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Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun)
BACKGROUND: The effectiveness of Long-Lasting Insecticidal Nets (LLINs) and indoor residual spraying (IRS) in controlling malaria vectors is hampered by the resistance of anopheles to insecticides. A good knowledge of the breeding sites and of the resistance profile of the vectors could facilitate t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MTSI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940278/ https://www.ncbi.nlm.nih.gov/pubmed/36815176 http://dx.doi.org/10.48327/mtsi.v2i4.2022.284 |
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author | NTONGA AKONO, Patrick MBONGUE, Roméo Serge FOKO DADJI, Gisèle Aurélie TSILA, Henri Gabriel OFFONO ENAMA, Léger NOPOWO TAKAP, Francis EKOKO, Wolfgang Eyisap MBIDA MBIDA, Jean Arthur |
author_facet | NTONGA AKONO, Patrick MBONGUE, Roméo Serge FOKO DADJI, Gisèle Aurélie TSILA, Henri Gabriel OFFONO ENAMA, Léger NOPOWO TAKAP, Francis EKOKO, Wolfgang Eyisap MBIDA MBIDA, Jean Arthur |
author_sort | NTONGA AKONO, Patrick |
collection | PubMed |
description | BACKGROUND: The effectiveness of Long-Lasting Insecticidal Nets (LLINs) and indoor residual spraying (IRS) in controlling malaria vectors is hampered by the resistance of anopheles to insecticides. A good knowledge of the breeding sites and of the resistance profile of the vectors could facilitate the development of an appropriate control strategy. This study looks at the larval ecology and the susceptibility profile of An. gambiae s.l. to insecticides in urban and rural areas in Kribi, South Region of Cameroon. METHODS: Mosquito breeding sites were categorized and geo-referenced. For each site, larvae were collected and reared and physicochemical parameters were measured in situ. The susceptibility of anopheles to dichlorodiphenyltrichloroethane (DDT), deltamethrin and permethrin, after pre-exposure to piperonyl butoxide (PBO) or not, was evaluated on the reared larvae. The Kdr mutation was detected using the Hot Oligonucleotide Ligation Assay (HOLA). RESULTS: Natural breeding sites of An. gambiae s.l. were tyre tracks (12%, n=10), unbuilt wells (5%, n=4), pools of residual water (57%, n=48), foot and hoof prints, gullies, streams and the banks of the Kienké River (15%, n=13). Artificial breeding sites were abandoned dugouts (11%, n=9). Breeding sites in urban areas were characterized by higher mean values of temperature, conductivity, salinity and turbidity compared to the breeding sites in the rural area. The breeding sites of An. gambiae s.l. in urban Kribi were found to be sunnier than those in rural Kribi. A total of 4320 adults were used for testing, 1 440 mosquitoes from rural Kribi, 1 440 from urban Kribi and 1 440 specimens from the laboratory Kisumu strain. For DDT and deltamethrin, susceptibility tests showed that mortality was lower in a situation of no pre-exposure to PBO than in a situation of pre-exposure to PBO in the two study areas. The frequency of the resistant allele (R) was high for the Kdr West mutation in both urban (0.94) and rural areas in Kribi (0.93). CONCLUSION: An. gambiae s.l. colonizes a wide range of breeding sites and develops metabolic and mutation resistance to recommended insecticides. The search of alternative molecules for vector control is a necessity. |
format | Online Article Text |
id | pubmed-9940278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MTSI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99402782023-02-21 Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) NTONGA AKONO, Patrick MBONGUE, Roméo Serge FOKO DADJI, Gisèle Aurélie TSILA, Henri Gabriel OFFONO ENAMA, Léger NOPOWO TAKAP, Francis EKOKO, Wolfgang Eyisap MBIDA MBIDA, Jean Arthur Med Trop Sante Int Entomologie Médicale BACKGROUND: The effectiveness of Long-Lasting Insecticidal Nets (LLINs) and indoor residual spraying (IRS) in controlling malaria vectors is hampered by the resistance of anopheles to insecticides. A good knowledge of the breeding sites and of the resistance profile of the vectors could facilitate the development of an appropriate control strategy. This study looks at the larval ecology and the susceptibility profile of An. gambiae s.l. to insecticides in urban and rural areas in Kribi, South Region of Cameroon. METHODS: Mosquito breeding sites were categorized and geo-referenced. For each site, larvae were collected and reared and physicochemical parameters were measured in situ. The susceptibility of anopheles to dichlorodiphenyltrichloroethane (DDT), deltamethrin and permethrin, after pre-exposure to piperonyl butoxide (PBO) or not, was evaluated on the reared larvae. The Kdr mutation was detected using the Hot Oligonucleotide Ligation Assay (HOLA). RESULTS: Natural breeding sites of An. gambiae s.l. were tyre tracks (12%, n=10), unbuilt wells (5%, n=4), pools of residual water (57%, n=48), foot and hoof prints, gullies, streams and the banks of the Kienké River (15%, n=13). Artificial breeding sites were abandoned dugouts (11%, n=9). Breeding sites in urban areas were characterized by higher mean values of temperature, conductivity, salinity and turbidity compared to the breeding sites in the rural area. The breeding sites of An. gambiae s.l. in urban Kribi were found to be sunnier than those in rural Kribi. A total of 4320 adults were used for testing, 1 440 mosquitoes from rural Kribi, 1 440 from urban Kribi and 1 440 specimens from the laboratory Kisumu strain. For DDT and deltamethrin, susceptibility tests showed that mortality was lower in a situation of no pre-exposure to PBO than in a situation of pre-exposure to PBO in the two study areas. The frequency of the resistant allele (R) was high for the Kdr West mutation in both urban (0.94) and rural areas in Kribi (0.93). CONCLUSION: An. gambiae s.l. colonizes a wide range of breeding sites and develops metabolic and mutation resistance to recommended insecticides. The search of alternative molecules for vector control is a necessity. MTSI 2022-10-25 /pmc/articles/PMC9940278/ /pubmed/36815176 http://dx.doi.org/10.48327/mtsi.v2i4.2022.284 Text en Copyright © 2022 SFMTSI https://creativecommons.org/licenses/by/4.0/Cet article en libre accès est distribué selon les termes de la licence Creative Commons CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Entomologie Médicale NTONGA AKONO, Patrick MBONGUE, Roméo Serge FOKO DADJI, Gisèle Aurélie TSILA, Henri Gabriel OFFONO ENAMA, Léger NOPOWO TAKAP, Francis EKOKO, Wolfgang Eyisap MBIDA MBIDA, Jean Arthur Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title | Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title_full | Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title_fullStr | Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title_full_unstemmed | Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title_short | Habitats larvaires d‘Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun) |
title_sort | habitats larvaires d‘anopheles gambiae s.l. et mécanismes de résistance à kribi (cameroun) |
topic | Entomologie Médicale |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940278/ https://www.ncbi.nlm.nih.gov/pubmed/36815176 http://dx.doi.org/10.48327/mtsi.v2i4.2022.284 |
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