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Diversity and behavioral activity of Anopheles mosquitoes on the slopes of Mount Cameroon



Malaria remains endemic in Cameroon, with heterogeneous transmission related to eco-climatic variations, vector diversity and spatial distribution. The intensification of malaria prevention and control through the free distribution of insecticide-treated nets in recent years may have altered the composition, geographic distribution and natural infection rate of Anopheles species, with implications for malaria transmission dynamics. The present study seeks to assess the vectorial diversity, dynamics and infectivity across different seasons and altitudes in relationship to parasite prevalence around the slopes of Mount Cameroon, southwestern region.


Mosquitoes were sampled (indoors and outdoors) in 11 eco-epidemiological settings at low (18–197 m), intermediate (371–584 m) and high (740–1067 m) altitude by nightly human landing catches. The mosquitoes were identified morphologically and Anopheles gambiae sibling species identified by PCR. Parity status was ascertained by examining the ovaries and the entomological inoculation rates (EIR) determined by Plasmodium falciparum circumsporozoite antigen ELISA of the head-thorax. The prevalence of Plasmodium infection across target communities was assessed using rapid diagnostic tests.


A total of 7327 (18.0 mosquitoes/trap/night) mosquitoes were trapped, mainly during the rainy season (5678, 77.5%) and at low altitude (3669, 50.1%). Anopheles spp. (5079, 69.3%) was the most abundant genera and An. gambiae complex (2691, 36.7%) the major vector, varying with altitude (χ2 = 183.87, df = 8, P < 0.001) and season (χ2 = 28.14, df = 4, P < 0.001). Only An. gambiae (s.s.) was identified following molecular analysis of An. gambiae complex siblings. The overall biting peak for An. gambiae complex was 2—3 a.m. Anopheles cinctus was the most abundant secondary vector in the area. The average EIR in the area was 2.08 infective bites per person per night (ib/p/n), higher at low (2.45 ib/p/n) than at intermediate altitude (1.39 ib/p/n) and during the rainy (1.76 ib/p/n) compared to the dry season (0.34 ib/p/n). Anopheles funestus was most infectious overall (28.1%, 16/57) while An. gambiae had the highest inoculation rates averaging 1.33 ib/p/n. Most Anopheles species across all altitudes and seasons were parous, highest in communities with the highest proportion of malaria parasite infections.


Anopheles gambiae (s.s.) remains the major malaria vector in the area and An. cinctus possibly a secondary vector of the disease in the slopes of Mt. Cameroon. The seasonal and altitudinal effects on the distribution of these mosquitoes may have implications for the transmission of malaria and its control strategies in the area. Regular monitoring of the bionomics of local Anopheles vector species and targeted control interventions in the ‘hotspots’ is necessary to curb the prevalence of the infection and incidence of disease.


Malaria remains a significant global health concern, especially in children < 5 years in sub-Saharan Africa (SSA), where 95% of cases and 96% of the deaths occur [1]. The disease is transmitted to people through the bites of infected female Anopheles mosquito, with 70 of the approximately 490 Anopheles species known to be malaria vectors [2]. In SSA, approximately 20 of the 140 Anopheles species are known to transmit malaria parasites to humans [3]. Of these, Anopheles gambiae sensu stricto (s.s.), An. gambiae sensu lato (s.l.), An. arabiensis, An. funestus group and An. nili group are the most widely distributed and important vector species in tropical Africa [2,3,4,5]. Furthermore, only 18 of these 140 have been documented and incriminated for malaria transmission in Cameroon [3, 6,7,8]. Anopheles arabiensis, An. coluzzii, An. gambiae and An. funestus (s.s.) are classified as primary vector species for Plamodium spp. transmission in Cameroon while An. carnevalei, An. coustani, An. hancocki, An. leesoni, An. marshallii, An. melas, An. moucheti, An. nili, An. paludis, An. pharoensis, An. ovengensis, An. rivulorum-like, An. wellcomei and An. ziemanni play a secondary role [9]. All these species display strong anthropophilic host-seeking behavior and longevity, causing many malaria cases [1].

Identifying vector species in different ecological zones is essential for the planning and implementation of vector control measures. In addition, assessments of malaria parasite transmission dynamics and the risk of human infection as well as the interaction among humans, parasite and vectors are also imperative. This depends on several factors, including the human biting rate (the frequency at which a human is exposed to mosquito bites), proportion of biting mosquitoes that are infectious, altitude, topography, hydrology and landscape occupied by humans and/or peridomestic animals [10,11,12]. Thus, the abundance of anopheline mosquito species is the most common entomological measure for determining the relationship between vectors and malaria incidence in any locality [13, 14].

Although a number of alternative sampling methods exist [15], human landing catches (HLCs) remains the most appropriate method for information about the actual behavioral activities of mosquitoes [16]. This is still the gold standard for measuring exposure of humans to mosquito bites [16] and estimating the human biting rate (HBR), a key determinant of the entomological inoculation rate (EIR) and a measure of malaria transmission [17]. In Cameroon, like in other parts of Africa, malaria transmission is very heterogeneous because of eco-climatic variations, seasonality, rainfall and precipitation [18]. Malaria transmission is seasonal in most parts of Cameroon, hyperendemic and hypoendemic during the rainy and dry season respectively around the slopes of Mount Cameroon in the southwestern region [18].

Malaria control hinges on vector control through the use of long-lasting insecticide-treated nets (LLINs) and indoor residual spraying (IRS). The concomitant reduction in malaria mortality following the scale-up in ITN coverage prompted the government of Cameroon, with support from Global Fund for the Fight against HIV, Malaria, and Tuberculosis, to distribute millions of LLINs to most households in the country, including the southwestern region, in line with the Roll Back Malaria (RBM) recommendation of universal coverage [19]. Mass and free distributions of LLINs remain the main national malaria vector control intervention strategy [20] and have been shown to effectively reduce the prevalence of the disease in the area [21] and country [18] and perhaps the vector population and their dynamics. In addition, the state sanitation company, Hysacam, contracted since 2011 to dispose of garbage and improve community environmental hygiene [22], has faced serious challenges in workflow over the last few years. This is due partly to the sociopolitical crisis that has affected the region since 2016, with implications for mosquito-breeding sites, anopheline density and malaria parasite transmission.

