Whole genome sequencing of field isolates reveals a common duplication of the Duffy binding protein gene in Malagasy Plasmodium vivax strains.

Didier Menard 1 Ernest R Chan 2 Christophe Benedet 1 Arsène Ratsimbasoa 3 Saorin Kim 1 Pheaktra Chim 1 Catherine Do 1 Benoit Witkowski 1 Remy Durand 4 Marc Thellier 5 Carlo Severini 6 Eric Legrand 7 Lise Musset 7 Bakri y M Nour 8 Odile Mercereau-Puijalon 9 David Serre 2 Peter A Zimmerman 10
1 Laboratoire d'épidémiologie moléculaire
2 Genomic Medicine Institute
3 Ministère de la Santé, du Planning Familial et de la Protection Sociale
4 Laboratoire de Parasitologie-Mycologie
5 Service de parasitologie - mycologie [CHU Pitié-Salpétrière]
6 Department of Infectious, Parasitic and Immunomediated Diseases
7 Institut Pasteur de la Guyane
8 Blue Nile National Institute for Communicable Diseases
9 Immunologie moléculaire des parasites
10 Center for Global Health and Diseases
Abstract : Plasmodium vivax is the most prevalent human malaria parasite, causing serious public health problems in malaria-endemic countries. Until recently the Duffy-negative blood group phenotype was considered to confer resistance to vivax malaria for most African ethnicities. We and others have reported that P. vivax strains in African countries from Madagascar to Mauritania display capacity to cause clinical vivax malaria in Duffy-negative people. New insights must now explain Duffy-independent P. vivax invasion of human erythrocytes. Through recent whole genome sequencing we obtained ≥ 70× coverage of the P. vivax genome from five field-isolates, resulting in ≥ 93% of the Sal I reference sequenced at coverage greater than 20×. Combined with sequences from one additional Malagasy field isolate and from five monkey-adapted strains, we describe here identification of DNA sequence rearrangements in the P. vivax genome, including discovery of a duplication of the P. vivax Duffy binding protein (PvDBP) gene. A survey of Malagasy patients infected with P. vivax showed that the PvDBP duplication was present in numerous locations in Madagascar and found in over 50% of infected patients evaluated. Extended geographic surveys showed that the PvDBP duplication was detected frequently in vivax patients living in East Africa and in some residents of non-African P. vivax-endemic countries. Additionally, the PvDBP duplication was observed in travelers seeking treatment of vivax malaria upon returning home. PvDBP duplication prevalence was highest in west-central Madagascar sites where the highest frequencies of P. vivax-infected, Duffy-negative people were reported. The highly conserved nature of the sequence involved in the PvDBP duplication suggests that it has occurred in a recent evolutionary time frame. These data suggest that PvDBP, a merozoite surface protein involved in red cell adhesion is rapidly evolving, possibly in response to constraints imposed by erythrocyte Duffy negativity in some human populations.
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Didier Menard, Ernest R Chan, Christophe Benedet, Arsène Ratsimbasoa, Saorin Kim, et al.. Whole genome sequencing of field isolates reveals a common duplication of the Duffy binding protein gene in Malagasy Plasmodium vivax strains.. PLoS Neglected Tropical Diseases, Public Library of Science, 2013, 7 (11), pp.e2489. ⟨10.1371/journal.pntd.0002489⟩. ⟨pasteur-01109627⟩

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