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Insecticide resistance in Anopheles gambiae from south-western Chad, Central Africa
Indoor residual spraying and insecticide-treated nets (ITN) are essential components of malaria vector control in Africa. Pyrethroids are the only recommended compounds for nets treatment because they are fast-acting insecticides with low mammalian toxicity. However, there is growing concern that py...
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Published in: | Malaria journal 2008-09, Vol.7 (1), p.192-192, Article 192 |
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description | Indoor residual spraying and insecticide-treated nets (ITN) are essential components of malaria vector control in Africa. Pyrethroids are the only recommended compounds for nets treatment because they are fast-acting insecticides with low mammalian toxicity. However, there is growing concern that pyrethroid resistance may threaten the sustainability of ITN scaling-up programmes. Here, insecticide susceptibility was investigated in Anopheles gambiae sensu lato from an area of large scale ITN distribution programme in south-western Chad.
Susceptibility to 4% DDT, 0.05% deltamethrin, 0.75% permethrin, 0.1% bendiocarb and 5% malathion was assessed using the WHO standard procedures for adult mosquitoes. Tests were carried out with two to four days-old, non-engorged female mosquitoes. The An. gambiae Kisumu strain was used as a reference. Knockdown effect was recorded every 5 min and mortality scored 24 h after exposure. Mosquitoes were identified to species and molecular form by PCR-RFLP and genotypes at the kdr locus were determined in surviving specimens by Hot Oligonucleotide Ligation Assay (HOLA).
During this survey, full susceptibility to malathion was recorded in all samples. Reduced susceptibility to bendiocarb (mortality rate of 96.1%) was found in one sample out of nine assayed. Increased tolerance to pyrethroids was detected in most samples (8/9) with mortality rates ranging from 70.2 to 96.6% for deltamethrin and from 26.7 to 96.3% for permethrin. Pyrethroid tolerance was not associated with a significant increase of knock-down times. Anopheles arabiensis was the predominant species of the An. gambiae complex in the study area, representing 75 to 100% of the samples. Screening for kdr mutations detected the L1014F mutation in 88.6% (N = 35) of surviving An. gambiae sensu stricto S form mosquitoes. All surviving An. arabiensis (N = 49) and M form An. gambiae s.s. (N = 1) carried the susceptible allele.
This first investigation of malaria vector susceptibility to insecticides in Chad revealed variable levels of resistance to pyrethroid insecticides (permethrin and deltamethrin) in most An. gambiae s.l. populations. Resistance was associated with the L1014F kdr mutation in the S form of An. gambiae s.s.. Alternative mechanisms, probably of metabolic origin are involved in An. arabiensis. These results emphasize the crucial need for insecticide resistance monitoring and in-depth investigation of resistance mechanisms in malaria vectors in Chad. The impac |
doi_str_mv | 10.1186/1475-2875-7-192 |
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Susceptibility to 4% DDT, 0.05% deltamethrin, 0.75% permethrin, 0.1% bendiocarb and 5% malathion was assessed using the WHO standard procedures for adult mosquitoes. Tests were carried out with two to four days-old, non-engorged female mosquitoes. The An. gambiae Kisumu strain was used as a reference. Knockdown effect was recorded every 5 min and mortality scored 24 h after exposure. Mosquitoes were identified to species and molecular form by PCR-RFLP and genotypes at the kdr locus were determined in surviving specimens by Hot Oligonucleotide Ligation Assay (HOLA).
During this survey, full susceptibility to malathion was recorded in all samples. Reduced susceptibility to bendiocarb (mortality rate of 96.1%) was found in one sample out of nine assayed. Increased tolerance to pyrethroids was detected in most samples (8/9) with mortality rates ranging from 70.2 to 96.6% for deltamethrin and from 26.7 to 96.3% for permethrin. Pyrethroid tolerance was not associated with a significant increase of knock-down times. Anopheles arabiensis was the predominant species of the An. gambiae complex in the study area, representing 75 to 100% of the samples. Screening for kdr mutations detected the L1014F mutation in 88.6% (N = 35) of surviving An. gambiae sensu stricto S form mosquitoes. All surviving An. arabiensis (N = 49) and M form An. gambiae s.s. (N = 1) carried the susceptible allele.