Potential reductions of the malaria burden in endemic and epidemic regions depend on knowledge of the malaria-transmitting mosquito species, populations behavioral characteristics and malaria exposure risks [6]. However, data on the susceptibility of Anopheles mosquitoes in the southwest region of Cameroon, home to the largest agro-industrial complex in the Central African Sub-Region, remain limited [9, 23, 24] and may not reflect the current dynamics. In addition, little is known about their seasonal and altitudinal distribution of the anopheline fauna in the area despite their documented impact on parasite prevalence [25]. The present study seeks to assess the vectorial diversity, dynamics and infectivity across different seasons and altitudes in relationship to parasite prevalence around the slopes of Mount Cameroon, southwestern region.


Study area

The study was carried out in the Buea, Limbe and Tiko health districts along the slopes of Mount Cameroon in the southwest region of Cameroon in selected eco-epidemiological settings at low (18–197 m), intermediate (371–584 m) and high (740–1067 m) altitude (Fig. 1). This forested region, located close to the Atlantic Ocean, is made up of low land and hilly areas, consisting of villages and towns, some of which are close to water bodies such as streams, ponds and rivers [24]. The southwest region of Cameroon has Buea as its capital, and as of 2015, its population was estimated to be 1,553,320. The area has an equatorial climate characterized by daily temperatures ranging between 20–33 °C, average annual rainfall of 2625 mm, high relative humidity (75–80%) and precipitation (2000–10,000 mm) [24] and two major seasons, a long rainy season (March–November) and a short dry season (November–February) [26], although the pattern is changing. Houses in the areas are made of plank/wood, mudbrick or cement blocks with aluminum metal sheets. Livestock like dogs, goats and fowl are the most common peridomestic animals and agriculture is the main occupation.

Fig. 1
figure 1

Study area and sampling sites

Study design and sites

This was a cross-sectional study carried out between April 2020 and September 2021. Following malaria parasite prevalence surveys, 11 communities across different altitudinal zones [low (18—197 m), intermediate (371—584 m) and high altitude (740—1067 m)] and localities (rural, semi-urban and urban) were selected (Table 1, Fig. 1) [21, 24], each community at least 5 km from the next. Mosquitoes were trapped at 68 randomly selected sites across all altitudes during the rainy and dry seasons. A total of 172 malaria rapid diagnostic test (mRDT)-negative collectors and 68 supervisors were involved in the study, with an average distance of 500 m maintained between the collection sites in every community.

Table 1 Geographic characteristics of the study sites in the Mount Cameroon area

Malaria rapid diagnostic testing

The malaria parasite prevalence of selected communities was determined by screening volunteer individuals by malaria rapid diagnostic test (mRDT) of the capillary blood using the PfHRP2/pLDH mRDT kit (SD Bioline, Alere, South Korea) and according to the manufacturer’s instructions. In addition to the community-wide cross-sectional survey, malaria tests were also done on prospective mosquito catchers, as described above, and all malaria-positive potential catchers excluded from the study.

Household survey

For mosquito sampling, each community was divided into 4 different sectors, each of which had a minimum of 20 houses. One house was then randomly selected from each sector for mosquito collection, subject to the consent of the household head, failing which, a neighboring household was chosen.

Mosquito sampling and identification

Mosquito collections were undertaken in most communities immediately following malaria prevalence survey. Mosquitoes were trapped monthly for 3 consecutive nights, both indoors and outdoors, by human landing catches (HLC), each collection period lasting for 12 h uninterrupted, from 6:00 p.m. to 6:00 a.m. To increase the effectiveness of the trapping and avoid catchers falling asleep, four catchers were used at every sector, two between 6:00 p.m.–12:00 a.m. and the other two from 12:00 a.m. to 6:00 a.m. The catchers used mouth aspirators, flashlights and stopwatches to trap mosquitoes from their exposed legs. To reduce bias due to individual differences in skill and attraction to mosquitoes, catchers were rotated between shifts and days of collection. The mosquitoes were then sorted by genus and the anophelines identified morphologically under a stereomicroscope (Olympus SZX10, Berlin, Germany) using the WHO pictorial identification key of important disease vectors [27] and the keys of Maureen Coetzee [28]. The parity status of a proportion of unfed mosquitoes was ascertain by dissecting their ovaries and examining the tracheoles as described previously [29]. This indicates the proportion of older mosquitoes within the population during the survey and is used as a proxy measure for the daily survival rate and average life span of the vector population.

Molecular identification of An. gambiae complex

A total of 160 mosquitoes of the An. gambiae complex were randomly selected (40 each per season at both the low and intermediate altitudes) for molecular speciation. Briefly, genomic DNA was extracted from the legs/abdomen of the mosquitoes using the DNAzol protocol as described [6]. The DNA was re-suspended in 10 μl sterile TE buffer (10 mM Tris–HCl pH 8.1, 1 mM EDTA) and the An. gambiae sibling species identified by multiplex PCR using predesigned ribosomal DNA-specific primers as described previously [30]. PCR products were subsequently separated on 2% agarose in TBE containing ethidium bromide at 10 mg/ml and visualized on a UV illuminator (TOYOBO Trans Modele TM-20) against a 1-kb ladder.

Estimation of entomological parameters

The head-thorax segment of a total of 313 randomly selected Anopheles species, including the 160 mosquitoes of the An. gambiae complex molecularly identified above, 51 each of An. funestus, An. nili and An. hancoki were tested for the P. falciparum circumsporozoite antigen by ELISA as described [31]. In each assay, test samples giving optical densities (OD) that exceeded the corresponding mean + 2 standard deviations for 4 negative control samples (male Anopheles mosquito) were considered seropositive.

