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首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Genetic diversity in the C-terminal 42 kDa region of merozoite surface protein-1 of Plasmodium vivax (PvMSP-1(42)) among Indian isolates.
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Genetic diversity in the C-terminal 42 kDa region of merozoite surface protein-1 of Plasmodium vivax (PvMSP-1(42)) among Indian isolates.

机译:印度分离株间日疟原虫裂殖子表面蛋白-1(PvMSP-1(42))的C末端42 kDa区域的遗传多样性。

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Plasmodium vivax merozoite surface protein 1 (PvMSP-1) is a leading malaria vaccine candidate. This protein is processed to give rise to various sized fragments during merozoite maturation. Here, we describe the analysis of genetic diversity in the 42 kDa C-terminal part of this protein among 33 Indian P. vivax isolates. A total of 27 haplotypes with 72 mutations and 0.0212+/-0.0005S.D. over all pi nucleotide diversity were observed among the isolates. Twenty-six of 27 haplotypes reported here were new as they have not been reported so far from any other country. The difference between non-synonymous (dN) and synonymous (dS) mutations was found to be positive (0.0081+/-0.0051) for the entire 42 kDa region. Further analysis revealed that 33 kDa (MSP-1(33)) fragment of the MSP-1(42) was highly polymorphic with pi nucleotide diversity 0.0290+/-0.0007S.D. The dN-dS for this region of MSP-1 was also positive (0.0114+/-0.0071S.E.). On the other hand, there was no non-synonymous mutation in the 19 kDa (MSP-1(19)) fragment of the MSP-1(42) and thus it was highly conserved. In conclusion, MSP-1(33) fragment was highly polymorphic and appeared to be under diversifying selection whereas there was no selection at MSP-1(19) region among the isolates. Present study will be helpful for the development of PvMSP-1 based vaccine against P. vivax malaria.
机译:间日疟原虫裂殖子表面蛋白1(PvMSP-1)是领先的疟疾疫苗候选者。在裂殖子成熟过程中,该蛋白质经过处理后会产生各种大小的片段。在这里,我们描述了33个印度间日疟原虫分离株中该蛋白42 kDa C末端部分的遗传多样性分析。共有27个单倍型,具有72个突变和0.0212 +/- 0.0005S.D。在分离株之间观察到所有π核苷酸的多样性。此处报告的27种单倍型中有26种是新的,因为到目前为止尚未从任何其他国家报告过。对于整个42 kDa区域,发现非同义(dN)和同义(dS)突变之间的差异为正(0.0081 +/- 0.0051)。进一步分析显示,MSP-1(42)的33 kDa(MSP-1(33))片段具有π核苷酸多样性0.0290 +/- 0.0007S.D的高度多态性。 MSP-1此区域的dN-dS也为阳性(0.0114 +/- 0.0071S.E。)。另一方面,MSP-1(42)的19 kDa(MSP-1(19))片段中没有非同义突变,因此高度保守。总之,MSP-1(33)片段高度多态性,似乎处于多样化选择之下,而在分离株中MSP-1(19)区域则没有选择。目前的研究将有助于开发基于PvMSP-1的抗间日疟原虫的疫苗。

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