A sensory appendage protein protects malaria vectors from pyrethroids
Pyrethroid-impregnated bed nets have driven considerable reductions in malaria-associated morbidity and mortality in Africa since the beginning of the century 1 . The intense selection pressure exerted by bed nets has precipitated widespread and escalating resistance to pyrethroids in African Anophe...
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description | Pyrethroid-impregnated bed nets have driven considerable reductions in malaria-associated morbidity and mortality in Africa since the beginning of the century
1
. The intense selection pressure exerted by bed nets has precipitated widespread and escalating resistance to pyrethroids in African
Anopheles
populations, threatening to reverse the gains that been made by malaria control
2
. Here we show that expression of a sensory appendage protein (SAP2), which is enriched in the legs, confers pyrethroid resistance to
Anopheles gambiae
. Expression of
SAP2
is increased in insecticide-resistant populations and is further induced after the mosquito comes into contact with pyrethroids.
SAP2
silencing fully restores mortality of the mosquitoes, whereas
SAP2
overexpression results in increased resistance, probably owing to high-affinity binding of SAP2 to pyrethroid insecticides. Mining of genome sequence data reveals a selective sweep near the
SAP2
locus in the mosquito populations of three West African countries (Cameroon, Guinea and Burkina Faso) with the observed increase in haplotype-associated single-nucleotide polymorphisms mirroring the increasing resistance of mosquitoes to pyrethroids reported in Burkina Faso. Our study identifies a previously undescribed mechanism of insecticide resistance that is likely to be highly relevant to malaria control efforts.
The leg-enriched sensory appendage protein, SAP2, confers pyrethroid resistance to
Anopheles gambiae
, through high-affinity binding of pyrethroid insecticides; an observed selective sweep in field mosquitoes mirrors the increasing resistance reported in Africa. |
doi_str_mv | 10.1038/s41586-019-1864-1 |
format | Article |
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1
. The intense selection pressure exerted by bed nets has precipitated widespread and escalating resistance to pyrethroids in African
Anopheles
populations, threatening to reverse the gains that been made by malaria control
2
. Here we show that expression of a sensory appendage protein (SAP2), which is enriched in the legs, confers pyrethroid resistance to
Anopheles gambiae
. Expression of
SAP2
is increased in insecticide-resistant populations and is further induced after the mosquito comes into contact with pyrethroids.
SAP2
silencing fully restores mortality of the mosquitoes, whereas
SAP2
overexpression results in increased resistance, probably owing to high-affinity binding of SAP2 to pyrethroid insecticides. Mining of genome sequence data reveals a selective sweep near the
SAP2
locus in the mosquito populations of three West African countries (Cameroon, Guinea and Burkina Faso) with the observed increase in haplotype-associated single-nucleotide polymorphisms mirroring the increasing resistance of mosquitoes to pyrethroids reported in Burkina Faso. Our study identifies a previously undescribed mechanism of insecticide resistance that is likely to be highly relevant to malaria control efforts.
The leg-enriched sensory appendage protein, SAP2, confers pyrethroid resistance to
Anopheles gambiae
, through high-affinity binding of pyrethroid insecticides; an observed selective sweep in field mosquitoes mirrors the increasing resistance reported in Africa.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/s41586-019-1864-1</identifier><identifier>PMID: 31875852</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38 ; 38/39 ; 45 ; 45/43 ; 45/61 ; 45/77 ; 631/208/182 ; 631/326/417/2548 ; 631/601/1466 ; 82 ; 82/80 ; Abdomen ; Africa, Central ; Analysis ; Animals ; Anopheles ; Anopheles - genetics ; Anopheles - metabolism ; Anopheles gambiae ; Aquatic insects ; Binding proteins ; Control ; Culicidae ; Cytochrome ; Distribution ; Female ; Forecasts and trends ; Genetic aspects ; Genomes ; Haplotypes ; Humanities and Social Sciences ; Insect Proteins - genetics ; Insect Proteins - metabolism ; Insecticide Resistance ; Insecticides ; Insecticides - pharmacology ; Laboratories ; Localization ; Malaria ; Metabolism ; Methods ; Morbidity ; Mortality ; Mosquito Control ; Mosquito Vectors - drug effects ; Mosquitoes ; multidisciplinary ; Nets ; Nucleotide sequence ; Nucleotides ; Pesticide resistance ; Physiological aspects ; Populations ; Proteins ; Pyrethrins - pharmacology ; Pyrethroids ; Science ; Science (multidisciplinary) ; Single-nucleotide polymorphism ; Variance analysis ; Vector control ; Vector-borne diseases ; Vectors</subject><ispartof>Nature (London), 2020-01, Vol.577 (7790), p.376-380</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2019</rights><rights>COPYRIGHT 2020 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jan 16, 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c675t-76efced9f2f02d50a4b6f7346ceefec17af962dfc2eea923fa48408a92dceaf23</citedby><cites>FETCH-LOGICAL-c675t-76efced9f2f02d50a4b6f7346ceefec17af962dfc2eea923fa48408a92dceaf23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41586-019-1864-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41586-019-1864-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31875852$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ingham, Victoria A.