Data analysis

All data were entered into Microsoft Excel 2019 and analyzed using SPSS Statistics 24 for windows (IBM, CA, USA). Associations between normally distributed qualitative parameters were assessed using the chi-square test while differences in group means were assessed using the Student t test or analysis of variance (ANOVA). Statistical significance level was set at P < 0.05.

The four main measures of malaria vector transmission include; human biting rate (HBR), sporozoite index (SI), parity rate (PR) and entomological inoculation rate (EIR) as stated previously [6].

  • HBR = number of mosquitoes caught per person per night of sampling.

  • SI = the proportion of anophelines with P. falciparum circumsporozoite antigen = (ELISA positive samples/total sample analyzed by ELISA) × 100.

  • PR = number of female anophelines that laid eggs at least once (parous) multiplied by 100 and divided by the total number of females dissected.

  • EIR, a key variable in expressing malaria transmission levels, was calculated as the product of anopheline-biting rate and SI.


Mosquito density and diversity

A total of 7327 (18.0 mosquitoes/trap/night) mosquitoes were trapped during the entire survey period, mainly during the rainy season (5678, 77.5%) and at low altitude (3669, 50.1%). Five genera were recorded (Fig. 2): Anopheles spp. (5079, 69.3%), Culex spp. (2024, 27.6%), Aedes spp. (165, 2.3%), Mansonia spp. (55, 0.8%) and Toxorhynchites spp. (4, 0.1%). There was a significant variation in mosquito diversity across the sampling communities (χ2 = 3557.91, df = 40, P < 0.001), altitudes (χ2 = 1535.87, df = 8, P < 0.001), and season (χ2 = 191.68, df = 4, P < 0.001), with Anopheles spp. most abundant in Misselele (87.4%, 298/341) and Dibanda (86.3%, 1952/2262) at intermediate altitude (77.4%, 2297/2969) and during the dry season (78.9%, 1301/1649). Nevertheless, Culex spp., the majority of which were Culex pipiens (71.7%, 1451/2024), dominated the mosquito fauna in Buea Town (95.1%, 196/206) and Bokwoango (92.3%, 286/306) at high altitude (82.7%, 570/689) and during the rainy season (30.9%, 1756/5678). Most Aedes mosquitoes were caught from sandpit (40.1%, 71/177) while all (100%, 4/4) Toxorhynchites spp. were caught from Tiko at low altitude during the rainy season. In all, very few anophelines were trapped at high altitude (6.8%, 47/689) compared to intermediate (77.4%, 2298/2969) and low (74.5%, 2735/3669) altitudes.

Fig. 2
figure 2

Distribution of the genera of mosquitoes around the slopes of Mount Cameroon. a Overall distribution in the survey. b Variation across altitude. c Variation across seasons. d Variation across sampling communities

Anopheline species diversity and biting density

A total of 5079 anophelines were trapped, giving an average density of 12.4 Anopheles mosquitoes/trap/night across all sites. In all, 81.4% (4136/5079) of the Anopheles spp. fauna were major malaria vectors. Anopheles gambiae complex (2691, 36.7%), An. funestus (560, 7.6%), An. nili (438, 6.0%), An. hancoki (270, 3.7%) and An. moucheti (177, 2.4%) distribution (Fig. 3) varied significantly with altitude (χ2 = 183.87, df = 8, P < 0.001) and season (χ2 = 28.14, df = 4, P < 0.001). Interestingly, the proportion of all major vectors, except An. moucheti, was higher in the dry season compared to the wet season. The density of An. gambiae complex was highest at low altitude, An. funestus group and An. nili complex at intermediate altitude while anophelines were almost nonexistent, overall at high altitude.

Fig. 3
figure 3

Variation in major malaria vector populations across the slope of Mount Cameroon. a Variation across seasons. b Variation across altitude. c Variation across sampling communities

Molecular analysis of Anopheles gambiae complex siblings revealed only the presence of An. gambiae (s.s.). Furthermore, An. cinctus (155), An. longipalpis (117), An. kingi (106), An. ziemanni (100) and An. marshalli (67) are proposed as secondary vectors of malaria in the area, constituting up to 10.7% (545/5079) of the population of anophelines caught. This is the first report of An. cinctus as a possible secondary malaria vector in the area. Some 173 (2.4%) of the anophelines did not match the characteristics of any known species according to the manual.

Anopheles biting behavior

The HLC collections indicated outdoor and indoor exposure of residents to host-seeking anophelines (Fig. 4). In this survey, there was a significant association between the trapping site and the mosquito genera (χ2 = 39.29, df = 4, P < 0.001) and major malaria vector species (χ2 = 52.58, df = 4, P < 0.001). Most (71.5%, 3924/5488) of the Anopheles species were caught outdoors (Fig. 4), indicative of the strongly exophagic biting habits of the anophelines. A greater proportion of all major vectors were trapped outdoors except for An. nili and An. moucheti, which were more abundant indoors. Most anoplelines were trapped outdoors in the rainy season (χ2 = 43.47, df = 4, P < 0.001) as well as at low (χ2 = 24.09, df = 4, P < 0.001) and intermediate (χ2 = 29.18, df = 3, P < 0.001) altitudes. However, most Anopheles spp. were trapped indoors in the dry season (χ2 = 46.11, df = 3, P < 0.001) and at high altitude (χ2 = 12.85, df = 3, P = 0.005). There was also a significant association between the major malaria vector species and the trapping site at low (χ2 = 15.67, df = 4, P = 0.003), intermediate (χ2 = 29.72, df = 4, P < 0.001) and high (χ2 = 8.37, df = 2, P = 0.015) altitude as well as in the dry (χ2 = 57.91, df = 4, P < 0.001) and rainy (χ2 = 16.58, df = 4, P = 0.002) seasons.

