated that the economic cost of invasive alien species reached at least US$ 2.168 trillion over the last 4 decades (see Living Figure in [22], and https://borisleroy.com/invacost/invacost_livingfigure.html), with Aedes mosquitoes being the most expensive genus among aquatic and semi-aquatic invaders, with a total cost of potentially US$ 311 billion [23]. This economic burden is expected to increase further if the worldwide proliferation and invasion by alien hematophagous arthropods that can vector disease are not halted.

Ongoing climate change may assist the invasion rates of alien species in addition to facilitating range-shifting species expanding beyond their native range (the so-called ‘neo-native’ species [24]; see Box 2 for additional information). It is important to bear in mind that changing climate and increasing travel and trade are interactive forces driving establishment success during introduction and making the invasiveness of alien hematophagous arthropods after introduction even more likely. Hence, the outcomes of complex interactions between climate change and biological invasions require far more consideration [25, 26]. The positive role of climate warming in the establishment rate of alien populations of insects in the period 1900–2005 was demonstrated by Huang et al. [27]. Using species distribution models, Bellard et al. [7] found that, on average, insects belonging to the IUCN’s list “100 of the world’s worst invasive alien species” would increase their suitable range by 18% in 2050. Similarly, invasive alien hematophagous arthropods will likely do so in the future [28, 29].

Owing to the long-standing invasion history of hematophagous arthropods, affecting human populations since the Paleolithic Era [30], their ecological consequences have been well documented [31, 32], and the magnitude of their impact can highly vary according to the species considered. Numerous studies have reported the negative outcomes incurred by these arthropods, including their major impacts on the survival of resident species [33,34,35], on local human communities [31], as well as on ecosystem functioning and services [36, 37]. Surprisingly, and despite the known health threat of invasive hematophagous arthropods, and their high diversity, our understanding of how global change will impact the population dynamics of existing and emerging invaders—and the epidemiology of the diseases they might transmit—remains poor [38, 39]. Also, there is an urgent need to compile information on the historical and social aspects of hematophagous arthropod invasions to inform policymakers and prepare robust risk mitigation strategies based on lessons learned and sound risk assessment. In this context, this review examines the different actions and roles that invasive hematophagous arthropods, vectors of disease, play in a rapidly changing world, considering a range of socioeconomic and ecological contexts and case studies. By “vector,” we refer to hematophagous arthropods which can spread pathogens and/or parasites that cause disease, belonging to insects (mosquitoes, phlebotomine sand-flies, culicoides, body lice, fleas, etc.) or ticks (hard Ixodidae ticks and soft Argasidae ticks) and mainly consuming blood from terrestrial mammals, birds, reptiles and/or amphibians. Importantly, this review focuses in scope on all invasive hematophagous arthropods, despite differences in their invasion ecology and behavior. In part, this allows us to highlight knowledge gaps in the study of these taxa as well as highlight the diversity of processes through which they are introduced, succeed and cause impact. However, given the uneven research effort that is predominantly targeted towards a few species of mosquitoes and ticks, as well as the expertise of the current authors, these taxa are most prominently exemplified in this review.

Previous reviews have examined the biology, ecology and health impacts for vertebrates as well as risks and management of important groups of invasive hematophagous arthropods and associated diseases [e.g. 38, 38, 38]. Here, our review provides a broader, overarching perspective that spans invasion dynamics, ecological and socioeconomic impacts, global change drivers and wider social and cultural dimensions in an integrative way across multiple taxa. Particularly, this review provides a novel synthesis of the historical contexts underpinning hematophagous arthropod invasions, by amalgamating, for the first time, a chronology of arrivals and pathways for these species and thereby allowing future management strategies to be informed by historical trajectories of past invasion dynamics alongside anticipated socioeconomic and environmental changes. First, we consider past and present invasions of hematophagous arthropods, assuming that ongoing globalization and climate change will drive and accelerate further proliferations in the future. In doing so, we construct a timeline of past disease vector invasions across hematophagous arthropod groups, considering individual species and socioeconomic drivers. Second, we explore the ecological, economic and health impacts of these taxa, anticipating a higher competitive ability of invasive alien species over natives, marked risks to native species through disease vectoring and substantial economic costs to activity sectors such as healthcare. Third, we discuss the combined threat of future climate change and invasions from hematophagous arthropods to human populations. Last, we explore the social-ethnological dimension of these invasions (i.e. we considered how the different cultural contexts and people living in different social contexts could drive the perception of invasive hematophagous arthropods), with the aim to highlight opportunities for collaboration among the health sector and environment researchers, alongside engagement with policymakers and citizens. Ultimately, this will contribute to placing hematophagous arthropod invasions and their management in a broader sustainability context, whereby management strategies considered by scientists, public health officials and communities are considered in tandem with, and do not compromise, environment quality, ecosystem services and conservation values.

Chrono-geography of invasions

Mosquito invasions in the Renaissance period and during European expeditions

By definition, organisms are considered to be alien when they occur in a novel region as a result of human transportation and activities [40]. For hematophagous arthropods, the majority of introductions have occurred by seas [41]. The transport and arrival of alien organisms by humans greatly increased during the fifteenth and sixteenth centuries through intensification in commercial trade, agricultural practices, decrease of forest cover and of fallows [42]. This land use change and intensification of trade and transport of goods and materials by sea, including the transport of livestock, also impacted hematophagous arthropods, as many are closely linked to humans or livestock for completing their life cycle. Changes in the geographic distributions of several disease-vectoring arthropods were recorded during that period, including the mosquitoes Aedes aegypti, Ae. albopictus, Culex pipiens and Cx. quinquefasciatus, the ticks Amblyomma breviscutatum and Rhipicephalus sanguineus, and the kissing bug Triatoma rubrofasciata (Fig. 1, Additional file 1: Appendix S1). Among these species, the invasion pathways of Ae. aegypti (see Powell et al. [43] for a comprehensive review of the invasion history of this mosquito species) and members of the Cx. pipiens complex (i.e. Cx. pipiens, Cx. quinquefasciatus) have been intensively studied and monitored.

Fig. 1
figure 1figure 1

Synthetic representation of the historical trajectory of the different waves of dispersal of hematophagous arthropods. The gray arrow at the top of the figure represents the years from 3000 BC to present time. The solid black lines within the arrow relate to important historical events linked to the dispersion of species (the dotted parts show events either ongoing or with no clear end). Hematophagous arthropod species are identified on the right side of the figure, followed by a symbol representing the taxon (see symbols legend). Each line represents a different wave of dispersal (species with several waves are shown with brackets). For each wave, the geographical details are written following the format “Native Area Alien Area.” Symbols represent the mode of introduction (mechanical and/or via animal hosts) for each wave (see symbols legend). The solid black line represents the time frame of the species’ presence in the alien area. The dotted parts at the end of the lines show either uncertainty in the establishment/extinction dates (particularly when the entire line is dotted) or introduction/extinction occurring during an extended period of time. When the species has become extinct in the alien area, a symbol at the right end of the line represents the mode of extinction (see symbols legend)

Both Ae. aegypti and the Cx. pipiens complex are associated with key historical events related to international trade and colonialism, such as the European colonization of the Americas and the slave trade. Accordingly, both of these hematophagous arthropods and their associated viruses likely arrived by ship during that period, though often the pathogen arrived after the mosquito [31] (Fig. 1). Historical outbreaks of yellow fever (vectored by Ae. aegypti, a species native to Africa) in the New World were recorded as far back as 1648 and as far north as New York City [44, 45]. Epidemics of West Nile virus from Cx. pipiens started later than yellow fever (from 1999 in North America [46]).

Long distance transport and livestock trade facilitated tick translocations

Unlike mosquitoes which feed only during the adult stage, ticks require blood meals to progress across each of their life history stages following hatching, and their full life cycle takes comparatively longer (up to 3 years), while constrained near the ground in the terrestrial realm. Consequently, the means of introduction of alien tick species differ from those of mosquitoes, which have a more complex aquatic life history stage. For ticks, introduction is often linked to specific vertebrate hosts used in agriculture. The translocation of several tick species (Amblyomma variegatum, Haemaphysalis longicornis and Rhipicephalus microplus) dates back to the eighteenth or nineteenth century. For A. variegatum, introduction to the Caribbean region was due to the human-mediated transport of their cattle hosts from west Africa [47], and introduction of other tick species was associated with the global trade of livestock [48].

Booming invasions with the early nineteenth century globalization

The next significant wave of disease vector species translocations occurred with the increase in air transport and traffic eventually connecting almost all continents by the early 1900s (Fig. 1). For example, in 1930, Anopheles arabiensis, belonging to the An. gambiae complex, was first observed in Brazil where it quickly established and expanded in the decades that followed its introduction [49, 50]. The vectorial capacity of this mosquito for Plasmodium falciparum, combined with rapid population proliferation, caused significant epidemic outbreaks resulting in the death of 14,000 people in Brazil during 1938–1939 [49]. It was nonetheless successfully eliminated from the continent through an integrated program, but one which relied overwhelmingly upon larval control [51]. The rise in air travel in the 1900s was also associated with range expansions of known and already established alien species, in addition to novel introductions [52, 53] (Fig. 1). For instance, Ae. aegypti was first recorded in Asia and Australia during the nineteenth century, despite being known as an invasive alien species in America since the fifteenth-seventeenth centuries [41]. Most of the other invasive mosquito species, Ae. albopictus [54], Cx. pipiens [55] and Cx. quinquefasciatus [56], were also and are still propagated by air transport nowadays. Similarly, Culicoides belkini was introduced in French Polynesia and further expanded its range within a few decades in the islands of the archipelago [57]. As a consequence, the expansion and re-emergence of associated vector-borne diseases has also increased [58].