This first investigation of malaria vector susceptibility to insecticides in Chad revealed variable levels of resistance to pyrethroid insecticides (permethrin and deltamethrin) in most An. gambiae s.l. populations. Resistance was associated with the L1014F kdr mutation in the S form of An. gambiae s.s.. Alternative mechanisms, probably of metabolic origin are involved in An. arabiensis. These results emphasize the crucial need for insecticide resistance monitoring and in-depth investigation of resistance mechanisms in malaria vectors in Chad. The impact of reduced susceptibility to pyrethroids on ITN efficacy should be further assessed.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/1475-2875-7-192</identifier><identifier>PMID: 18823537</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Amino Acid Substitution - genetics ; Animals ; Anopheles - classification ; Anopheles - drug effects ; Anopheles - genetics ; Care and treatment ; Chad ; Demographic aspects ; Drug Resistance ; Genotype ; Insect Proteins - genetics ; Insecticide resistance ; Insecticides - pharmacology ; Malaria ; Mutation, Missense ; Polymorphism, Restriction Fragment Length ; Pyrethrins - pharmacology ; Survival Analysis</subject><ispartof>Malaria journal, 2008-09, Vol.7 (1), p.192-192, Article 192</ispartof><rights>COPYRIGHT 2008 BioMed Central Ltd.</rights><rights>Copyright © 2008 Kerah-Hinzoumbé et al; licensee BioMed Central Ltd. 2008 Kerah-Hinzoumbé et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b555t-993325fe00e58804eb2d9a2a6638684136680b9ce31e2fe863ac05c8b5e9929b3</citedby><cites>FETCH-LOGICAL-b555t-993325fe00e58804eb2d9a2a6638684136680b9ce31e2fe863ac05c8b5e9929b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566574/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566574/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18823537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kerah-Hinzoumbé, Clément</creatorcontrib><creatorcontrib>Péka, Mallaye</creatorcontrib><creatorcontrib>Nwane, Philippe</creatorcontrib><creatorcontrib>Donan-Gouni, Issa</creatorcontrib><creatorcontrib>Etang, Josiane</creatorcontrib><creatorcontrib>Samè-Ekobo, Albert</creatorcontrib><creatorcontrib>Simard, Frédéric</creatorcontrib><title>Insecticide resistance in Anopheles gambiae from south-western Chad, Central Africa</title><title>Malaria journal</title><addtitle>Malar J</addtitle><description>Indoor residual spraying and insecticide-treated nets (ITN) are essential components of malaria vector control in Africa. Pyrethroids are the only recommended compounds for nets treatment because they are fast-acting insecticides with low mammalian toxicity. However, there is growing concern that pyrethroid resistance may threaten the sustainability of ITN scaling-up programmes. Here, insecticide susceptibility was investigated in Anopheles gambiae sensu lato from an area of large scale ITN distribution programme in south-western Chad.
Susceptibility to 4% DDT, 0.05% deltamethrin, 0.75% permethrin, 0.1% bendiocarb and 5% malathion was assessed using the WHO standard procedures for adult mosquitoes. Tests were carried out with two to four days-old, non-engorged female mosquitoes. The An. gambiae Kisumu strain was used as a reference. Knockdown effect was recorded every 5 min and mortality scored 24 h after exposure. Mosquitoes were identified to species and molecular form by PCR-RFLP and genotypes at the kdr locus were determined in surviving specimens by Hot Oligonucleotide Ligation Assay (HOLA).
During this survey, full susceptibility to malathion was recorded in all samples. Reduced susceptibility to bendiocarb (mortality rate of 96.1%) was found in one sample out of nine assayed. Increased tolerance to pyrethroids was detected in most samples (8/9) with mortality rates ranging from 70.2 to 96.6% for deltamethrin and from 26.7 to 96.3% for permethrin. Pyrethroid tolerance was not associated with a significant increase of knock-down times. Anopheles arabiensis was the predominant species of the An. gambiae complex in the study area, representing 75 to 100% of the samples. Screening for kdr mutations detected the L1014F mutation in 88.6% (N = 35) of surviving An. gambiae sensu stricto S form mosquitoes. All surviving An. arabiensis (N = 49) and M form An. gambiae s.s. (N = 1) carried the susceptible allele.
