Behavioural divergence of sympatric Anopheles funestus populations in Burkina Faso
© Guelbeogo et al.; licensee BioMed Central Ltd. 2014
Received: 21 January 2014
Accepted: 20 February 2014
Published: 24 February 2014
In Burkina Faso, two chromosomal forms of the malaria vector Anopheles funestus, Folonzo and Kiribina, are distinguished by contrasting frequencies of shared polymorphic chromosomal inversions. Sympatric and synchronous populations of Folonzo and Kiribina mate assortatively, as indicated by a significant deficit of heterokaryotypes, and genetic associations among inversions on independently segregating chromosome arms. The present study aimed to assess, by intensive longitudinal sampling, whether sympatric Folonzo and Kiribina populations are characterized by behavioural differences in key malaria vectorial parameters.
The study was conducted in two adjacent villages near Ouagadougou, in the dry savanna of central Burkina Faso. Mosquito adult resting behaviour of both forms was compared based on parallel indoor/outdoor collections across six breeding seasons; 8,235 fully karyotyped samples of half-gravid females were analysed in total. Additionally, indoor/outdoor human biting behaviour, host selection, and Plasmodium falciparum sporozoite rate was assessed and compared between chromosomal forms.
The Kiribina form was numerically predominant in the area. However, the Folonzo form was significantly over-represented in indoor resting collections and showed stronger post-prandial endophily, while Kiribina predominated outdoors. Neither form was statistically distinguishable in human biting behaviour, and both were more likely to seek human blood meals indoors than outside. The human blood index and sporozoite rate were comparably high in both chromosomal forms in indoor collections (>89% and >8%, respectively).
Both Kiribina and Folonzo chromosomal forms are formidable malaria vectors in Burkina Faso. However, the significantly greater tendency for the Kiribina form to rest outdoors despite its pronounced anthropophily suggests that uniform exposure of the overall An. funestus population to indoor-based vector control tools cannot be expected; Kiribina is more likely to evade indoor interventions and escape unharmed outdoors, reducing the efficacy of malaria control. Accordingly, more efficient methods to detect Kiribina and Folonzo, and a more complete understanding of their distribution and behaviour in Africa are advocated.
The malaria vectorial system in tropical Africa is dominated by four species of major importance, Anopheles gambiae, Anopheles coluzzii, Anopheles arabiensis and Anopheles funestus, which are broadly codistributed across much of tropical Africa in close association with humans[1, 2]. The first three species belong to the same cryptic species complex (the An. gambiae complex) whose members cannot be distinguished morphologically at any developmental stage, although they differ in aquatic larval ecology and adult behaviours relevant to malaria transmission and control (e.g., degree of anthropophily and tendency to blood-feed or rest indoors)[3, 4]. Anopheles funestus and its presently recognized closest relatives are classified into a group and subgroup[5, 6] rather than a species complex, owing to slight morphological distinctions mainly at immature stages. However, further cryptic taxonomic complexities within the group have recently come to light and more can be anticipated as An. funestus research emerges from a period of neglect[7–11]. Malaria transmission by the Funestus Subgroup is overwhelmingly attributed to An. funestus sensu stricto, owing to its strong preference for human blood meals (see reviews by[7, 12]).
Anopheles funestus s.s. is characterized by abundant genetic polymorphism, exemplified by at least 17 chromosomal re-arrangements segregating within and among populations across Africa[13, 14]. Although this species is generally considered to be uniformly anthropophilic and endophilic throughout its range, complex and incompletely understood patterns of population structure based on cytogenetic and DNA markers have been detected[15–20]. In particular, two chromosomal forms designated “Folonzo” and “Kiribina” have been described in West Africa. First discovered in Burkina Faso and most intensively characterized in that country, Folonzo and Kiribina populations carry markedly different frequencies of shared polymorphic chromosomal inversions, mainly involving arm 3R[16, 17]. In localities where the chromosomal forms are synchronous and stably sympatric across successive breeding seasons and years, there are highly significant departures from Hardy Weinberg equilibrium and significant genetic associations among physically unlinked inversion systems; alternative homokaryotypes are more frequent than expected under random mating, and there are significant deficits of heterozygotes in virtually all population samples, consistent with assortative mating by form[16, 17].
