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Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII

SIMPLE SUMMARY: An. funestus is a major vector of human malaria and is responsible for high transmissions in sub-Saharan Africa. In the malaria endemic region of western Kenya, it has adapted and colonized different ecological niches owing to its high resistance to pyrethroids and changing breeding...

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Autores principales: Debrah, Isaiah, Ochwedo, Kevin O., Otambo, Wilfred O., Machani, Maxwell G., Magomere, Edwin O., Onyango, Shirley A., Zhong, Daibin, Amoah, Linda E., Githeko, Andrew K., Afrane, Yaw A., Yan, Guiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052146/
https://www.ncbi.nlm.nih.gov/pubmed/36975958
http://dx.doi.org/10.3390/insects14030273
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author Debrah, Isaiah
Ochwedo, Kevin O.
Otambo, Wilfred O.
Machani, Maxwell G.
Magomere, Edwin O.
Onyango, Shirley A.
Zhong, Daibin
Amoah, Linda E.
Githeko, Andrew K.
Afrane, Yaw A.
Yan, Guiyun
author_facet Debrah, Isaiah
Ochwedo, Kevin O.
Otambo, Wilfred O.
Machani, Maxwell G.
Magomere, Edwin O.
Onyango, Shirley A.
Zhong, Daibin
Amoah, Linda E.
Githeko, Andrew K.
Afrane, Yaw A.
Yan, Guiyun
author_sort Debrah, Isaiah
collection PubMed
description SIMPLE SUMMARY: An. funestus is a major vector of human malaria and is responsible for high transmissions in sub-Saharan Africa. In the malaria endemic region of western Kenya, it has adapted and colonized different ecological niches owing to its high resistance to pyrethroids and changing breeding environments. The genetic basis of its ecological adaptations to various settings, which could enrich our understanding of how the population is structured or segregated, is poorly understood. This study sought to evaluate the population structure and genetic diversity of Anopheles funestus in different landscapes in western Kenya. To achieve this, the cytochrome oxidase subunit II gene (COII) was PCR-amplified and sequenced. This study revealed an excess of low-frequency variations that are likely due to population expansion or possibly negative selection pressure. Our findings could serve as a guide for future genomic research to facilitate the design of control strategies. ABSTRACT: The mitochondrial marker, COII, was employed to assess the genetic structure and diversity of Anopheles funestus, a very important malaria vector in Africa that adapt and colonize different ecological niches in western Kenya. Mosquitoes were collected using mechanical aspirators in four areas (Bungoma, Port Victoria, Kombewa, and Migori) in western Kenya. Following morphological identification, PCR was used to confirm the species. The COII gene was amplified, sequenced, and analyzed to determine genetic diversity and population structure. A total of 126 (Port Victoria-38, Migori-38, Bungoma-22, and Kombewa-28) sequences of COII were used for population genetic analysis. Anopheles funestus had a high haplotype diversity (Hd = 0.97 to 0.98) but low nucleotide diversity (Π = 0.004 to 0.005). The neutrality test revealed negative Tajima’s D and Fs values indicating an excess of low-frequency variation. This could be attributed to either population expansion or negative selection pressure across all the populations. No genetic or structural differentiation (Fst = −0.01) and a high level of gene flow (Gamma St, Nm = 17.99 to 35.22) were observed among the populations. Population expansion suggests the high adaptability of this species to various ecological requirements, hence sustaining its vectorial capacity and malaria transmission.
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spelling pubmed-100521462023-03-30 Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII Debrah, Isaiah Ochwedo, Kevin O. Otambo, Wilfred O. Machani, Maxwell G. Magomere, Edwin O. Onyango, Shirley A. Zhong, Daibin Amoah, Linda E. Githeko, Andrew K. Afrane, Yaw A. Yan, Guiyun Insects Article SIMPLE SUMMARY: An. funestus is a major vector of human malaria and is responsible for high transmissions in sub-Saharan Africa. In the malaria endemic region of western Kenya, it has adapted and colonized different ecological niches owing to its high resistance to pyrethroids and changing breeding environments. The genetic basis of its ecological adaptations to various settings, which could enrich our understanding of how the population is structured or segregated, is poorly understood. This study sought to evaluate the population structure and genetic diversity of Anopheles funestus in different landscapes in western Kenya. To achieve this, the cytochrome oxidase subunit II gene (COII) was PCR-amplified and sequenced. This study revealed an excess of low-frequency variations that are likely due to population expansion or possibly negative selection pressure. Our findings could serve as a guide for future genomic research to facilitate the design of control strategies. ABSTRACT: The mitochondrial marker, COII, was employed to assess the genetic structure and diversity of Anopheles funestus, a very important malaria vector in Africa that adapt and colonize different ecological niches in western Kenya. Mosquitoes were collected using mechanical aspirators in four areas (Bungoma, Port Victoria, Kombewa, and Migori) in western Kenya. Following morphological identification, PCR was used to confirm the species. The COII gene was amplified, sequenced, and analyzed to determine genetic diversity and population structure. A total of 126 (Port Victoria-38, Migori-38, Bungoma-22, and Kombewa-28) sequences of COII were used for population genetic analysis. Anopheles funestus had a high haplotype diversity (Hd = 0.97 to 0.98) but low nucleotide diversity (Π = 0.004 to 0.005). The neutrality test revealed negative Tajima’s D and Fs values indicating an excess of low-frequency variation. This could be attributed to either population expansion or negative selection pressure across all the populations. No genetic or structural differentiation (Fst = −0.01) and a high level of gene flow (Gamma St, Nm = 17.99 to 35.22) were observed among the populations. Population expansion suggests the high adaptability of this species to various ecological requirements, hence sustaining its vectorial capacity and malaria transmission. MDPI 2023-03-09 /pmc/articles/PMC10052146/ /pubmed/36975958 http://dx.doi.org/10.3390/insects14030273 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Debrah, Isaiah
Ochwedo, Kevin O.
Otambo, Wilfred O.
Machani, Maxwell G.
Magomere, Edwin O.
Onyango, Shirley A.
Zhong, Daibin
Amoah, Linda E.
Githeko, Andrew K.
Afrane, Yaw A.
Yan, Guiyun
Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title_full Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title_fullStr Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title_full_unstemmed Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title_short Genetic Diversity and Population Structure of Anopheles funestus in Western Kenya Based on Mitochondrial DNA Marker COII
title_sort genetic diversity and population structure of anopheles funestus in western kenya based on mitochondrial dna marker coii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052146/
https://www.ncbi.nlm.nih.gov/pubmed/36975958
http://dx.doi.org/10.3390/insects14030273
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