Fig. 4
figure 4

Outdoor and indoor exposure of residents to host-seeking anophelines and biting behavior. a Anopheline density at different trapping sites. b Overall biting behavior. c Indoor biting behavior. d Outdoor biting behavior

In the dry season at low and intermediate altitudes, there was a significant association between the proportion of the major malaria vectors and the site of collection, with all except An. gambiae complex trapped indoors. No major malaria vector was caught at high altitude during the dry season, although very few anophelines (73) were trapped, mostly outdoors (62), during the survey. The major vector population also varied significantly with the site of collection during the dry season, with all mosquitoes except An. gambiae complex at low (χ2 = 33.01, df = 4, P < 0.001) and intermediate (χ2 = 29.11, df = 4, P < 0.001) altitude caught indoors.

Of the very few major malaria vectors (27) trapped at high altitude during the rainy season, most (12) of the An. gambiae complex (16) as well as the only An. hancocki were caught outdoors. Nevertheless, eight of the ten An. funestus were trapped indoors at high altitude in the rainy season. The biting cycle of Anopheles species overall as well as both indoors and outdoors was slightly similar for the major malaria vectors. The overall biting peaks for An. gambiae complex, An. funestus, An. nili, An. hancoki and An. moucheti were at 2–3 a.m., 5–6 a.m., 10–11 p.m., 9–10 p.m. and 1–2 a.m. respectively. However, the biting activities of An. gambiae complex were slightly different indoors and outdoors as its peak biting period was at 11 p.m. and 2–3 a.m./4–5 a.m. indoors and outdoors respectively (Fig. 4).

Infection and entomological inoculation rates

Fifty-two (16.6%) of the 313 anophelines tested for P. falciparum circumsporozoite antigen by ELISA at intermediate and low altitudes in both the rainy and dry season were infected (Table 2). The overall average infection rate was 20.2% (42/208) and 9.5 (10/105) during the rainy and dry seasons respectively. Of these, An. funestus was the most infectious in the area overall (28.1%, 16/57), with higher rates in the rainy (30.4%, 14/46) compared to the dry (18.2%, 2/11) season. Apart from the An. hancocki, which was not infectious in the dry season (n = 12), all the other anophelines carried P. falciparum circumsporozoite antigen, with 24 (16.4%) of the tested An. gambiae (s.s.) seropositive overall (Table 2). The infectivity rate of the vectors was higher overall at low (19.7%, 37/188) compared to intermediate altitude (12.0%, 15/125) and in the rainy compared to the dry season at low altitude (23.5%, 32/136 vs. 9.6%, 5/52) and at intermediate altitude (13.9%, 10/72 vs. 9.4%, 5/53).

Table 2 Infection and entomological inoculation rates of major anophelines in the Mount Cameroon region

The human biting and entomological inoculation rates are shown in Table 2. The average EIR in the study area was 2.08 infective bites per person per night (ib/p/n), almost two fold higher at low (2.45 ib/p/n) than at intermediate altitude (1.39 ib/p/n) and five times higher during the rainy (1.76 ib/p/n) compared to the dry season (0.34 ib/p/n). Anopheles gambiae (s.s.) had the highest inoculation rates averaging 1.33ib/p/n for the two seasons and up to 1.58 ib/p/n in the rainy season at low altitude.

Malaria parasite prevalence and Anopheles behavior

A total of 1233 participants in 6 communities were screened for Plasmodium spp. infection, the majority (990, 80.3%) of which were > 5 years of age. The overall prevalence of malaria parasite infection was 31.5%, higher in children at most 5 years of age (39.9%) compared to older participants (31.3%) (Table 3). The prevalence of malaria parasite infection was lowest in Mutengene and highest in Misellele, where almost half (48.6%) of the participants were shown to harbor the parasite. Incidentally, more than half of the children ≤ 5 years old in three out of the six communities (Misellele, Ombe and Tiko) were parasite positive (Table 3).

Table 3 Malaria parasite prevalence and Anopheles biting rate and parity status in different communities around the slopes of Mount Cameroon

Of the 31.1% (1573/5065) randomly selected and dissected Anopheles species across all three altitudinal zones and both seasons, 971 (61.7%) were parous (Fig. 5). There was a significant variation in the parity status across different communities overall (χ2 = 23.84, df = 8, P = 0.002) as well as in the rainy (χ2 = 56.04, df = 8, P < 0.001) and dry (χ2 = 23.78, df = 4, P < 0.001) season. Although the overall proportions of parous anophelines in the dry [317 (64.8%)] and rainy [654 (60.3%)] seasons were similar (χ2 = 2.88, df = 1, P = 0.090), there was a significant association between parity status and altitude (χ2 = 10.30, df = 2, P = 0.006), highest at low altitude (447, 64.8%) and lowest at high altitude (5, 31.2%). Parity status was associated with altitude in the rainy season (χ2 = 7.80, df = 2, P = 0.020) but not in the dry season (χ2 = 1.62, df = 1, P = 0.203). There was no relationship between Anopheles biting or parity rate and malaria parasite prevalence in the selected communities for which both were simultaneously assessed (Table 3). Biting rates varied from 3.5 in Ombe to 20.3 bite/person/night in Dibanda while the proportion of parous Anopheles mosquitoes ranged from 41.4% in Moliwe to 71.4% in Misellele, where the prevalence of malaria parasite infection was highest (Table 3). All (100%, 5/5) An. moucheti dissected were parous compared to 65.6% (257/392), 64.3% (552/859) and 49.5% (156/315) of An. funestus, An. gambiae complex and An. nili respectively. Parity rate varied with altitude (P = 0.006) but not with season (P = 0.090) and site of collection (P = 0.990). The highest proportions of parous An. gambiae (83.9%, 26/31) were recorded between 8 and 9 p.m. while up to 81.8% (18/22) and 83.3% (60/72) of An. funestus between 7 and 8 p.m. and 1–2 a.m. respectively and 61.9% (13/21) and all three (100%) An. nili between 9 and 10 p.m. and 5–6 a.m. respectively were parous.

