Ren Tongwei, Mo Qingrong, Wang Yuxu, Wang Hao, Nong Zuorong, Wang Jinglong, Niu Chenxia, Liu Chang, Chen Ying, Ouyang Kang, Huang Weijian, Wei Zuzhang
Laboratory of Animal Infectious Diseases and Molecular Immunology, College of Animal Science and Technology, Guangxi University, Nanning, China.
Front Vet Sci. 2020 Dec 3;7:552517. doi: 10.3389/fvets.2020.552517. eCollection 2020.
Getah virus (GETV) has caused many outbreaks in animals in recent years. Monitoring of the virus and its related diseases is crucial to control the transmission of the virus. In the summer of 2018, we conducted routine tests on clinical samples from different pig farms in Guangxi province, South China, and isolated and characterized a GETV strain, named GX201808. Cytopathic effects were observed in BHK-21 cells inoculated with GX201808. The expression of E2 protein of GETV could be detected in virus-infected cells by indirect immunofluorescence assays. Electron microscopic analysis showed that the virus particles were spherical and ~70 nm in diameter with featured surface fibers. The multistep growth curves showed the virus propagated well in the BHK-21 cells. Molecular genetic analysis revealed that GX201808 belongs to Group 3, represented by Kochi-01-2005 isolated in Japan in 2005, and it clustered closely with the recently reported Chinese strains isolated from pigs, cattle, and foxes. A comparison of the identities of nucleotides and amino acids in the coding regions demonstrated that the GX201808 showed the highest amino acid identity (99.6%) with the HuN1 strain, a highly pathogenic isolate resulting in an outbreak of GETV infection in swine herds in Hunan province in 2017. In the present study, GETV was identified and isolated for the first time in Guangxi province of southern China, suggesting that future surveillance of this virus should be strengthened.
近年来,盖塔病毒(GETV)在动物中引发了多次疫情。对该病毒及其相关疾病进行监测对于控制病毒传播至关重要。2018年夏季,我们对中国南方广西不同猪场的临床样本进行了常规检测,分离并鉴定了一株GETV毒株,命名为GX201808。在接种GX201808的BHK - 21细胞中观察到细胞病变效应。通过间接免疫荧光试验可在病毒感染细胞中检测到GETV的E2蛋白表达。电子显微镜分析表明,病毒粒子呈球形,直径约70 nm,表面有特征性纤维。多步生长曲线显示该病毒在BHK - 21细胞中增殖良好。分子遗传学分析表明,GX201808属于第3组,以2005年在日本分离的高知 - 01 - 2005为代表,它与最近报道的从猪、牛和狐狸中分离的中国毒株紧密聚类。编码区核苷酸和氨基酸同一性比较表明,GX201808与HuN1毒株的氨基酸同一性最高(99.6%),HuN1是一株高致病性毒株,于2017年在湖南省猪群中引发了GETV感染疫情。在本研究中,首次在中国南方广西省鉴定并分离出GETV,这表明未来应加强对该病毒的监测。