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      <title>GSG6-P1 salivary biomarker discriminates micro-geographical heterogeneity of human exposure to Anopheles bites in low and seasonal malaria areas</title>
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    <abstract>Background: Over the past decade, a sharp decline of malaria burden has been observed in several countries. Consequently, the conventional entomological methods have become insufficiently sensitive and probably underestimate micro-geographical heterogeneity of exposure and subsequent risk of malaria transmission. In this study, we investigated whether the human antibody (Ab) response to Anopheles salivary gSG6-P1 peptide, known as a biomarker of Anopheles exposure, could be a sensitive and reliable tool for discriminating human exposure to Anopheles bites in area of low and seasonal malaria transmission. Methods: A multi-disciplinary survey was performed in Northern Senegal where An. gambiae s.l. is the main malaria vector. Human IgG Ab response to gSG6-P1 salivary peptide was compared according to the season and villages in children from five villages in the middle Senegal River valley, known as a low malaria transmission area. Results: IgG levels to gSG6-P1 varied considerably according to the villages, discriminating the heterogeneity of Anopheles exposure between villages. Significant increase of IgG levels to gSG6-P1 was observed during the peak of exposure to Anopheles bites, and decreased immediately after the end of the exposure season. In addition, differences in the season-dependent specific IgG levels between villages were observed after the implementation of Long-Lasting Insecticidal Nets by The National Malaria Control Program in this area. Conclusion: The gSG6-P1 salivary peptide seems to be a reliable tool to discriminate the micro-geographical heterogeneity of human exposure to Anopheles bites in areas of very low and seasonal malaria transmission. A biomarker such as this could also be used to monitor and evaluate the possible heterogeneous effectiveness of operational vector control programs in low-exposure areas.</abstract>
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    <subject>
      <topic>Malaria</topic>
      <topic>Salivary peptide</topic>
      <topic>Biomarker</topic>
      <topic>Low transmission</topic>
      <topic>Anopheles exposure</topic>
      <topic>Antibodies</topic>
    </subject>
    <subject authority="local">
      <geographic>SENEGAL</geographic>
    </subject>
    <classification authority="local">052</classification>
    <classification authority="local">050</classification>
    <classification authority="local">020</classification>
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      <titleInfo>
        <title>Parasites and Vectors</title>
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        <detail type="volume">
          <number>6</number>
        </detail>
        <extent unit="pages">
          <list> 68</list>
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      <originInfo>
        <dateIssued>2013</dateIssued>
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      <identifier type="issn">1756-3305</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010060845</identifier>
    <identifier type="doi">10.1186/1756-3305-6-68</identifier>
    <identifier type="issn">1756-3305</identifier>
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      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/fdi:010060845</url>
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      <recordCreationDate encoding="w3cdtf">2013-05-31</recordCreationDate>
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