Measuring local genetic variation in permethrin-resistant head lice (Phthiraptera: Pediculidae) from Buenos Aires, Argentina
The cosmopolitan ectoparasite humanheadlouse, Pediculus humanuscapitis (DeGeer)(Phthiraptera:Pediculidae), affects mostly school-aged children, with infestations reported every year mainly due to louse resistance to pyrethroids. One of the main resistance mechanisms of pyrethroids is the target site...
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description | The cosmopolitan ectoparasite humanheadlouse, Pediculus humanuscapitis (DeGeer)(Phthiraptera:Pediculidae), affects mostly school-aged children, with infestations reported every year mainly due to louse resistance to pyrethroids. One of the main resistance mechanisms of pyrethroids is the target site insensitivity (kdr), which is caused by single-nucleotide point mutations (SNPs) located in the voltage-sensitive sodium channel gene. In this study, we analyzed individual head lice toxicologically via the description of their susceptibility profile to permethrin and genetically through the genotypification of their kdr alleles as well as nuclear microsatellite loci. Lice were collected from 4 schools in the city of Buenos Aires, Argentina. The resistance ratios varied from 33.3% to 71.4%, with a frequency of the T917I kdr mutation of 87.31% and with 83.6% of the head lice being homozygous resistant to pyrethroids. Microsatellite data indicated that all the louse school populations had genotype proportions that deviated from Hardy–Weinberg expectations, with FIS > 0 reflecting a deficit of heterozygotes. Bottleneck analysis suggested that all louse school populations underwent a recent reduction in population sizes, while 3 of the 4 schools had gene flow values around 1, indicating ongoing gene flow among those schools. Our study suggests that school louse populations in the city of Buenos Aires may form a metapopulation, where each school represents a small population that undergoes extinction and recolonization processes under strong permethrin selection. This is the first multilevel analysis integrating toxicological, kdr-genotyping, and microsatellite data in human louse populations. Graphical Abstract |
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One of the main resistance mechanisms of pyrethroids is the target site insensitivity (kdr), which is caused by single-nucleotide point mutations (SNPs) located in the voltage-sensitive sodium channel gene. In this study, we analyzed individual head lice toxicologically via the description of their susceptibility profile to permethrin and genetically through the genotypification of their kdr alleles as well as nuclear microsatellite loci. Lice were collected from 4 schools in the city of Buenos Aires, Argentina. The resistance ratios varied from 33.3% to 71.4%, with a frequency of the T917I kdr mutation of 87.31% and with 83.6% of the head lice being homozygous resistant to pyrethroids. Microsatellite data indicated that all the louse school populations had genotype proportions that deviated from Hardy–Weinberg expectations, with FIS > 0 reflecting a deficit of heterozygotes. Bottleneck analysis suggested that all louse school populations underwent a recent reduction in population sizes, while 3 of the 4 schools had gene flow values around 1, indicating ongoing gene flow among those schools. Our study suggests that school louse populations in the city of Buenos Aires may form a metapopulation, where each school represents a small population that undergoes extinction and recolonization processes under strong permethrin selection. This is the first multilevel analysis integrating toxicological, kdr-genotyping, and microsatellite data in human louse populations. Graphical Abstract</description><identifier>ISSN: 0022-2585</identifier><identifier>ISSN: 1938-2928</identifier><identifier>EISSN: 1938-2928</identifier><identifier>DOI: 10.1093/jme/tjae048</identifier><identifier>PMID: 38635291</identifier><language>eng</language><publisher>US: Entomological Society of America</publisher><subject>Argentina ; Ectoparasites ; Gene flow ; Genetic diversity ; Genotypes ; Genotyping ; Head ; Heterozygotes ; human head lice ; insecticide resistance ; Insecticides ; kdr ; KDR gene ; Lice ; Metapopulations ; Mutation ; Nucleotides ; Pediculidae ; Permethrin ; Phthiraptera ; Point mutation ; population genetic structure ; Population genetics ; Population studies ; Populations ; Pyrethroids ; Recolonization ; Schools ; Single-nucleotide polymorphism ; Sodium channels ; Sodium channels (voltage-gated) ; Species extinction ; VECTOR CONTROL, PEST MANAGEMENT, RESISTANCE, REPELLENTS</subject><ispartof>Journal of medical entomology, 2024-04, Vol.61 (4), p.984-994</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-b270t-cece1f6ab193cbb0cd395b9af7faf22563b301982851f3b8f62c42365eb519263</cites><orcidid>Vector Control, Pest Management, Resistance, Repellents ; 0000-0003-2090-2135 ; 0000-0002-5239-3585</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38635291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Severson, David</contributor><creatorcontrib>Toloza, Ariel C.