Complex non-falciparum transmission and widespread insecticide resistance in Penka-Michel, a hyperendemic malaria focus of the Cameroon highlands.

Authors

Belinda Claire Kiam, Ibrahima Ibrahima, Jean Arthur Mbida Mbida, Aline Gaëlle Bouopda-Tuedom, Luc Abate, Samuel J White, Charlène Tina Nanssong-Vomo, Brigitte Fotso Tumamo, Isabelle Morlais, Lawrence Ayong, Jessica T Lin, Innocent Mbulli Ali, Jonathan J Juliano, Rhoel R Dinglasan, Sandrine Eveline Nsango

Published in

Research square. May 25, 2026. Epub May 25, 2026.

Abstract

A 12-month longitudinal entomological study (September 2023-August 2024) in the Western Highlands of Cameroon (Penka-Michel) investigated malaria transmission dynamics and insecticide resistance markers, including knockdown resistance mutations (L1014F, N1575Y) and metabolic resistance genes (G119S-Ace1, E205D-CYP6P3, L119F-GSTe2, CYP6P9a/b). Malaria transmission has depended on the coexistence of three species: Anopheles funestus (43.7%), Anopheles gambiae (42.9%), and Anopheles ziemanni (13.5%). The site was hyperendemic with annual EIR of 839.5 infective-bites/human/night. Plasmodium falciparum predominated (70.2%), yet a significant non-falciparum burden was observed (P. malariae, 27.5%; P. ovale, 22.1%). An. funestus was the principal driver (IR=7.8%, EIR=0.9 infective bites/human/night), with P. falciparum and P. ovale curtisi peaking in the later rainy season (November), while An. gambiae (IR=5.4%; EIR=0.6 ib/h/n) vectored P. malariae (14.5%) primarily, followed by a sustained peak in the dry season (January). Widespread insecticide resistance was observed, with resistant homozygotes detected in 70% of infected mosquito samples. We observed associations of L119F-GSTe2 mutations with P. ovale curtisi transmission (IRR=1.15, p=0.03), and L1014F-kdr with P. malariae (IRR=2.2, p=0.04). These dynamics highlight a complex multi-species system in which seasonal vector efficiency and insecticide resistance sustain hyperendemicity of the often-overlooked non-falciparum malaria species.

PMID:
42245801
Bibliographic data and abstract were imported from PubMed on 02 Oct 2026.

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