首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >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
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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

机译:疟原虫和食蟹猕猴的达菲结合蛋白基因的序列多样性和阳性选择:泰国分离株的完整编码序列分析

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摘要

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 PkDBP alpha, PkDBP beta and PkDBP gamma, 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 PkDBP alpha (n = 11), PkDBP beta (n = 11), PkDBP gamma (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 PkDBPa, 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 PkDBPa and PkDBP. with those from Peninsular Malaysia, consistent with their geographic proximity. (C) 2016 Elsevier B.V. All rights reserved.
机译:诺氏疟原虫和食蟹猴疟原虫是能够引起人类症状性感染的猿猴疟原虫。诺氏疟原虫裂殖子上的达菲结合蛋白α与人和猕猴红细胞膜上趋化因子的达菲抗原受体(DARC)之间的相互作用是建立血液阶段感染的先决条件,而食蟹猴侵袭红细胞不需要DARC 。为了深入了解PkDBP基因家族的进化,包括PkDBP alpha,PkDBP beta和PkDBP gamma,以及食蟹猴(PcyDBP1)的DBP基因家族的成员,从泰国田间分离株中分析了这些基因的完整编码序列。并将其与间日疟原虫的公开DBP序列(PvDBP)进行比较。从PCR产物的直接测序获得了PkDBP alpha(n = 11),PkDBP beta(n = 11),PkDBP gamma(n = 10)和PcyDBP1(n = 11)的完整编码序列。在疟疾物种之间,DBP的核苷酸多样性差异很大。 PcyDBP1表现出最大的核苷酸多样性水平,而所有PkDBP基因成员表现出可比较的多样性水平。正选择发生在PvDBP的域I,II和IV和PcyDBP1的域V中。尽管在PkDBPa的结构域II中未检测到偏离中性,但是在该结构域的推定DARC结合位点中鉴定出阳性选择的特征。 DBP基因家族似乎遵循了协调进化的模式,因为旁系同源物而非直系同源物聚集在系统发生树中。 PkDBP基因家族专有的相同或紧密相关重复序列的存在表明,基因成员的复制推迟了其与祖先PcyDBP和PvDBP世系的分歧。在这些疟疾物种的所有DBP基因中均检测到了基因内重组。尽管分离株的数量有限,但是来自泰国的诺氏疟原虫共享PkDBPa和PkDBP的系统发育相关的结构域II序列。与来自马来西亚半岛的游客,与其地理位置相近。 (C)2016 Elsevier B.V.保留所有权利。

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