Fig. 5
figure 5

Variation in the proportion of parous anophelines in the rainy and dry season along the slopes of Mount Cameroon. a Variation with altitude. Variation across sampling sites. No Anopheles species were caught at high altitude during the dry season


Malaria remains the leading cause of death to children < 5 years and pregnant women in most countries in SSA [1] with favourable malaria vectorial specificity and eco-climatic factors. Better understanding of the bio-ecology and spatiotemporal distribution of vectors is essential to design effective strategies for sustaining malaria control and elimination [32]. This study assessed key entomological parameters such as mosquito species composition, abundance, distribution and anopheline feeding behavior and biting activity in the rainy and dry season across different altitudinal zones 6 years following the intensification of vector control through the mass distribution of LLINs.

The study documents several different mosquito species and anopheline fauna around the forested slopes of Mount Cameroon, consistent with previous reports [9, 23, 24, 33]. The facts that Anopheles was the most abundant mosquito genera and several major Anopeles species were present all year round explain the high malaria burden in the region. The unequal distribution of the Anopheles species within the communities studied further confirms that mosquito occurrence is influenced by macro- and micro-environmental differences exhibited by different bio-ecological areas [24]. Culex spp. was the second most abundant mosquito genus in this study, in contrast to Amvongo-Adji et al. (2018) [9] who reported Mansonia as the second most common species. The increased density of Culicines, the primary host of several viruses, has implications for the transmission of West Nile fever, St. Louis encephalitis, Japanese encephalitis and lymphatic filariasis in the area.

The densities of both anophelines and culicines were greatly influenced by altitude and season, consistent with studies in the city of Yaoundé, Cameroon [34, 35], with the abundance of mosquitoes and anopheline fauna highest at low/intermediate altitudes and in the dry season. Previous studies around the slopes of Mount Cameroon have also reported more Anopheles species during the dry season [23, 36] compared to the rainy season, during which mosquito breeding is expected to be higher owing to increased rainfall and the presence of unwanted water bodies. This may accrue to the ever-enduring larval habitats in these villages but could also be explained by the ability of anopheline species to adapt and breed in several alternative water bodies. The Ndongo River that runs from Dibanda to Mutengene, for instance, is ever present while other streams run from Moliwe through Ombe, converging at the Tiko health district. The proportion of mosquitoes in the dry season may have been elevated by breeding sources left during the rainy season since some surveys were undertaken just at the end of the rains.

Consistent with previous reports [24], A. gambiae complex, An. funestus, An. nili, An. hancoki and An. moucheti were the first five major Anopheles species in decreasing order of prevalence. Of the anophelines whose densities were slightly lower than those of the major vectors, An. cinctus, An. longipalpis, An. kingi, An. ziemanni and An. marshalli are the proposed secondary vectors of malaria in the area. Anopheles ziemanni has been well characterized in several entomological studies as a major malaria vector in the northwestern region [37] or secondary vector elsewhere in the country [36] while this is the first report of An. cinctus as a possible secondary malaria vector in the southwestern part of the country.

Mosquito species of the An. gambiae complex are known to be heterogeneous in their biting behavior and could be endophilic, exophilic, anthropophilic or zoophagic, characteristics that enable the assessment of malaria transmission from vector biting rates. With up to 71.5% of the anopheline fauna caught outdoors, plenty of the Anopheles species still prefer resting outdoors as opposed to indoors as reported previously in the area and elsewhere [9, 24, 38]. Exophagic activity was the dominant behavior of the An. gambiae complex mosquitoes in this study, at a degree consistent with previous reports of mostly exophagous An. gambiae populations during the rainy season [6, 9]. However, An. nili and An. moucheti were mainly trapped indoors suggestive of a strongly endophagic behavior and contrary to previous studies [6, 9]. This modification in host-seeking behavior may have been induced by years of vector control through ITNs/LLINs and IRS and hence the need to change or augment these intervention strategies.

The overall biting activities of the major malaria vectors recorded in this study are consistent with others studies [9, 39], with members of the An. gambiae complex (2–3 am) and An. funestus group (5–6 am) biting late at night, between midnight and the early hours of the morning. This behavior clearly suggests increased biting activity when places are calm and the host is stable, coinciding with the resting periods (deep sleep) of their host. The slightly different indoor and outdoor biting peaks of An. gambiae complex may be due to the nocturnal habits of the hosts in the study area.

Most mosquitoes caught during both seasons were parous in accordance with previous studies [40]. In addition, most of the parous mosquitoes were trapped during the early evening hours. This coincides with the time Anopheles species start feeding and could be explained by the fact that the period corresponds to the time when an increased number of persons return home after diurnal activities. Overall, the transmission intensity was high, as shown by the parity rates, which also coincided with the high density of An. gambiae complex and other Anopheles species which are established as the primary malaria vector in the region and also in so many parts of Africa.

Multiple vectors are known to transmit malaria in the area [9, 23, 24], with the presence of An. gambiae complex together with An. funestus and An. hancocki at all altitudes as well as with An. funestus and An. nili at low and intermediate altitudes, consistent with the sympatric co-existence of these anophelines. However, the fact that only An. gambiae (s.s.) of the An. gambiae complex sibling species was identified following molecular characterization contradicts previous studies [9, 24]. It is possible that temporary rainfall-dependent larval habitats that could support breeding of An. gambiae (s.s.) [41] might have increased with increased amount of rainfall over the period, thus reducing potential An. coluzzii breeding sites [42].

