Insecticide resistance allele frequencies in Anopheles gambiae before and after anti-vector interventions in continental Equatorial Guinea
Anti-malaria interventions that rely on insecticides can be compromised by insecticide-resistance alleles among malaria vectors. We examined frequency changes of resistance alleles at two loci, knockdown resistance (kdr) and acetylcholinesterase-1 (ace-1), which confer resistance to pyrethroids and...
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Veröffentlicht in: | The American journal of tropical medicine and hygiene 2013-05, Vol.88 (5), p.897-907 |
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creator | Reddy, Michael R Godoy, Adrian Dion, Kirstin Matias, Abrahan Callender, Kevin Kiszewski, Anthony E Kleinschmidt, Immo Ridl, Frances C Powell, Jeffrey R Caccone, Adalgisa Slotman, Michel A |
description | Anti-malaria interventions that rely on insecticides can be compromised by insecticide-resistance alleles among malaria vectors. We examined frequency changes of resistance alleles at two loci, knockdown resistance (kdr) and acetylcholinesterase-1 (ace-1), which confer resistance to pyrethroids and DDT, and carbamates, respectively. A total of 7,059 Anopheles gambiae sensu stricto mosquitoes were analyzed from multiple sites across continental Equatorial Guinea. A subset of sites included samples collected pre-intervention (2007) and post-intervention (2009-2011). Both L1014S and L1014F resistance alleles were observed in almost all pre-intervention collections. In particular, L1014F was already at substantial frequencies in M form populations (17.6-74.6%), and at high frequencies (> 50%) in all but two S form populations. Comparison before and throughout anti-vector interventions showed drastic increases in L1014F, presumably caused by intensified selection pressure imposed by pyrethroids used in vector control efforts. In light of these findings, inclusion of other insecticide classes in any anti-vector intervention can be considered prudent. |
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We examined frequency changes of resistance alleles at two loci, knockdown resistance (kdr) and acetylcholinesterase-1 (ace-1), which confer resistance to pyrethroids and DDT, and carbamates, respectively. A total of 7,059 Anopheles gambiae sensu stricto mosquitoes were analyzed from multiple sites across continental Equatorial Guinea. A subset of sites included samples collected pre-intervention (2007) and post-intervention (2009-2011). Both L1014S and L1014F resistance alleles were observed in almost all pre-intervention collections. In particular, L1014F was already at substantial frequencies in M form populations (17.6-74.6%), and at high frequencies (> 50%) in all but two S form populations. Comparison before and throughout anti-vector interventions showed drastic increases in L1014F, presumably caused by intensified selection pressure imposed by pyrethroids used in vector control efforts. 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We examined frequency changes of resistance alleles at two loci, knockdown resistance (kdr) and acetylcholinesterase-1 (ace-1), which confer resistance to pyrethroids and DDT, and carbamates, respectively. A total of 7,059 Anopheles gambiae sensu stricto mosquitoes were analyzed from multiple sites across continental Equatorial Guinea. A subset of sites included samples collected pre-intervention (2007) and post-intervention (2009-2011). Both L1014S and L1014F resistance alleles were observed in almost all pre-intervention collections. In particular, L1014F was already at substantial frequencies in M form populations (17.6-74.6%), and at high frequencies (> 50%) in all but two S form populations. Comparison before and throughout anti-vector interventions showed drastic increases in L1014F, presumably caused by intensified selection pressure imposed by pyrethroids used in vector control efforts. In light of these findings, inclusion of other insecticide classes in any anti-vector intervention can be considered prudent.</description><subject>Acetylcholinesterase - genetics</subject><subject>Alleles</subject><subject>Animals</subject><subject>Anopheles - drug effects</subject><subject>Anopheles - genetics</subject><subject>Anopheles gambiae</subject><subject>Gene Frequency</subject><subject>Insect Vectors - genetics</subject><subject>Insecticide Resistance - genetics</subject><subject>Insecticides - administration & dosage</subject><subject>Insecticides - pharmacology</subject><subject>Malaria - transmission</subject><subject>Mosquito Control - methods</subject><subject>Pyrethrins - administration & dosage</subject><subject>Pyrethrins - pharmacology</subject><issn>0002-9637</issn><issn>1476-1645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctuFDEQRS0EIkNgyRZ5yaaDH-3HbJCiKIRIkdjA2nK7yxlH3fbE7h6JX8hXU5OECFYuXZ-6VapLyEfOznqht1_83TLvzrjoWK_NK7LhvdEd1716TTaMMdFttTQn5F1rd4xxKzh_S06E7KU12m7Iw3VuEJYU0gi0Qktt8TkA9dMEE9BY4X6FHBI0mjI9z2W_Q73RWz8PyQMdIJaKeB6pjwtUrJbUHdCyVOxA5QColPzYHwrWGQU_0cv71SOUsLxaUfTvyZvopwYfnt9T8uvb5c-L793Nj6vri_ObLvSCLZ2KXtqwVdoOwWwtyMELIyGCGayVvYgwKt5rPQqhlLXcxNEKNXg5SBFt1PKUfH3y3a_DDGPAdaqf3L6m2dffrvjk_v_Jaeduy8FJo4RRCg0-PxvUgtdpi5tTCzBNPkNZm8PrG8Y1k0e0e0JDLa1ViC9jOHPH_Nxjfo4Ld8wP-U__7vZC_w1M_gG2SJwH</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Reddy, Michael