The Anthropocene Era: human-made artificial habitats as significant sources of hematophagous arthropods and their associated diseases

Most alien mosquitoes are highly adapted to synanthropic contexts and are highly efficient in exploiting human-made water containers for larval breeding sites. In general, life history traits often assist the invasive potential of hematophagous arthropods. For instance, Ae. albopictus is able to produce drought- and freeze-resistant eggs. Human-made microhabitats have amplified translocation rates and establishment possibilities for mosquito species with such adaptations. The worldwide development in the trade of used tires since the 1950s, and of certain ornamental plants, such as lucky bamboo (Dracaena sanderiana) [2], have become the principal points of entry within Europe and other continents. This is particularly true for temperate species capable of producing dormant eggs in discarded automobile tires, like for Aedes spp. [59, 60]. For example, used tire exports from countries such as Japan have been responsible for the introduction of Ae. albopictus to countries such as the USA [61] and have been regarded as an important introduction pathway for this species, alongside sea transport, plant translocations and ground vehicles [62]. For ornamental plants, lucky bamboo was identified as an important introduction pathway in Belgium, and plant nurseries were subsequently targeted for control measures [63]. Other goods have been implicated in the transportation of Ae. albopictus, such as repatriated military equipment from Vietnam and stone fountains from China [64].

Prediction and prevention of future invasions

Connectivity among cities, international trade and anthropogenic environmental disturbances are likely to increase in the future, providing novel opportunities and generating ecological conditions propitious for the expansion or new introduction of hematophagous arthropods that may vector disease (Fig. 1, Additional file 1: Appendix S1), which can subsequently proliferate in their new ranges [65]. The “Belt and Road Initiative” (BRI) proposed by China is a prominent example, as this unprecedented global development project may promote further invasions by hematophagous arthropods. In particular, 14 hotspots in the world have been identified as being at considerable risk of invasions [5], and these mainly fall along the economic corridors proposed in China’s BRI project, thus placing 68 countries at high risk of invasion [5]. While Liu et al. [5] focused on the potential risk of invasion by terrestrial vertebrates—and did not consider invertebrates such as hematophagous arthropods—we suggest that hematophagous arthropods will also increase their range in response to such an increase in connectivity. This assumption is supported by the example of Ae. albopictus, whose dispersal is amplified by road traffic [66, 67].

After arrival, expansion from introduction points can be further enabled by passive transportation of mated females through road traffic [67], with petrol stations and highway parking lots, as well as seaports, railway stations and airports, subject to heightened surveillance [64]. Recent mathematical models have found that better prevention (e.g. surveillance and early detection) could have made multi-billion dollar savings for Aedes spp. alone, by mitigating future damages and control efforts [68]. However, this particular focus on mosquitoes involves only a subset of potential proactive approaches to manage invasions, which remain to be optimized for a range of taxonomic groups (and also see Box 1).

Climate change in shaping invasions, diseases and socioeconomic impacts

Climate change and the opening of novel thermal niches

Climate warming may have a major role in fostering hematophagous arthropod invasions by increasing the number of favorable thermal niches for their development, including towards formerly cold and restrictive environments, such as at higher latitudes and altitudes [80]. Even if the outcomes of future distribution forecasts should be considered carefully and include different scenarios, Carvalho et al. [81] showed that many disease vectors are expected to expand their range, especially towards the poles. As a consequence, climate change is likely to worsen health risks by increasing zoonotic diseases, transmission and disease vector population growth after the arrival of alien hematophagous arthropods (e.g. Ae. albopictus and Ixodes ricinus [82]) (also see Box 2 for additional information).

For the highly invasive yellow fever mosquito Ae. aegypti, Iwamura et al. [9] suggested an increasing global suitability for life cycle completion of + 1.5% (in terms of periods suitable for mosquito development) per decade between 1950 and 2000, with that trend predicted to accelerate and increase by + 3.2% per decade, and even up to + 4.4% per decade, by 2050. In southern Europe, future climatic predictions suggest a northward expansion of Ae. aegypti from the limited remnant population in the Black Sea area, introduced over a century ago [83], and particularly to container ports of the Alboran, Balearic and Aegean Sea areas [84]. For Ae. albopictus and the Asian rock pool mosquito Aedes japonicus, Cunze et al. [85] predicted differential habitat suitability and range shifts under future climate change scenarios up to 2080 in Europe, with Ae. albopictus expected to expand its range and Ae. japonicus expected to contract its range. Aedes albopictus, native to the tropical and temperate forests of southeast Asia [86], has already extended its distribution range to all temperate zones of the planet in response to global warming and the increase in human-mediated trade and transport. The proliferation of Ae. albopictus in temperate regions is partly due to its eggs being able to enter diapause during winter. Eggs do not hatch until the following spring, when they likely exist in a quiescent state until environmental conditions become favorable for hatching [87]. Given that climate is expected to warm at least by 3 °C by 2100, cold-related stresses will disappear in many habitats of the world, and Ae. albopictus will no longer have to go through the winter diapause stage to survive [88].

Similarly, we suggest that the lessening of thermal barriers could permit Ae. aegypti and tick species, such as those from the Ixodes genus, to expand their range into warming temperate regions, increasing disease risks [89]. Importantly, such predictions can present substantial heterogeneity, and species-specific differences may occur, as reported for tick species dynamics [90], and for tick-borne and mosquito-borne diseases [91]. While mosquitoes can be affected by extreme weather events and climatic variability in the short term, ticks will respond to climate change through long-term changes in their spatiotemporal occurrence [91].

Many alien hematophagous arthropods, currently introduced but apparently not spreading or causing impact yet [92, 93], will likely transition to invasive species in the future, owing to the concept of invasion debts (i.e. time lags to alien species spread and impact following arrival [94]). Indeed, the impact on the environment of an alien species recently introduced to a new ecosystem, though initially benign, can be the premise of a proliferation detrimental to the invaded habitats or society. In this context, the assessment of population dynamics and distributions of hematophagous arthropods is key, as this then allows development of reliable predictions for the effects of climate change on disease transmission, and thus robust estimates of the populations that are at highest epidemiological risks. Modeling efforts should therefore concentrate on the worldwide projections of vector-borne diseases under different future scenarios involving climate change, pollution and urbanization. This would mean that regions, including polar and high altitude areas, and populations at higher epidemiological risks can be better equipped, whilst currently there is low awareness, unprepared medical systems and immune naiveté of the population to the disease [95]. Furthermore, the increasing rates of sea level rise caused by global warming will significantly increase the area of coastal marshes by incursions inland [96]; those coastal marshes are historical habitats for mosquitoes [97] and their expansion would thus foster their re-emergence alongside diseases.

Finally, the risk of native vertebrate species extinction due to alien exotic pathogens, including alien hematophagous arthropods, is particularly acute within insular systems harboring endemic fauna composed of immunologically naïve species. For example, the mosquito Cx. quinquefasciatus, a vector of avian malaria (Plasmodium sp.), represents a serious threat to the Galapagos and Hawaii bird diversity [34, 35].

Climate change will worsen economic costs

The impact of hematophagous arthropods on human societies is often assessed either as an economic cost (in monetary currency) or in disability-adjusted life year (DALY), which represents the life expectancy lost because of the burden of insect-borne diseases. While the costs in terms of human lives and suffering should be sufficient to warrant effective measures against the spread of hematophagous insects and the pathogens they carry [115], it is in fact the huge economic costs incurred by the spread of hematophagous insects that ironically provide powerful and more tangible metrics for actions by international authorities. Economic costs therefore appear to be more straightforward to use for synthetic and applied purposes, and especially in the context of invasive alien species [20], including hematophagous arthropods [4, 23].

Economic studies on invasive hematophagous arthropods revealed heterogeneous, either direct (e.g. [116]) or indirect (e.g. [117]), cost figures worldwide. However, global syntheses are still scarce and evidenced a spatially biased repartition of these costs (e.g. [116]). Similarly, the number of reported vector-borne diseases considered in such existing studies is very limited and underrepresents the reality, with dengue representing up to 84% of total health costs, the West Nile virus representing 15% and Chikungunya and Zika together representing < 1% [18]. The existing knowledge reveals that only 15% of the economic costs incurred by hematophagous arthropods are devoted to their control (6% being of unknown use), the remaining being medical care (52%) or both medical care and control (27%) [18, 20]. The part of the control that is allocated to biosecurity and early detection of newly introduced species remains unknown (information retrieved from the public database InvaCost v5, https://doi.org/10.6084/m9.figshare.12668570.v5). This is surprising, as a recent economic evaluation of the cost-effectiveness of disease vector control in six countries showed that control expenditures would cost less than the outbreak response, with populations reduced by up to 90% [118]. Warmer conditions will likely increase mosquito populations and abundance, in turn increasing biting rates. As incubation periods for the parasites and viruses they carry are also temperature-dependent, climate change will certainly contribute to a switch from occasional to frequent disease outbreaks (for instance, malaria and dengue), in parallel to providing more regions where the vectors and their associated diseases could arrive and spread. Almost 2 decades ago, Cumming and Van Vuuren [119] were already pointing out the significant impact that climate change could have on the occurrence of tick-borne diseases and the extremely high economic importance this could have.

Rapid response to eradicate invaders post-invasion as well as the implementation of effective biosecurity control pre-invasion (i.e. biosurveillance and intensive monitoring) are up to ten times cheaper for mosquito-borne diseases than waiting and paying for accrued damages [120]. A recent modeling study using logistic response curves to resemble impact dynamics showed that for the Aedes genus, current management delays of 55 years have led to an additional cost of US$ 4.57 billion that could have been avoided, showing the crucial importance of acting early against future invasions and other global changes [68, 121]. With climate change projections over the next 3 decades likely to increase the area occupied by current arthropod invaders by 18%, the need for better biosecurity control to mitigate hematophagous arthropod nuisance biting and disease has never been stronger [7]. Moreover, knowledge needs around the potential synergistic links between climate change and invasive alien species impacts are pervasive, both concerning ecosystems and economies [25]. Yet, even if additional investigations on the influence of temperature on disease transmission are required, there are lines of evidence suggesting that vectorial capacity and vector competence could be increased in certain circumstances [122], further increasing medical costs.