Neither inversions nor inversion combinations are diagnostic taxonomic characters. However, the Kiribina form is predominantly homokaryotypic for the standard chromosomal arrangements, while Folonzo, the more chromosomally polymorphic taxon, carries high frequencies of inversions 3Ra and 3Rb, and presumably corresponds to An. funestus from East Africa, where Kiribina has not been recorded. Strongly reminiscent of the chromosomal forms of An. gambiae, these alternative karyotypes show cyclical patterns of seasonal variation in relative abundance linked to temperature and rainfall, likely reflecting differences in geographic distribution modulated by larval habitat utilization. Although direct evidence is lacking, the Folonzo form is associated with natural larval habitats such as marshes, while Kiribina is associated with larval habitats created by the practice of agriculture, notably rice fields. Molecular genetic studies using mtDNA and microsatellite markers revealed very slight but significant divergence between sympatric samples of Folonzo and Kiribina across Burkina Faso, although nuclear divergence was not genome-wide and could be explained by loci on chromosome 3R inside and outside inversions[23, 24]. These data are suggestive of an incipient process of ecological divergence and lineage splitting, similar to, but less advanced than, that responsible for the divergence of An. coluzzii and An. gambiae (formerly recognized as chromosomal or molecular forms[25, 26]).
Previous studies in Burkina Faso and Senegal have reported similarly high rates of anthropophily and comparable Plasmodium falciparum infection rates in sympatric Folonzo and Kiribina populations[23, 24, 27]. However, there were indications of differences in indoor resting behaviour, leading to the suggestion that the Kiribina form may be more easily diverted to outdoor resting and biting, particularly in localities where alternative hosts such as cattle outnumber the local human population. If the ecological and genetic heterogeneities between Folonzo and Kiribina indeed extend to behavioural differences of importance to malaria epidemiology and control, these vectorial differences must be understood more deeply. Toward that end, resting and biting behaviour were assessed separately for sympatric and synchronous Folonzo and Kiribina populations in the rural villages of Kuiti and Koubri near Ouagadougou, Burkina Faso. Observations spanned six breeding seasons and 8,235 fully karyotyped Folonzo and Kiribina adult half-gravid females.
The study was carried out in the arid Sudan savanna vegetation belt of West Africa, in adjacent rural villages located 35 km south of Ouagadougou, the capital of Burkina Faso. Koubri (12°11′54 N; 1°23′43 W) and Kuiti (12°11′36 N; 1°23′11 W) lie about 1 km apart on opposite margins of an artificial lake bordered by permanent swamps. A detailed map and additional information about the study area can be found elsewhere[17, 24]. In this region, the An. funestus breeding season commences at the end of the rainy season (September), extends throughout the cool dry season (October-February), and ends in April, mid-way through the hot dry season (March-May). Folonzo peaks in relative abundance following the rains, in October-December.
Chromosomal form identification
Adult Funestus Group females were sorted morphologically in the field under a dissecting microscope. Ovaries from females at the appropriate gonotrophic stage were immediately dissected and preserved by individual mosquito in 1.5 ml microcentrifuge tubes using Carnoy’s fixative (ethanol:glacial acetic acid, 3:1), while the associated carcass was placed in a correspondingly labelled microcentrifuge tube with desiccant. Molecular taxonomic identification of An. funestus based on DNA extracted from the carcass was performed with a modified rDNA-based PCR assay. Ovaries in Carnoy’s were held on ice until they could be stored at -20°C for later polytene chromosome analysis. Polytene chromosomes of An. funestus were spread and examined under a phase-contrast microscope. Karyotypes were assigned using the cytogenetic map of Sharakhov et al.. Of all karyotyped samples, 92% were successfully scored for all inversions. Chromosomal form assignment followed the deterministic algorithm of Guelbeogo et al.. Using a probabilistic assignment test as an alternative method of classification of karyotypes sampled from the same localities as the present study, these authors estimated the rate of mis-classification to be very low, about 0.7%.
An estimate of the odds of adult females of the Folonzo or Kiribina forms resting indoors was calculated by comparing the relative abundance of each form in resting collections that were conducted indoors and outdoors in parallel. Indoor resting mosquitoes were sampled in the afternoon inside multiple huts and compounds in both villages, by insecticide spray-sheet catches (ISC) three times per week; mosquitoes resting outdoors in the villages were sampled at least twice weekly from four Muirhead-Thompson style pit-shelters with manual aspirators. In addition, an estimate of the odds of post-prandial indoor-resting by outdoor-biting Folonzo or Kiribina was calculated based on blood meal identifications performed on indoor/outdoor-resting collections made between 2005–2007 (described below). As cattle do not share the domestic environment with humans in the study area, mosquitoes with exclusively bovine blood meals must have fed outdoors on cattle. Accordingly, the numbers of each form that fed solely on cattle were compared between indoor-resting (ISC) and outdoor-resting (PIT) collections from the same time period.
Human biting behaviour
Human biting behaviour of Folonzo and Kiribina was assessed by human landing catches (HLC). Two teams of trained collectors worked in two different compounds in eight-hour shifts (21:00–05:00), twice per week from October 2002-January 2003. Each team consisted of a pair of collectors, one of whom performed an indoor landing catch while the other did the same outdoors, reversing positions on a subsequent night to control for collector-specific effects. To identify the chromosomal form of host-seeking An. funestus captured by HLC, mosquitoes were blood-fed on rabbits the same night of capture, and held in the insectary until they reached the stage of ovarian development appropriate for polytene chromosome analysis.
