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诺氏疟原虫和食蟹猴疟原虫达菲结合蛋白基因的序列多样性与正选择:泰国分离株完整编码序列分析

Sequence diversity and positive selection at the Duffy-binding protein genes of Plasmodium knowlesi and P. cynomolgi: Analysis of the complete coding sequences of Thai isolates.

作者信息

Putaporntip Chaturong, Kuamsab Napaporn, Jongwutiwes Somchai

机构信息

Molecular Biology of Malaria and Opportunistic Parasites Research Unit, Department of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Molecular Biology of Malaria and Opportunistic Parasites Research Unit, Department of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Infect Genet Evol. 2016 Oct;44:367-375. doi: 10.1016/j.meegid.2016.07.040. Epub 2016 Jul 30.

Abstract

Plasmodium knowlesi and P. cynomolgi are simian malaria parasites capable of causing symptomatic human infections. The interaction between the Duffy binding protein alpha on P. knowlesi merozoite and the Duffy-antigen receptor for chemokine (DARC) on human and macaque erythrocyte membrane is prerequisite for establishment of blood stage infection whereas DARC is not required for erythrocyte invasion by P. cynomolgi. To gain insights into the evolution of the PkDBP gene family comprising PkDBPα, PkDBPβ and PkDBPγ, and a member of the DBP gene family of P. cynomolgi (PcyDBP1), the complete coding sequences of these genes were analyzed from Thai field isolates and compared with the publicly available DBP sequences of P. vivax (PvDBP). The complete coding sequences of PkDBPα (n=11), PkDBPβ (n=11), PkDBPγ (n=10) and PcyDBP1 (n=11) were obtained from direct sequencing of the PCR products. Nucleotide diversity of DBP is highly variable across malaria species. PcyDBP1 displayed the greatest level of nucleotide diversity while all PkDBP gene members exhibited comparable levels of diversity. Positive selection occurred in domains I, II and IV of PvDBP and in domain V of PcyDBP1. Although deviation from neutrality was not detected in domain II of PkDBPα, a signature of positive selection was identified in the putative DARC binding site in this domain. The DBP gene families seem to have arisen following the model of concerted evolution because paralogs rather than orthologs are clustered in the phylogenetic tree. The presence of identical or closely related repeats exclusive for the PkDBP gene family suggests that duplication of gene members postdated their divergence from the ancestral PcyDBP and PvDBP lineages. Intragenic recombination was detected in all DBP genes of these malaria species. Despite the limited number of isolates, P. knowlesi from Thailand shared phylogenetically related domain II sequences of both PkDBPα and PkDBPγ with those from Peninsular Malaysia, consistent with their geographic proximity.

摘要

诺氏疟原虫和食蟹猴疟原虫是能够引起人类有症状感染的猿类疟原虫。诺氏疟原虫裂殖子上的达菲结合蛋白α与人类和猕猴红细胞膜上的趋化因子达菲抗原受体(DARC)之间的相互作用是建立血液阶段感染的先决条件,而食蟹猴疟原虫侵入红细胞则不需要DARC。为了深入了解由诺氏疟原虫的PkDBPα、PkDBPβ和PkDBPγ以及食蟹猴疟原虫的DBP基因家族成员(PcyDBP1)组成的PkDBP基因家族的进化情况,对这些基因的完整编码序列进行了泰国野外分离株分析,并与公开可得的间日疟原虫(PvDBP)的DBP序列进行了比较。通过对PCR产物的直接测序获得了PkDBPα(n = 11)、PkDBPβ(n = 11)、PkDBPγ(n = 10)和PcyDBP1(n = 11)的完整编码序列。DBP的核苷酸多样性在不同疟原虫物种中高度可变。PcyDBP1显示出最高水平的核苷酸多样性,而所有PkDBP基因成员表现出相当的多样性水平。正向选择发生在PvDBP的结构域I、II和IV以及PcyDBP1的结构域V中。虽然在PkDBPα的结构域II中未检测到偏离中性的情况,但在该结构域的假定DARC结合位点中鉴定出了正向选择的特征。DBP基因家族似乎是按照协同进化模型产生的,因为旁系同源物而非直系同源物聚集在系统发育树中。PkDBP基因家族特有的相同或密切相关重复序列的存在表明,基因成员的复制发生在它们与祖先PcyDBP和PvDBP谱系分化之后。在这些疟原虫物种的所有DBP基因中都检测到了基因内重组。尽管分离株数量有限,但来自泰国的诺氏疟原虫与来自马来西亚半岛的诺氏疟原虫在系统发育上共享PkDBPα和PkDBPγ的相关结构域II序列,这与它们的地理接近性一致。

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