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Vivax malaria in Mauritania includes infection of a Duffy-negative individual

BACKGROUND: Duffy blood group polymorphisms are important in areas where Plasmodium vivax is present because this surface antigen is thought to act as a key receptor for this parasite. In the present study, Duffy blood group genotyping was performed in febrile uninfected and P. vivax-infected patien...

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Detalles Bibliográficos
Autores principales: Wurtz, Nathalie, Mint Lekweiry, Khadijetou, Bogreau, Hervé, Pradines, Bruno, Rogier, Christophe, Ould Mohamed Salem Boukhary, Ali, Hafid, Jamal Eddine, Ould Ahmedou Salem, Mohamed Salem, Trape, Jean-François, Basco, Leonardo K, Briolant, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228859/
https://www.ncbi.nlm.nih.gov/pubmed/22050867
http://dx.doi.org/10.1186/1475-2875-10-336
Descripción
Sumario:BACKGROUND: Duffy blood group polymorphisms are important in areas where Plasmodium vivax is present because this surface antigen is thought to act as a key receptor for this parasite. In the present study, Duffy blood group genotyping was performed in febrile uninfected and P. vivax-infected patients living in the city of Nouakchott, Mauritania. METHODS: Plasmodium vivax was identified by real-time PCR. The Duffy blood group genotypes were determined by standard PCR followed by sequencing of the promoter region and exon 2 of the Duffy gene in 277 febrile individuals. Fisher's exact test was performed in order to assess the significance of variables. RESULTS: In the Moorish population, a high frequency of the FYB(ES)/FYB(ES )genotype was observed in uninfected individuals (27.8%), whereas no P. vivax-infected patient had this genotype. This was followed by a high level of FYA/FYB, FYB/FYB, FYB/FYB(ES )and FYA/FYB(ES )genotype frequencies, both in the P. vivax-infected and uninfected patients. In other ethnic groups (Poular, Soninke, Wolof), only the FYB(ES)/FYB(ES )genotype was found in uninfected patients, whereas the FYA/FYB(ES )genotype was observed in two P. vivax-infected patients. In addition, one patient belonging to the Wolof ethnic group presented the FYB(ES)/FYB(ES )genotype and was infected by P. vivax. CONCLUSIONS: This study presents the Duffy blood group polymorphisms in Nouakchott City and demonstrates that in Mauritania, P. vivax is able to infect Duffy-negative patients. Further studies are necessary to identify the process that enables this Duffy-independent P. vivax invasion of human red blood cells.