All major vectors tested in this study were found to be infected by P. falciparum, with higher infectivity (and lower EIR) for An. funestus compared to An. gambiae (s.s.). Anopheles gambiae (s.s.) was clearly the most aggressive vector, with the higher EIR recorded, consistent with previous studies in the forested region of Cameroon [6, 23, 43]. Although higher infectivity of An. funestus relative to An. gambiae has been recorded previously in the area [44], this may accrue to the relatively fewer numbers of vector species trapped and tested during the survey, perhaps because of their low longevity, with most dying before the parasites can develop to infective stage [45, 46]. Also, higher EIRs obtained in rural areas were likely due to a high biting rate of An. gambiae (s.s.) and An. funestus. This should result from an exponential proliferation in breeding sites in rural settings, meeting optimum conditions for development, in contrast to urban areas where the larval habitats are generally quite polluted and therefore more conducive for the development of Culicines [47]. Transmission was shown to occur during both the dry and wet seasons, consistent with the perennial pattern in the area. Higher EIR in the rainy season and at lower altitude compared to the dry season and intermediate altitude is in line with previous reports of peak transmission during the heavy rains and at low altitude [21, 44]. Interventions such as IRS will thus be more impactful in the area if scheduled appropriately in line with varying transmission.

The fact that communities such as Misellele and Tiko with the highest malaria parasite prevalence in participants surveyed had the highest Anopheles fauna, biting and parity rates reaffirms the role of the vector in malaria morbidity. Targeted control interventions in some of these ‘hotspots’ may be indispensable in curbing the prevalence of the infection and incidence of disease in the area and region as a whole. However, the fact that almost half of the population of a community harbors the malaria parasite despite the tremendous and continuous deployment of LLINs, the main vector control strategy [48, 49] is concerning. This is because the massive scale up of LLIN, IRS and ITBN prevention tools between 2000 and 2016 resulted in substantial decrease of malaria morbidity and mortality across Africa (WHO 2018). It is possible that the emergence and rapid spread of malaria vectors resistant to pyrethroids, the most effective and rapidly acting single insecticide class used for impregnation of LLINs in the recent past [50] in several parts of Africa [51, 52] may have limited the impact of the intervention.


Anopheles gambiae complex, An. funestus, An. nili, An. hancoki and An. moucheti were the most common Anopheles species around the slope of Mount Cameroon while An. cinctus was identified for the first time as a possible secondary vector for malaria transmission in the area. The biting cycles of Anopheles species overall as well as both indoors and outdoors were slightly similar for the major malaria vectors. Most Anopheles species across all three altitudinal zones and both seasons were parous, with the highest parity rate in communities with the highest proportion of individuals with malaria parasite infections. Regular monitoring of the bionomics of local Anopheles vector species and targeted control interventions in the ‘hotspots’ is necessary to curb the prevalence of the infection and the incidence of disease in the area and region as a whole.

Availability of data and materials

All data are provided within the manuscript.



Comite national D’ethique de la research pour la sante humaine


Entomological inoculation rate


Enzyme-linked immunosorbent assay


Human biting rate


Human landing catches


Insecticide-treated nets


Long lasting insecticide-treated nets


Malaria rapid diagnostic test


Optical density


Polymerase chain reaction


Parity rate


Sporozoite index


Sub-Saharan Africa


  1. World Health Organization. World malaria report 2021. Geneva: World Health Organization; 2021 [cited 2022 Jan 18]. Available from:

  2. Foley DH, Wilkerson RC, Birney I, Harrison S, Christensen J, Rueda LM. MosquitoMap and the Mal-area calculator: new web tools to relate mosquito species distribution with vector borne disease. Int J Health Geogr. 2010;9:11.

    Article  PubMed  PubMed Central  Google Scholar 

  3. 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. Parasit Vectors. 2010;3:117.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Gillies M, Coetzee M. A supplement to the Anophelinae of Africa south of the Sahara (Afrotropical Region). undefined. 1987 [cited 2022 Jan 18]; Available from:

  5. Coetzee M, Hunt RH, Wilkerson R, Della Torre A, Coulibaly MB, Besansky NJ. Anopheles coluzzii and Anopheles amharicus, new members of the Anopheles gambiae complex. Zootaxa. 2013;3619:246–74.

    Article  PubMed  Google Scholar 

  6. Bigoga JD, Nanfack FM, Awono-Ambene PH, Patchoké S, Atangana J, Otia VS, et al. Seasonal prevalence of malaria vectors and entomological inoculation rates in the rubber cultivated area of Niete. South Region of Cameroon Parasit Vectors. 2012;5:197.

    Article  PubMed  Google Scholar 

  7. Fontenille D, Simard F. Unravelling complexities in human malaria transmission dynamics in Africa through a comprehensive knowledge of vector populations. Comp Immunol Microbiol Infect Dis. 2004;27:357–75.

    Article  PubMed  Google Scholar 

  8. Ayala D, Costantini C, Ose K, Kamdem GC, Antonio-Nkondjio C, Agbor J-P, et al. Habitat suitability and ecological niche profile of major malaria vectors in Cameroon. Malar J. 2009;8:307.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Amvongo-Adjia N, Wirsiy EL, Riveron JM, Chounna Ndongmo WP, Enyong PA, Njiokou F, et al. Bionomics and vectorial role of anophelines in wetlands along the volcanic chain of Cameroon. Parasit Vectors. 2018;11:471.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Garrett-Jones C. Prognosis for interruption of malaria transmission through assessment of the mosquito’s vectorial capacity. Nature. 1964;204:1173–5.

    Article  CAS  PubMed  Google Scholar 

  11. Pascual M, Ahumada JA, Chaves LF, Rodó X, Bouma M. Malaria resurgence in the East African highlands: temperature trends revisited. Proc Natl Acad Sci USA. 2006;103:5829–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Nmor JC, Sunahara T, Goto K, Futami K, Sonye G, Akweywa P, et al. Topographic models for predicting malaria vector breeding habitats: potential tools for vector control managers. Parasit Vectors. 2013;6:14.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Muturi EJ, Shililu J, Jacob B, Gu W, Githure J, Novak R. Mosquito species diversity and abundance in relation to land use in a riceland agroecosystem in Mwea, Kenya. J Vector Ecol J Soc Vector Ecol. 2006;31:129–37.

    Article  Google Scholar 

  14. Zimmerman R, Galardo A, Lounibos LP, Arruda M, Wirtz R. Bloodmeal hosts of Anopheles species (Diptera: Culicidae) in a Malaria-endemic area of the Brazilian Amazon. J Med Entomol. 2006;43:947.