This first investigation of malaria vector susceptibility to insecticides in Chad revealed variable levels of resistance to pyrethroid insecticides (permethrin and deltamethrin) in most An. gambiae s.l. populations. Resistance was associated with the L1014F kdr mutation in the S form of An. gambiae s.s.. Alternative mechanisms, probably of metabolic origin are involved in An. arabiensis. These results emphasize the crucial need for insecticide resistance monitoring and in-depth investigation of resistance mechanisms in malaria vectors in Chad. The impact of reduced susceptibility to pyrethroids on ITN efficacy should be further assessed.</description><subject>Amino Acid Substitution - genetics</subject><subject>Animals</subject><subject>Anopheles - classification</subject><subject>Anopheles - drug effects</subject><subject>Anopheles - genetics</subject><subject>Care and treatment</subject><subject>Chad</subject><subject>Demographic aspects</subject><subject>Drug Resistance</subject><subject>Genotype</subject><subject>Insect Proteins - genetics</subject><subject>Insecticide resistance</subject><subject>Insecticides - pharmacology</subject><subject>Malaria</subject><subject>Mutation, Missense</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Pyrethrins - pharmacology</subject><subject>Survival Analysis</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1klmLFDEQx4Mo7qHPvkl_AHs3R-d6EcbBY2DBB_U5JOnKTJbpZEh6Fb-9GXvZ3QElkBR1_CrFvxB6Q_AVIUpck0Hynqp2yZ5o-gydP3ieP7HP0EWttxgTqSR9ic6IUpRxJs_Rt02q4Ofo4whdgRrrbJOHLqZulfJhB3uo3dZOLlroQslTV_PdvOt_QZ2hpG69s-O7bg1pLnbfrUKJ3r5CL4LdV3h9_16iH58-fl9_6W--ft6sVze945zPvdaMUR4AY-BK4QEcHbWlVgimhBoIE0Jhpz0wAjSAEsx6zL1yHLSm2rFLtFm4Y7a35lDiZMtvk200fx25bI0tbbQ9GKw1kQzcYDEZvBBWa0914I4CpdweWe8X1uHOTTD6ZaAT6GkkxZ3Z5p-GciG4HBrgwwJwMf8HcBrxeTJHgcxRICNNk69BrhbI1rZPxxRyS_XtjDBFnxOE2PyrprxUgnDdCq6XAl9yrQXCQ0OCzXFD_tHi7dNBH_PvV4L9AZIetwA</recordid><startdate>20080929</startdate><enddate>20080929</enddate><creator>Kerah-Hinzoumbé, Clément</creator><creator>Péka, Mallaye</creator><creator>Nwane, Philippe</creator><creator>Donan-Gouni, Issa</creator><creator>Etang, Josiane</creator><creator>Samè-Ekobo, Albert</creator><creator>Simard, Frédéric</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20080929</creationdate><title>Insecticide resistance in Anopheles gambiae from south-western Chad, Central Africa</title><author>Kerah-Hinzoumbé, Clément ; Péka, Mallaye ; Nwane, Philippe ; Donan-Gouni, Issa ; Etang, Josiane ; Samè-Ekobo, Albert ; Simard, Frédéric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b555t-993325fe00e58804eb2d9a2a6638684136680b9ce31e2fe863ac05c8b5e9929b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amino Acid Substitution - genetics</topic><topic>Animals</topic><topic>Anopheles - classification</topic><topic>Anopheles - drug effects</topic><topic>Anopheles - genetics</topic><topic>Care and treatment</topic><topic>Chad</topic><topic>Demographic aspects</topic><topic>Drug Resistance</topic><topic>Genotype</topic><topic>Insect Proteins - genetics</topic><topic>Insecticide resistance</topic><topic>Insecticides - pharmacology</topic><topic>Malaria</topic><topic>Mutation, Missense</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Pyrethrins - pharmacology</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kerah-Hinzoumbé, Clément</creatorcontrib><creatorcontrib>Péka, Mallaye</creatorcontrib><creatorcontrib>Nwane, Philippe</creatorcontrib><creatorcontrib>Donan-Gouni, Issa</creatorcontrib><creatorcontrib>Etang, Josiane</creatorcontrib><creatorcontrib>Samè-Ekobo, Albert</creatorcontrib><creatorcontrib>Simard, Frédéric</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kerah-Hinzoumbé, Clément</au><au>Péka, Mallaye</au><au>Nwane, Philippe</au><au>Donan-Gouni, Issa</au><au>Etang, Josiane</au><au>Samè-Ekobo, Albert</au><au>Simard, Frédéric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insecticide