</creatorcontrib><creatorcontrib>Anthousi, Amalia</creatorcontrib><creatorcontrib>Douris, Vassilis</creatorcontrib><creatorcontrib>Harding, Nicholas J.</creatorcontrib><creatorcontrib>Lycett, Gareth</creatorcontrib><creatorcontrib>Morris, Marion</creatorcontrib><creatorcontrib>Vontas, John</creatorcontrib><creatorcontrib>Ranson, Hilary</creatorcontrib><title>A sensory appendage protein protects malaria vectors from pyrethroids</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Pyrethroid-impregnated bed nets have driven considerable reductions in malaria-associated morbidity and mortality in Africa since the beginning of the century
1
. The intense selection pressure exerted by bed nets has precipitated widespread and escalating resistance to pyrethroids in African
Anopheles
populations, threatening to reverse the gains that been made by malaria control
2
. Here we show that expression of a sensory appendage protein (SAP2), which is enriched in the legs, confers pyrethroid resistance to
Anopheles gambiae
. Expression of
SAP2
is increased in insecticide-resistant populations and is further induced after the mosquito comes into contact with pyrethroids.
SAP2
silencing fully restores mortality of the mosquitoes, whereas
SAP2
overexpression results in increased resistance, probably owing to high-affinity binding of SAP2 to pyrethroid insecticides. Mining of genome sequence data reveals a selective sweep near the
SAP2
locus in the mosquito populations of three West African countries (Cameroon, Guinea and Burkina Faso) with the observed increase in haplotype-associated single-nucleotide polymorphisms mirroring the increasing resistance of mosquitoes to pyrethroids reported in Burkina Faso. Our study identifies a previously undescribed mechanism of insecticide resistance that is likely to be highly relevant to malaria control efforts.
The leg-enriched sensory appendage protein, SAP2, confers pyrethroid resistance to
Anopheles gambiae
, through high-affinity binding of pyrethroid insecticides; an observed selective sweep in field mosquitoes mirrors the increasing resistance reported in Africa.</description><subject>38</subject><subject>38/39</subject><subject>45</subject><subject>45/43</subject><subject>45/61</subject><subject>45/77</subject><subject>631/208/182</subject><subject>631/326/417/2548</subject><subject>631/601/1466</subject><subject>82</subject><subject>82/80</subject><subject>Abdomen</subject><subject>Africa, Central</subject><subject>Analysis</subject><subject>Animals</subject><subject>Anopheles</subject><subject>Anopheles - genetics</subject><subject>Anopheles - metabolism</subject><subject>Anopheles gambiae</subject><subject>Aquatic insects</subject><subject>Binding proteins</subject><subject>Control</subject><subject>Culicidae</subject><subject>Cytochrome</subject><subject>Distribution</subject><subject>Female</subject><subject>Forecasts and trends</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Haplotypes</subject><subject>Humanities and Social Sciences</subject><subject>Insect Proteins - genetics</subject><subject>Insect Proteins - metabolism</subject><subject>Insecticide Resistance</subject><subject>Insecticides</subject><subject>Insecticides - pharmacology</subject><subject>Laboratories</subject><subject>Localization</subject><subject>Malaria</subject><subject>Metabolism</subject><subject>Methods</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Mosquito Control</subject><subject>Mosquito Vectors - drug effects</subject><subject>Mosquitoes</subject><subject>multidisciplinary</subject><subject>Nets</subject><subject>Nucleotide sequence</subject><subject>Nucleotides</subject><subject>Pesticide resistance</subject><subject>Physiological aspects</subject><subject>Populations</subject><subject>Proteins</subject><subject>Pyrethrins - pharmacology</subject><subject>Pyrethroids</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Single-nucleotide polymorphism</subject><subject>Variance analysis</subject><subject>Vector control</subject><subject>Vector-borne 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sensory appendage protein protects malaria vectors from pyrethroids</title><author>Ingham, Victoria A. ; Anthousi, Amalia ; Douris, Vassilis ; Harding, Nicholas J. ; Lycett, Gareth ; Morris, Marion ; Vontas, John ; Ranson, Hilary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c675t-76efced9f2f02d50a4b6f7346ceefec17af962dfc2eea923fa48408a92dceaf23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>38</topic><topic>38/39</topic><topic>45</topic><topic>45/43</topic><topic>45/61</topic><topic>45/77</topic><topic>631/208/182</topic><topic>631/326/417/2548</topic><topic>631/601/1466</topic><topic>82</topic><topic>82/80</topic><topic>Abdomen</topic><topic>Africa, Central</topic><topic>Analysis</topic><topic>Animals</topic><topic>Anopheles</topic><topic>Anopheles - genetics</topic><topic>Anopheles - metabolism</topic><topic>Anopheles gambiae</topic><topic>Aquatic insects</topic><topic>Binding proteins</topic><topic>Control</topic><topic>Culicidae</topic><topic>Cytochrome</topic><topic>Distribution</topic><topic>Female</topic><topic>Forecasts and trends</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Haplotypes</topic><topic>Humanities and Social Sciences</topic><topic>Insect Proteins - genetics</topic><topic>Insect Proteins - metabolism</topic><topic>Insecticide Resistance</topic><topic>Insecticides</topic><topic>Insecticides - pharmacology</topic><topic>Laboratories</topic><topic>Localization</topic><topic>Malaria</topic><topic>Metabolism</topic><topic>Methods</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Mosquito Control</topic><topic>Mosquito Vectors - drug effects</topic><topic>Mosquitoes</topic><topic>multidisciplinary</topic><topic>Nets</topic><topic>Nucleotide sequence</topic><topic>Nucleotides</topic><topic>Pesticide resistance</topic><topic>Physiological 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(London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2020-01-16</date><risdate>2020</risdate><volume>577</volume><issue>7790</issue><spage>376</spage><epage>380</epage><pages>376-380</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>Pyrethroid-impregnated bed nets have driven considerable reductions in malaria-associated morbidity and mortality in Africa since the beginning of the century
1
. The intense selection pressure exerted by bed nets has precipitated widespread and escalating resistance to pyrethroids in African
Anopheles
populations, threatening to reverse the gains that been made by malaria control
2
. Here we show that expression of a sensory appendage protein (SAP2), which is enriched in the legs, confers pyrethroid resistance to
Anopheles gambiae
. Expression of
SAP2
is increased in insecticide-resistant populations and is further induced after the mosquito comes into contact with pyrethroids.
SAP2
silencing fully restores mortality of the mosquitoes, whereas
SAP2
overexpression results in increased resistance, probably owing to high-affinity binding of SAP2 to pyrethroid insecticides. Mining of genome sequence data reveals a selective sweep near the
SAP2
locus in the mosquito populations of three West African countries (Cameroon, Guinea and Burkina Faso) with the observed increase in haplotype-associated single-nucleotide polymorphisms mirroring the increasing resistance of mosquitoes to pyrethroids reported in Burkina Faso. Our study identifies a previously undescribed mechanism of insecticide resistance that is likely to be highly relevant to malaria control efforts.
The leg-enriched sensory appendage protein, SAP2, confers pyrethroid resistance to
Anopheles gambiae
, through high-affinity binding of pyrethroid insecticides; an observed selective sweep in field mosquitoes mirrors the increasing resistance reported in Africa.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31875852</pmid><doi>10.1038/s41586-019-1864-1</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | MEDLINE; Springer Nature - Complete Springer Journals; Nature |
subjects | 38 38/39 45 45/43 45/61 45/77 631/208/182 631/326/417/2548 631/601/1466 82 82/80 Abdomen Africa, Central Analysis Animals Anopheles Anopheles - genetics Anopheles - metabolism Anopheles gambiae Aquatic insects Binding proteins Control Culicidae Cytochrome Distribution Female Forecasts and trends Genetic aspects Genomes Haplotypes Humanities and Social Sciences Insect Proteins - genetics Insect Proteins - metabolism Insecticide Resistance Insecticides Insecticides - pharmacology Laboratories Localization Malaria Metabolism Methods Morbidity Mortality Mosquito Control Mosquito Vectors - drug effects Mosquitoes multidisciplinary Nets Nucleotide sequence Nucleotides Pesticide resistance Physiological aspects Populations Proteins Pyrethrins - pharmacology Pyrethroids Science Science (multidisciplinary) Single-nucleotide polymorphism Variance analysis Vector control Vector-borne diseases Vectors |
title | A sensory appendage protein protects malaria vectors from pyrethroids |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A08%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20sensory%20appendage%20protein%20protects%20malaria%20vectors%20from%20pyrethroids&rft.jtitle=Nature%20(London)&rft.au=Ingham,%20Victoria%20A.&rft.date=2020-01-16&rft.volume=577&rft.issue=7790&rft.spage=376&rft.epage=380&rft.pages=376-380&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/s41586-019-1864-1&rft_dat=%3Cgale_pubme%3EA648895935%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2345781742&rft_id=info:pmid/31875852&rft_galeid=A648895935&rfr_iscdi=true |