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Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020
BACKGROUND: Insecticide resistance is a serious threat to the continued effectiveness of insecticide-based malaria vector control measures, such as long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS). This paper describes trends and dynamics of insecticide resistance and its un...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024418/ https://www.ncbi.nlm.nih.gov/pubmed/36932400 http://dx.doi.org/10.1186/s12936-023-04508-3 |
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author | Tungu, Patrick Kabula, Bilali Nkya, Theresia Machafuko, Pendael Sambu, Edward Batengana, Bernard Sudi, Wema Derua, Yahaya A. Mwingira, Victor Masue, Denis Malima, Robert Kitojo, Chonge Serbantez, Naomi Reaves, Erik J. Mwalimu, Charles Nhiga, Samwel L. Ally, Mohamed Mkali, Humphrey R. Joseph, Joseph J. Chan, Adeline Ngondi, Jeremiah Lalji, Shabbir Nyinondi, Ssanyu Eckert, Erin Reithinger, Richard Magesa, Stephen Kisinza, William N. |
author_facet | Tungu, Patrick Kabula, Bilali Nkya, Theresia Machafuko, Pendael Sambu, Edward Batengana, Bernard Sudi, Wema Derua, Yahaya A. Mwingira, Victor Masue, Denis Malima, Robert Kitojo, Chonge Serbantez, Naomi Reaves, Erik J. Mwalimu, Charles Nhiga, Samwel L. Ally, Mohamed Mkali, Humphrey R. Joseph, Joseph J. Chan, Adeline Ngondi, Jeremiah Lalji, Shabbir Nyinondi, Ssanyu Eckert, Erin Reithinger, Richard Magesa, Stephen Kisinza, William N. |
author_sort | Tungu, Patrick |
collection | PubMed |
description | BACKGROUND: Insecticide resistance is a serious threat to the continued effectiveness of insecticide-based malaria vector control measures, such as long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS). This paper describes trends and dynamics of insecticide resistance and its underlying mechanisms from annual resistance monitoring surveys on Anopheles gambiae sensu lato (s.l.) populations conducted across mainland Tanzania from 2004 to 2020. METHODS: The World Health Organization (WHO) standard protocols were used to assess susceptibility of the wild female An. gambiae s.l. mosquitoes to insecticides, with mosquitoes exposed to diagnostic concentrations of permethrin, deltamethrin, lambdacyhalothrin, bendiocarb, and pirimiphos-methyl. WHO test papers at 5× and 10× the diagnostic concentrations were used to assess the intensity of resistance to pyrethroids; synergist tests using piperonyl butoxide (PBO) were carried out in sites where mosquitoes were found to be resistant to pyrethroids. To estimate insecticide resistance trends from 2004 to 2020, percentage mortalities from each site and time point were aggregated and regression analysis of mortality versus the Julian dates of bioassays was performed. RESULTS: Percentage of sites with pyrethroid resistance increased from 0% in 2004 to more than 80% in the 2020, suggesting resistance has been spreading geographically. Results indicate a strong negative association (p = 0.0001) between pyrethroids susceptibility status and survey year. The regression model shows that by 2020 over 40% of An. gambiae mosquitoes survived exposure to pyrethroids at their respective diagnostic doses. A decreasing trend of An. gambiae susceptibility to bendiocarb was observed over time, but this was not statistically significant (p = 0.8413). Anopheles gambiae exhibited high level of susceptibility to the pirimiphos-methyl in sampled sites. CONCLUSIONS: Anopheles gambiae Tanzania’s major malaria vector, is now resistant to pyrethroids across the country with resistance increasing in prevalence and intensity and has been spreading geographically. This calls for urgent action for efficient malaria vector control tools to sustain the gains obtained in malaria control. Strengthening insecticide resistance monitoring is important for its management through evidence generation for effective malaria vector control decision. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-023-04508-3. |
format | Online Article Text |