Even aside from direct health costs, invasions by hematophagous arthropods can cause substantial impacts through nuisance biting that affects recreational and real estate values which yield an economic return [123]. As lagging effects in population dynamics are the rule during the invasion process, invasive populations may grow undetected for many generations before reaching a threshold where they become abundant enough for economic damages to occur or be noticed. Indeed, Cuthbert et al. [124] found that invasion costs relate positively to the time duration a species has been present, signaling that failing to respond rapidly could prove more costly in the future.

The global economic burden associated with invasive hematophagous arthropods that vector diseases is most likely underestimated, often excluding indirect economic impacts on productivity and income [125], tourism [126], blood-supply system [127], personal protection [128] and quality of life [129], not to mention the contribution of each disease to DALY, which seldom include monetary values [18]. With climate change likely to provide opportunity for new invasions and exacerbate current ones, future economic impacts from hematophagous arthropods that vector diseases will likely rise substantially.

Hematophagous arthropod invasions in the anthropocene

Urbanization and heat islands

Four and a half billion people currently live in cities, about 55% of the world population [130]. This represents a growing opportunity for the development of invasive mosquito populations [131, 132] due to: (i) human-generated dumping sites in both public and private spaces; (ii) the deterioration of roads; (iii) the pollution of surface and ground waters, which some arthropod disease vectors (e.g. Cx. pipiens) use as resources. Growing urbanization also results in large numbers of construction sites, often offering additional microhabitats for the proliferation of mosquito populations [133, 134]. Mosquito communities in urban areas have also been shown to be less diverse, but also more abundant, being dominated by a few species that are adapted to develop effectively in artificial environments [135]. In cities, larvae of most alien mosquitoes, including Ae. aegypti, Ae. albopictus and Cx. pipiens, largely benefit from the presence of scrap tires, plates under flower pots, clogged roof gutters, cement tanks, metal pots, cemetery urns and many other water storage containers [136, 137]. In these human-made habitats, often associated with private gardens and urbanized areas, water collections support larval development and are available in similar forms worldwide, thus representing a significant predictor of the presence of Ae. albopictus [138]. Moreover, they often contain a smaller suite of natural enemies due to their frequent inability to colonize very small, often transient, urban aquatic habitats.

In urban environments, females of Cx. pipiens (Cx. pipiens and Cx. quinquefasciatus) often oviposit in the polluted waters collected in sections of ditches and many other sites contaminated by urban effluents [139, 140]. There is growing evidence that major human malaria vectors in Africa, and especially An. coluzzi and An. arabiensis within the An. gambiae complex, are also thriving in rapidly expanding urban metropoles, where non-specific insecticide resistance mechanisms selected in agricultural settings may promote adaptation to polluted waters [141, 142]. Aedes aegypti and Ae. albopictus, two other urban mosquito vectors of dengue, chikungunya and Zika viruses, more frequently oviposit in clear, domestic and peridomestic water collections before their inundation from rainfall [143]. Of note, the recent invasion of major cities in easternmost Africa (i.e. Djibouti, Ethiopia and Sudan) by the Asian urban malaria vector Anopheles stephensi breeding in water tanks has already given rise to severe malaria epidemics and is potentially threatening over 126 million people in its novel predicted range in Africa [144]. The presence of larval microhabitats for Ae. aegypti, in the form of unsealed urban water storage containers, can also greatly improve connectivity among mosquito populations and thus favor the spread within urban environments [145]. Moreover, mathematical simulations have evidenced that high unsealed tank densities and the presence of non-compliant tanks can bolster the invasiveness of the species by reducing habitat fragmentation [146].

While not necessarily causing a difference among native and alien mosquito populations, urbanization may have different effects on the distribution of mosquito species. For example, in Guangzhou (China), urbanization providing human-made container habitats is beneficial to Ae. albopictus [147] in the absence of domestic populations from Ae. aegypti. Conversely, the more heat-sensitive species Ae. japonicus suffers from urbanization in Fukuoka city (Japan) and especially from the urban heat island effect [148]. Furthermore, for Aedes koreicus, human population density has been found to negatively affect mosquito abundances, suggesting that they rely on other blood meal sources [149]. However, the urban heat island effect in cities can also be beneficial, by causing shifts in phenology, promoting more rapid development associated with increased temperature and causing earlier seasonal population peaks in temperate areas [135] as well as acting as stepping stones to foster alien range expansion. Notably, the population density of the alien species Ae. albopictus in its invaded range can be inversely related to the distance to the nearest vegetation border [150], almost suggesting a niche inversion (i.e. reversal of niche characteristics between native and invaded regions) compared with the original habitat of the same species within its native range, as invasive alien populations can prefer urban areas over vegetated ones. Human environments can also foster the potential evolution of sub-populations, exemplified by the supposed “London Underground” subspecies of Cx. pipiens, with surface and subterranean populations genetically distinct and displaying different reproductive and feeding behaviors [151] (but see [152]).

Environmental pollution

The effects of light pollution, i.e. artificial light at night in urban areas, on the life cycle and physiology of mosquitoes and other hematophagous arthropods that vector diseases are also becoming a growing research topic, possibly further strengthening the invasion potential of alien species. A recent study indeed evidenced the alteration of the seasonal phenology of Cx. pipiens, whose females have prolonged reproduction and biting seasons when exposed to urban light pollution [153], thus increasing the proliferation of alien mosquitoes and their epidemiological significance. It is thus expected that the ongoing worldwide urbanization, and the increasing problem of water storage by households in areas exposed to light pollution at night, will further support mosquito proliferation.

In agricultural lands, the fertilization of rice and vegetable crops usually takes place in warm and sun-lit waters, already propitious to the development of Anopheles and Culex mosquitoes. Importantly, NPK fertilizers (N for nitrogen, P for phosphorus and K for potassium) strongly attract gravid females of mosquitoes searching for nutrient-rich oviposition sites [154,155,156,157]. While the NPK fertilizer is not directly assimilated by the mosquito larvae, the three minerals enhance the development of bacteria, algae and fungi, increasing the food biomass of the breeding sites [158]. The larvae of mosquitoes exploit this additional biomass to proliferate. Laboratory studies found the survival rates of Ae. aegypti and An. gambiae in waters contaminated by fertilizers to be two-to-three times as great as in the uncontaminated waters [159, 160]. Direct nutrient inputs from grazing cattle also increase mosquito proliferation [161].

Finally, in regions of intensive monoculture, where pests and parasites represent a real threat to plants, there has been a sustained use of fungicides, herbicides and insecticides. Those substances, used repeatedly, favor the emergence of multiple lines of resistance among pests and mosquitoes, while causing the decline of predatory insects, amphibians, reptiles and fishes [162]. In sum, the growing human population requiring increased agricultural productivity will lead to increased insecticide resistance and proliferation of mosquito populations associated with these activities [140].

Social ethnology to improve health and environment quality

Transformational change and paradigm shift in perceptions

Until recently, the sociological and ethnological literature on hematophagous arthropods tended to fit into two distinct sectors: ‘health specialists’ dealing with disease and epidemic risks to humans and ‘environment specialists’ dealing with the relations between insects and their ecosystems [163, 164]. This ‘health’ versus ‘environment’ distinction can be paralleled with a ‘tropical’ versus ‘temperate’ contrast in the geographical space. In tropical regions, populations are still heavily burdened by the diseases that hematophagous arthropods transmit, with mosquitoes remaining one of the deadliest disease vectors. That is despite the considerable progress achieved in recent decades, owing to the distribution of insecticide-treated mosquito nets for malaria control (http://www.who.int/malaria/en), in particular. Until the 1990/2000s, in temperate regions, the health issues related to hematophagous arthropods were considered a thing of the past. In this context, research rather focused on environmental issues and on perceptions towards these insects, the identity attachments they may be involved in and the socio-technical controversies related to their management—particularly those concerning comfort-based mosquito control policies [163, 165,166,167].

In recent decades, however, several factors have called into question this tropical/temperate division. In temperate regions, the introduction of alien vector species, which subsequently became invasive, exposed populations to new epidemic risks and high levels of nuisance. The case of Ae. albopictus is particularly representative of the crossover between environmental and health issues. The introduction of this mosquito species into southern Europe in the early 2000s disrupted the vernacular taxonomies associating mosquitoes with polluted urban places (i.e. sewage) or to wilderness (i.e. wetlands). Aedes albopictus, conversely, prefers habitats in proximity to domestic spaces in clear waters and consequently has provoked reactions of denial or responsibility shifts among the human population [168]. In addition, the ability of Ae. albopictus to proliferate and harm human health challenges ecological belief in European populations, further widening the gap between their ecological discourses and practices [169, 170]. This ‘ladybird syndrome’ [171] leads the same individuals to declare themselves highly sensitive to the protection of nature, while demanding the eradication of Ae. albopictus by a biocide. In a further paradox, human populations use the health risk argument to justify their requests for mosquito control, while expressing relatively little concern about the occurrence of an epidemic of dengue, chikungunya or Zika in their region [172].

As populations gain awareness of the adverse ecological and health effects of biocides, the increasingly ineffective insecticide treatments, which apply to mosquitoes that vector disease first and foremost [173, 174], are the subject of burgeoning protests. These environmental concerns are accompanied by growing aspirations for genuine consultation with local populations, for instance, prior to the testing of genetically modified mosquitoes in various southern countries [175]. In this nexus between environment and health, the progressive changes in the wording defining Lyme disease transmitted by ticks of the Ixodes genus—from infectious, to vectorial and then zoonotic—have exemplified the progressive ecologization of health issues [176]. In other words, human populations are increasingly aiming to improve environmental safety by limiting human-made environmental threats, including the reconsidering of management of invasive hematophagous vectors of disease with chemicals. Requests for integrating environmental protection measures in the discussions around management of outbreaks of invasive hematophagous arthropods have gained particular traction in tropical regions, where ecological framing of health issues has been progressively paired with democratic demands. In recent decades, the constantly increasing connection between environment and planetary health has contributed to the development of the now well-known One Health approach [177], whose definition was revised in 2022 [178].

