Ebrahimzadeh Adel, Mohammadi Saeed, Jamshidi Ali
Department of Parasitology and Mycology, Zahedan University of Medical Sciences, Zahedan, IR Iran.
Department of Molecular Medicine, Golestan University of Medical Sciences, Gorgan, IR Iran.
Jundishapur J Microbiol. 2014 May;7(5):e9829. doi: 10.5812/jjm.9829. Epub 2014 May 1.
Genetic diversity has provided Plasmodium falciparum with the potential capacity of avoiding the immune response, and possibly supported the natural selection of drug or vaccine-resistant parasites. Merozoite surface protein-3 (MSP-3) has been used to develop vaccines and investigate the genetic diversity regarding P. falciparum malaria in Iran.
The main goal of this study was to analyze the polymorphic antigen MSP-3 genes across southeast of Iran among four different districts, to identify the differences in the allele frequency and genetic diversity.
Nested polymerase chain reaction amplification was used to determine polymorphisms of N-terminal region of the MSP-3 gene. A total of 85 microscopically positive P. falciparum infected individuals from southeast of Iran were included in this study.
Of the 85 confirmed P. falciparum samples obtained from four different districts, 72 were successfully scored for MSP-3.The MSP-3 allele classes (K1 and 3D7 types) showed comparable prevalence in all districts. Overall frequencies of K1 and 3D7 allele classes were 94.5 % for both.
Since no study has yet looked at the extent of P. falciparum MSP-3 in this geographic region, these data can be helpful to support development of a vaccine based on MSP-3 against malaria. There should be a comparative analysis in different seasonal peaks to indicate the allelic polymorphism of MSP-3 over a period.
遗传多样性赋予恶性疟原虫逃避免疫反应的潜在能力,并可能支持对药物或疫苗耐药寄生虫的自然选择。裂殖子表面蛋白3(MSP-3)已被用于开发疫苗,并研究伊朗恶性疟原虫疟疾的遗传多样性。
本研究的主要目的是分析伊朗东南部四个不同地区的多态性抗原MSP-3基因,以确定等位基因频率和遗传多样性的差异。
采用巢式聚合酶链反应扩增法测定MSP-3基因N端区域的多态性。本研究共纳入了85名来自伊朗东南部的经显微镜检查确诊为恶性疟原虫感染的个体。
从四个不同地区获得的85份确诊恶性疟原虫样本中,72份成功进行了MSP-3分型。MSP-3等位基因类别(K1和3D7型)在所有地区的流行率相当。K1和3D7等位基因类别的总体频率均为94.5%。
由于尚未有研究关注该地理区域恶性疟原虫MSP-3的情况,这些数据有助于支持开发基于MSP-3的抗疟疾疫苗。应在不同季节高峰进行比较分析,以表明一段时间内MSP-3基因的等位基因多态性。