R</creator><creator>Godoy, Adrian</creator><creator>Dion, Kirstin</creator><creator>Matias, Abrahan</creator><creator>Callender, Kevin</creator><creator>Kiszewski, Anthony E</creator><creator>Kleinschmidt, Immo</creator><creator>Ridl, Frances C</creator><creator>Powell, Jeffrey R</creator><creator>Caccone, Adalgisa</creator><creator>Slotman, Michel A</creator><general>The American Society of Tropical Medicine and Hygiene</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>7QL</scope><scope>7SS</scope><scope>7T2</scope><scope>7U2</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>201305</creationdate><title>Insecticide resistance allele frequencies in Anopheles gambiae before and after anti-vector interventions in continental Equatorial Guinea</title><author>Reddy, Michael R ; Godoy, Adrian ; Dion, Kirstin ; Matias, Abrahan ; Callender, Kevin ; Kiszewski, Anthony E ; Kleinschmidt, Immo ; Ridl, Frances C ; Powell, Jeffrey R ; Caccone, Adalgisa ; Slotman, Michel A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-5fa38c9568bc798e3ba273efe7b88342fed51466d22558817fd825ba3b32f8f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acetylcholinesterase - genetics</topic><topic>Alleles</topic><topic>Animals</topic><topic>Anopheles - drug effects</topic><topic>Anopheles - genetics</topic><topic>Anopheles gambiae</topic><topic>Gene Frequency</topic><topic>Insect Vectors - genetics</topic><topic>Insecticide Resistance - genetics</topic><topic>Insecticides - administration & dosage</topic><topic>Insecticides - pharmacology</topic><topic>Malaria - transmission</topic><topic>Mosquito Control - methods</topic><topic>Pyrethrins - administration & dosage</topic><topic>Pyrethrins - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reddy, Michael R</creatorcontrib><creatorcontrib>Godoy, Adrian</creatorcontrib><creatorcontrib>Dion, Kirstin</creatorcontrib><creatorcontrib>Matias, Abrahan</creatorcontrib><creatorcontrib>Callender, Kevin</creatorcontrib><creatorcontrib>Kiszewski, Anthony E</creatorcontrib><creatorcontrib>Kleinschmidt, Immo</creatorcontrib><creatorcontrib>Ridl, Frances C</creatorcontrib><creatorcontrib>Powell, Jeffrey R</creatorcontrib><creatorcontrib>Caccone, Adalgisa</creatorcontrib><creatorcontrib>Slotman, Michel A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of tropical medicine and hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reddy, Michael R</au><au>Godoy, Adrian</au><au>Dion, Kirstin</au><au>Matias, Abrahan</au><au>Callender, Kevin</au><au>Kiszewski, Anthony E</au><au>Kleinschmidt, Immo</au><au>Ridl, Frances C</au><au>Powell, Jeffrey R</au><au>Caccone, Adalgisa</au><au>Slotman, Michel A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insecticide resistance allele frequencies in Anopheles gambiae before and after anti-vector interventions in continental Equatorial Guinea</atitle><jtitle>The American journal of tropical medicine and hygiene</jtitle><addtitle>Am J Trop Med Hyg</addtitle><date>2013-05</date><risdate>2013</risdate><volume>88</volume><issue>5</issue><spage>897</spage><epage>907</epage><pages>897-907</pages><issn>0002-9637</issn><eissn>1476-1645</eissn><abstract>Anti-malaria interventions that rely on insecticides can be compromised by insecticide-resistance alleles among malaria vectors. We examined frequency changes of resistance alleles at two loci, knockdown resistance (kdr) and acetylcholinesterase-1 (ace-1), which confer resistance to pyrethroids and DDT, and carbamates, respectively. A total of 7,059 Anopheles gambiae sensu stricto mosquitoes were analyzed from multiple sites across continental Equatorial Guinea. A subset of sites included samples collected pre-intervention (2007) and post-intervention (2009-2011). Both L1014S and L1014F resistance alleles were observed in almost all pre-intervention collections. In particular, L1014F was already at substantial frequencies in M form populations (17.6-74.6%), and at high frequencies (> 50%) in all but two S form populations. Comparison before and throughout anti-vector interventions showed drastic increases in L1014F, presumably caused by intensified selection pressure imposed by pyrethroids used in vector control efforts. 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subjects | Acetylcholinesterase - genetics Alleles Animals Anopheles - drug effects Anopheles - genetics Anopheles gambiae Gene Frequency Insect Vectors - genetics Insecticide Resistance - genetics Insecticides - administration & dosage Insecticides - pharmacology Malaria - transmission Mosquito Control - methods Pyrethrins - administration & dosage Pyrethrins - pharmacology |
title | Insecticide resistance allele frequencies in Anopheles gambiae before and after anti-vector interventions in continental Equatorial Guinea |
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