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Impact of changing drug treatment and malaria endemicity on the heritability of malaria phenotypes in a longitudinal family-based cohort study

Identifieur interne : 000231 ( France/Analysis ); précédent : 000230; suivant : 000232

Impact of changing drug treatment and malaria endemicity on the heritability of malaria phenotypes in a longitudinal family-based cohort study

Auteurs : Cheikh Loucoubar [France] ; Bronner Gonçalves [France] ; Adama Tall [Sénégal] ; Cheikh Sokhna [Sénégal] ; Jean-Francois Trape [Sénégal] ; Fatoumata Diene Sarr [Sénégal] ; Joseph Faye [Sénégal] ; Abdoulaye Badiane [Sénégal] ; Alioune Badara Ly [Sénégal] ; Aliou Diop [Sénégal] ; Avner Bar-Hen [France] ; Jean-François Bureau [France] ; Anavaj Sakuntabhai [Thaïlande] ; Richard Paul [France]

Source :

RBID : Hal:pasteur-02076528

Abstract

Despite considerable success of genome wide association (GWA) studies in identifying causal variants for many human diseases, their success in unraveling the genetic basis to complex diseases has been more mitigated. Pathogen population structure may impact upon the infectious phenotype, especially with the intense short-term selective pressure that drug treatment exerts on pathogens. Rigorous analysis that accounts for repeated measures and disentangles the influence of genetic and environmental factors must be performed. Attempts should be made to consider whether pathogen diversity will impact upon host genetic responses to infection.We analyzed the heritability of two Plasmodium falciparum phenotypes, the number of clinical malaria episodes (PFA) and the proportion of these episodes positive for gametocytes (Pfgam), in a family-based cohort followed for 19 years, during which time there were four successive drug treatment regimes, with documented appearance of drug resistance. Repeated measures and variance components analyses were performed with fixed environmental, additive genetic, intra-individual and maternal effects for each drug period. Whilst there was a significant additive genetic effect underlying PFA during the first drug period of study, this was lost in subsequent periods. There was no additive genetic effect for Pfgam. The intra-individual effect increased significantly in the chloroquine period.The loss of an additive genetic effect following novel drug treatment may result in significant loss of power to detect genes in a GWA study. Prior genetic analysis must be a pre-requisite for more detailed GWA studies. The temporal changes in the individual genetic and the intra-individual estimates are consistent with those expected if there were specific host-parasite interactions. The complex basis to the human response to malaria parasite infection likely includes dominance/epistatic genetic effects encompassed within the intra-individual variance component. Evaluating their role in influencing the outcome of infection through host genotype by parasite genotype interactions warrants research effort.


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DOI: 10.1371/journal.pone.0026364


