Evidence map›Paper›PMID 41639761›Full record

ArticleBMC microbiology2026

The L1014F Kdr mutation is associated with a higher prevalence and load of the Plasmodium-blocking symbiont Microsporidia MB In Anopheles Gambiae s.l. In Benin.

Arthur Sovi, Minassou Juvenal Ahouandjinou, Rock Aïkpon, Gérard S Totongnon, Boulais Yovogan, Thomas Syme, Abdramane Dembélé, Come Zinsou Koukpo, Hermann Sagbohan, Razaki Ossè and 13 more

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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

23 authors.

Arthur SoviFaculty of Agronomy, University of Parakou, Parakou, Benin.
Minassou Juvenal AhouandjinouCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Rock AïkponNational University of Sciences, Technologies, Engineering and Mathematics, Abomey, Benin.
Gérard S TotongnonCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Boulais YovoganCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Thomas SymeDisease Control Department, Faculty of Infectious and Tropical Diseases, The London School of Hygiene and Tropical Medicine, London, UK.
Abdramane DembéléUniversity of Sciences, Techniques, and Technologies of Bamako, Bamako, Mali. mamadoukamanabdramane@gmail.com.
Come Zinsou KoukpoCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Hermann SagbohanCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Razaki OssèCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Andil Agbo-OlaCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Virgile GnanguenonGnanguenon Global Health Consulting, Porto-Novo, Bénin.
Ulrick ToffodjiLaboratory of Functional and Evolutionary Entomology, University of Liège, Gembloux Agro-Bio Tech, Gembloux, 5030, Belgium.
Rudy Caparros MegidoLaboratory of Functional and Evolutionary Entomology, University of Liège, Gembloux Agro-Bio Tech, Gembloux, 5030, Belgium.
Steve Zinsou HougbeCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
David Mahouton ZoungbédjiCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Alphonse Keller KonkonCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Jackie CookMRC International Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.
Germain Gil PadonouCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Natacha ProtopopoffDisease Control Department, Faculty of Infectious and Tropical Diseases, The London School of Hygiene and Tropical Medicine, London, UK.
Martin C AkogbétoCentre de Recherche Entomologique de Cotonou, Cotonou, Benin.
Louisa A Messenger *Disease Control Department, Faculty of Infectious and Tropical Diseases, The London School of Hygiene and Tropical Medicine, London, UK.
Constantin J Adoha *Centre de Recherche Entomologique de Cotonou, Cotonou, Benin.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe Plasmodium transmission-blocking endosymbiont Microsporidia MB was previously identified in Anopheles gambiae s.l., but its association with the carriage of the genotypes of the L1014F kdr mutation, as well as the ecological factors driving its geographical distribution remain understudied.

methodsAdult mosquitoes were field-collected using human landing catches (HLCs) across 60 villages in the Covè, Ouinhi, and Zangnanado communes of southern Benin. After morphological identification, a sub-sample of An. gambiae s.l. were molecularly speciated, and genotypied for the L1014F kdr mutation by Polymerase Chain Reaction (PCR). Enzyme-Linked Immunosorbent Assay (ELISA) and qPCR were also used to assess infection with Plasmodium falciparum sporozoites and Microsporidia MB, respectively. The environmental variables that drive the habitat suitability for Microsporidia MB were also assessed using Maximum Entropy (MaxEnt) modelling.

resultsThe An. gambiae complex (N = 1040) was composed of 93.7% An. coluzzii, 4.4% An. gambiae s.s., 0.2% An. gambiae s.s./coluzzii hybrids, while the rest failed to amplify. Infection prevalence with Microsporidia MB was 1.6% (95% CI: 0.7–3.3) in An. coluzzii and 2.2% (95% CI: 0.1–13.2) in An. gambiae s.s. The P. falciparum sporozoite rate was 2% (95% CI: 1.2–3.1, N = 974) in An. coluzzii, and null in An. gambiae s.s. (N = 46). None of the mosquitoes infected with Microsporidia MB were infected with P. falciparum. The frequency of the L1014F kdr mutation was 75.1% (95% CI: 73.1–76.9) in An. coluzzii and 91.3% (95% CI: 83.1–95.9) in An. gambiae s.s. Microsporidia MB was absent in kdr-SS mosquitoes but was present in low proportions in both kdr-RS and kdr-RR mosquitoes (1.9%, 95% CI: 0.6–5.1). The mean load of Microsporidia MB DNA was higher in kdr-RR (23.23 ng/µl, 95% CI: 18.77–28.48) compared to kdr-RS (10.13 ng/µl, 95% CI: 7.36–13.91) mosquitoes. The elevation and soil contributed to explain, at 78% and 20% respectively, the habitat suitability for Microsporidia MB.

conclusionIn this study, we demonstrated that An. gambiae s.l. mosquitoes bearing the L1014F kdr resistant allele was associated with a higher prevalence and load of Microsporidia MB than their susceptible counterparts. Moreover, the geographical distribution of Microsporidia MB was found to be influenced by certain environmental conditions, which warrant further large-scale investigations.

Indexed as

AnophelesMicrosporidiaAnimalsBeninFemaleGenotypeHumansMutationPlasmodium falciparumPrevalenceSymbiosisL1014F Kdr mutationMicrosporidia MBPlasmodium

Identifiers

PMID41639761
PMCPMC12964893

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.