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Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar

BACKGROUND: Low-level of malaria transmission persist in Zanzibar despite high coverage of core vector control interventions. This study was carried out in hot-spot sites to better understand entomological factors that may contribute to residual malaria transmission in Zanzibar. METHODS: A total of...

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Autores principales: Musiba, Revocatus M., Tarimo, Brian B., Monroe, April, Msaky, Dickson, Ngowo, Halfan, Mihayo, Kimberly, Limwagu, Alex, Chilla, Godlove T., Shubis, Gasper K., Ibrahim, Ahmada, Greer, George, Mcha, Juma H., Haji, Khamis A., Abbas, Faiza B., Ali, Abdullah, Okumu, Fredros O., Kiware, Samson S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171934/
https://www.ncbi.nlm.nih.gov/pubmed/35672768
http://dx.doi.org/10.1186/s12936-022-04200-y
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author Musiba, Revocatus M.
Tarimo, Brian B.
Monroe, April
Msaky, Dickson
Ngowo, Halfan
Mihayo, Kimberly
Limwagu, Alex
Chilla, Godlove T.
Shubis, Gasper K.
Ibrahim, Ahmada
Greer, George
Mcha, Juma H.
Haji, Khamis A.
Abbas, Faiza B.
Ali, Abdullah
Okumu, Fredros O.
Kiware, Samson S.
author_facet Musiba, Revocatus M.
Tarimo, Brian B.
Monroe, April
Msaky, Dickson
Ngowo, Halfan
Mihayo, Kimberly
Limwagu, Alex
Chilla, Godlove T.
Shubis, Gasper K.
Ibrahim, Ahmada
Greer, George
Mcha, Juma H.
Haji, Khamis A.
Abbas, Faiza B.
Ali, Abdullah
Okumu, Fredros O.
Kiware, Samson S.
author_sort Musiba, Revocatus M.
collection PubMed
description BACKGROUND: Low-level of malaria transmission persist in Zanzibar despite high coverage of core vector control interventions. This study was carried out in hot-spot sites to better understand entomological factors that may contribute to residual malaria transmission in Zanzibar. METHODS: A total of 135 households were randomly selected from six sites and consented to participate with 20–25 households per site. Mosquito vector surveillance was carried out indoors and outdoors from 6:00 pm–7:00 am using miniaturized double net trap (DN-Mini™). Additional collections were done indoors using mouth aspirators to retrieve resting mosquitoes from wall and ceiling surfaces, and outdoors using resting bucket and pit traps. All collected mosquitoes were morphologically and genetically (PCR) analysed in the laboratory. All collected anopheline and blood-fed mosquitoes were analysed for sporozoite infection and blood meal host preferences by Circumsporozoite Protein ELISA and blood meal ELISA, respectively. The differences between indoor and outdoor mosquito biting rates were analysed using generalized linear mixed models. Levels of resistance to commonly used insecticides were quantified by WHO susceptibility tests. RESULTS: Out of 704 malaria vectors collected across 135 households, PCR analysis shows that 98.60% were Anopheles arabiensis, 0.6% Anopheles merus and 0.6% Anopheles gambiae sensu stricto. Sporozoite ELISA analysis indicates that all mosquitoes were negative for the malaria parasite. The results show that more An. arabiensis were collected outdoor (~ 85%) compared to indoor (~ 15%). Furthermore, large numbers of An. arabiensis were caught in outdoor resting sites, where the pit trap (67.2%) collected more mosquitoes compared to the outdoor DN-Mini trap (32.8%). Nearly two-thirds (60.7%) of blood-fed mosquitoes had obtained blood meals from non-human hosts. Mosquitoes displayed non-uniform susceptibility status and resistance intensity among the tested insecticides across the study sites to all WHO recommended insecticides across the study sites. CONCLUSION: This study suggests that in contexts such as Zanzibar, testing of novel techniques to complement indoor protection and targeting outdoor biting and/or resting mosquitoes, may be warranted to complement existing interventions and contribute to malaria elimination efforts. The study highlights the need to implement novel interventions and/or adaptations of strategies that can target outdoors biting mosquitoes.
