Abstract

BackgroundMost malaria vectors belong to species complexes. Sibling species often exhibit divergent behaviors dictating the measures that can be deployed effectively in their control. Despite the importance of the Anopheles funestus complex in malaria transmission in sub-Saharan Africa, sibling species have rarely been identified in the past and their vectoring potential remains understudied.MethodsWe analyzed 1149 wild-caught An. funestus (senso lato) specimens from 21 sites in Kenya, covering the major malaria endemic areas including western, central and coastal areas. Indoor and outdoor collection tools were used targeting host-seeking and resting mosquitoes. The identity of sibling species, infection with malaria Plasmodium parasites, and the host blood meal sources of engorged specimens were analyzed using PCR-based and sequencing methods.ResultsThe most abundant sibling species collected in all study sites were Anopheles funestus (59.8%) and Anopheles rivulorum (32.4%) among the 1062 successfully amplified specimens of the An. funestus complex. Proportionally, An. funestus dominated in indoor collections whilst An. rivulorum dominated in outdoor collections. Other species identified were Anopheles leesoni (4.6%), Anopheles parensis (2.4%), Anopheles vaneedeni (0.1%) and for the first time in Kenya, Anopheles longipalpis C (0.7%). Anopheles funestus had an overall Plasmodium infection rate of 9.7% (62/636), predominantly Plasmodium falciparum (59), with two infected with Plasmodium ovale and one with Plasmodium malariae. There was no difference in the infection rate between indoor and outdoor collections. Out of 344 An. rivulorum, only one carried P. falciparum. We also detected P. falciparum infection in two non-blood-fed An. longipalpis C (2/7) which is the first record for this species in Kenya. The mean human blood indices for An. funestus and An. rivulorum were 68% (93/136) and 64% (45/70), respectively, with feeding tendencies on a broad host range including humans and domestic animals such as cow, goat, sheep, chicken and pig.ConclusionsOur findings underscore the importance of active surveillance through application of molecular approaches to unravel novel parasite-vector associations possibly contributed by cryptic species with important implications for effective malaria control and elimination.

Highlights

  • Most malaria vectors belong to species complexes

  • The major African malaria vectors belong to two species complexes: Anopheles gambiae and Anopheles funestus [4, 5]

  • At the sites in Ahero, Tana Delta, Kapkuikui, collections were limited to outdoors only using Centers for Disease Control and Prevention (CDC) light traps (10) while in Kamnarok, Usenge, Mageta, Njoro and Kiwalwa, collections were limited to indoors using pyrethrum spray catches (PSC) or backpack aspiration (ASP) targeting resting mosquitoes

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Summary

Introduction

Most malaria vectors belong to species complexes. Despite the importance of the Anopheles funestus complex in malaria transmission in sub-Saharan Africa, sibling species have rarely been identified in the past and their vectoring potential remains understudied. Recent reports of novel Plasmodium falciparum sporozoite associations in An. vaneedeni [7], as well as yet-to-be-identified species [8, 9], suggest the possibility of adaptive changes in vector systems among the group. This underscores the importance of active surveillance of vector populations for potential emerging threats as malaria is being controlled

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