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<idno type="IdRef">027936643</idno>
<idno type="ISNI">0000 0001 2353 6535</idno>
<orgName>Institut Pasteur [Paris]</orgName>
<date type="start">1887-06-04</date>
<desc>
<address>
<addrLine>25-28, rue du docteur Roux, 75724 Paris cedex 15</addrLine>
<country key="FR"></country>
</address>
<ref type="url">https://www.pasteur.fr</ref>
</desc>
</org>
</tutelle>
<tutelle name="URA3012" active="#struct-441569" type="direct">
<org type="institution" xml:id="struct-441569" status="VALID">
<idno type="IdRef">02636817X</idno>
<idno type="ISNI">0000000122597504</idno>
<orgName>Centre National de la Recherche Scientifique</orgName>
<orgName type="acronym">CNRS</orgName>
<date type="start">1939-10-19</date>
<desc>
<address>
<country key="FR"></country>
</address>
<ref type="url">http://www.cnrs.fr/</ref>
</desc>
</org>
</tutelle>
</tutelles>
</hal:affiliation>
<country>France</country>
</affiliation>
</author>
</analytic>
<idno type="DOI">10.1371/journal.pone.0026364</idno>
<series>
<title level="j">PLoS ONE</title>
<idno type="ISSN">1932-6203</idno>
<imprint>
<date type="datePub">2011-11-03</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Despite considerable success of genome wide association (GWA) studies in identifying causal variants for many human diseases, their success in unraveling the genetic basis to complex diseases has been more mitigated. Pathogen population structure may impact upon the infectious phenotype, especially with the intense short-term selective pressure that drug treatment exerts on pathogens. Rigorous analysis that accounts for repeated measures and disentangles the influence of genetic and environmental factors must be performed. Attempts should be made to consider whether pathogen diversity will impact upon host genetic responses to infection.We analyzed the heritability of two Plasmodium falciparum phenotypes, the number of clinical malaria episodes (PFA) and the proportion of these episodes positive for gametocytes (Pfgam), in a family-based cohort followed for 19 years, during which time there were four successive drug treatment regimes, with documented appearance of drug resistance. Repeated measures and variance components analyses were performed with fixed environmental, additive genetic, intra-individual and maternal effects for each drug period. Whilst there was a significant additive genetic effect underlying PFA during the first drug period of study, this was lost in subsequent periods. There was no additive genetic effect for Pfgam. The intra-individual effect increased significantly in the chloroquine period.The loss of an additive genetic effect following novel drug treatment may result in significant loss of power to detect genes in a GWA study. Prior genetic analysis must be a pre-requisite for more detailed GWA studies. The temporal changes in the individual genetic and the intra-individual estimates are consistent with those expected if there were specific host-parasite interactions. The complex basis to the human response to malaria parasite infection likely includes dominance/epistatic genetic effects encompassed within the intra-individual variance component. Evaluating their role in influencing the outcome of infection through host genotype by parasite genotype interactions warrants research effort.</p>
</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>France</li>
<li>Sénégal</li>
<li>Thaïlande</li>
</country>
</list>
<tree>
<country name="France">
<noRegion>
<name sortKey="Loucoubar, Cheikh" sort="Loucoubar, Cheikh" uniqKey="Loucoubar C" first="Cheikh" last="Loucoubar">Cheikh Loucoubar</name>
</noRegion>
<name sortKey="Bar Hen, Avner" sort="Bar Hen, Avner" uniqKey="Bar Hen A" first="Avner" last="Bar-Hen">Avner Bar-Hen</name>
<name sortKey="Bureau, Jean Francois" sort="Bureau, Jean Francois" uniqKey="Bureau J" first="Jean-François" last="Bureau">Jean-François Bureau</name>
<name sortKey="Goncalves, Bronner" sort="Goncalves, Bronner" uniqKey="Goncalves B" first="Bronner" last="Gonçalves">Bronner Gonçalves</name>
<name sortKey="Paul, Richard" sort="Paul, Richard" uniqKey="Paul R" first="Richard" last="Paul">Richard Paul</name>
</country>
<country name="Sénégal">
<noRegion>
<name sortKey="Tall, Adama" sort="Tall, Adama" uniqKey="Tall A" first="Adama" last="Tall">Adama Tall</name>
</noRegion>
<name sortKey="Badara Ly, Alioune" sort="Badara Ly, Alioune" uniqKey="Badara Ly A" first="Alioune" last="Badara Ly">Alioune Badara Ly</name>
<name sortKey="Badiane, Abdoulaye" sort="Badiane, Abdoulaye" uniqKey="Badiane A" first="Abdoulaye" last="Badiane">Abdoulaye Badiane</name>
<name sortKey="Diene Sarr, Fatoumata" sort="Diene Sarr, Fatoumata" uniqKey="Diene Sarr F" first="Fatoumata" last="Diene Sarr">Fatoumata Diene Sarr</name>
<name sortKey="Diop, Aliou" sort="Diop, Aliou" uniqKey="Diop A" first="Aliou" last="Diop">Aliou Diop</name>
<name sortKey="Faye, Joseph" sort="Faye, Joseph" uniqKey="Faye J" first="Joseph" last="Faye">Joseph Faye</name>
<name sortKey="Sokhna, Cheikh" sort="Sokhna, Cheikh" uniqKey="Sokhna C" first="Cheikh" last="Sokhna">Cheikh Sokhna</name>
<name sortKey="Trape, Jean Francois" sort="Trape, Jean Francois" uniqKey="Trape J" first="Jean-Francois" last="Trape">Jean-Francois Trape</name>
</country>
<country name="Thaïlande">
<noRegion>
<name sortKey="Sakuntabhai, Anavaj" sort="Sakuntabhai, Anavaj" uniqKey="Sakuntabhai A" first="Anavaj" last="Sakuntabhai">Anavaj Sakuntabhai</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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