Co-constructive and deliberative approaches

The recent sociological and ethnological literature on hematophagous arthropods is increasingly considering the interactions among human, animal and environmental health [172, 179,180,181,182]. Novel research questions will arise from the comparative analyses of the emergence and re-emergence of ecological and/or health concerns as well as shifts in priorities in diverse socio-ecological contexts. These will pave the way for novel generations of sociologists and ethnologists to bridge together ecologists, entomologists, virologists and other public health and environment specialists to securely anchor their working hypotheses on solid biological roots. In turn, biologists interested in hematophagous arthropod invasion biology and its ecological and evolutionary tenets should benefit from strengthened interactions with social scientists. This will allow them to better integrate sociological and ethnological dimensions when performing risk assessment analyses and/or formulating scenarios and hypotheses for vector evolution as well as associated disease emergence and spread [183]. Altogether, this will increase uptake of research results by non-academic stakeholders, including civil societies, regulators and authorities, by providing data and recommendations for evidence-based decisions. The importance of considering biodiversity and environmental value pluralism in management action discussions has been recently advocated by Meinard et al. [184], who proposed solutions aimed at implementing consensual plans for biological invasion mitigation efforts.

Conclusions

  1. (1)

    The worldwide invasion of hematophagous arthropods is a longstanding and pervasive problem, which is predicted to further increase with climate change. In addition to global climate change, our review highlights the importance of shipping and air traffic, the transport of vertebrates (i.e. livestock and pets) and worn tires as prominent factors and sources assisting the introduction of hematophagous arthropods that vector diseases. The management of invasive hematophagous arthropods should be more proactive and consider expected changes in socioeconomic activity patterns worldwide so that new potential pathways and species source pools for introduction could be identified. Given the focus on a few groups here (principally mosquitoes and ticks), future works should consider invasion dynamics and impacts of additional, understudied hematophagous arthropod taxa.

  2. (2)

    Several hematophagous arthropods have exhibited strong ecological niche shifts, including niche inversion phenomenon, during the invasion process. The opportunistic development of populations in a large variety of human-made microhabitats is increasingly reported. Here, we alert decision-makers and politicians to the knowledge gaps and growing risks posed by accelerated worldwide urbanization and interconnectivity, which could further support mosquito proliferation and adaptations to human-modified environments.

  3. (3)

    Surveillance systems and strong political commitment are required to set-up and maintain proactive disease prevention programs and preparedness for rapid responses to outbreaks.

  4. (4)

    Finally, social-ethnological approaches represent a valuable perspective for setting mitigation measures aiming at improving health and environments in the context of proliferations of hematophagous arthropods that vector diseases. By encouraging the dialogue between experts of health and environmental topics, including epidemiologists, policymakers and researchers, and considering social perception, the chances of exploring issues related to encounters between hematophagous arthropods and humans, including new encounters, would improve. Beside the significant health and economic concerns posed to human populations, our review demonstrates several nuisances to wildlife, highlighting the importance of placing the management of these arthropods in a wider biodiversity context, i.e. by the consideration of a multispecies well‐being.

Availability of data and materials

No data were collected for this study (review). All data and information synthesized in the review are already published and publicly available, and those publications are properly cited in this submission.

References

  1. Vasilakis N, Tesh RB. Insect-specific viruses and their potential impact on arbovirus transmission. Curr Opin Virol. 2015;15:69–74.

    PubMed  PubMed Central  Google Scholar 

  2. Medlock JM, Hansford KM, Schaffner F, Versteirt V, Hendrickx G, Zeller H, et al. Review of the invasive mosquitoes in Europe: ecology, public health risks, and control options. Vector Borne Zoonotic Dis. 2012;12:435–47.

    PubMed  PubMed Central  Google Scholar 

  3. Bath S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, et al. The global distribution and burden of dengue. Nature. 2013;496:504–7.

    Google Scholar 

  4. Cuthbert RN, Pattison Z, Taylor NG, Verbrugge L, Diagne C, Ahmed DA, et al. Global economic costs of aquatic invasive alien species. Sci Total Environ. 2021;775:145238.

    CAS  PubMed  Google Scholar 

  5. Liu X, Blackburn TM, Song T, Li X, Huang C, Li Y. Risks of biological invasion on the belt and road. Curr Biol. 2019;29:499–505.

    CAS  PubMed  Google Scholar 

  6. Ramalho-Ortigao M, Gubler DJ. Human diseases associated with vectors (arthropods in disease transmission). In: Ryan ET, Hill DR, Solomon T, Endy TP, Aronson N, editors. Hunter’s tropical medicine and emerging infectious diseases. Amsterdam: Elsevier; 2020. p. 1063–169.

    Google Scholar 

  7. Bellard C, Thuillier W, Leroy B, Genovesi P, Baklenes M, Courchamp F. Will climate change promote future invasions? Glob Chang Biol. 2013;19:3740–8.

    PubMed  PubMed Central  Google Scholar 

  8. Caminade C, Mcintyre KM, Jones AE. Impact of recent and future climate change on vector-borne diseases. Ann NY Acad Sci. 2019;1436:157–73.

    PubMed  Google Scholar 

  9. Iwamura T, Guzman-Holst A, Murray KA. Accelarating invasion potential of disease vector Aedes aegypti under climate change. Nat Commun. 2020;11:2130.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. Lenoir J, Bertrand R, Comte L, Bourgeaud L, Hattab T, Murienne J, et al. Species better track climate warming in the oceans than on land. Nat Ecol Evol. 2020;4:1044–59.

    PubMed  Google Scholar 

  11. Semenchuk P, Moser D, Essl F, Schindler S, Wessely J, Gattringer A, et al. Future representation of species’ climatic niches in protected areas: a case study with Austrian endemics. Front Ecol Evol. 2021;9:685753.

    Google Scholar 

  12. Daly EZ, Gerlich HS, Frenot Y, Høye TT, Holmstrup M, Renault D. Climate change helps polar invasives establish and flourish: evidence from long-term monitoring of the blowfly Calliphora vicina. Biology. 2023;12:111.

    PubMed  PubMed Central  Google Scholar 

  13. Pyšek P, Jarošik V, Pergl J. Alien plants introduced by different pathways differ in invasion success: unintentional introductions as a threat to natural areas. PLoS ONE. 2011;6:e24890.

    PubMed  PubMed Central  Google Scholar 

  14. Lambdon PW, Pyšek P, Basnou C, Arianoutsou M, Essl F, Hejda M, et al. Alien flora of Europe: species diversity, temporal trends, geographical patterns and research needs. Preslia. 2008;80:101–49.

    Google Scholar 

  15. Haubrock PJ, Turbelin AJ, Cuthbert RN, Novoa A, Taylor NG, Angulo E, et al. Economic costs of invasive alien species across Europe. NeoBiota. 2021;67:153–90.

    Google Scholar 

  16. Kourantidou M, Cuthbert RN, Haubrock PJ, Novoa A, Taylor N, Leroy B, et al. Economic costs of invasive alien species in the Mediterranean basin. NeoBiota. 2021;67:427–58.

    Google Scholar 

  17. Hudgins EJ, Cuthbert RN, Haubrock PJ, Taylor NG, Kourantidou M, Nguyen D, et al. Unevenly distributed biological invasion costs among origin and recipient regions. Nat Sustain. 2023. https://doi.org/10.1038/s41893-023-01124-6.

    Article  Google Scholar 

  18. Bradshaw C, Leroy B, Bellard C, Roiz D, Albert C, Fournier A, et al. Massive yet grossly underestimated global costs of invasive insects. Nat Commun. 2016;7:12986.

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Jeschke JM, Heger T. Invasion biology: hypotheses and evidence. Boston: CABI International; 2018.

    Google Scholar 

  20. Diagne C, Leroy B, Gozlan RE, Vaissiere AC, Assailly C, Nuninger L, et al. InvaCost, a public database of the economic costs of biological invasions worldwide. Sci Data. 2020;7:277.

    CAS  PubMed  PubMed Central  Google Scholar 

  21. Cuthbert RN, Diagne C, Haubrock PJ, Turbelin AJ, Courchamp F. Are the “100 of the world’s worst” invasive species also the costliest? Biol Invasions. 2022;24:1895–904.

    Google Scholar 

  22. Diagne C, Leroy B, Vaissière AC, Gozlan RE, Roiz D, Jarić I, et al. High and rising economic costs of biological invasions worlwide. Nature. 2021;592:571–6.

    CAS  PubMed  Google Scholar 

  23. Roiz D, Pontifes P, Jourdain F, Diagne C, Leroy B, Vaissière A-C, Tolsá MJ, Salles J-M, Simard F, Courchamp F. 2023. The rising global economic costs of Aedes and Aedes-borne diseases. ResearchSquare (pre-print): https://doi.org/10.21203/rs.3.rs-2679030/v1

  24. Essl F, Dullinger S, Genovesi P, Hulme PE, Jeschke JM, Katsanevakis S, et al. A conceptual framework for range-expanding species that track human-induced environmental change. Bio Sci. 2019;69:908–19.

    Google Scholar 

  25. Ricciardi A, Iacarella JC, Aldridge DC, Blackburn TM, Carlton JT, Catford JA, et al. Four priority areas to advance invasion science in the face of rapid environmental change. Environ Rev. 2021;29:119–41.

    Google Scholar 

  26. Lopez BE, Allen JM, Dukes JS, Lenoir J, Vilà M, Blumenthal DM, et al. Global environmental changes more frequently offset than intensify detrimental effects of biological invasions. Proc Natl Acad Sci USA. 2022;119:e2117389119.

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Huang D, Haack RA, Zhang R. Does global warming increase establishment rates of invasive alien species? A centurial time series analysis. PLoS ONE. 2011;6:e24733.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Mazza G, Tricarico E, Genovesi P, Gherardi F. Biological invaders are threats to human health: an overview. Ethol Ecol Evol. 2014;26:112–29.

