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Plasmodium falciparum susceptibility to standard and potential anti-malarial drugs in Dakar, Senegal, during the 2013–2014 malaria season

Identifieur interne : 000E54 ( Main/Exploration ); précédent : 000E53; suivant : 000E55

Plasmodium falciparum susceptibility to standard and potential anti-malarial drugs in Dakar, Senegal, during the 2013–2014 malaria season

Auteurs : Bécaye Fall [Sénégal] ; Cheikhou Camara [Sénégal] ; Mansour Fall [Sénégal] ; Aminata Nakoulima [Sénégal] ; Pierre Dionne [Sénégal] ; Bakary Diatta [Sénégal] ; Yaya Diemé [Sénégal] ; Boubacar Wade [Sénégal] ; Bruno Pradines [Sénégal]

Source :

RBID : Hal:hal-01220028

Descripteurs français

English descriptors

Abstract

Background: In 2006, the Senegalese National Malaria Control Programme recommended artemisinin-based combination therapy (ACT) as the first-line treatment for uncomplicated malaria. Since the introduction of ACT, there have been very few reports on the level of Plasmodium falciparum resistance to anti-malarial drugs. An ex vivo susceptibility study was conducted on local isolates obtained from the Hôpital Principal de Dakar (Dakar, Senegal) from November 2013 to January 2014. Methods: Eighteen P. falciparum isolates were sussessfully assessed for ex vivo susceptibility to chloroquine (CQ), quinine (QN), monodesethylamodiaquine (MDAQ), the active metabolite of amodiaquine, mefloquine (MQ), lumefantrine (LMF), artesunate (AS), dihydroartemisinin (DHA), the active metabolite of artemisinin derivatives, pyronaridine (PND), piperaquine (PPQ), and, Proveblue (PVB), a methylene blue preparation, using the HRP2-based ELISA test. Results: The prevalence of isolates with reduced susceptibility was 55.6% for MQ, 50% for CQ, 5.6% for QN and MDAQ, and 0% for DHA, AS and LMF. The mean IC 50 for PND, PPQ and PVB were 5.8 nM, 32.2 nM and 5.3 nM, respectively. Conclusions: The prevalence of isolates with a reduced susceptibility to MQ remains high and stable in Dakar. Since 2004, the prevalence of CQ resistance decreased, but rebounded in 2013 in Dakar. PND, PPQ and PVB showed high in vitro activity in P. falciparum parasites from Dakar.


