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优势隐孢子虫亚型 IIaA15G2R1 的种群遗传特征。

Population genetic characterisation of dominant Cryptosporidium parvum subtype IIaA15G2R1.

机构信息

State Key Laboratory of Bioreactor Engineering, School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

Int J Parasitol. 2013 Dec;43(14):1141-7. doi: 10.1016/j.ijpara.2013.09.002. Epub 2013 Oct 12.

Abstract

The subtype IIaA15G2R1 at the 60 kDa glycoprotein (gp60) gene locus is the most dominant Cryptosporidium parvum infecting dairy cattle and humans in industrialised nations. The reasons for its high transmissibility are not clear, and it remains to be determined whether this subtype represents a homogeneous parasite population. In this study, we sequence-characterised 26 IIaA15G2R subtype specimens and 26 non-IIaA15G2R subtype specimens from the United States, Canada, United Kingdom and Spain at seven other known polymorphic loci, including CP47, CP56, DZ-HRGP, MSC6-5, MSC6-7, RPGR and ZPT. Extensive heterogeneity within IIaA15G2R1 and discordance in typing results between gp60 and other genetic markers were observed. Results of inter-locus and intra-ZPT linkage disequilibrium and recombination analyses indicated that the heterogeneity within IIaA15G2R1 and discordance in typing results among genetic loci were largely due to the occurrence of genetic recombination, mostly within the gp60 subtype IIaA15G2R1. Although there was no clear population diversion between IIaA15G2R and non-IIaA15G2R subtypes, results of STRUCTURE and FST analyses suggested the presence of at least two subpopulations; subpopulation 1 had an epidemic population structure and was widely distributed, whereas subpopulation 2 had a clonal population structure and consisted of geographically segregated multilocus subtypes. Genetic recombination between epidemic and geographically segregated C. parvum populations appeared to be a driving force in the emergence of a hyper-transmissible IIaA15G2R1 subtype. Genetic recombination was observed even between the zoonotic IIa subtype family and anthroponotic subtype family IIc at CP56, MSC6-7 and ZPT. Thus, the IIaA15G2R1 subtype at gp60 is likely a fitness marker for C. parvum and the wide spread of IIaA15G2R1 subtype around the world is probably independent of the sequence characteristics at other genetic loci.

摘要

IIaA15G2R1 亚型是在 60 kDa 糖蛋白(gp60)基因座上最占优势的感染工业化国家奶牛和人类的微小隐孢子虫。其高传染性的原因尚不清楚,仍有待确定该亚型是否代表一个同质的寄生虫种群。在这项研究中,我们对来自美国、加拿大、英国和西班牙的 26 个 IIaA15G2R 亚型样本和 26 个非 IIaA15G2R 亚型样本在其他七个已知多态性基因座(CP47、CP56、DZ-HRGP、MSC6-5、MSC6-7、RPGR 和 ZPT)进行了测序特征分析。在 IIaA15G2R1 内部观察到广泛的异质性,并且在 gp60 和其他遗传标记之间的分型结果不一致。基因座间和 ZPT 内的连锁不平衡和重组分析结果表明,IIaA15G2R1 内部的异质性以及遗传标记之间的分型结果不一致主要是由于遗传重组的发生,主要发生在 gp60 亚型 IIaA15G2R1 内部。尽管在 IIaA15G2R 和非 IIaA15G2R 亚型之间没有明显的种群分化,但 STRUCTURE 和 FST 分析的结果表明至少存在两个亚群;亚群 1 具有流行种群结构且分布广泛,而亚群 2 具有克隆种群结构且由地理隔离的多基因座亚型组成。流行的微小隐孢子虫种群和地理隔离的微小隐孢子虫种群之间的遗传重组似乎是高传染性 IIaA15G2R1 亚型出现的驱动力。在 CP56、MSC6-7 和 ZPT 等基因座,甚至观察到了从动物源 IIa 亚型家族到人类源 IIc 亚型家族的遗传重组。因此,gp60 上的 IIaA15G2R1 亚型可能是微小隐孢子虫的适应度标志,IIaA15G2R1 亚型在世界各地的广泛传播可能与其他遗传基因座的序列特征无关。

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