Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Exp Parasitol. 2012 Apr;130(4):456-62. doi: 10.1016/j.exppara.2012.01.006. Epub 2012 Jan 28.
The apical membrane antigen-1 (AMA-1) of Plasmodium falciparum is a prime malaria asexual blood-stage vaccine candidate. Antigenic variation is one of the main obstacles in the development of a universal effective malaria vaccine. The extracellular region of P. falciparum AMA-1 (PfAMA-1) consists of three domains (I-III), of which the domain I is the most diverse region of this antigen. The objective of our study was to investigate and analyze the extent of genetic diversity and the effectiveness of natural selection at the AMA-1 domain I of P. falciparum in isolates from Iran. A fragment of ama-1 gene spanning domain I was amplified by nested PCR from 48 P. falciparum isolates collected from two major malaria endemic areas of Iran during 2009 to August 2010 and sequenced. Genetic polymorphism and statistical analyses were performed using DnaSP and MEGA software packages. Analysis of intrapopulation diversity revealed relatively high nucleotide and haplotype diversity at the PfAMA-1 domain I of Iranian isolates. Neutrality tests provided strong evidence of positive natural selection acting on the sequenced gene region. The findings also demonstrated that, in addition to natural selection, intragenic recombination may contribute to the diversity observed at the domain I. The results obtained will have significant implications in the design and the development of an AMA-1-based vaccine against falciparum malaria.
疟原虫顶膜抗原-1(AMA-1)是主要的恶性疟无性血期疫苗候选抗原。抗原变异是开发通用有效疟疾疫苗的主要障碍之一。恶性疟原虫 AMA-1(PfAMA-1)的细胞外区由三个结构域(I-III)组成,其中结构域 I 是该抗原中最多样化的区域。本研究的目的是调查和分析 2009 年 8 月至 2010 年期间从伊朗两个主要疟疾流行地区采集的 48 株疟原虫分离株中 PfAMA-1 结构域 I 的遗传多样性和自然选择的有效性。采用巢式 PCR 从 48 株疟原虫分离株中扩增 ama-1 基因跨越结构域 I 的片段,并对其进行测序。采用 DnaSP 和 MEGA 软件包进行遗传多态性和统计分析。群体内多样性分析显示,伊朗分离株 PfAMA-1 结构域 I 的核苷酸和单倍型多样性相对较高。中性检验提供了强有力的证据表明,在测序基因区域存在正自然选择。研究结果还表明,除自然选择外,基因内重组可能导致观察到的结构域 I 多样性。研究结果将对基于 AMA-1 的抗恶性疟疫苗的设计和开发具有重要意义。