Positively Selected G6PD -Mahidol Mutation Reduces Plasmodium vivax Density in Southeast Asians

Author:

Louicharoen Chalisa12,Patin Etienne3,Paul Richard1,Nuchprayoon Issarang4,Witoonpanich Bhee1,Peerapittayamongkol Chayanon1,Casademont Isabelle1,Sura Thanyachai5,Laird Nan M.6,Singhasivanon Pratap7,Quintana-Murci Lluis3,Sakuntabhai Anavaj15

Affiliation:

1. Institut Pasteur, Laboratoire de la Génétique de la réponse aux infections chez l'homme, 75724 Paris, France.

2. Interdepartmental Program of Biomedical Science, Faculty of the Graduate School, Chulalongkorn University, Bangkok, Thailand.

3. Institut Pasteur, Human Evolutionary Genetics Unit, CNRS, URA3012, 75015 Paris, France.

4. Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

5. Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

6. Department of Biostatistics, Harvard School of Public Health, 655 Huntington Avenue, Boston, MA 02115, USA.

7. Department of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

Abstract

Ghosts of Selection Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency of humans, and it has been long suspected to exert an effect on Plasmodium falciparum malaria in Africa. Likewise, the increase in prevalence of the G6PD-Mahidol 487 A allele among Karen people in Thailand, who only in the past few thousand years have migrated into malarious zones, may be the result of selection by Plasmodium vivax malaria. P. vivax has recently been implicated in more severe disease than previously suspected, providing both a direct selective effect through mortality and an indirect selective effect through morbidity and reproductive failure. Louicharoen et al. (p. 1546 ) link population-genetic evidence for positive selection in an 8-year family-based study of 3000 Karen individuals and reveal that there is an association between the presence of the G6PD-Mahidol 487 A allele and a reduction in the density of P. vivax parasites circulating in the bloodstreams of infected individuals. The mutation appears to exert its effect on the physiology of immature red blood cells, which are the preferred niche for P. vivax but not of P. falciparum .

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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