</creatorcontrib><creatorcontrib>Ascunce, Marina S.</creatorcontrib><creatorcontrib>Reed, David L.</creatorcontrib><title>Measuring local genetic variation in permethrin-resistant head lice (Phthiraptera: Pediculidae) from Buenos Aires, Argentina</title><title>Journal of medical entomology</title><addtitle>J Med Entomol</addtitle><description>The cosmopolitan ectoparasite humanheadlouse, Pediculus humanuscapitis (DeGeer)(Phthiraptera:Pediculidae), affects mostly school-aged children, with infestations reported every year mainly due to louse resistance to pyrethroids. One of the main resistance mechanisms of pyrethroids is the target site insensitivity (kdr), which is caused by single-nucleotide point mutations (SNPs) located in the voltage-sensitive sodium channel gene. In this study, we analyzed individual head lice toxicologically via the description of their susceptibility profile to permethrin and genetically through the genotypification of their kdr alleles as well as nuclear microsatellite loci. Lice were collected from 4 schools in the city of Buenos Aires, Argentina. The resistance ratios varied from 33.3% to 71.4%, with a frequency of the T917I kdr mutation of 87.31% and with 83.6% of the head lice being homozygous resistant to pyrethroids. Microsatellite data indicated that all the louse school populations had genotype proportions that deviated from Hardy–Weinberg expectations, with FIS > 0 reflecting a deficit of heterozygotes. Bottleneck analysis suggested that all louse school populations underwent a recent reduction in population sizes, while 3 of the 4 schools had gene flow values around 1, indicating ongoing gene flow among those schools. Our study suggests that school louse populations in the city of Buenos Aires may form a metapopulation, where each school represents a small population that undergoes extinction and recolonization processes under strong permethrin selection. This is the first multilevel analysis integrating toxicological, kdr-genotyping, and microsatellite data in human louse populations. Graphical Abstract</description><subject>Argentina</subject><subject>Ectoparasites</subject><subject>Gene flow</subject><subject>Genetic diversity</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Head</subject><subject>Heterozygotes</subject><subject>human head lice</subject><subject>insecticide resistance</subject><subject>Insecticides</subject><subject>kdr</subject><subject>KDR gene</subject><subject>Lice</subject><subject>Metapopulations</subject><subject>Mutation</subject><subject>Nucleotides</subject><subject>Pediculidae</subject><subject>Permethrin</subject><subject>Phthiraptera</subject><subject>Point mutation</subject><subject>population genetic structure</subject><subject>Population genetics</subject><subject>Population studies</subject><subject>Populations</subject><subject>Pyrethroids</subject><subject>Recolonization</subject><subject>Schools</subject><subject>Single-nucleotide polymorphism</subject><subject>Sodium channels</subject><subject>Sodium channels (voltage-gated)</subject><subject>Species extinction</subject><subject>VECTOR CONTROL, PEST MANAGEMENT, RESISTANCE, REPELLENTS</subject><issn>0022-2585</issn><issn>1938-2928</issn><issn>1938-2928</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqF0c9PFDEUB_DGSGRFT95NExMCgZH-mJltua1EkAQjBz1P2s4r281MO7QdEhL-eKu7ePCgp14-_b738kXoHSUfKZH8bDPCWd4oILV4gRZUclExycRLtCCEsYo1otlHr1PaEEIEreUrtM9Fyxsm6QI9fQWV5uj8HR6CUQO-Aw_ZGfygolPZBY-dxxPEEfK6sCpCcikrn_EaVI8HZwAf3a7z2kU1ZYjqHN9C78w8uF7BMbYxjPjTDD4kvHLl9ylexTIkO6_eoD2rhgRvd-8B-nH5-fvFl-rm29X1xeqm0mxJcmXAALWt0uU2ozUxPZeNlsourbKMNS3XnFApmGio5VrYlpma8bYB3VDJWn6Ajra5Uwz3M6TcjS4ZGAblIcyp46SmjPP2N_3wF92EOfqyXccpE4Tymi2LOtkqE0NKEWw3RTeq-NhR0v0qpSuldLtSin6_y5z1CP0f-9xCAYdbEObpP0nHW6hdCB7-aX8CUmukyA</recordid><startdate>20240418</startdate><enddate>20240418</enddate><creator>Toloza, Ariel C.</creator><creator>Ascunce, Marina S.</creator><creator>Reed, David L.