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Genetic Diversity of MSP1 Block 2 of Plasmodium vivax Isolates from Manaus (Central Brazilian Amazon)

机译:Manaus(巴西亚马逊中央巴西亚马逊)疟原虫分离株MSP1块2的遗传多样性

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摘要

The diversity of MSP1 in both Plasmodium falciparum and P. vivax is presumed be associated to parasite immune evasion. In this study, we assessed genetic diversity of the most variable domain of vaccine candidate N-terminal PvMSP1 (Block 2) in field isolates of Manaus. Forty-seven blood samples the polymorphism of PvMSP1 Block 2 generates four fragment sizes. In twenty-eight of them, sequencing indicated seven haplotypes of PvMSP1 Block 2 circulating among field isolates. Evidence of striking exchanges was observed with two stretches flanking the repeat region and two predicted recombination sites were described. Single nucleotide polymorphisms determined with concurrent infections per patient indicated that nonsynonymous substitutions occurred preferentially in the repeat-rich regions which also were predicted as B-cell epitopes. The comprehensive understanding of the genetic diversity of the promising Block 2 associated with clinical immunity and a reduced risk of infection by Plasmodium vivax would be important for the rationale of malaria vaccine designs.
机译:假定疟原虫和P.Vivax两种疟原虫和P.Vivax中的MSP1的多样性与寄生虫免疫逃避相关。在这项研究中,我们评估了Manaus的场分离株中最可变的疫苗候选N-末端PVMSP1(框2)的遗传多样性。四十七个血样PVMSP1块2的多态性产生四个片段尺寸。在其中二十八个中,测序指示PVMSP1块2的七个单倍型,在野外分离物之间循环。用两个伸展的侧翼观察到触发交换的证据,并描述了两个预测的重组位点。每位患者的同时感染测定的单核苷酸多态性表明,在重复的地区中优先发生不纯的取代,这也预测为B细胞表位。综合了解与临床免疫相关的有前途块2的遗传多样性以及降低疟疾vivax风险降低对疟疾疫苗设计的基本原理是重要的。

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