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Two Nonrecombining Sympatric Forms of the Human Malaria Parasite Plasmodium ovale Occur Globally

Identifieur interne : 001F06 ( PascalFrancis/Checkpoint ); précédent : 001F05; suivant : 001F07

Two Nonrecombining Sympatric Forms of the Human Malaria Parasite Plasmodium ovale Occur Globally

Auteurs : Colin J. Sutherland [Royaume-Uni] ; Naowarat Tanomsing [Thaïlande] ; Debbie Noider [Royaume-Uni] ; Mary Oguike [Royaume-Uni] ; Charlie Jennison [Royaume-Uni] ; Sasithon Pukrittayakamee [Thaïlande] ; Christiane Dolecek [Viêt Nam] ; TRAN TINH HEN [Viêt Nam] ; Virgilio E. Do Rosario [Portugal] ; Ana Paula Arez [Portugal] ; João Pinto [Portugal] ; Pascal Michon [Papouasie-Nouvelle-Guinée] ; Ananias A. Escalante [États-Unis] ; Francois Nosten [Royaume-Uni, Thaïlande] ; Martina Burke [Royaume-Uni] ; Rogan Lee [Australie] ; Marie Blaze [Royaume-Uni] ; Thomas Dan Otto [Royaume-Uni] ; John W. Barnwell [États-Unis] ; Arnab Pain [Royaume-Uni] ; John Williams [Royaume-Uni] ; Nicholas J. White [Royaume-Uni, Thaïlande] ; Nicholas P. J. Day [Royaume-Uni, Thaïlande] ; Georges Snounou [France, Singapour] ; Peter J. Lockhart [Nouvelle-Zélande] ; Peter L. Chiodini [Royaume-Uni] ; Mallika Imwong [Thaïlande] ; Spencer D. Polley [Royaume-Uni]

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RBID : Pascal:10-0249353

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English descriptors

Abstract

Background. Malaria in humans is caused by apicomplexan parasites belonging to 5 species of the genus Plasmodium. Infections with Plasmodium ovale are widely distributed but rarely investigated, and the resulting burden of disease is not known. Dimorphism in defined genes has led to P. ovale parasites being divided into classic and variant types. We hypothesized that these dimorphs represent distinct parasite species. Methods. Multilocus sequence analysis of 6 genetic characters was carried out among 55 isolates from 12 African and 3 Asia-Pacific countries. Results. Each genetic character displayed complete dimorphism and segregated perfectly between the 2 types. Both types were identified in samples from Ghana, Nigeria, São Tomé, Sierra Leone, and Uganda and have been described previously in Myanmar. Splitting of the 2 lineages is estimated to have occurred between 1.0 and 3.5 million years ago in hominid hosts. Conclusions. We propose that P. ovale comprises 2 nonrecombining species that are sympatric in Africa and Asia. We speculate on possible scenarios that could have led to this speciation. Furthermore, the relatively high frequency of imported cases of symptomatic P. ovale infection in the United Kingdom suggests that the morbidity caused by ovale malaria has been underestimated.


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<name sortKey="Tran Tinh Hen" sort="Tran Tinh Hen" uniqKey="Tran Tinh Hen" last="Tran Tinh Hen">TRAN TINH HEN</name>
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<name sortKey="Lee, Rogan" sort="Lee, Rogan" uniqKey="Lee R" first="Rogan" last="Lee">Rogan Lee</name>
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<country>Australie</country>
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<settlement type="city">Sydney</settlement>
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<s1>Sanger Genome Centre</s1>
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<s1>Health Protection Agency Malaria Reference Laboratory, London School of Hygiene and Tropical Medicine</s1>
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<s1>Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Churchill Hospital</s1>
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<sZ>23 aut.</sZ>
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<country>Thaïlande</country>
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<s1>Centre for Tropical Medicine, Nuffield Department of Clinical Medicine, Churchill Hospital</s1>
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<settlement type="city">Oxford</settlement>
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<sZ>23 aut.</sZ>
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<country>Thaïlande</country>
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<name sortKey="Snounou, Georges" sort="Snounou, Georges" uniqKey="Snounou G" first="Georges" last="Snounou">Georges Snounou</name>
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<s1>Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche S945</s1>
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<sZ>24 aut.</sZ>
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<country>France</country>
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<s1>Université Pierre and Marie Curie, Faculté de Médecine Pitié-Salpêtrière</s1>
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<sZ>24 aut.</sZ>
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<country>France</country>
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<region type="region">Île-de-France</region>
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<s1>Department of Microbiology, National University of Singapore</s1>
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<title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
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<term>Homme</term>
<term>Plasmodium ovale</term>
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<div type="abstract" xml:lang="en">Background. Malaria in humans is caused by apicomplexan parasites belonging to 5 species of the genus Plasmodium. Infections with Plasmodium ovale are widely distributed but rarely investigated, and the resulting burden of disease is not known. Dimorphism in defined genes has led to P. ovale parasites being divided into classic and variant types. We hypothesized that these dimorphs represent distinct parasite species. Methods. Multilocus sequence analysis of 6 genetic characters was carried out among 55 isolates from 12 African and 3 Asia-Pacific countries. Results. Each genetic character displayed complete dimorphism and segregated perfectly between the 2 types. Both types were identified in samples from Ghana, Nigeria, São Tomé, Sierra Leone, and Uganda and have been described previously in Myanmar. Splitting of the 2 lineages is estimated to have occurred between 1.0 and 3.5 million years ago in hominid hosts. Conclusions. We propose that P. ovale comprises 2 nonrecombining species that are sympatric in Africa and Asia. We speculate on possible scenarios that could have led to this speciation. Furthermore, the relatively high frequency of imported cases of symptomatic P. ovale infection in the United Kingdom suggests that the morbidity caused by ovale malaria has been underestimated.</div>
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