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斯里兰卡间日疟原虫环子孢子蛋白(Pvcsp)的种群遗传结构。

Population genetic structure of the Plasmodium vivax circumsporozoite protein (Pvcsp) in Sri Lanka.

机构信息

Department of Zoology, Faculty of Science, University of Colombo, Colombo 03, Sri Lanka.

出版信息

Gene. 2013 Apr 15;518(2):381-7. doi: 10.1016/j.gene.2013.01.003. Epub 2013 Jan 17.

Abstract

Molecular methods elucidate evolutionary and ecological processes in parasites, where interaction between hosts and parasites enlighten the evolution of parasite lifestyles and host defenses. Population genetics of Plasmodium vivax parasites accurately describe transmission dynamics of the parasites and evaluation of malaria control measures. As a first generation vaccine candidate against malaria, the Circumsporozoite Protein (CSP) has demonstrated significant potential in P. falciparum. Extensive polymorphism hinders the development of a potent malaria vaccine. Hence, the genetic diversity of Pvcsp was investigated for the first time in 60 Sri Lankan clinical isolates by obtaining the nucleotide sequence of the central repeat (CR) domain and examining the polymorphism of the peptide repeat motifs (PRMs), the genetic diversity indices and phylogenetic relationships. PCR amplicons determined size polymorphism of 610, 700 and 710 bp in Pvcsp of Sri Lanka where all amino acid sequences obtained were of the VK210 variant, consisting variable repeats of 4 different PRMs. The two most abundant PRMs of the CR domain, GDRADGQPA and GDRAAGQPA consisted ~2-4 repeats, while GNRAAGQPA was unique to the island. Though, different nucleotide sequences termed repeat allotypes (RATs) were observed for each PRM, these were synonymous contributing to a less polymorphic CR domain. The genetic diversity of Pvcsp in Sri Lanka was due to the number of repetitive peptide repeat motifs, point mutations, and intragenic recombination. The 19 amino acid haplotypes defined were exclusive to Sri Lanka, whereas the 194 Pvcsp sequences of global isolates generated 57 more distinct a.a. haplotypes of the VK210 variant. Strikingly, the CR domain of both VK210 and VK247 variants was under purifying selection interpreting the scarcity of CSP non-synonymous polymorphisms. Insights to the distribution of RATs in the CR region with geographic clustering of the P. vivax VK210 variant were revealed. The cladogram reiterated this unique geographic clustering of local (VK210) and global isolates (VK210 and VK247), which was further validated by the elevated fixation index values of the VK210 variant.

摘要

分子方法阐明了寄生虫的进化和生态过程,其中宿主和寄生虫之间的相互作用揭示了寄生虫生活方式和宿主防御的进化。间日疟原虫寄生虫的种群遗传学准确描述了寄生虫的传播动态,并评估了疟疾控制措施。作为针对疟疾的第一代疫苗候选物,环子孢子蛋白(CSP)在恶性疟原虫中表现出了显著的潜力。广泛的多态性阻碍了有效疟疾疫苗的开发。因此,首次在 60 个斯里兰卡临床分离株中研究了 Pvcsp 的遗传多样性,方法是获得中央重复(CR)结构域的核苷酸序列,并检查肽重复基序(PRM)的多态性、遗传多样性指数和系统发育关系。PCR 扩增子确定了斯里兰卡 Pvcsp 的 610、700 和 710bp 大小多态性,所有获得的氨基酸序列均为 VK210 变体,由 4 种不同 PRM 的可变重复组成。CR 结构域中最丰富的两个 PRM,GDRADGQPA 和 GDRAAGQPA 由~2-4 个重复组成,而 GNRAAGQPA 是该岛所特有的。尽管观察到每个 PRM 的不同核苷酸序列称为重复等位基因(RAT),但这些都是同义的,导致 CR 结构域的多态性较低。斯里兰卡 Pvcsp 的遗传多样性归因于重复肽重复基序的数量、点突变和基因内重组。定义的 19 个氨基酸单倍型是斯里兰卡特有的,而来自全球分离株的 194 个 Pvcsp 序列则产生了 VK210 变体的 57 个更多独特的 a.a.单倍型。值得注意的是,VK210 和 VK247 变体的 CR 结构域都受到纯化选择的影响,这解释了 CSP 非同义多态性的稀缺性。揭示了 CR 区域中 RAT 分布的见解,并显示了间日疟原虫 VK210 变体的地理聚类。系统发育树再次强调了本地(VK210)和全球分离株(VK210 和 VK247)的这种独特地理聚类,这进一步通过 VK210 变体的高固定指数值得到验证。

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