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    <titleInfo>
      <title>CCR5 polymorphism and plague resistance in natural populations of the black rat in Madagascar</title>
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    <name type="personnal">
      <namePart type="family">Tollenaere</namePart>
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      <namePart type="family">Rahalison</namePart>
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    <name type="personnal">
      <namePart type="family">Ranjalahy</namePart>
      <namePart type="given">M.</namePart>
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        <roleTerm type="text">auteur</roleTerm>
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    <name type="personnal">
      <namePart type="family">Rahelinirina</namePart>
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    <name type="personnal">
      <namePart type="family">Duplantier</namePart>
      <namePart type="given">Jean-Marc</namePart>
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    <name type="personnal">
      <namePart type="family">Brouat</namePart>
      <namePart type="given">Carine</namePart>
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    <abstract>Madagascar remains one of the world's largest plague foci. The black rat, Rattus rattus, is the main reservoir of plague in rural areas. This species is highly susceptible to plague in plague-free areas (low-altitude regions), whereas rats from the plague focus areas (central highlands) have evolved a disease-resistance polymorphism. We used the candidate gene CCR5 to investigate the genetic basis of plague resistance in R. rattus. We found a unique non-synonymous substitution (H184R) in a functionally important region of the gene. We then compared (i) CCR5 genotypes of dying and surviving plague-challenged rats and (ii) CCR5 allelic frequencies in plague focus and plague-free populations. Our results suggested a higher prevalence of the substitution in resistant animals compared to susceptible individuals, and a tendency for higher frequencies in plague focus areas compared to plague-free areas. Therefore, the CCR5 polymorphism may be involved in Malagasy black rat plague resistance. CCR5 and other undetermined plague resistance markers may provide useful biological information about host evolution and disease dynamics.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <subject>
      <topic>Infectious disease resistance</topic>
      <topic>Yersinia pestis</topic>
      <topic>Chemokine receptor</topic>
      <topic>Candidate gene</topic>
      <topic>Immunogenetics</topic>
    </subject>
    <classification authority="local">080</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Infection Genetics and Evolution</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>8</number>
        </detail>
        <detail type="volume">
          <number>6</number>
        </detail>
        <extent unit="pages">
          <list> 891-897</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2008</dateIssued>
      </originInfo>
      <identifier type="issn">1567-1348</identifier>
    </relatedItem>
    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010044159</identifier>
    <identifier type="doi">10.1016/j.meegid.2008.07.005</identifier>
    <identifier type="issn">1567-1348</identifier>
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      <url access="row object">https://www.documentation.ird.fr/intranet/publi/2009/01/010044159.pdf</url>
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      <recordContentSource>IRD - Base Horizon / Pleins textes</recordContentSource>
      <recordCreationDate encoding="w3cdtf">2009-02-06</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2017-08-23</recordChangeDate>
      <recordIdentifier>fdi:010044159</recordIdentifier>
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        <languageTerm authority="iso639-2b">fre</languageTerm>
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