Li Yuying, Huang Haixin, Lan Tian, Wang Wei, Zhang Jie, Zheng Min, Cao Liang, Sun Wenchao, Lu Huijun
Institute of Virology, Wenzhou University, Wenzhou, 325035, China.
Institute of Military Veterinary Medicine, The Academy of Military Medical Sciences, Changchun, 130122, China.
Virus Genes. 2021 Jun;57(3):284-288. doi: 10.1007/s11262-021-01840-1. Epub 2021 May 10.
Lyon IARC polyomavirus (LIPyV), a newly discovered polyomavirus (PyV), was first identified in 2017 in human skin samples in the USA. Later, it was detected in several other countries in samples of human and feline origin. Our aim was to find out if the virus occurs in China. To this end, 100 fecal samples were collected from cats with diarrhea in Guangxi Province during 2016 and 2018 and tested with polymerase chain reaction (PCR). Only 2 samples that originated from two related individuals were found to be positive. Based on the sequence identity of the 240-bp PCR products, the two positive samples supposedly contained identical viruses. Therefore, only one of them, which was designated as LIPyV-GXNN01, was selected for full genome amplification, cloning, sequencing and analysis. LIPyV-GXNN01, which comprises 5,263 nucleotides, has an early region that consists of small T antigen (ST-Ag) and large T antigen (LT-Ag) and a late region coding for the VP1, VP2, and VP3 structural proteins. Moreover, the LIPyV-GXNN01 strain structural proteins share 95.9-99.4%, 97.6-99.2%, and 97.1-99.2% nucleic acid identity with the VP1, VP2, and VP3of other LIPyV reference strains, respectively. A phylogenetic analysis revealed that GXNN01 clustered together with previously reported LIPyV strain. This present study is the first report of LIPyV in China.
里昂多瘤病毒(LIPyV)是一种新发现的多瘤病毒(PyV),于2017年首次在美国的人类皮肤样本中被鉴定出来。后来,在其他几个国家的人类和猫科动物来源的样本中也检测到了该病毒。我们的目的是查明该病毒在中国是否存在。为此,在2016年至2018年期间从广西省腹泻的猫身上采集了100份粪便样本,并采用聚合酶链反应(PCR)进行检测。仅发现来自两个相关个体的2份样本呈阳性。基于240 bp PCR产物的序列同一性,这两份阳性样本推测含有相同的病毒。因此,仅选择其中一份被命名为LIPyV-GXNN01的样本进行全基因组扩增、克隆、测序和分析。LIPyV-GXNN01由5263个核苷酸组成,有一个早期区域,由小T抗原(ST-Ag)和大T抗原(LT-Ag)组成,还有一个晚期区域编码VP1、VP2和VP3结构蛋白。此外,LIPyV-GXNN01菌株的结构蛋白与其他LIPyV参考菌株的VP1、VP2和VP3的核酸同一性分别为95.9 - 99.4%、97.6 - 99.2%和97.1 - 99.2%。系统发育分析表明,GXNN01与先前报道的LIPyV菌株聚集在一起。本研究是LIPyV在中国的首次报道。