Population genetic analysis of large sequence polymorphisms in Plasmodium falciparum blood-stage antigens


Autoria(s): AHOUIDI, Ambroise D.; BEI, Amy K.; NEAFSEY, Daniel E.; SARR, Ousmane; VOLKMAN, Sarah; MILNER, Dan; COX-SINGH, Janet; FERREIRA, Marcelo U.; NDIR, Omar; PREMJI, Zul; MBOUP, Souleymane; DURAISINGH, Manoj T.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Plasmodium falciparum, the causative agent of human malaria, invades host erythrocytes using several proteins on the surface of the invasive merozoite, which have been proposed as potential vaccine candidates. Members of the multi-gene PfRh family are surface antigens that have been shown to play a central role in directing merozoites to alternative erythrocyte receptors for invasion. Recently, we identified a large structural polymorphism, a 0.58 Kb deletion, in the C-terminal region of the PfRh2b gene, present at a high frequency in parasite populations from Senegal. We hypothesize that this region is a target of humoral immunity. Here, by analyzing 371 P. falciparum isolates we show that this major allele is present at varying frequencies in different populations within Senegal, Africa, and throughout the world. For allelic dimorphisms in the asexual stage antigens, Msp-2 and EBA-175, we find minimal geographic differentiation among parasite populations from Senegal and other African localities, suggesting extensive gene flow among these populations and/or immune-mediated frequency-dependent balancing selection. In contrast, we observe a higher level of inter-population divergence (as measured by F(st)) for the PfRh2b deletion, similar to that observed for SNPs from the sexual stage Pfs45/48 loci, which is postulated to be under directional selection. We confirm that the region containing the PfRh2b polymorphism is a target of humoral immune responses by demonstrating antibody reactivity of endemic sera. Our analysis of inter-population divergence suggests that in contrast to the large allelic dimorphisms in EBA-175 and Msp-2, the presence or absence of the large PfRh2b deletion may not elicit frequency-dependent immune selection, but may be under positive immune selection, having important implications for the development of these proteins as vaccine candidates. (C) 2009 Elsevier B.V. All rights reserved.

National Institute of Health (NIH)[5D43TW001503-09]

U.S. National Institutes of Health (NIH)

U.S. National Institutes of Health (NIH)

National Institute of Health (NIH)[RO1A1057919]

National Institute of Health (NIH)[1R03TW008053]

U.S. National Institutes of Health (NIH)

Harvard Institute for Global Health fellowship

Harvard Institute for Global Health fellowship

Identificador

INFECTION GENETICS AND EVOLUTION, v.10, n.2, p.200-206, 2010

1567-1348

http://producao.usp.br/handle/BDPI/28501

10.1016/j.meegid.2009.11.008

http://dx.doi.org/10.1016/j.meegid.2009.11.008

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Infection Genetics and Evolution

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Plasmodium falciparum #F(st) #Selection #Immunity #PfRh2b #Antigen #ERYTHROCYTE BINDING ANTIGEN #MALARIA-VACCINE CANDIDATE #MEROZOITE SURFACE PROTEIN-2 #NATURAL-SELECTION #GEOGRAPHICAL-DISTRIBUTION #HUMAN-ANTIBODIES #INVASION #DIVERSITY #EXPRESSION #EPITOPE #Infectious Diseases
Tipo

article

original article

publishedVersion