    Article  PubMed  Google Scholar 

  15. Smallegange RC, Schmied WH, van Roey KJ, Verhulst NO, Spitzen J, Mukabana WR, et al. Sugar-fermenting yeast as an organic source of carbon dioxide to attract the malaria mosquito Anopheles gambiae. Malar J. 2010;9:292.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Briët OJT, Huho BJ, Gimnig JE, Bayoh N, Seyoum A, Sikaala CH, et al. Applications and limitations of centers for disease control and prevention miniature light traps for measuring biting densities of African malaria vector populations: a pooled-analysis of 13 comparisons with human landing catches. Malar J. 2015;14:247.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Beier J, Killeen G, Githure J. Short report: Entomologic inoculation rates and Plasmodium falciparum malaria prevalence in Africa. Am J Trop Med Hyg. 1999;61:109–13.

    Article  CAS  PubMed  Google Scholar 

  18. Antonio-Nkondjio C, Ndo C, Njiokou F, Bigoga JD, Awono-Ambene P, Etang J, et al. Review of malaria situation in Cameroon: technical viewpoint on challenges and prospects for disease elimination. Parasit Vectors. 2019;12:501.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Kilian A, Boulay M, Koenker H, Lynch M. How many mosquito nets are needed to achieve universal coverage? Recommendations for the quantification and allocation of long-lasting insecticidal nets for mass campaigns. Malar J. 2010;9:330.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Boussougou-Sambe ST, Eyisap WE, Tasse GCT, Mandeng SE, Mbakop LR, Enyong P, et al. Insecticide susceptibility status of Anopheles gambiae (sl) in South-West Cameroon four years after long-lasting insecticidal net mass distribution. Parasit Vectors. 2018;11:391.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Apinjoh TO, Anchang-Kimbi JK, Mugri RN, Tangoh DA, Nyingchu RV, Chi HF, et al. 2015. The Effect of Insecticide Treated Nets (ITNs) on Plasmodium falciparum Infection in Rural and Semi-Urban Communities in the South West Region of Cameroon. Culleton R, editor. PLOS ONE. 10:e0116300.

  22. Nyasa RB, Zofou D, Kimbi HK, Kum KM, Ngu RC, Titanji VPK. The current status of malaria epidemiology in Bolifamba, atypical Cameroonian rainforest zone: an assessment of intervention strategies and seasonal variations. BMC Public Health. 2015;15:1105.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Bigoga JD, Manga L, Titanji VP, Coetzee M, Leke RG. Malaria vectors and transmission dynamics in coastal south-western Cameroon. Malar J BioMed Central. 2007;6:5.

    Google Scholar 

  24. Wanji S, Tanke T, Atanga SN, Ajonina C, Nicholas T, Fontenille D. Anopheles species of the Mount Cameroon region: biting habits, feeding behaviour and entomological inoculation rates. Trop Med Int Health. 2003;8:643–9.

    Article  PubMed  Google Scholar 

  25. Achidi EA, Apinjoh TO, Mbunwe E, Besingi R, Yafi C, Wenjighe Awah N, et al. Febrile status, malarial parasitaemia and gastro-intestinal helminthiases in schoolchildren resident at different altitudes, in south-western Cameroon. Ann Trop Med Parasitol. 2008;102:103–18.

    Article  CAS  PubMed  Google Scholar 

  26. Apinjoh TO, Tata RB, Anchang-Kimbi JK, Chi HF, Fon EM, Mugri RN, et al. Plasmodium falciparum merozoite surface protein 1 block 2 gene polymorphism in field isolates along the slope of Mount Cameroon: a cross-sectional study. BMC Infect Dis. 2015;15:309.

    Article  PubMed  PubMed Central  Google Scholar 

  27. World Health Organization. Regional Office for South-East Asia. Pictorial identification key of important disease vectors in the WHO South-East Asia Region. World Health Organization. Regional Office for South-East Asia; 2020 [cited 2022 May 21]. Available from:

  28. Coetzee M. Key to the females of Afrotropical Anopheles mosquitoes (Diptera: Culicidae). Malar J. Malar J; 2020 [cited 2022 Jan 18];19. Available from:

  29. Detinova TS, Bertram DS, Organization WH. Age-grouping methods in diptera of medical importance, with special reference to some vectors of malaria. World Health Organization; 1962. Available from:

  30. Scott JA, Brogdon WG, Collins FH. Identification of single specimens of the Anopheles Gambiae complex by the polymerase chain reaction. Am J Trop Med Hyg. 1993;49:520–9.

    Article  CAS  PubMed  Google Scholar 

  31. Burkot T, Williams J, Schneider I. Identification of Plasmodium Falciparum-infected mosquitoes by a double antibody enzyme-linked immunosorbent assay *. Am J Trop Med Hyg. 1984;33:783–8.

    Article  CAS  PubMed  Google Scholar 

  32. Moiroux N, Damien GB, Egrot M, Djenontin A, Chandre F, Corbel V, et al. Human exposure to early morning anopheles funestus biting behavior and personal protection provided by long-lasting insecticidal nets. PLoS ONE. 2014;9:e104967.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Nkuo-Akenji T, Ntonifor N, Ndukum M, Kimbi H, Abongwa E, Nkwescheu A, et al. Environmental factors affecting malaria parasite prevalence in rural Bolifamba, South- West Cameroon. Afr J Health Sci. 2008 [cited 2022 Jan 18]:13. Available from:

  34. Doumbe-Belisse P, Ngadjeu Cs, Sonhafouo-Chiana N, Talipouo A, Djamouko-Djonkam L, Kopya E, et al. High malaria transmission sustained by Anopheles gambiae s.l. occurring both indoors and outdoors in the city of Yaoundé, Cameroon. Wellcome Open Res; 2018 [cited 2022 Jan 18];3. Available from:

  35. Lwetoijera DW, Kiware SS, Mageni ZD, Dongus S, Harris C, Devine GJ, et al. A need for better housing to further reduce indoor malaria transmission in areas with high bed net coverage. Parasit Vectors; 2013 [cited 2022 Jan 18]:6. Available from:

  36. Antonio-Nkondjio C, Kerah CH, Simard F, Awono-Ambene P, Chouaibou M, Tchuinkam T, et al. Complexity of the malaria vectorial system in Cameroon: contribution of secondary vectors to malaria transmission. J Med Entomol. 2006;43:1215–21.

