Cargando…

Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso

The decline in malaria across Africa has been largely attributed to vector control using long-lasting insecticidal nets (LLINs). However, this intervention has prompted widespread insecticide resistance (IR) and been associated with changes in mosquito behaviour that reduce their contact with LLINs....

Descripción completa

Detalles Bibliográficos
Autores principales: Sanou, Antoine, Nelli, Luca, Guelbéogo, W. Moussa, Cissé, Fatoumata, Tapsoba, Madou, Ouédraogo, Pierre, Sagnon, N’falé, Ranson, Hilary, Matthiopoulos, Jason, Ferguson, Heather M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413378/
https://www.ncbi.nlm.nih.gov/pubmed/34475470
http://dx.doi.org/10.1038/s41598-021-96759-w
_version_ 1783747651481632768
author Sanou, Antoine
Nelli, Luca
Guelbéogo, W. Moussa
Cissé, Fatoumata
Tapsoba, Madou
Ouédraogo, Pierre
Sagnon, N’falé
Ranson, Hilary
Matthiopoulos, Jason
Ferguson, Heather M.
author_facet Sanou, Antoine
Nelli, Luca
Guelbéogo, W. Moussa
Cissé, Fatoumata
Tapsoba, Madou
Ouédraogo, Pierre
Sagnon, N’falé
Ranson, Hilary
Matthiopoulos, Jason
Ferguson, Heather M.
author_sort Sanou, Antoine
collection PubMed
description The decline in malaria across Africa has been largely attributed to vector control using long-lasting insecticidal nets (LLINs). However, this intervention has prompted widespread insecticide resistance (IR) and been associated with changes in mosquito behaviour that reduce their contact with LLINs. The relative importance and rate at which IR and behavioural adaptations emerge are poorly understood. We conducted surveillance of mosquito behaviour and IR at 12 sites in Burkina Faso to assess the magnitude and temporal dynamics of insecticide, biting and resting behaviours in vectors in the 2-year period following mass LLIN distribution. Insecticide resistance was present in all vector populations and increased rapidly over the study period. In contrast, no longitudinal shifts in LLIN-avoidance behaviours (earlier or outdoor biting and resting) were detected. There was a moderate but statistically significant shift in vector species composition from Anopheles coluzzii to Anopheles gambiae which coincided with a reduction in the proportion of bites preventable by LLINs; possibly driven by between-species variation in behaviour. These findings indicate that adaptations based on insecticide resistance arise and intensify more rapidly than behavioural shifts within mosquito vectors. However, longitudinal shifts in mosquito vector species composition were evident within 2 years following a mass LLIN distribution. This ecological shift was characterized by a significant increase in the exophagic species (An. gambiae) and coincided with a predicted decline in the degree of protection expected from LLINs. Although human exposure fell through the study period due to reducing vector densities and infection rates, such ecological shifts in vector species along with insecticide resistance were likely to have eroded the efficacy of LLINs. While both adaptations impact malaria control, the rapid increase of the former indicates this strategy develops more quickly in response to selection from LLINS. However, interventions targeting both resistance strategies will be needed.
format Online
Article
Text
id pubmed-8413378
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-84133782021-09-07 Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso Sanou, Antoine Nelli, Luca Guelbéogo, W. Moussa Cissé, Fatoumata Tapsoba, Madou Ouédraogo, Pierre Sagnon, N’falé Ranson, Hilary Matthiopoulos, Jason Ferguson, Heather M. Sci Rep Article The decline in malaria across Africa has been largely attributed to vector control using long-lasting insecticidal nets (LLINs). However, this intervention has prompted widespread insecticide resistance (IR) and been associated with changes in mosquito behaviour that reduce their contact with LLINs. The relative importance and rate at which IR and behavioural adaptations emerge are poorly understood. We conducted surveillance of mosquito behaviour and IR at 12 sites in Burkina Faso to assess the magnitude and temporal dynamics of insecticide, biting and resting behaviours in vectors in the 2-year period following mass LLIN distribution. Insecticide resistance was present in all vector populations and increased rapidly over the study period. In contrast, no longitudinal shifts in LLIN-avoidance behaviours (earlier or outdoor biting and resting) were detected. There was a moderate but statistically significant shift in vector species composition from Anopheles coluzzii to Anopheles gambiae which coincided with a reduction in the proportion of bites preventable by LLINs; possibly driven by between-species variation in behaviour. These findings indicate that adaptations based on insecticide resistance arise and intensify more rapidly than behavioural shifts within mosquito vectors. However, longitudinal shifts in mosquito vector species composition were evident within 2 years following a mass LLIN distribution. This ecological shift was characterized by a significant increase in the exophagic species (An. gambiae) and coincided with a predicted decline in the degree of protection expected from LLINs. Although human exposure fell through the study period due to reducing vector densities and infection rates, such ecological shifts in vector species along with insecticide resistance were likely to have eroded the efficacy of LLINs. While both adaptations impact malaria control, the rapid increase of the former indicates this strategy develops more quickly in response to selection from LLINS. However, interventions targeting both resistance strategies will be needed. Nature Publishing Group UK 2021-09-02 /pmc/articles/PMC8413378/ /pubmed/34475470 http://dx.doi.org/10.1038/s41598-021-96759-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Sanou, Antoine
Nelli, Luca
Guelbéogo, W. Moussa
Cissé, Fatoumata
Tapsoba, Madou
Ouédraogo, Pierre
Sagnon, N’falé
Ranson, Hilary
Matthiopoulos, Jason
Ferguson, Heather M.
Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title_full Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title_fullStr Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title_full_unstemmed Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title_short Insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the Cascades region of Burkina Faso
title_sort insecticide resistance and behavioural adaptation as a response to long-lasting insecticidal net deployment in malaria vectors in the cascades region of burkina faso
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413378/
https://www.ncbi.nlm.nih.gov/pubmed/34475470
http://dx.doi.org/10.1038/s41598-021-96759-w
work_keys_str_mv AT sanouantoine insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT nelliluca insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT guelbeogowmoussa insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT cissefatoumata insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT tapsobamadou insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT ouedraogopierre insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT sagnonnfale insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT ransonhilary insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT matthiopoulosjason insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso
AT fergusonheatherm insecticideresistanceandbehaviouraladaptationasaresponsetolonglastinginsecticidalnetdeploymentinmalariavectorsinthecascadesregionofburkinafaso