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Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe

BACKGROUND: Two mitochondrial DNA clades have been described in Anopheles funestus populations from southern Africa. Clade I is common across the continent while clade II is known only from Mozambique and Madagascar. The specific biological status of these clades is at present unknown. We investigat...

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Autores principales: Choi, Kwang S, Christian, Riann, Nardini, Luisa, Wood, Oliver R, Agubuzo, Eunice, Muleba, Mbanga, Munyati, Shungu, Makuwaza, Aramu, Koekemoer, Lizette L, Brooke, Basil D, Hunt, Richard H, Coetzee, Maureen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197278/
https://www.ncbi.nlm.nih.gov/pubmed/25293669
http://dx.doi.org/10.1186/s13071-014-0464-z
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author Choi, Kwang S
Christian, Riann
Nardini, Luisa
Wood, Oliver R
Agubuzo, Eunice
Muleba, Mbanga
Munyati, Shungu
Makuwaza, Aramu
Koekemoer, Lizette L
Brooke, Basil D
Hunt, Richard H
Coetzee, Maureen
author_facet Choi, Kwang S
Christian, Riann
Nardini, Luisa
Wood, Oliver R
Agubuzo, Eunice
Muleba, Mbanga
Munyati, Shungu
Makuwaza, Aramu
Koekemoer, Lizette L
Brooke, Basil D
Hunt, Richard H
Coetzee, Maureen
author_sort Choi, Kwang S
collection PubMed
description BACKGROUND: Two mitochondrial DNA clades have been described in Anopheles funestus populations from southern Africa. Clade I is common across the continent while clade II is known only from Mozambique and Madagascar. The specific biological status of these clades is at present unknown. We investigated the possible role that each clade might play in the transmission of Plasmodium falciparum and the insecticide resistance status of An. funestus from Zimbabwe and Zambia. METHODS: Mosquitoes were collected inside houses from Nchelenge District, Zambia and Honde Valley, Zimbabwe in 2013 and 2014. WHO susceptibility tests, synergist assays and resistance intensity tests were conducted on wild females and progeny of wild females. ELISA was used to detect Plasmodium falciparum circumsporozoite protein. Specimens were identified to species and mtDNA clades using standard molecular methods. RESULTS: The Zimbabwean samples were all clade I while the Zambian population comprised 80% clade I and 20% clade II in both years of collection. ELISA tests gave an overall infection rate of 2.3% and 2.1% in 2013, and 3.5% and 9.2% in 2014 for Zimbabwe and Zambia respectively. No significant difference was observed between the clades. All populations were resistant to pyrethroids and carbamates but susceptible to organochlorines and organophosphates. Synergist assays indicated that pyrethroid resistance is mediated by cytochrome P450 mono-oxygenases. Resistance intensity tests showed high survival rates after 8-hrs continuous exposure to pyrethroids but exposure to bendiocarb gave the same results as the susceptible control. CONCLUSIONS: This is the first record of An. funestus mtDNA clade II occurring in Zambia. No evidence was found to suggest that the clades are markers of biologically separate populations. The ability of An. funestus to withstand prolonged exposure to pyrethroids has serious implications for the use of these insecticides, either through LLINs or IRS, in southern Africa in general and resistance management strategies should be urgently implemented.
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spelling pubmed-41972782014-10-16 Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe Choi, Kwang S Christian, Riann Nardini, Luisa Wood, Oliver R Agubuzo, Eunice Muleba, Mbanga Munyati, Shungu Makuwaza, Aramu Koekemoer, Lizette L Brooke, Basil D Hunt, Richard H Coetzee, Maureen Parasit Vectors Research BACKGROUND: Two mitochondrial DNA clades have been described in Anopheles funestus populations from southern Africa. Clade I is common across the continent while clade II is known only from Mozambique and Madagascar. The specific biological status of these clades is at present unknown. We investigated the possible role that each clade might play in the transmission of Plasmodium falciparum and the insecticide resistance status of An. funestus from Zimbabwe and Zambia. METHODS: Mosquitoes were collected inside houses from Nchelenge District, Zambia and Honde Valley, Zimbabwe in 2013 and 2014. WHO susceptibility tests, synergist assays and resistance intensity tests were conducted on wild females and progeny of wild females. ELISA was used to detect Plasmodium falciparum circumsporozoite protein. Specimens were identified to species and mtDNA clades using standard molecular methods. RESULTS: The Zimbabwean samples were all clade I while the Zambian population comprised 80% clade I and 20% clade II in both years of collection. ELISA tests gave an overall infection rate of 2.3% and 2.1% in 2013, and 3.5% and 9.2% in 2014 for Zimbabwe and Zambia respectively. No significant difference was observed between the clades. All populations were resistant to pyrethroids and carbamates but susceptible to organochlorines and organophosphates. Synergist assays indicated that pyrethroid resistance is mediated by cytochrome P450 mono-oxygenases. Resistance intensity tests showed high survival rates after 8-hrs continuous exposure to pyrethroids but exposure to bendiocarb gave the same results as the susceptible control. CONCLUSIONS: This is the first record of An. funestus mtDNA clade II occurring in Zambia. No evidence was found to suggest that the clades are markers of biologically separate populations. The ability of An. funestus to withstand prolonged exposure to pyrethroids has serious implications for the use of these insecticides, either through LLINs or IRS, in southern Africa in general and resistance management strategies should be urgently implemented. BioMed Central 2014-10-08 /pmc/articles/PMC4197278/ /pubmed/25293669 http://dx.doi.org/10.1186/s13071-014-0464-z Text en © Choi et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Choi, Kwang S
Christian, Riann
Nardini, Luisa
Wood, Oliver R
Agubuzo, Eunice
Muleba, Mbanga
Munyati, Shungu
Makuwaza, Aramu
Koekemoer, Lizette L
Brooke, Basil D
Hunt, Richard H
Coetzee, Maureen
Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title_full Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title_fullStr Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title_full_unstemmed Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title_short Insecticide resistance and role in malaria transmission of Anopheles funestus populations from Zambia and Zimbabwe
title_sort insecticide resistance and role in malaria transmission of anopheles funestus populations from zambia and zimbabwe
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197278/
https://www.ncbi.nlm.nih.gov/pubmed/25293669
http://dx.doi.org/10.1186/s13071-014-0464-z
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