</creator><general>Entomological Society of America</general><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/Vector Control, Pest Management, Resistance, Repellents</orcidid><orcidid>https://orcid.org/0000-0003-2090-2135</orcidid><orcidid>https://orcid.org/0000-0002-5239-3585</orcidid></search><sort><creationdate>20240418</creationdate><title>Measuring local genetic variation in permethrin-resistant head lice (Phthiraptera: Pediculidae) from Buenos Aires, Argentina</title><author>Toloza, Ariel C. ; Ascunce, Marina S. ; Reed, David L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b270t-cece1f6ab193cbb0cd395b9af7faf22563b301982851f3b8f62c42365eb519263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Argentina</topic><topic>Ectoparasites</topic><topic>Gene flow</topic><topic>Genetic diversity</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>Head</topic><topic>Heterozygotes</topic><topic>human head lice</topic><topic>insecticide resistance</topic><topic>Insecticides</topic><topic>kdr</topic><topic>KDR gene</topic><topic>Lice</topic><topic>Metapopulations</topic><topic>Mutation</topic><topic>Nucleotides</topic><topic>Pediculidae</topic><topic>Permethrin</topic><topic>Phthiraptera</topic><topic>Point mutation</topic><topic>population genetic structure</topic><topic>Population genetics</topic><topic>Population studies</topic><topic>Populations</topic><topic>Pyrethroids</topic><topic>Recolonization</topic><topic>Schools</topic><topic>Single-nucleotide polymorphism</topic><topic>Sodium channels</topic><topic>Sodium channels (voltage-gated)</topic><topic>Species extinction</topic><topic>VECTOR CONTROL, PEST MANAGEMENT, RESISTANCE, REPELLENTS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toloza, Ariel C.</creatorcontrib><creatorcontrib>Ascunce, Marina S.</creatorcontrib><creatorcontrib>Reed, David L.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical entomology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Toloza, Ariel C.</au><au>Ascunce, Marina S.</au><au>Reed, David L.</au><au>Severson, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measuring local genetic variation in permethrin-resistant head lice (Phthiraptera: Pediculidae) from Buenos Aires, Argentina</atitle><jtitle>Journal of medical entomology</jtitle><addtitle>J Med Entomol</addtitle><date>2024-04-18</date><risdate>2024</risdate><volume>61</volume><issue>4</issue><spage>984</spage><epage>994</epage><pages>984-994</pages><issn>0022-2585</issn><issn>1938-2928</issn><eissn>1938-2928</eissn><abstract>The cosmopolitan ectoparasite humanheadlouse, Pediculus humanuscapitis (DeGeer)(Phthiraptera:Pediculidae), affects mostly school-aged children, with infestations reported every year mainly due to louse resistance to pyrethroids. One of the main resistance mechanisms of pyrethroids is the target site insensitivity (kdr), which is caused by single-nucleotide point mutations (SNPs) located in the voltage-sensitive sodium channel gene. In this study, we analyzed individual head lice toxicologically via the description of their susceptibility profile to permethrin and genetically through the genotypification of their kdr alleles as well as nuclear microsatellite loci. Lice were collected from 4 schools in the city of Buenos Aires, Argentina. The resistance ratios varied from 33.3% to 71.4%, with a frequency of the T917I kdr mutation of 87.31% and with 83.6% of the head lice being homozygous resistant to pyrethroids. Microsatellite data indicated that all the louse school populations had genotype proportions that deviated from Hardy–Weinberg expectations, with FIS > 0 reflecting a deficit of heterozygotes. Bottleneck analysis suggested that all louse school populations underwent a recent reduction in population sizes, while 3 of the 4 schools had gene flow values around 1, indicating ongoing gene flow among those schools. Our study suggests that school louse populations in the city of Buenos Aires may form a metapopulation, where each school represents a small population that undergoes extinction and recolonization processes under strong permethrin selection. This is the first multilevel analysis integrating toxicological, kdr-genotyping, and microsatellite data in human louse populations. Graphical Abstract</abstract><cop>US</cop><pub>Entomological Society of America</pub><pmid>38635291</pmid><doi>10.1093/jme/tjae048</doi><tpages>11</tpages><orcidid>https://orcid.org/Vector Control, Pest Management, Resistance, Repellents</orcidid><orcidid>https://orcid.org/0000-0003-2090-2135</orcidid><orcidid>https://orcid.org/0000-0002-5239-3585</orcidid></addata></record> |
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subjects | Argentina Ectoparasites Gene flow Genetic diversity Genotypes Genotyping Head Heterozygotes human head lice insecticide resistance Insecticides kdr KDR gene Lice Metapopulations Mutation Nucleotides Pediculidae Permethrin Phthiraptera Point mutation population genetic structure Population genetics Population studies Populations Pyrethroids Recolonization Schools Single-nucleotide polymorphism Sodium channels Sodium channels (voltage-gated) Species extinction VECTOR CONTROL, PEST MANAGEMENT, RESISTANCE, REPELLENTS |
title | Measuring local genetic variation in permethrin-resistant head lice (Phthiraptera: Pediculidae) from Buenos Aires, Argentina |
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