    Google Scholar 

  29. Pecl GT, Araújo MB, Bell JD, Blanchard J, Bonebrake TC, Chen IC, et al. Biodiversity redistribution under climate change: impacts on ecosystems and human well-being. Science. 2017;355:6332.

    Google Scholar 

  30. Athni TS, Shocket MS, Couper LI, Nova N, Caldwell IR, Caldwell JM, et al. The influence of vector-borne disease on human history: socio-ecological mechanisms. Ecol Lett. 2021;24:829–46.

    PubMed  PubMed Central  Google Scholar 

  31. Juliano SA, Lounobos LP. Ecology of invasive mosquitoes: effects on resident species and on human health. Ecol Lett. 2005;8:558–74.

    PubMed  PubMed Central  Google Scholar 

  32. Burridge MJ. Alien and invasive ticks: threats to human and animal health in the United States. Gainesville: University Press of Florida; 2011.

    Google Scholar 

  33. Rosen L, Rozeboom LE, Reeves WC, Saugrain J, Gubler DJ. A field trial of competitive displacement of Aedes polynesiensis by Aedes albopictus on a Pacific atoll. Am J Trop Med Hyg. 1976;25:906–13.

    CAS  PubMed  Google Scholar 

  34. Wikelski M, Foufopoulos J, Vargas H, Snell H. Galápagos birds and diseases: invasive pathogens as threats for island species. Ecol Soc. 2004;9:5.

    Google Scholar 

  35. Samuel MD, Woodworth BL, Atkinson CT, Hart PJ, Lapointe DA. Avian malaria in Hawaiian forest birds: infection and population impact across species and elevations. Ecosphere. 2015;6:1–21.

    Google Scholar 

  36. Ala-Hulkko T, Kotavaara O, Alahuhta J, Kesälä M, Hjort J. Accessibility analysis in evaluating exposure risk to an ecosystem disservice. Appl Geogr. 2019;113:102098.

    Google Scholar 

  37. Crowl TA, Crist TO, Parmenter RR, Belovsky G, Lugo AE. The spread of invasive species and infectious disease as drivers of ecosystem change. Front Ecol Environ. 2008;6:238–46.

    Google Scholar 

  38. Mordecai EA, Caldwell JM, Grossman MK, Lippi CA, Johnson LR, Neira M, et al. Thermal biology of mosquito-borne disease. Ecol Lett. 2019;22:1690–708.

    PubMed  PubMed Central  Google Scholar 

  39. Shocket MS, Verwillow AB, Numazu MG, Slamani H, Cohen JM, El Moustaid F, et al. Transmission of West Nile and five other temperate mosquito-borne viruses peaks at temperatures between 23°C and 26°C. eLife. 2020;9:e58511.

    CAS  PubMed  PubMed Central  Google Scholar 

  40. Blackburn TM, Pysek P, Bacher S, Carlton JT, Duncan RP, Jarošik V, et al. A proposed unified framework for biological invasions. Trends Ecol Evol. 2011;26:333–9.

    PubMed  Google Scholar 

  41. Lounibos LP. Invasions by insect vectors of human disease. Annu Rev Entomol. 2002;47:233–66.

    CAS  PubMed  Google Scholar 

  42. Hopcroft RL. The social origin of agrarian change in late medieval England. Am J Sociol. 1994;99:1559–95.

    Google Scholar 

  43. Powell JR, Gloria-Soria A, Kotsakiozi P. Recent History of Aedes aegypti: Vector genomics and epidemiology records. Bioscience. 2018;68:854–60.

    PubMed  PubMed Central  Google Scholar 

  44. McNeill WH. Plagues and Peoples. New York: Anchor Books; 1976.

    Google Scholar 

  45. Klitting R, Goukd EA, Paupy C, Lamballerie X. What does the future hold for yellow fever virus? (I). Genes. 2018;9:291.

    PubMed  PubMed Central  Google Scholar 

  46. Nash D, Mostashari F, Fine A, Miller J, O’Leary D, Murray K, et al. The outbreak of west Nile virus Infection in the New York city area in 1999. N Engl J Med. 2001;344:1807–14.

    CAS  PubMed  Google Scholar 

  47. Jongejan F, Uilenberg G. The global importance of ticks. Parasitology. 2004;129:3–14.

    Google Scholar 

  48. Hart E. From field to plate: the colonial livestock trade and the development of an American economic culture. William Mary Q. 2016;73:107–40.

    Google Scholar 

  49. Soper FL, Wilson DB. Anopheles gambiae in Brasil, 1930 to 1940. Rockfeller Foundation, New-York. 1943.

  50. Parmakelis A, Russelo MA, Caccone A, Marcondes CB, Costa J, Forattini OP, et al. Historical analysis of a near disaster: Anopheles gambiae in Brazil. Am J Trop Med Hyg. 2008;78:176–8.

    PubMed  Google Scholar 

  51. Killeen GF, Fillinger U, Kiche I, Gouagna LC, Knols BGJ. Eradication of Anopheles gambiae from Brazil: lessons from malaria control in Africa? Lancet Infect Dis. 2002;2:618–27.

    PubMed  Google Scholar 

  52. Kilpatrick AM, Randolph SE. Drivers, dynamics, and control of emerging vector-borne zoonotic diseases. Lancet. 2012;380:1946–55.

    PubMed  PubMed Central  Google Scholar 

  53. Tatem AJ, Hay SI, Rogers DJ. Global traffic and disease vector dispersal. Proc Natl Acad Sci USA. 2006;1003:6242–7.

    Google Scholar 

  54. Șuleșco T, Bușmachiu G, Lange U, Schmidt-Chanasit J, Lühken R. The first record of the invasive mosquito species Aedes albopictus in Chişinӑu, Republic of Moldova, 2020. Parasites Vectors. 2021;14:565.

    PubMed  PubMed Central  Google Scholar 

  55. Bakran-Lebl K, Jerrentrup H, Daroglou E, Pfitzner WP, Fuehrer HP, Allerberger F. First records of Aedes pulcritarsis (Rondani, 1872)(Diptera: Culicidae) in Austria. Parasitol Res. 2022;121:765–8.

    PubMed  PubMed Central  Google Scholar 

  56. Scholte EJ, Mars MH, Braks M, Den Hartog W, Ibañez-Justicia A, Koopmans M, et al. No evidence for the persistence of Schmallenberg virus in overwintering mosquitoes. Med Vet Entomol. 2014;28:110–5.

    CAS  PubMed  Google Scholar 

  57. Mouchet J, Giacomini T, Julvez J. La diffusion anthropique des arthropodes vecteurs de maladie dans le monde. Cahiers santé. 1995;5:293–8.

    CAS  PubMed  Google Scholar 

  58. Harrus S, Baneth G. Drivers for the emergence and re-emergence of vector-borne protozoal and bacterial diseases. Int J Parasitol. 2005;35:1309–18.

    CAS  PubMed  Google Scholar 

  59. Bennett KL, Martinez CG, Almanza A, Rovira JR, Mcmillan WO, Enrique V, et al. High infestation of invasive Aedes mosquitoes in used tires along the local transport network of Panama. Parasites Vectors. 2019;12:264.

    PubMed  PubMed Central  Google Scholar 

  60. Wilke AB, Vasquez C, Petrie W, Beier JC. Tire shops in Miami-Dade county, Florida are important producers of vector mosquitoes. PLoS ONE. 2019;14:e0217177.

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Hawley WA, Reiter P, Copeland RS, Pumpuni CB, Craig GB. Aedes albopictus in North America: probable introduction in used tires from northern Asia. Science. 1987;236:1114–6.

    CAS  PubMed  Google Scholar 

  62. Swan T, Russell TL, Staunton KM, Field MA, Ritchie SA, Burkot TR. A literature review of dispersal pathways of Aedes albopictus across different spatial scales: implications for vector surveillance. Parasit Vectors. 2022;15:303.

    PubMed  PubMed Central  Google Scholar 

  63. Deblauwe I, Demeulemeester J, De Witte J, Hendy A, Sohier C, Madder M. Increased detection of Aedes albopictus in Belgium: no overwintering yet, but an intervention strategy is still lacking. Parasitol Res. 2015;114:3469–77.

    PubMed  Google Scholar 

  64. European Centre for Disease Prevention and Control (EDC). 2012 Guidelines for the surveillance of invasive mosquitoes in Europe. Stockholm: ECDC.

  65. Balogun EO, Nok AJ, Kita K. Global warming and the possible globalization of vector-borne diseases: a call for increased awareness and action. Trop Med Health. 2016;44:38.

    PubMed  PubMed Central  Google Scholar 

  66. Medley KA, Jenkins DG, Hoffman EA. Human-aided and natural dispersal drive gene flow across the range of an invasive mosquito. Mol Ecol. 2014;24:284–95.

    PubMed  Google Scholar 

  67. Eritja R, Palmer JRB, Roiz D, Sanpera-Calbet I, Bartemus F. Direct evidence of adult Aedes albopictus Dispersal by Car. Sci Rep. 2017;7:14399.

    PubMed  PubMed Central  Google Scholar 

  68. Ahmed DA, Hudgins EJ, Cuthbert RN, Kourantidou M, Diagne C, Haubrock PJ, et al. Managing biological invasions: the cost of inaction. Biol Invasions. 2022;24:1927–46.

    Google Scholar 

  69. FAO, UNEP WHO, and WOAH. Global Plan of Action on One Health. Towards a more comprehensive One Health, approach to global health threats at the human-animal-environment interface. Rome. 2022.

  70. Cameron MM, Ramesh A. The use of molecular xenomonitoring for surveillance of mosquito-borne diseases. Philos Trans R Soc B. 2021;376:20190816.

    CAS  Google Scholar 

  71. Murindahabi MM, Takken W, Misago X, Niyituma E, Umupfasoni J, Hakizimana E, et al. Monitoring mosquito nuisance for the development of a citizen science approach for malaria vector surveillance in Rwanda. Malar J. 2021;20:36.