Url:
DOI: 10.1186/s12936-015-0589-3


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<relation active="#struct-338318" type="direct"></relation>
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<tutelles>
<tutelle active="#struct-338318" type="direct">
<org type="institution" xml:id="struct-338318" status="VALID">
<orgName>Hôpital Principal de Dakar</orgName>
<desc>
<address>
<addrLine> 1, avenue Nelson Mandéla - B.P. 3006 - DAKAR (Sénégal)</addrLine>
<country key="SN"></country>
</address>
<ref type="url">http://www.hopitalprincipal.sn/</ref>
</desc>
</org>
</tutelle>
</tutelles>
</hal:affiliation>
<country>Sénégal</country>
</affiliation>
</author>
<author>
<name sortKey="Pradines, Bruno" sort="Pradines, Bruno" uniqKey="Pradines B" first="Bruno" last="Pradines">Bruno Pradines</name>
<affiliation wicri:level="1">
<hal:affiliation type="laboratory" xml:id="struct-214449" status="INCOMING">
<orgName>Laboratoire d'étude de la chimiosensibilité du paludisme</orgName>
<desc>
<address>
<addrLine>Rte de la Corniche Est, Dakar</addrLine>
<country key="SN"></country>
</address>
</desc>
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<relation active="#struct-338318" type="direct"></relation>
<relation active="#struct-352262" type="direct"></relation>
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<tutelles>
<tutelle active="#struct-338318" type="direct">
<org type="institution" xml:id="struct-338318" status="VALID">
<orgName>Hôpital Principal de Dakar</orgName>
<desc>
<address>
<addrLine> 1, avenue Nelson Mandéla - B.P. 3006 - DAKAR (Sénégal)</addrLine>
<country key="SN"></country>
</address>
<ref type="url">http://www.hopitalprincipal.sn/</ref>
</desc>
</org>
</tutelle>
<tutelle active="#struct-352262" type="direct">
<org type="institution" xml:id="struct-352262" status="INCOMING">
<orgName>Fédération des laboratoires</orgName>
<desc>
<address>
<country key="FR"></country>
</address>
</desc>
</org>
</tutelle>
</tutelles>
</hal:affiliation>
<country>Sénégal</country>
</affiliation>
</author>
</analytic>
<idno type="DOI">10.1186/s12936-015-0589-3</idno>
<series>
<title level="j">Malaria Journal</title>
<idno type="ISSN">1475-2875</idno>
<imprint>
<date type="datePub">2015-02-16</date>
</imprint>
</series>
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<textClass>
<keywords scheme="mix" xml:lang="en">
<term>Anti-malarial</term>
<term>In vitro</term>
<term>Malaria</term>
<term>Methylene blue</term>
<term>Plasmodium falciparum</term>
<term>Proveblue</term>
<term>Resistance</term>
<term>Senegal</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Sénégal</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Background: In 2006, the Senegalese National Malaria Control Programme recommended artemisinin-based combination therapy (ACT) as the first-line treatment for uncomplicated malaria. Since the introduction of ACT, there have been very few reports on the level of Plasmodium falciparum resistance to anti-malarial drugs. An ex vivo susceptibility study was conducted on local isolates obtained from the Hôpital Principal de Dakar (Dakar, Senegal) from November 2013 to January 2014. Methods: Eighteen P. falciparum isolates were sussessfully assessed for ex vivo susceptibility to chloroquine (CQ), quinine (QN), monodesethylamodiaquine (MDAQ), the active metabolite of amodiaquine, mefloquine (MQ), lumefantrine (LMF), artesunate (AS), dihydroartemisinin (DHA), the active metabolite of artemisinin derivatives, pyronaridine (PND), piperaquine (PPQ), and, Proveblue (PVB), a methylene blue preparation, using the HRP2-based ELISA test. Results: The prevalence of isolates with reduced susceptibility was 55.6% for MQ, 50% for CQ, 5.6% for QN and MDAQ, and 0% for DHA, AS and LMF. The mean IC 50 for PND, PPQ and PVB were 5.8 nM, 32.2 nM and 5.3 nM, respectively. Conclusions: The prevalence of isolates with a reduced susceptibility to MQ remains high and stable in Dakar. Since 2004, the prevalence of CQ resistance decreased, but rebounded in 2013 in Dakar. PND, PPQ and PVB showed high in vitro activity in P. falciparum parasites from Dakar.</p>
</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Sénégal</li>
</country>
</list>
<tree>
<country name="Sénégal">
<noRegion>
<name sortKey="Fall, Becaye" sort="Fall, Becaye" uniqKey="Fall B" first="Bécaye" last="Fall">Bécaye Fall</name>
</noRegion>
<name sortKey="Camara, Cheikhou" sort="Camara, Cheikhou" uniqKey="Camara C" first="Cheikhou" last="Camara">Cheikhou Camara</name>
<name sortKey="Diatta, Bakary" sort="Diatta, Bakary" uniqKey="Diatta B" first="Bakary" last="Diatta">Bakary Diatta</name>
<name sortKey="Dieme, Yaya" sort="Dieme, Yaya" uniqKey="Dieme Y" first="Yaya" last="Diemé">Yaya Diemé</name>
<name sortKey="Dionne, Pierre" sort="Dionne, Pierre" uniqKey="Dionne P" first="Pierre" last="Dionne">Pierre Dionne</name>
<name sortKey="Fall, Mansour" sort="Fall, Mansour" uniqKey="Fall M" first="Mansour" last="Fall">Mansour Fall</name>
<name sortKey="Nakoulima, Aminata" sort="Nakoulima, Aminata" uniqKey="Nakoulima A" first="Aminata" last="Nakoulima">Aminata Nakoulima</name>
<name sortKey="Pradines, Bruno" sort="Pradines, Bruno" uniqKey="Pradines B" first="Bruno" last="Pradines">Bruno Pradines</name>
<name sortKey="Wade, Boubacar" sort="Wade, Boubacar" uniqKey="Wade B" first="Boubacar" last="Wade">Boubacar Wade</name>
</country>
</tree>
</affiliations>
</record>

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