Abstract
Background
Anopheles funestus
is one of the major malaria vectors in sub-Saharan Africa. In Senegal, it is found across nearly all biogeographical areas, often replacing
An. gambiae
s.l. and sustaining malaria transmission during the dry season. Despite its recognized role as a major vector, the specific contribution of
An. funestus
to malaria transmission in many malaria-endemic areas remains underexplored. This study aims to assess the contribution of
An. funestus
in malaria transmission in two health districts in Central Senegal.
Methods
Adult mosquitoes were collected from July 2018 to November 2019 in the health districts of Nioro (Ndramé Ndimb) and Ndoffane (Tawa Mboudaye) using Human Landing Catches (HLCs) and Pyrethrum Spray Catches (PSCs). Anopheline specimens were identified morphologically using standard dichotomous keys, with species confirmation performed by polymerase chain reaction (PCR).
Plasmodium falciparum
infection and blood meals sources were determined using Enzyme-Linked Immunosorbent Assay (ELISA) techniques.
Results
A total of 6,932
Anopheles
mosquitoes were collected. Of these, 73.7% (5,108/6,932) were identified as
An. funestus
, which was the predominant species at both study sites, with 1,364 specimens collected in Nioro and 3,744 in Ndoffane. Molecular analysis confirmed that
An. funestus
sensu stricto (s.s) was the only member of the
An. funestus
group recorded. In Ndramé Ndimb, the mean human biting rate and indoor resting density were 2.8 bites per person per night (b/p/n) and 9.0 females per room (f/r), respectively, compared to 12.4 b/p/n and 19.1 f/r in Tawa Mboudaye. The
P. falciparum
circumsporozoite rate was 0.3% in both villages, resulting in estimated entomological inoculation rates (EIRs) of 0.008 and 0.038 infected bites per person per night in Ndramé Ndimb and Tawa Mboudaye, respectively. The human blood index was relatively low, with only 22.3% (324/1,452) of
An. funestus
specimens found to have fed on humans.
Conclusions
This study highlights the predominance of
An. funestus
and its important role in sustaining residual malaria transmission in central Senegal, even where overall transmission intensity remains low.