Blood meal identification and Plasmodium falciparum detection
Samples of blood-fed mosquitoes collected in the 2005–2006 and 2006–2007 breeding seasons were cut transversely between the thorax and the abdomen. The origin of the blood meal (human, bovine, mixed) in the posterior portion was identified by an enzyme-linked immunosorbent assay (ELISA) using specific monoclonal antibodies. The presence of P. falciparum circumsporozoite protein (CSP) in the anterior portion (head + thorax) also was detected by ELISA in these samples.
The human blood index (HBI) of each chromosomal form was calculated as the proportion of human and mixed blood meals identified relative to all blood meals identified by ELISA in samples of that form. The sporozoite rate of each form was calculated as the proportion of mosquitoes in a sample that were positive for P. falciparum CSP by ELISA. The odds ratio (OR;), the ratio of the odds of an event occurring in one group to the odds of it occurring in another, was used to compare vectorial parameters between the chromosomal forms. The precision of the OR was estimated using the 95% confidence interval (CI). P-values are reported based on the Pearson Chi-square test of association for 2×2 contingency tables, with P <0.05 considered as significant.
The study protocols were reviewed and approved by the institutional health ethical review board of Burkina Faso. Informed consent was obtained from participants.
Resting behaviour of Anopheles funestus chromosomal forms in Burkina Faso
Post-prandial resting behaviour of outdoor-feeding Anopheles funestus chromosomal forms in Burkina Faso (2005–2007)
Human biting behaviour of Anopheles funestus chromosomal forms in Burkina Faso (2002–2003)
Host selection of Anopheles funestus chromosomal forms in Burkina Faso (2005–2007)
Human + Mixed
191 + 21 (212)
232 + 11 (243)
Human + Mixed
2 + 1 (3)
13 + 25 (38)
Plasmodium falciparum sporozoite rate of Anopheles funestus chromosomal forms in Burkina Faso (2005–2007)
Intensive longitudinal sampling of An. funestus from adjacent villages in the Sudan savanna of Burkina Faso, West Africa, affirms and extends the previous findings by Costantini et al. of behavioural divergence between sympatric and synchronous chromosomal forms known as Folonzo and Kiribina. The high rate of anthropophagy by both forms (>89% of indoor samples), coupled with comparably high rates of P. falciparum infection (>8% of indoor samples) emphasize the fact that Folonzo and Kiribina both are formidable malaria vectors in this part of Africa. The Kiribina form often outnumbered Folonzo. Yet, Folonzo was disproportionately represented in indoor versus outdoor resting samples and was more inclined to post-prandial endophily, while Kiribina was over-represented outdoors in pit shelters. This suggests that the overall An. funestus population is not uniformly exposed to indoor-based malaria interventions such as insecticide-treated nets and house spraying by residual insecticides, and that those indoor interventions are less effective against the Kiribina form.
There is precedence for chromosomal inversion-associated heterogeneity in mosquito resting behaviour in the West African savanna, uncovered by Coluzzi and colleagues through polytene chromosome analysis of An. gambiae and An. arabiensis populations during the Garki Project in Nigeria[3, 32]. Such behavioural heterogeneity was responsible for the failure to interrupt malaria transmission during the course of the Project, despite rigorous insecticide applications and simultaneous administration of anti-malarial drugs to the human population. Indeed, there are hints that this same phenomenon has been witnessed previously with respect to An. funestus in the West African savanna, where Kiribina co-exists with Folonzo. In the absence of Kiribina in eastern and southern Africa, historical house spraying campaigns not only locally eliminated An. funestus, but the effect was maintained for several years following the cessation of spraying, due to the apparent inability of An. funestus to recolonize some areas. Likewise, An. funestus was eliminated from humid forest and degraded forest areas in West Africa where malaria is meso- or hypo-endemic, an environment where Folonzo is predicted to dominate[16, 35–37]. However, in the savannas of West Africa where malaria is holo- or hyperendemic, similar historical indoor spraying campaigns failed to eliminate the species. Exophilic populations persisted which, despite marked anthropophily, continued to feed outdoors on cattle as well as humans, and also entered sprayed houses to bite humans, but escaped unharmed to rest outdoors. These exophilic populations likely represented what would now be recognized as the Kiribina form of An. funestus.
More recently, further epidemiologically significant behavioural heterogeneities in An. funestus from the same biogeographical area have been recognized following large-scale implementation of indoor-based vector control interventions. After mass deployment of insecticide-treated bed nets, the biting cycle of An. funestus shifted from its usual peak between 02:00 and 04:00 toward a later peak between dawn and early morning hours, when human hosts are less likely to be protected by nets. Unfortunately, it is not known whether this behavioural shift was associated with a change in the chromosomal composition of the local An. funestus population.