    PubMed  PubMed Central  Google Scholar 

  72. Pernat N, Kampen H, Jeschke JM, Werner D. Citizen science versus professional data collection: comparison of approaches to mosquito monitoring in Germany. J Appl Ecol. 2021;58:214–23.

    Google Scholar 

  73. Pataki BA, Garriga J, Eritja R, Palmer JRB, Bartumeus F, Casbai I. Deep learning identification for citizen science surveillance of tiger mosquitoes. Sci Rep. 2021;11:4718.

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Santos LM, Mutsaers M, Garcia GA, David MR, Pavan MG, Petersen MT, et al. High throughput estimates of Wolbachia, Zika and chikungunya infection in Aedes aegypti by near-infrared spectroscopy to improve arbovirus surveillance. Commun Biol. 2021;4:1–9.

    Google Scholar 

  75. Nuñez MA, Pauchard A, Riccardi A. Invasion science and the global spread of SARS-CoV-2. Trends Ecol Evol. 2020;35:642–5.

    PubMed  PubMed Central  Google Scholar 

  76. Suckling DM. Can we replace toxicants, achieve biosecurity, and generate market position with semiochemicals? Front Ecol Evol. 2015;3:17.

    Google Scholar 

  77. Mweresa CK, Mukabana WR, Van Loon JJA, Dicke M, Takken W. Use of semiochemicals for surveillance and control of hematophagous insects. Chemoecology. 2020;30:277–86.

    Google Scholar 

  78. Hoch G, Connell J, Roques A. Testing multi-lure traps for surveillance of native and alien longhorn beetles (Coleoptera, Cerambycidae) at ports of entry and in forests in Austria. Manag Biol Invasions. 2020;11:677–88.

    Google Scholar 

  79. Faccoli M, Galleggo D, Branco M, Brockerhoff EG, Corley J, Coyle DR, et al. A first worldwide multispecies survey of invasive Mediterranean pine bark beetles (Coleoptera: Curculionidae, Scolytinae). Biol Invasions. 2020;22:1785–99.

    Google Scholar 

  80. Pauchard A, Milbau A, Albihn A, Alexander J, Burgess T, Daehler C, et al. Non-native and native organisms moving into high elevation and high latitude ecosystems in an era of climate change: new challenges for ecology and conservation. Biol Invasions. 2016;18:345–53.

    Google Scholar 

  81. Carvalho BM, Rangel EF, Vale MM. Evaluation of the impacts of climate change on disease vectors through ecological niche modeling. Bull Entomol Res. 2017;107:419–30.

    CAS  PubMed  Google Scholar 

  82. Semenza JC, Suk JE. Vector-borne diseases and climate change: a European perspective. FEMS Microbiol Lett. 2018;365:244.

    Google Scholar 

  83. Kotsakiozi P, Gloria-Soria A, Schaffner F, Robert V, Powell JR. Aedes aegypti in the Black Sea: recent introduction or ancient remnant? Parasites Vectors. 2018;11:396.

    PubMed  PubMed Central  Google Scholar 

  84. Trájer AJ. Aedes aegypti in the Mediterranean container ports at the time of climate change: a time bomb on the mosquito map of Europe. Heliyon. 2021;7:E07981.

    PubMed  PubMed Central  Google Scholar 

  85. Cunze S, Koch LK, Klimpel S. Aedes albopictus and Aedes japonicas—two invasive mosquito species with different temperature niches in Europe. Parasites Vectors. 2016;9:573.

    PubMed  PubMed Central  Google Scholar 

  86. Smith CEG. The history of dengue in tropical Asia and its probable relationship to the mosquito Aedes aegypti. Am J Trop Med Hyg. 1956;59:243–51.

    CAS  Google Scholar 

  87. Armbruster PA. Photoperiodic diapauses and the establishment of Aedes albopictus (Diptera: Culicidae) in North America. J Med Entomol. 2016;53:1013–23.

    PubMed  PubMed Central  Google Scholar 

  88. Caminade C, Medlock JM, Ducheyne E, McIntyre KM, Leach S, Baylis M, et al. Suitability of European climate for the Asian tiger Aedes albopictus: recent trends and future scenario. J R Soc Interface. 2012;9:2708–17.

    PubMed  PubMed Central  Google Scholar 

  89. Ostfeld RS, Brunner JL. Climate change and Ixodes tick-borne diseases of humans. Phil Trans R Soc B. 2015;370:2014005120140051.

    Google Scholar 

  90. Gilbert L. The impacts of climate change on ticks and tick-borne disease risk. Annu Rev Entomol. 2021;66:373–88.

    CAS  PubMed  Google Scholar 

  91. Ogden NH, Lindsay LR. Effects of climate and climate change on vectors and vector-borne diseases: ticks are different. Trends Parasitol. 2016;32:646–56.

    PubMed  Google Scholar 

  92. de Wolf K, Vanderheyden A, Deblauwe I, Smitz N, Gombeer S, Vanslembrouck A, et al. First record of the West Nile virus bridge vector Culex modestus Ficalbi (Diptera: Culicidae) in Belgium, validated by DNA barcoding. Zootaxa. 2021;4920:131–9.

    Google Scholar 

  93. Kwak ML, Ng A. The detection of three new Haemaphysalis ticks (Acari: Ixodidae) in Singapore and their potential threat for public health, companion animals, and wildlife. Acarologia. 2022;62:927–40.

    Google Scholar 

  94. Essl F, Dullinger S, Rabitsch W, Hulme PE, Hülber K, Jarošik V, et al. Socioeconomic legacy yields and invasion debt. Proc Natl Acad Sci USA. 2011;108:203–7.

    CAS  PubMed  Google Scholar 

  95. Colón-González FJ, Sewe MO, Tompkins AM, Sjödin H, Casallas A, Rocklöv J, et al. Projecting the risk of mosquito-borne diseases in a warmer and more populated world: a multi-model, multi-scenario intercomparison modelling study. Lancet Planet Health. 2021;5:e404–14.

    PubMed  PubMed Central  Google Scholar 

  96. Meirland A, Gallet-Moron E, Rybarczyk H, Dubois F, Chabrerie O. Predicting the effects of sea level rise on salt marsh plant communities: does vegetation age matter more than sea level? Plant Ecol Evol. 2015;148:5–18.

    Google Scholar 

  97. Wolfe R, Zarebicki P, Meredith W. The evolution of saltmarsh mosquito control water management practices relative to coastal resiliency in the Mid-Atlantic and northeastern United States. Wetl Ecol Manag. 2022;30:1099–108.

    Google Scholar 

  98. Wilson JRU. Definitions can confuse: why the “neonative” neologism is bad for conservation. Bioscience. 2020;70:110–1.

    Google Scholar 

  99. Urban MC. Climate-tracking species are not invasive. Nat Clim Change. 2020;10:382–4.

    Google Scholar 

  100. Wallingford PD, Morelli TL, Allen JM, Beaury EM, Blumenthal DM, Bradley BA, et al. Adjusting the lens of invasion biology to focus on the impacts of climate-driven range shifts. Nat Clim Change. 2020;10:398–405.

    Google Scholar 

  101. Lindgren E, Tälleklint L, Polfelft T. Impact of climatic change on the northern latitude limit and population density of the disease-transmitting European tick Ixodes ricinus. Environ Health Perspect. 2000;108:119–23.

    CAS  PubMed  PubMed Central  Google Scholar 

  102. Lindgren E, Gustafson R. Tick-borne encephalitis in Sweden and climate change. Lancet. 2001;358:16–8.

    CAS  PubMed  Google Scholar 

  103. Jore S, Vilugrein H, Holshagen M, Brun-Hansen H, Kristoffersen AB, Nygård K, et al. Multi-source analysis reveals latitudinal and altitudinal shifts in range of Ixodes ricinus at its northern distribution limit. Parasit Vectors. 2011;4:84.

    PubMed  PubMed Central  Google Scholar 

  104. Jaenson TG, Jaenson DG, Eisen L, Petersson E, Lindgren E. Changes in the geographical distribution and abundance of the tick Ixodes ricinus during the past 30 years in Sweden. Parasites Vectors. 2012;5:8.

    PubMed  PubMed Central  Google Scholar 

  105. Jaenson TG, Lindgren E. The range of Ixodes ricinus and the risk of contracting Lyme borreliosis will increase northwards when the vegetation period becomes longer. Ticks Tick Borne Dis. 2011;2:44–9.

    PubMed  Google Scholar 

  106. Ogden NH, Maarouf A, Barker IK, Bigras-Poulin M, Lindsay LR, Morshed MG, et al. Climate change and the potential for range expansion of the Lyme disease vector Ixodes scapularis in Canada. Int J Parasitol. 2006;36:63–70.

    CAS  PubMed  Google Scholar 

  107. Parkinson AJ, Evengård B. Climate change, its impact on human health in the Arctic and the public health response to threats of emerging infectious diseases. Glob Health Action. 2009;2:2075.

    Google Scholar 

  108. Siraj AS, Santos-Vega M, Bouma MJ, Yadeta D, Ruiz Carrascal D, Pascual M. Altitudinal changes in malaria incidence in highlands of Ethiopia and Colombia. Science. 2014;343:1154–8.

    CAS  PubMed  Google Scholar 

  109. Pergolizzi JJ, LeQuang JA, Umeda-Raffa S, Fleischer C, Pergolizzi J III, Pergolizzi C, et al. The Zika virus: lurking behind the COVID-19 pandemic? J Clin Pharm Ther. 2021;46:267–76.

    CAS  PubMed  Google Scholar 

  110. Mouchet J, Carnevale P, Coosemans M, Julvez J, Manguin S, Richard-Lenoble D, et al. Biodiversité du paludisme dans le monde. Paris: Editions John Libbey Eurotext; 2004.

    Google Scholar 

  111. Sinka ME, Bangs MJ, Manguin S, Coetzee M, Mbogo CM, Hemingway J, et al. The dominant Anopheles vectors of human malaria in Africa, Europe and the Middle East: occurrence data, distribution maps and bionomic précis. Parasites Vectors. 2010;3:117.

