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鉴定、定位新型 RhopH2 保守跨物种表位及其遗传多样性与 的关系

Identification, Mapping, and Genetic Diversity of Novel Conserved Cross-Species Epitopes of RhopH2 in With .

机构信息

Indian Council of Medical Research (ICMR)-Regional Medical Research Centre, North East Region (NER), Dibrugarh, India.

Department of Biotechnology and Microbiology, National College, Tiruchirapalli, India.

出版信息

Front Cell Infect Microbiol. 2022 Jan 13;11:810398. doi: 10.3389/fcimb.2021.810398. eCollection 2021.

Abstract

Malaria is a major public health concern, and any tangible intervention during the pre-elimination phase can result in a significant reduction in infection rates. Recent studies have reported that antigens producing cross-protective immunity can play an important role as vaccines and halt malaria transmission in different endemic regions. In this study, we studied the genetic diversity, natural selection, and discovered novel conserved epitopes of a high molecular weight rhoptry protein 2 (RhopH2) in clinical samples of and cross-protective domains, which has been proven to produce cross-protective immunity in both species. We found low levels of nucleotide diversity (; π ~ 0.0093, SNPs = 49 and π ~ 0.0014, SNPs = 23) in (n = 40) and (n = 65) samples in the cross-protective domain. Strong purifying selection was observed for both species ( knowlesi; dS - dN = 2.41, p < 0.009, ; dS - dN = 1.58, p < 0.050). epitope prediction in identified 10 potential epitopes, of which 7 epitopes were 100% conserved within clinical samples. Of these epitopes, an epitope with 10 amino acids (QNSKHFKKEK) was found to be fully conserved within all and clinical samples and 80%-90% conservation within simian malaria ortholog species, i.e., and . Phylogenetic analysis of the PkRhopH2 cross-protective domain showed geographical clustering, and three subpopulations of were identified of which two subpopulations originated from Sarawak, Malaysian Borneo, and one comprised only the laboratory lines from Peninsular Malaysia. This study suggests that RhopH2 could be an excellent target for cross-protective vaccine development with potential for outwitting strain as well as species-specific immunity. However, more detailed studies on genetic diversity using more clinical samples from both species as well as the functional role of antibodies specific to the novel conserved epitope identified in this study can be explored for protection against infection.

摘要

疟疾是一个主要的公共卫生关注点,在消除前阶段的任何切实可行的干预措施都可以显著降低感染率。最近的研究表明,产生交叉保护免疫的抗原可以作为疫苗发挥重要作用,并阻止不同流行地区的疟疾传播。在这项研究中,我们研究了临床样本中一种高分子量的裂殖体蛋白 2(RhopH2)的遗传多样性、自然选择,并发现了一种新的保守表位,该蛋白已被证明在两种物种中都能产生交叉保护免疫。我们发现,在 (n = 40)和 (n = 65)样本的 交叉保护域中,核苷酸多样性水平较低(;π0.0093,SNP = 49和π0.0014,SNP = 23)。在这两个物种中都观察到强烈的纯化选择(knowlesi;dS-dN = 2.41,p < 0.009,;dS-dN = 1.58,p < 0.050)。在 中,10 个潜在表位的预测,其中 7 个表位在临床样本中 100%保守。在这些表位中,一个含有 10 个氨基酸(QNSKHFKKEK)的表位被发现完全保守于所有 和 临床样本中,在灵长类疟原虫直系同源物物种中保守 80%-90%,即 和 。PkRhopH2 交叉保护域的系统发育分析显示出地理聚类,鉴定出 有三个亚群,其中两个亚群起源于马来西亚婆罗洲的沙捞越,一个仅由马来西亚半岛的实验室株组成。本研究表明,RhopH2 可能是一种很好的交叉保护疫苗开发靶点,具有逃避株和种特异性免疫的潜力。然而,需要使用更多来自两种物种的临床样本进行遗传多样性的更详细研究,以及对本研究中鉴定的新保守表位的特异性抗体的功能作用进行研究,以探索针对感染的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4492/8793677/981abb6923f7/fcimb-11-810398-g001.jpg

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