The Folonzo and Kiribina chromosomal forms have been well characterized across several hundred kilometres and all ecozones of Burkina Faso[16, 23]. However, their broader geographical distribution in Africa is poorly known. Certainly, they occur as far west as Senegal[15, 27, 39]. A recent study of sympatric populations of these forms, the first of its kind in Senegal, found stable co-existence of the forms across three successive breeding seasons and concluded, in accord with the present study, that Kiribina predominated, and rates of anthropophagy and sporozoite infection were comparable between forms, although both metrics were considerably lower in Senegal (~30 and ~3%, respectively) than they were in Burkina Faso. Unfortunately, due to very low outdoor resting sample size (five total, of which only three could be identified chromosomally as Kiribina), indoor/outdoor resting behaviour was difficult to compare between forms, and thus, between studies. Cameroon is the most easterly country in which An. funestus chromosomal forms have been reported, but their vectorial heterogeneities (if any) are essentially uncharacterized. Available cytogenetic data suggest that these forms are largely allopatric in Cameroon, with Folonzo occurring in the mesic, forested south and Kiribina to the north in the dry savannas, except for a central contact zone at the forest-savanna transition, where stable sympatric co-existence of the two forms has not been clearly resolved[35–37]. In another parallel with the An. gambiae chromosomal forms, there is no evidence for the co-occurrence of An. funestus chromosomal forms in East Africa; existing populations of An. funestus in eastern Africa are hypothesized to be allied with the Folonzo form, although that proposal has yet to be tested genetically.
Ample indication now exists of the practical importance of population structure and behavioural heterogeneities hidden within An. funestus, for malaria epidemiology and control in West Africa, if not beyond. In this light, the dearth of information about the wider geographic distribution and associated bionomics and vectorial parameters of the Folonzo and Kiribina forms is a problem that must be remedied as a matter of priority. The polytene chromosomes of An. funestus are considerably more difficult to spread and analyse than those of An. gambiae, a factor that has impeded past research on An. funestus. The demanding and specialized task of polytene chromosome-based identification, the restrictive sex and life stage from which favourable chromosomes are obtained, and the absence of any known DNA-based diagnostics to distinguish the chromosomal forms, all but prohibit deeper field investigation of Folonzo and Kiribina, particularly studies of their larval biology which is presumed to be a driver of their ecological and behavioural divergence. Genome sequencing of An. gambiae in 2002, and the discovery of molecular forms of An. gambiae detectable by a simple PCR assay, greatly transformed understanding of the complexities of An. gambiae population structure and its impacts on malaria transmission. Recent whole genome sequencing and a newly available reference assembly for An. funestus offer a platform that will support a more detailed understanding of An. funestus population structure across Africa, as well as an efficient means to discover genomic sequences potentially useful for molecular taxonomy of Folonzo and Kiribina.
For decades, patterns of chromosomal inversion polymorphism have guided discovery of population structure and even species boundaries hidden inside otherwise morphologically indistinguishable groups of anopheline mosquitoes i.e.,[16, 43–46]. Such an association of inversions with population substructure could be an incidental consequence of genetic drift owing to reduced gene flow, or the result of demographic history, but the observation that polymorphic inversions are often clinally distributed with respect to environmental gradients and subject to repeating seasonal fluctuations in frequency suggests that they are subject to strong selective forces. In anopheline mosquitoes, as in many animal and plant species, chromosomal inversions are implicated in local adaptation to environmental heterogeneities[35, 48–51]. To the extent that speciation may occur as a by-product of adaptive divergence, chromosomal inversions may also be instrumental in lineage splitting, as proposed by Coluzzi for anopheline mosquitoes. That Kiribina and Folonzo forms are characterized by alternative arrangements of chromosomal inversions, and that these alternative arrangements shift in relative frequency according to geography, season, and larval habitat availability, suggests a direct role for chromosomal rearrangements in adaptation to heterogeneous and changing environments (see also[35, 50]). Thus, beyond simply serving as markers for epidemiologically relevant population structure, alternative chromosomal arrangements some how condition different physiological and behavioural responses to the environment. A mechanistic understanding of what the adaptations are and how they evolved could prove instrumental in predicting how An. funestus may be capable of responding to future environmental challenges, including anthropogenic changes to climate and landscape, and exposure to new means of vector control.
We thank the inhabitants of Koubri and Kuiti for their collaboration, and the entomological team of CNRFP for their efforts during the course of this study. M A Yameogo, O Grushko and D Boccolini were instrumental in polytene chromosome analysis. This research was financially supported by grant R01 AI48842 from the US National Institutes of Health to NJB; re-entry grant A 41413 to WG from WHO/TDR; and WHO MIM/TDR grant 50090 to NFS.
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