...
首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >A comparative study of the genetic diversity of the 42kDa fragment of the merozoite surface protein 1 in Plasmodium falciparum and P. vivax
【24h】

A comparative study of the genetic diversity of the 42kDa fragment of the merozoite surface protein 1 in Plasmodium falciparum and P. vivax

机译:恶性疟原虫和间日疟原虫裂殖子表面蛋白1 42kDa片段遗传多样性的比较研究

获取原文
获取原文并翻译 | 示例
           

摘要

We investigated the genetic diversity of the 42kDa fragment of the merozoite surface protein 1 (MSP-1) antigen in Plasmodium falciparum and P. vivax, as well as in non-human primate malarial parasites. This fragment undergoes a proteolytic cleavage generating two fragments of 19kDa (MSP-1(19)) and 33kDa (MSP-1(33)) that are critical in erythrocyte invasion. We found that overall the MSP-1(33) fragment exhibits greater genetic diversity than the MSP-1(19) regardless of the species. We have found evidence for positive natural selection only in the human malaria parasites by comparing the rate of non-synonymous versus synonymous substitutions. In addition, we found clear differences between the two major human malaria parasites. In the case of P. falciparum, positive natural selection is acting on the MSP-1(19) region while the MSP-1(33) is neutral or under purifying selection. The opposite pattern was observed in P. vivax. Our results suggest different roles of this antigen in the host-parasite immune interaction in each of the major human malarial parasites.
机译:我们调查了恶性疟原虫和间日疟原虫以及非人类灵长类疟疾寄生虫中裂殖子表面蛋白1(MSP-1)抗原42kDa片段的遗传多样性。此片段进行蛋白水解切割,生成两个19kDa(MSP-1(19))和33kDa(MSP-1(33))片段,这两个片段对红细胞的入侵至关重要。我们发现,总体而言,MSP-1(33)片段显示出比MSP-1(19)更高的遗传多样性,而与物种无关。通过比较非同义替换与同义替换的比率,我们已经发现仅在人类疟疾寄生虫中具有积极自然选择的证据。此外,我们发现两种主要的人类疟疾寄生虫之间存在明显差异。对于恶性疟原虫,当MSP-1(33)为中性或纯化选择时,阳性自然选择作用于MSP-1(19)区域。在间日疟原虫中观察到相反的模式。我们的结果表明,该抗原在每个主要人类疟疾寄生虫的宿主-寄生虫免疫相互作用中的不同作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号