Kinya, FionaMutero, Clifford MainaSang, RosemaryOwino, EuniceRotich, GilbertOgola, Edwin O.Wondji, CharlesTorto, BaldwynTchouassi, David2022-11-022022-11-022022-05-03Kinya, F., Mutero, C.M., Sang, R. et al. Outdoor malaria vector species profile in dryland ecosystems of Kenya. Scientific Reports 12, 7131 (2022). https://doi.org/10.1038/s41598-022-11333-2.2045-2322 (online)10.1038/s41598-022-11333-2https://repository.up.ac.za/handle/2263/88101Outdoor biting by anopheline mosquitoes is one of the contributors to residual malaria transmission, but the profle of vectors driving this phenomenon is not well understood. Here, we studied the bionomics and genetically characterized populations of An. gambiae and An. funestus complexes trapped outdoors in three selected dryland areas including Kerio Valley, Nguruman and Rabai in Kenya. We observed a higher abundance of Anopheles funestus group members (n= 639, 90.6%) compared to those of the An. gambiae complex (n= 66, 9.4%) with An. longipalpis C as the dominant vector species with a Plasmodium falciparum sporozoite rate (Pfsp) of 5.2% (19/362). The known malaria vectors including An. funestus s.s. (8.7%, 2/23), An. gambiae (14.3%, 2/14), An. rivulorum (14.1%, 9/64), An. arabiensis (1.9%, 1/52) occurred in low densities and displayed high Pfsp rates, which varied with the site. Additionally, six cryptic species found associated with the An. funestus group harbored Pf sporozoites (cumulative Pfsp rate = 7.2%, 13/181). We detected low frequency of resistant 119F-GSTe2 alleles in An. funestus s.s. (15.6%) and An. longipalpis C (3.1%) in Kerio Valley only. Evidence of outdoor activity, emergence of novel and divergent vectors and detection of mutations conferring metabolic resistance to pyrethroid/DDT could contribute to residual malaria transmission posing a threat to efective malaria control.en© The Author(s) 2022. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.Outdoor malariaDryland ecosystemsArticle