id | pubmed-10024418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100244182023-03-19 Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 Tungu, Patrick Kabula, Bilali Nkya, Theresia Machafuko, Pendael Sambu, Edward Batengana, Bernard Sudi, Wema Derua, Yahaya A. Mwingira, Victor Masue, Denis Malima, Robert Kitojo, Chonge Serbantez, Naomi Reaves, Erik J. Mwalimu, Charles Nhiga, Samwel L. Ally, Mohamed Mkali, Humphrey R. Joseph, Joseph J. Chan, Adeline Ngondi, Jeremiah Lalji, Shabbir Nyinondi, Ssanyu Eckert, Erin Reithinger, Richard Magesa, Stephen Kisinza, William N. Malar J Research BACKGROUND: Insecticide resistance is a serious threat to the continued effectiveness of insecticide-based malaria vector control measures, such as long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS). This paper describes trends and dynamics of insecticide resistance and its underlying mechanisms from annual resistance monitoring surveys on Anopheles gambiae sensu lato (s.l.) populations conducted across mainland Tanzania from 2004 to 2020. METHODS: The World Health Organization (WHO) standard protocols were used to assess susceptibility of the wild female An. gambiae s.l. mosquitoes to insecticides, with mosquitoes exposed to diagnostic concentrations of permethrin, deltamethrin, lambdacyhalothrin, bendiocarb, and pirimiphos-methyl. WHO test papers at 5× and 10× the diagnostic concentrations were used to assess the intensity of resistance to pyrethroids; synergist tests using piperonyl butoxide (PBO) were carried out in sites where mosquitoes were found to be resistant to pyrethroids. To estimate insecticide resistance trends from 2004 to 2020, percentage mortalities from each site and time point were aggregated and regression analysis of mortality versus the Julian dates of bioassays was performed. RESULTS: Percentage of sites with pyrethroid resistance increased from 0% in 2004 to more than 80% in the 2020, suggesting resistance has been spreading geographically. Results indicate a strong negative association (p = 0.0001) between pyrethroids susceptibility status and survey year. The regression model shows that by 2020 over 40% of An. gambiae mosquitoes survived exposure to pyrethroids at their respective diagnostic doses. A decreasing trend of An. gambiae susceptibility to bendiocarb was observed over time, but this was not statistically significant (p = 0.8413). Anopheles gambiae exhibited high level of susceptibility to the pirimiphos-methyl in sampled sites. CONCLUSIONS: Anopheles gambiae Tanzania’s major malaria vector, is now resistant to pyrethroids across the country with resistance increasing in prevalence and intensity and has been spreading geographically. This calls for urgent action for efficient malaria vector control tools to sustain the gains obtained in malaria control. Strengthening insecticide resistance monitoring is important for its management through evidence generation for effective malaria vector control decision. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-023-04508-3. BioMed Central 2023-03-17 /pmc/articles/PMC10024418/ /pubmed/36932400 http://dx.doi.org/10.1186/s12936-023-04508-3 Text en © The Author(s) 2023 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 Tungu, Patrick Kabula, Bilali Nkya, Theresia Machafuko, Pendael Sambu, Edward Batengana, Bernard Sudi, Wema Derua, Yahaya A. Mwingira, Victor Masue, Denis Malima, Robert Kitojo, Chonge Serbantez, Naomi Reaves, Erik J. Mwalimu, Charles Nhiga, Samwel L. Ally, Mohamed Mkali, Humphrey R. Joseph, Joseph J. Chan, Adeline Ngondi, Jeremiah Lalji, Shabbir Nyinondi, Ssanyu Eckert, Erin Reithinger, Richard Magesa, Stephen Kisinza, William N. Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title | Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title_full | Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title_fullStr | Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title_full_unstemmed | Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title_short | Trends of insecticide resistance monitoring in mainland Tanzania, 2004–2020 |
title_sort | trends of insecticide resistance monitoring in mainland tanzania, 2004–2020 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024418/ https://www.ncbi.nlm.nih.gov/pubmed/36932400 http://dx.doi.org/10.1186/s12936-023-04508-3 |
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