    PubMed  PubMed Central  Google Scholar 

  112. Toty C, Barre H, Le Goff G, Larget-Thiery I, Rahola N, Couret D, et al. Malaria risk in Corsica, former hot spot of malaria in France. Malar J. 2010;9:231.

    PubMed  PubMed Central  Google Scholar 

  113. D’Alessandro G, Bruno Smiraglia C, Lavagnino A. Further studies on the biology of Anopheles labranchiae labranchiae Falleroni in Sicily. World Health Organization WHO-MAL-71.754. 1971.

  114. Di Luca M, Boccolini D, Severini F, Toma L, Mancini Barbieri F, Massa A, et al. A 2-year entomological study of potential malaria vectors in Central Italy. Vector Borne Zoonotic Dis. 2009;9:703–11.

    PubMed  Google Scholar 

  115. Patz JA, Campbell-Lendrum D, Holloway T, Foley JA. Impact of regional climate change on human health. Nature. 2005;438:310.

    CAS  PubMed  Google Scholar 

  116. Shepard DS, Undurraga EA, Halasa YA, Stanaway JD. The global economic burden of dengue: a systematic analysis. Lancet Infect Dis. 2016;16:935–41.

    PubMed  Google Scholar 

  117. Gopalan SS, Das A. Household economic impact of an emerging disease in terms of catastrophic out-of-pocket health care expenditure and loss of productivity: investigation of an outbreak of chikungunya in Orissa. India J Vector Borne Dis. 2009;46:57–64.

    PubMed  Google Scholar 

  118. Fitzpatrick C, Haines A, Bangert M, Farlow A, Hemingway J, Velayudhan R. An economic evaluation of vector control in the age of a dengue vaccine. PLoS Negl Trop Dis. 2017;11:e0005785.

    PubMed  PubMed Central  Google Scholar 

  119. Cumming GS, Van Vuuren DP. Will climate change affect ectoparasite species ranges? Glob Ecol Biogeogr. 2006;15:486–97.

    Google Scholar 

  120. Vazquez-Prokopec GM, Chaves LF, Ritchie SA, Davis J, Kitron U. Unforeseen Costs of Cutting Mosquito Surveillance Budgets. PLoS Negl Trop Dis. 2010;4:e858.

    PubMed  PubMed Central  Google Scholar 

  121. Cuthbert RN, Diagne C, Hudgins EJ, Turbelin A, Ahmed DA, Albert C, et al. Biological invasion costs reveal insufficient proactive management worldwide. Sci Total Environ. 2022;819:153404.

    CAS  PubMed  Google Scholar 

  122. Bellone R, Failloux A-B. The role of temperature in shaping mosquito-borne viruses transmission. Front Microbiol. 2020;11:584846.

    PubMed  PubMed Central  Google Scholar 

  123. Claeys-mekdade C, Morales A. Moustiques et démoustication: une enquête sociologique auprès des Arlésiens et des Camarguais, Rapport final sur l'étude d'impact d'un éventuel traitement au BTI sur le territoire du Parc Naturel Régional de Camargue, DESMID-IMEP : 6–72. 2002.

  124. Cuthbert RN, Bartlett AC, Turbelin A, Haubrock PJ, Diagne C, Pattison Z, et al. Economic costs of biological invasions in the United Kingdom. NeoBiota. 2021;67:299–328.

    Google Scholar 

  125. Selck FW, Adalja AA, Boddie CR. An estimate of the global health care and lost productivity costs of dengue. Vector Borne Zoonotic Dis. 2014;14:824–6.

    PubMed  Google Scholar 

  126. Fontenille D, Lagneau C, Yébakima A, Lecollinet S, Robin RL, Setbon M, Tirel B. La lutte antivectorielle en France. IRD Editions, Collection expertise collégiale, Marseille. 2009.

  127. Liumbruno GM, Calteri D, Petropulacos K, Mattivi A, Po C, Macini P, et al. The Chikungunya epidemic in Italy and its repercussion on the blood system. Blood Transfus. 2008;6:199–210.

    PubMed  PubMed Central  Google Scholar 

  128. Thuilliez J, Bellia C, Dehecq JS, Reilhes O. Household-level expenditure on protective measures against mosquitoes on the Island of La Réunion. France PLoS Negl Trop Dis. 2014;8:e2609.

    PubMed  Google Scholar 

  129. Halasa YA, Shepard DS, Fonseca DM, Farajohally A, Healy S, Gaugler R, et al. Quantifying the impact of mosquitoes on quality of life and enjoyment of yard and porch activities in new jersey. PlosOne. 2014;9:e89221.

    Google Scholar 

  130. UN World Urbanization Prospects. 2018. https://esa.un.org/unpd/wup/Download/.

  131. Lee JM, Wasserman RJ, Gan JY, Wilson RF, Rahman S, Yek SH. Human activities attract harmful mosquitoes in a tropical urban landscape. Eco Health. 2020;17:52–63.

    CAS  PubMed  Google Scholar 

  132. Kache PA, Santos-Vega M, Stewart-Ibarra AM, Cook EM, Seto KC, Diuk-Wasser MA. Bridging landscape ecology and urban science to respond to the rising threat of mosquito-borne diseases. Nat Ecol Evol. 2022;6:1601–16.

    PubMed  Google Scholar 

  133. Kraemer MU, Sinka ME, Duda KA, Mylne AQ, Shearer FM, Barker CM, et al. The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus. Elife. 2015;4:e08347.

    PubMed  PubMed Central  Google Scholar 

  134. Samy AM, Elaagipn AH, Kenawy MA, Ayres CFJ, Peterson AT, Soliman DE. Climate change influences on the global potential distribution of the mosquito Culex quinquefasciatus, vector of West Nile virus and lymphatic filariasis. PLoS ONE. 2016;11:e0163863.

    PubMed  PubMed Central  Google Scholar 

  135. Townroe S, Callaghan A. British container breeding mosquitoes: The impact of urbanization and climate change on community composition and phenology. PLoS ONE. 2014;9:e95325.

    PubMed  PubMed Central  Google Scholar 

  136. Vezzani D. Artificial container-breeding mosquitoes and cemeteries: a perfect match. Trop Med Int Health. 2007;12:299–313.

    PubMed  Google Scholar 

  137. Delatte H, Toty C, Boyer S, Bouetard A, Bastien F, Fontenille F. Evidence of habitat structuring Aedes albopictus populations in Réunion Island. PLoS Negl Trop Dis. 2013;7:e2111.

    PubMed  PubMed Central  Google Scholar 

  138. Sanz-Aguilar A, Rosseló R, Bengoa M, Ruiz-Pérez M, Gonzàles-Calleja M, Barceló C, et al. Water associated with residential areas and tourist resorts is the key predictor of Asian tiger mosquito presence on a Mediterranean island. Med Vet Entomol. 2018;32:443–50.

    CAS  PubMed  Google Scholar 

  139. Darriet F. Des moustiques et des hommes. Chronique d’une pullulation annoncée. IRD Éditions, collection Didactiques, Marseille. 2014.

  140. Darriet F. When urban and agricultural activities favor the proliferation of mosquito nuisance and vectors of pathogens to humans. Bull Soc Pathol Exot. 2019;112:96–104.

    CAS  PubMed  Google Scholar 

  141. 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.

    CAS  PubMed  PubMed Central  Google Scholar 

  142. Longo-Pendy NM, Tene-Fossog B, Tawedi RE, Akone-Ella O, Toty C, Rahola N, et al. Ecological plasticity to ions concentration determines genetic response and dominance of Anopheles coluzzii larvae in urban coastal habitats of Central Africa. Sci Rep. 2021;11:1–13.

    Google Scholar 

  143. Bartlett-Healy K, Unlu I, Obenauer P, Hughes T, Healy S, Crepeau T, et al. Larval mosquito habitat utilization and community dynamics of Aedes albopictus and Aedes japonicus (Diptera: Culicidae). J Med Entomol. 2012;49:813–24.

    PubMed  Google Scholar 

  144. Sinka ME, Pironon S, Massey NC, Longbottom J, Hemingway J, Moyes CL, et al. A new malaria vector in Africa: Predicting the expansion range of Anopheles stephensi and identifying the urban populations at risk. Proc Natl Acad Sci USA. 2020;117:24900–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  145. Trewin BJ, Pagendam DE, Johnson BJ, Paton C, Snoad N, Ritchie SA, et al. Mark-release-recapture of male Aedes aegypti (Diptera: Culicidae): use of rhodamine B to estimate movement, mating and population parameters in preparation for an incompatible male program. PLoS Negl Trop Dis. 2021;15:e0009357.

    PubMed  PubMed Central  Google Scholar 

  146. Trewin BJ, Parry HR, Pagendam DE, Devine GJ, Zalucki MP, Darbro JM, et al. Simulating an invasion: unsealed water storage (rainwater tanks) and urban block design facilitate the spread of the dengue fever mosquito, Aedes aegypti, in Brisbane. Australia Biol Invasions. 2021;23:3891–906.

    PubMed  Google Scholar 

  147. Li Y, Kamara F, Zhou G, Puthiyakunnon S, Li C, Liu Y, et al. Urbanization increases Aedes albopictus larval habitats and accelerates mosquito development and survivorship. PLoS Negl Trop Dis. 2014;8:e3301.

    PubMed  PubMed Central  Google Scholar 

  148. Mogi M, Armbruster PA, Tuno N. Differences in responses to urbanization between invasive mosquitoes, Aedes japonicus japonicus (Diptera: Culicidae) and Aedes albopictus, in their native range. Japan J Med Entomol. 2019;57:104–12.

    Google Scholar 

  149. Kurucz K, Manica M, Delucchi L, Kemenesi G, Marini G. Dynamics and distribution of the invasive mosquito Aedes koreicus in a temperate European city. Int J Environ Res Public Health. 2020;17:2728.