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spelling pubmed-91719342022-06-08 Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar Musiba, Revocatus M. Tarimo, Brian B. Monroe, April Msaky, Dickson Ngowo, Halfan Mihayo, Kimberly Limwagu, Alex Chilla, Godlove T. Shubis, Gasper K. Ibrahim, Ahmada Greer, George Mcha, Juma H. Haji, Khamis A. Abbas, Faiza B. Ali, Abdullah Okumu, Fredros O. Kiware, Samson S. Malar J Research BACKGROUND: Low-level of malaria transmission persist in Zanzibar despite high coverage of core vector control interventions. This study was carried out in hot-spot sites to better understand entomological factors that may contribute to residual malaria transmission in Zanzibar. METHODS: A total of 135 households were randomly selected from six sites and consented to participate with 20–25 households per site. Mosquito vector surveillance was carried out indoors and outdoors from 6:00 pm–7:00 am using miniaturized double net trap (DN-Mini™). Additional collections were done indoors using mouth aspirators to retrieve resting mosquitoes from wall and ceiling surfaces, and outdoors using resting bucket and pit traps. All collected mosquitoes were morphologically and genetically (PCR) analysed in the laboratory. All collected anopheline and blood-fed mosquitoes were analysed for sporozoite infection and blood meal host preferences by Circumsporozoite Protein ELISA and blood meal ELISA, respectively. The differences between indoor and outdoor mosquito biting rates were analysed using generalized linear mixed models. Levels of resistance to commonly used insecticides were quantified by WHO susceptibility tests. RESULTS: Out of 704 malaria vectors collected across 135 households, PCR analysis shows that 98.60% were Anopheles arabiensis, 0.6% Anopheles merus and 0.6% Anopheles gambiae sensu stricto. Sporozoite ELISA analysis indicates that all mosquitoes were negative for the malaria parasite. The results show that more An. arabiensis were collected outdoor (~ 85%) compared to indoor (~ 15%). Furthermore, large numbers of An. arabiensis were caught in outdoor resting sites, where the pit trap (67.2%) collected more mosquitoes compared to the outdoor DN-Mini trap (32.8%). Nearly two-thirds (60.7%) of blood-fed mosquitoes had obtained blood meals from non-human hosts. Mosquitoes displayed non-uniform susceptibility status and resistance intensity among the tested insecticides across the study sites to all WHO recommended insecticides across the study sites. CONCLUSION: This study suggests that in contexts such as Zanzibar, testing of novel techniques to complement indoor protection and targeting outdoor biting and/or resting mosquitoes, may be warranted to complement existing interventions and contribute to malaria elimination efforts. The study highlights the need to implement novel interventions and/or adaptations of strategies that can target outdoors biting mosquitoes. BioMed Central 2022-06-07 /pmc/articles/PMC9171934/ /pubmed/35672768 http://dx.doi.org/10.1186/s12936-022-04200-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Musiba, Revocatus M.
Tarimo, Brian B.
Monroe, April
Msaky, Dickson
Ngowo, Halfan
Mihayo, Kimberly
Limwagu, Alex
Chilla, Godlove T.
Shubis, Gasper K.
Ibrahim, Ahmada
Greer, George
Mcha, Juma H.
Haji, Khamis A.
Abbas, Faiza B.
Ali, Abdullah
Okumu, Fredros O.
Kiware, Samson S.
Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title_full Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title_fullStr Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title_full_unstemmed Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title_short Outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in Zanzibar
title_sort outdoor biting and pyrethroid resistance as potential drivers of persistent malaria transmission in zanzibar
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171934/
https://www.ncbi.nlm.nih.gov/pubmed/35672768
http://dx.doi.org/10.1186/s12936-022-04200-y
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