    Article  PubMed  Google Scholar 

  37. Tabue RN, Nem T, Atangana J, Bigoga JD, Patchoke S, Tchouine F, et al. Anopheles ziemanni a locally important malaria vector in Ndop health district, north west region of Cameroon. Parasit Vectors. 2014;7:262.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Mojahedi AR, Safari R, Yarian M, Pakari A, Raeisi A, Edalat H, et al. Biting and resting behaviour of malaria vectors in Bandar-Abbas county, islamic Republic of Iran. East Mediterr Health J Rev Sante Mediterr Orient Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit. 2020;26:1218–26.

    Google Scholar 

  39. Kabbale FG, Akol AM, Kaddu JB, Onapa AW. Biting patterns and seasonality of anopheles gambiae sensu lato and Anopheles funestus mosquitoes in Kamuli District. Uganda Parasit Vectors. 2013;6:340.

    Article  PubMed  Google Scholar 

  40. Ngadjeu CS, Doumbe-Belisse P, Talipouo A, Djamouko-Djonkam L, Awono-Ambene P, Kekeunou S, et al. Influence of house characteristics on mosquito distribution and malaria transmission in the city of Yaoundé. Cameroon Malar J. 2020;19:53.

    Article  CAS  PubMed  Google Scholar 

  41. Abdoulaye D, Thierry B, Chandre C, Roch DK, Pierre K, Robert GT, et al. KDR mutation, a genetic marker to assess events of introgression between the molecular M and S forms of Anopheles gambiae (Diptera: Culicidae) in the tropical Savannah area of West Africa. J Med Entomol Entomol Soc Am. 2003;40:195–8.

    Article  CAS  Google Scholar 

  42. Wondji C, Simard F, Fontenille D. Evidence for genetic differentiation between the molecular forms M and S within the forest chromosomal form of Anopheles gambiae in an area of sympatry. Insect Mol Biol. 2002;11:11–9.

    Article  CAS  PubMed  Google Scholar 

  43. Manga L, Toto J, Goff GL, Brunhes J. The bionomics of Anopheles funestus and its role in malaria transmission in a forested area of southern Cameroon. undefined. 1997 [cited 2022 Apr 16];

  44. Eyong EEJ, Kengne-Ouafo AJ, Chounna PWN, Wanji S. Altitudinal variation in the parasitological and entomological indices of malaria around Mount Cameroon, South West region of Cameroon. J Parasitol Vector Biol. 2016;8:13.

    Google Scholar 

  45. Tchuinkam T, Simard F, Lélé-Defo E, Téné-Fossog B, Tateng-Ngouateu A, Antonio-Nkondjio C, et al. Bionomics of Anopheline species and malaria transmission dynamics along an altitudinal transect in Western Cameroon. BMC Infect Dis BioMed Central. 2009;10:119.

    Article  Google Scholar 

  46. Sarah C, Watson H, Allen A, Donna OM, Charlie I, Hugo B, et al. Changes in vector species composition and current vector biology and behaviour will favour malaria elimination in Santa Isabel province Solomon islands. Malar J BMC. 2011;10:287.

    Article  Google Scholar 

  47. Omumbo J, Guerra C, Hay S, Snow R. The influence of urbanisation on measures of Plasmodium falciparum infection prevalence in East Africa. Acta Trop. 2005;93:11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. 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.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. 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.

    Article  CAS  PubMed  Google Scholar 

  50. Sovi A, Govoétchan R, Ossé R, Koukpo CZ, Salako AS, Syme T, et al. Resistance status of Anopheles gambiae s.l. to insecticides following the, mass distribution campaign of long-lasting insecticidal nets (LLINs) in the plateau department, south-eastern Benin. Malar J. 2011;2020:19–26.

    Google Scholar 

  51. Aïkpon RY, Padonou G, Dagnon F, Ossè R, Ogouyemi Hounto A, Tokponon F, et al. Upsurge of malaria transmission after indoor residual spraying withdrawal in Atacora region in Benin. West Africa Malar J. 2020;19:3.

    PubMed  Google Scholar 

  52. Camara S, Koffi AA, Ahoua Alou LP, Koffi K, Kabran J-PK, Koné A, et al. Mapping insecticide resistance in Anopheles gambiae (s.l.) from Côte d’Ivoire. Parasit Vectors. 2018;11:19.

    Article  PubMed  PubMed Central  Google Scholar 

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We thank the participants from the various communities who made this study possible and the mosquito trappers, Chiefs, Quarter Heads, administrative and health personnel who assisted with this work. Special thanks to Ernest Oriero for his help with the map in Fig. 1.


AA and TOA received funding from the H3Africa through the Alliance for the African Academy of Science, grant no. H3AFull/17/008. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.

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PNK: coordinated the study, performed field and laboratory experiments and drafted the manuscript. EEE performed field survey and laboratory experiment. MNM performed field survey and provided substantial improvement in manuscript. LNT and VNN performed laboratory experiment. FZ performed laboratory experiment. EAA, DDSF, FC, AA and JDB contributed reagents and materials. TOA conceived, designed and coordinated the study, performed the statistical analysis and drafted the manuscript. All authors read and approved the final manuscript.

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Correspondence to Tobias O. Apinjoh.

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Kwi, P.N., Ewane, E.E., Moyeh, M.N. et al. Diversity and behavioral activity of Anopheles mosquitoes on the slopes of Mount Cameroon. Parasites Vectors 15, 344 (2022).

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  • Malaria
  • Anopheles
  • Diversity
  • Altitude
  • Infectivity