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Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique
BACKGROUND: The dual problems of rising insecticide resistance in the malaria vectors and increasing human malaria cases since 2001 in southern Mozambique are cause for serious concern. The selection of insecticides for use in indoor residual spraying (IRS) programmes is highly dependent on the exte...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050845/ https://www.ncbi.nlm.nih.gov/pubmed/21306631 http://dx.doi.org/10.1186/1756-3305-4-16 |
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author | Kloke, R Graham Nhamahanga, Eduardo Hunt, Richard H Coetzee, Maureen |
author_facet | Kloke, R Graham Nhamahanga, Eduardo Hunt, Richard H Coetzee, Maureen |
author_sort | Kloke, R Graham |
collection | PubMed |
description | BACKGROUND: The dual problems of rising insecticide resistance in the malaria vectors and increasing human malaria cases since 2001 in southern Mozambique are cause for serious concern. The selection of insecticides for use in indoor residual spraying (IRS) programmes is highly dependent on the extent to which local mosquitoes are susceptible to the approved classes of insecticides. The insecticide resistance status and role in malaria transmission of Anopheles funestus was evaluated at the Maragra Sugar Estate in southern Mozambique where an IRS vector control programme has been in operation for seven years using the carbamate insecticide bendiocarb. RESULTS: No Anopheles species were captured inside the sugar estate control area. Anopheles funestus group captured outside of the estate represented 90% (n = 475) of the total collections. Of the specimens identified to species by PCR (n = 167), 95% were An. funestus s.s. One An. rivulorum was identified and seven specimens did not amplify. The Anopheles gambiae complex was less abundant (n = 53) and of those identified (n = 33) 76% were An. arabiensis and 24% An. merus. Insecticide susceptibility tests showed that wild-caught and F-1 family An. funestus were resistant to deltamethrin (32.5% mortality) and lambda-cyhalothrin (14.6% mortality), less so to bendiocarb (71.5% mortality) and fully susceptible to both malathion and DDT (100%). Bendiocarb and pyrethroid resistance was nullified using 4% piperonyl butoxide (Pbo), strongly suggesting that both are mediated by P450 monooxygenase detoxification. ELISA tests of An. funestus for Plasmodium falciparum, gave a sporozoite rate of 6.02% (n = 166). One unidentified member of the An. gambiae complex tested positive for P. falciparum sporozoites. CONCLUSION: Anopheles funestus was found to be the most abundant and principle vector of malaria in this area, with members of the An. gambiae complex being secondary vectors. Despite the continual use of bendiocarb within the estate for seven years and the level of An. funestus resistance to this insecticide, the IVC programme is still effective against this and other Anopheles in that no vectors were found inside the control area. However, the Mozambique National Malaria Control Programme ceased the use of DDT and bendiocarb in this area of its operations in 2009, and replaced these insecticides with a pyrethroid which will increase insecticide resistance selection pressure and impact on control programmes such as the Maragra IVC. |
format | Text |
id | pubmed-3050845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30508452011-03-09 Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique Kloke, R Graham Nhamahanga, Eduardo Hunt, Richard H Coetzee, Maureen Parasit Vectors Research BACKGROUND: The dual problems of rising insecticide resistance in the malaria vectors and increasing human malaria cases since 2001 in southern Mozambique are cause for serious concern. The selection of insecticides for use in indoor residual spraying (IRS) programmes is highly dependent on the extent to which local mosquitoes are susceptible to the approved classes of insecticides. The insecticide resistance status and role in malaria transmission of Anopheles funestus was evaluated at the Maragra Sugar Estate in southern Mozambique where an IRS vector control programme has been in operation for seven years using the carbamate insecticide bendiocarb. RESULTS: No Anopheles species were captured inside the sugar estate control area. Anopheles funestus group captured outside of the estate represented 90% (n = 475) of the total collections. Of the specimens identified to species by PCR (n = 167), 95% were An. funestus s.s. One An. rivulorum was identified and seven specimens did not amplify. The Anopheles gambiae complex was less abundant (n = 53) and of those identified (n = 33) 76% were An. arabiensis and 24% An. merus. Insecticide susceptibility tests showed that wild-caught and F-1 family An. funestus were resistant to deltamethrin (32.5% mortality) and lambda-cyhalothrin (14.6% mortality), less so to bendiocarb (71.5% mortality) and fully susceptible to both malathion and DDT (100%). Bendiocarb and pyrethroid resistance was nullified using 4% piperonyl butoxide (Pbo), strongly suggesting that both are mediated by P450 monooxygenase detoxification. ELISA tests of An. funestus for Plasmodium falciparum, gave a sporozoite rate of 6.02% (n = 166). One unidentified member of the An. gambiae complex tested positive for P. falciparum sporozoites. CONCLUSION: Anopheles funestus was found to be the most abundant and principle vector of malaria in this area, with members of the An. gambiae complex being secondary vectors. Despite the continual use of bendiocarb within the estate for seven years and the level of An. funestus resistance to this insecticide, the IVC programme is still effective against this and other Anopheles in that no vectors were found inside the control area. However, the Mozambique National Malaria Control Programme ceased the use of DDT and bendiocarb in this area of its operations in 2009, and replaced these insecticides with a pyrethroid which will increase insecticide resistance selection pressure and impact on control programmes such as the Maragra IVC. BioMed Central 2011-02-09 /pmc/articles/PMC3050845/ /pubmed/21306631 http://dx.doi.org/10.1186/1756-3305-4-16 Text en Copyright ©2011 Kloke et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kloke, R Graham Nhamahanga, Eduardo Hunt, Richard H Coetzee, Maureen Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title | Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title_full | Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title_fullStr | Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title_full_unstemmed | Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title_short | Vectorial status and insecticide resistance of Anopheles funestus from a sugar estate in southern Mozambique |
title_sort | vectorial status and insecticide resistance of anopheles funestus from a sugar estate in southern mozambique |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050845/ https://www.ncbi.nlm.nih.gov/pubmed/21306631 http://dx.doi.org/10.1186/1756-3305-4-16 |
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