resistance in Anopheles gambiae from south-western Chad, Central Africa</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2008-09-29</date><risdate>2008</risdate><volume>7</volume><issue>1</issue><spage>192</spage><epage>192</epage><pages>192-192</pages><artnum>192</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>Indoor residual spraying and insecticide-treated nets (ITN) are essential components of malaria vector control in Africa. Pyrethroids are the only recommended compounds for nets treatment because they are fast-acting insecticides with low mammalian toxicity. However, there is growing concern that pyrethroid resistance may threaten the sustainability of ITN scaling-up programmes. Here, insecticide susceptibility was investigated in Anopheles gambiae sensu lato from an area of large scale ITN distribution programme in south-western Chad.
Susceptibility to 4% DDT, 0.05% deltamethrin, 0.75% permethrin, 0.1% bendiocarb and 5% malathion was assessed using the WHO standard procedures for adult mosquitoes. Tests were carried out with two to four days-old, non-engorged female mosquitoes. The An. gambiae Kisumu strain was used as a reference. Knockdown effect was recorded every 5 min and mortality scored 24 h after exposure. Mosquitoes were identified to species and molecular form by PCR-RFLP and genotypes at the kdr locus were determined in surviving specimens by Hot Oligonucleotide Ligation Assay (HOLA).
During this survey, full susceptibility to malathion was recorded in all samples. Reduced susceptibility to bendiocarb (mortality rate of 96.1%) was found in one sample out of nine assayed. Increased tolerance to pyrethroids was detected in most samples (8/9) with mortality rates ranging from 70.2 to 96.6% for deltamethrin and from 26.7 to 96.3% for permethrin. Pyrethroid tolerance was not associated with a significant increase of knock-down times. Anopheles arabiensis was the predominant species of the An. gambiae complex in the study area, representing 75 to 100% of the samples. Screening for kdr mutations detected the L1014F mutation in 88.6% (N = 35) of surviving An. gambiae sensu stricto S form mosquitoes. All surviving An. arabiensis (N = 49) and M form An. gambiae s.s. (N = 1) carried the susceptible allele.
This first investigation of malaria vector susceptibility to insecticides in Chad revealed variable levels of resistance to pyrethroid insecticides (permethrin and deltamethrin) in most An. gambiae s.l. populations. Resistance was associated with the L1014F kdr mutation in the S form of An. gambiae s.s.. Alternative mechanisms, probably of metabolic origin are involved in An. arabiensis. These results emphasize the crucial need for insecticide resistance monitoring and in-depth investigation of resistance mechanisms in malaria vectors in Chad. The impact of reduced susceptibility to pyrethroids on ITN efficacy should be further assessed.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>18823537</pmid><doi>10.1186/1475-2875-7-192</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Substitution - genetics Animals Anopheles - classification Anopheles - drug effects Anopheles - genetics Care and treatment Chad Demographic aspects Drug Resistance Genotype Insect Proteins - genetics Insecticide resistance Insecticides - pharmacology Malaria Mutation, Missense Polymorphism, Restriction Fragment Length Pyrethrins - pharmacology Survival Analysis |
title | Insecticide resistance in Anopheles gambiae from south-western Chad, Central Africa |
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