    PubMed  PubMed Central  Google Scholar 

  150. Ayllón T, Câmara DCP, Morone FC, Da Silva GL, De Barros FSM, Brasil P, et al. Dispersion and oviposition of Aedes albopictus in a Brazilian slum: initial evidence of Asian tiger mosquito domiciliation in urban environments. PLoS ONE. 2018;13:e0195014.

    PubMed  PubMed Central  Google Scholar 

  151. Byrne K, Nichols R. Culex pipiens in London underground tunnels: differentiation between surface and subterranean populations. Heredity. 1999;82:7–15.

    PubMed  Google Scholar 

  152. Haba Y, McBride L. Origin and status of Culex pipiens mosquito ecotypes. Curr Biol. 2022;32:R237–46.

    CAS  PubMed  PubMed Central  Google Scholar 

  153. Fyie LR, Gardiner MM, Meuti M. Artificial light at night alters the seasonal responses of biting mosquitoes. J Insect Physiol. 2021;129:104194.

    CAS  PubMed  Google Scholar 

  154. Darriet F, Corbel V. Aedes aegypti oviposition in response to NPK fertilizers. Parasite. 2008;15:89–92.

    CAS  PubMed  Google Scholar 

  155. Darriet F, Zumbo B, Corbel V, Chandre F. Influence of plant matter and NPK fertilizer on the biology of Aedes aegypti (Diptera: Culicidae). Parasite. 2010;17:149–54.

    CAS  PubMed  Google Scholar 

  156. Young GB, Golladay S, Covich A, Blackmore M. Nutrient enrichment affects immature mosquito abundance and species composition in field-based mesocosms in the coastal plain of Georgia. Environ Entomol. 2014;43:1–8.

    CAS  PubMed  Google Scholar 

  157. Kibuthu TW, Njenga SM, Mbugua AK, Muturi MJ. Agricultural chemicals: life changer for mosquito vectors in agricultural landscapes? Parasites Vectors. 2016;9:500.

    PubMed  PubMed Central  Google Scholar 

  158. Hao XH, Hu RG, Wu JS, Tang SR, Luo XQ. Effects of long-term fertilization on paddy soils organic nitrogen, microbial biomass, and microbial functional diversity. J Appl Ecol. 2010;21:1477–84.

    CAS  Google Scholar 

  159. Darriet F, Rossignol M, Chandre F. The combination of NPK fertilizer and deltamethrin insecticide favors the proliferation of pyrethroid-resistant Anopheles gambiae (Diptera: Culicidae). Parasite. 2012;19:159–64.

    CAS  PubMed  PubMed Central  Google Scholar 

  160. Darriet F. Synergistic effect of fertilizer and plant material combinations on the development of Aedes aegypti (Diptera: Culicidae) and Anopheles gambiae (Diptera: Culicidae). J Med Entomol. 2018;55:496–500.

    CAS  PubMed  Google Scholar 

  161. Buxton M, Cuthbert RN, Dalu T, Nyamukondiwa C, Wasserman R. Cattle induced eutrophisation favours disease-vector mosquitoes. Sci Total Environ. 2020;715:136952.

    CAS  PubMed  Google Scholar 

  162. FAO. Aquatic biodiversity in rice field. International year of rice. http://www.fao.org/rice2004/en/f-sheet/factsheet7.pdf Food and Agriculture Organization. Rome, Italy. 2004.

  163. Claeys C. Les controverses relatives à la démoustication de la Camargue: rapports à l’animal et au territoire. Espaces et Sociétés. 2003;110–111:147–66.

    Google Scholar 

  164. Baxerres C, Le Hesran JY. Quelles ressources familiales financent la santé des enfants? Les difficultés du recours aux soins pour traiter le paludisme en milieu rural sénégalais. Revue Tiers Monde. 2010;202:149–65.

    Google Scholar 

  165. Davey G, McDonald A, Prabhu G, Iwawaki S, Im Jim C, Merckelbach H, et al. A cross-cultural study of animal fears. Behav Res Ther. 1998;36:735–50.

    CAS  PubMed  Google Scholar 

  166. Huneau V. Étude Socio-environnementale de la présence des Moustiques dans l’est du Golfe du Morbihan (56, France). Bull Soc Sci Nat Ouest Fr. 2008;30:201–15.

    Google Scholar 

  167. Lidskog R, Olausson U. To spray or not to spray: the discursive construction of contested environmental issues in the news media. Discourse Context Media. 2013;2:123–30.

    Google Scholar 

  168. Claeys C, Mieulet E. The spread of Asian tiger mosquitoes and related health risks along the French Riviera: an analysis of reactions and concerns amongst the local population. Int Rev Soc Sci. 2013;3:151–73.

    Google Scholar 

  169. Martinez-Alier J. The environmentalism of the poor a study of ecological conflicts and valuation. Cheltenham: Edward Elgar Publishing; 2002.

    Google Scholar 

  170. Bozonnet JP. De la conscience écologique aux pratiques: Comment expliquer le hiatus entre attitudes environnementalistes et les comportements. Grenoble-Toulouse, Pacte IEP Grenoble-Toulouse. 2007.

  171. Claeys C. Mosquitoes management environmental issues and health concerns. Brussels: Peter Lang S.A; 2019.

    Google Scholar 

  172. Claeys C, Mieulet E. Climate change, biological invasion and emerging diseases: a longitudinal sociological study monitoring the spread of the Asian tiger mosquitoes in a European region. Socijalna ekologija Zagreb. 2016;25:143–66.

    Google Scholar 

  173. Hemingway J, Ranson H, Magill A, Kolaczinski J, Fornadel C, Gimming J, et al. Averting a malaria disaster: will insecticide resistance derail malaria control? Lancet. 2016;387:1785–8.

    PubMed  PubMed Central  Google Scholar 

  174. Moyes CL, Vontas J, Martins AJ, Ng LC, Koou SY, Dusfour I, et al. Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans. PLoS Negl Trop Dis. 2017;11:e0005625.

    PubMed  PubMed Central  Google Scholar 

  175. Beisel U, Boëte C. The flying public health tool: genetically modified mosquitoes and malaria control. Sci Cult. 2013;22:38–60.

    Google Scholar 

  176. La MC. maladie de Lyme entre cadrage infectieux, vectoriel et zoonotique: vers une écologisation des problèmes sanitaires. VertigO. 2013;13:3.

    Google Scholar 

  177. Destoumieux-Garzón D, Mavingui P, Boetsch G, Boissier J, Darriet F, Duboz P, et al. The one health concept: 10 years old and a long road ahead. Front Vet Sci. 2018;5:14.

    PubMed  PubMed Central  Google Scholar 

  178. OHHLEP—One Health High-Level Expert Panel, Adisasmito WB, Almuhairi S, Behravesh CB, Bilivogui P, Bukachi SA, et al. One Health: a new definition for a sustainable and healthy future. PLoS Pathog. 2022;18:e1010537.

    Google Scholar 

  179. Raude J, Setbon M. The role of environmental and individual factors in the social epidemiology of chikungunya disease on Mayotte island. Health Place. 2009;15:689–99.

    Google Scholar 

  180. Shaw I, Robbins P, Jones JP. A Bug’s Life and the spatial ontologies of mosquito management. Ann Assoc Am Geogr. 2010;100:373–92.

    Google Scholar 

  181. Beisel U. The blue warriors: ecology, participation and public health in malaria control experiments in Ghana. In: Geissler PW, editor. Para-states and medical science. Durham: Duke University Press; 2015. p. 281–302.

    Google Scholar 

  182. Ojala M, Lidskog R. Mosquitoes as a threat to humans and the community: the role of place identity, social norms, environmental concerns and ecocentric values in public risk perception. Local Environ. 2017;22:172–84.

    Google Scholar 

  183. Hernandez E, Torres R, Joyce AL. Environmental and sociological factors associated with the incidence of West Nile virus cases in the Northern San Joaquin valley of California, 2011–2015. Vector Borne Zoonotic Dis. 2019;19:851–8.

    PubMed  PubMed Central  Google Scholar 

  184. Meinard Y, Dereniowska M, Glatron S, Maris V, Philippot V, Georges J-Y. A heuristic for innovative invasive species management actions and strategies. Ecol Soc. 2022;27:24.

    Google Scholar 

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Acknowledgements

We thank Dr Paride Balzani for his inputs to the preparation of the manuscript.

Funding

The authors were supported by InEE-CNRS via a funded network dedicated to Biological Invasions (GdR CNRS 3647 Invasions Biologiques). DR is funded by the ASICS project (ANR-20-EBI5-0004, BiodivERsA, BiodivClim call 2019–2020). RNC acknowledges funding from the Leverhulme Trust (ECF-2021-001). DA is supported by the ANR grant WILDING (ANR-18-CE35-0002-01). FC acknowledges the AXA Research Fund Chair of Invasion Biology of University Paris Saclay. CD was funded by the BiodivERsA-Belmont Forum Project “Alien Scenarios” (BMBF/PT DLR 01LC1807C). SM is funded by French ANR project FutureHealthSEA (ANR-17-CE35-0003-01).

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Conceptualization: DR, FC, FD, JL, OC, VR; Project administration: DR, FD; Funding acquisition: DR; Visualization: OC, FJ, RU; all co-authors wrote the original draft, reviewed and edited the text, which was led by RNC, FD and DR.

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Correspondence to Ross N. Cuthbert.

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Additional file 1:

List of invasive hematophagous arthropods (species name). For each species, the following information, whenever available, is mentioned: native area (i.e. the known native geographic zone of the species), the invaded area, date or period of introduction, the date of extinction, the introduction pathway, the diseases / pathogens that are hosted by the species, the ecological impact, the description of the larval and adult habitats, and for ticks and fleas the mammals vectoring the species.

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Cuthbert, R.N., Darriet, F., Chabrerie, O. et al. Invasive hematophagous arthropods and associated diseases in a changing world. Parasites Vectors 16, 291 (2023). https://doi.org/10.1186/s13071-023-05887-x

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