Molecular characterization and genotype distribution of thioester‑containing protein 1 gene in Anopheles gambiae mosquitoes in western Kenya

dc.contributor.authorOnyango, S.A.
dc.contributor.authorOchwedo, K.O.
dc.contributor.authorMachani, M.G.
dc.contributor.authorOlumeh, J.O.
dc.contributor.authorAfrane, Y.A.
dc.contributor.authorDebrah, I.
dc.contributor.authoret al.
dc.date.accessioned2023-03-13T16:19:44Z
dc.date.available2023-03-13T16:19:44Z
dc.date.issued2022
dc.descriptionResearch articleen_US
dc.description.abstractAbstract Background: Evolutionary pressures lead to the selection of efficient malaria vectors either resistant or susceptible to Plasmodium parasites. These forces may favour the introduction of species genotypes that adapt to new breeding habitats, potentially having an impact on malaria transmission. Thioester-containing protein 1 (TEP1) of Anopheles gambiae complex plays an important role in innate immune defenses against parasites. This study aims to characterize the distribution pattern of TEP1 polymorphisms among populations of An. gambiae sensu lato (s.l.) in western Kenya. Methods: Anopheles gambiae adult and larvae were collected using pyrethrum spray catches (PSC) and plastic dippers respectively from Homa Bay, Kakamega, Bungoma, and Kisumu counties between 2017 and 2020. Collected adults and larvae reared to the adult stage were morphologically identified and then identified to sibling species by PCR. TEP1 alleles were determined in 627 anopheles mosquitoes using restriction fragment length polymorphismspolymerase chain reaction (RFLP-PCR) and to validate the TEP1 genotyping results, a representative sample of the alleles was sequenced. Results: Two TEP1 alleles (TEP1*S1 and TEP1*R2) and three corresponding genotypes (*S1/S1, *R2/S1, and *R2/R2) were identified. TEP1*S1 and TEP1*R2 with their corresponding genotypes, homozygous *S1/S1 and heterozygous *R2/S1 were widely distributed across all sites with allele frequencies of approximately 80% and 20%, respectively both in Anopheles gambiae and Anopheles arabiensis. There was no significant difference detected among the populations and between the two mosquito species in TEP1 allele frequency and genotype frequency. The overall low levels in population structure (FST = 0.019) across all sites corresponded to an effective migration index (Nm = 12.571) and low Nei’s genetic distance values (< 0.500) among the subpopulation. The comparative fixation index values revealed minimal genetic differentiation between species and high levels of gene flow among populations.Conclusion: Genotyping TEP1 has identified two common TEP1 alleles (TEP1*S1 and TEP1*R2) and three corresponding genotypes (*S1/S1, *R2/S1, and *R2/R2) in An. gambiae s.l. The TEP1 allele genetic diversity and population structure are low in western Kenya. Keywords: Anopheles gambiae, Thioester-containing protein 1, Genetic diversity, Population structure, Signature of selection, Malaria transmissionen_US
dc.identifier.otherhttps://doi.org/10.1186/s12936-022-04256-w
dc.identifier.urihttp://ugspace.ug.edu.gh:8080/handle/123456789/38760
dc.language.isoenen_US
dc.publisherMalaria Journalen_US
dc.subjectAnopheles gambiaeen_US
dc.subjectThioester-containing protein 1en_US
dc.subjectGenetic diversityen_US
dc.subjectPopulation structureen_US
dc.subjectSignature of selectionen_US
dc.subjectMalaria transmissionen_US
dc.titleMolecular characterization and genotype distribution of thioester‑containing protein 1 gene in Anopheles gambiae mosquitoes in western Kenyaen_US
dc.typeArticleen_US

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