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描述加利福尼亚海狮多瘤病毒 1:多瘤病毒科对食肉目动物宿主范围的扩展。

Characterization of California sea lion polyomavirus 1: expansion of the known host range of the Polyomaviridae to Carnivora.

机构信息

Marine Animal Disease Laboratory, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.

出版信息

Infect Genet Evol. 2011 Jul;11(5):987-96. doi: 10.1016/j.meegid.2011.03.010. Epub 2011 Mar 29.

DOI:10.1016/j.meegid.2011.03.010
PMID:21453794
Abstract

The genome of a novel polyomavirus first identified in a proliferative tongue lesion of a California sea lion (Zalophus californianus) is reported. This is only the third described polyomavirus of laurasiatherian mammals, is the first of the three associated with a lesion, and is the first known polyomavirus of a host in the order Carnivora. Predicted large T, small t, VP1, VP2, and VP3 genes were identified based on homology to proteins of known polyomaviruses, and a putative agnoprotein was identified based upon its location in the genome. Phylogenetic analysis of the predicted late region proteins found that the laurasiatherian polyomaviruses, together with Squirrel monkey polyomavirus and Murine pneumotropic virus, form a monophyletic clade. Phylogenetic analysis of the early region was more ambiguous. The noncoding control region of California sea lion polyomavirus 1 is unusual in that only two apparent large T binding sites are present; this is less than any other known polyomavirus. The VP1 of this virus has an unusually long carboxy-terminal region. A quantitative polymerase chain reaction was developed and utilized on various samples from 79 additional animals from either managed or wild stranded California sea lion populations, and California sea lion polyomavirus 1 infection was found in 24% of stranded animals. Sequence of additional samples identified four sites of variation in the t antigens, three of which resulted in predicted coding changes.

摘要

一种新型多瘤病毒的基因组首次在加利福尼亚海狮(Zalophus californianus)的增殖性舌病变中被发现。这是仅有的三种描述的劳亚兽类哺乳动物多瘤病毒中的第三种,与病变有关的三种中的第一种,也是已知的食肉目宿主的第一种多瘤病毒。根据与已知多瘤病毒蛋白的同源性,预测了大 T、小 t、VP1、VP2 和 VP3 基因,并根据其在基因组中的位置预测了推定的 agnoprotein。预测的晚期区蛋白的系统发育分析表明,劳亚兽多瘤病毒与松鼠猴多瘤病毒和鼠肺转移病毒一起形成一个单系分支。早期区的系统发育分析更为模糊。加利福尼亚海狮多瘤病毒 1 的非编码调控区是不寻常的,因为只有两个明显的大 T 结合位点;这比任何其他已知的多瘤病毒都要少。该病毒的 VP1 具有异常长的羧基末端区域。开发并利用来自管理或野生搁浅加利福尼亚海狮种群的 79 只以上动物的各种样本进行了定量聚合酶链反应,发现 24%的搁浅动物感染了加利福尼亚海狮多瘤病毒 1。对其他样本的序列分析确定了 t 抗原的四个变异位点,其中三个导致了预测的编码变化。

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