Kim Yongkwan, Son Kidong, Kim Young-Sik, Lee Sook-Young, Jheong Weonhwa, Oem Jae-Ku
Environmental Health Research Department, National Institute of Environmental Research, Hwangyeong-ro 42, Seo-gu, Incheon, Republic of Korea.
Department of Veterinary Infectious Diseases, College of Veterinary Medicine, Chonbuk National University, Jeonju, Republic of Korea.
Virus Genes. 2019 Aug;55(4):545-549. doi: 10.1007/s11262-019-01668-w. Epub 2019 May 10.
Bats have been widely known as natural reservoir hosts of zoonotic diseases, such as severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS) caused by coronaviruses (CoVs). In the present study, we investigated the whole genomic sequence of a SARS-like bat CoV (16BO133) and found it to be 29,075 nt in length with a 40.9% G+C content. Phylogenetic analysis using amino acid sequences of the ORF 1ab and the spike gene showed that the bat coronavirus strain 16BO133 was grouped with the Beta-CoV lineage B and was closely related to the JTMC15 strain isolated from Rhinolophus ferrumequinum in China. However, 16BO133 was distinctly located in the phylogenetic topology of the human SARS CoV strain (Tor2). Interestingly, 16BO133 showed complete elimination of ORF8 regions induced by a frame shift of the stop codon in ORF7b. The lowest amino acid identity of 16BO133 was identified at the spike region among various ORFs. The spike region of 16BO133 showed 84.7% and 75.2% amino acid identity with Rf1 (SARS-like bat CoV) and Tor2 (human SARS CoV), respectively. In addition, the S gene of 16BO133 was found to contain the amino acid substitution of two critical residues (N479S and T487 V) associated with human infection. In conclusion, we firstly carried out whole genome characterization of the SARS-like bat coronavirus discovered in the Republic of Korea; however, it presumably has no human infectivity. However, continuous surveillance and genomic characterization of coronaviruses from bats are necessary due to potential risks of human infection induced by genetic mutation.
蝙蝠一直被广泛认为是人畜共患病的天然宿主,例如由冠状病毒(CoV)引起的严重急性呼吸综合征(SARS)和中东呼吸综合征(MERS)。在本研究中,我们调查了一种类SARS蝙蝠冠状病毒(16BO133)的全基因组序列,发现其长度为29,075个核苷酸,G+C含量为40.9%。使用开放阅读框1ab(ORF 1ab)和刺突基因的氨基酸序列进行的系统发育分析表明,蝙蝠冠状病毒株16BO133与β冠状病毒谱系B归为一类,并且与在中国从马铁菊头蝠分离出的JTMC15株密切相关。然而,16BO133在人类SARS冠状病毒株(Tor2)的系统发育拓扑结构中位置明显不同。有趣的是,16BO133显示出ORF7b中终止密码子移码诱导的ORF8区域完全缺失。在各个开放阅读框中,16BO133的刺突区域氨基酸同一性最低。16BO133的刺突区域与Rf1(类SARS蝙蝠冠状病毒)和Tor2(人类SARS冠状病毒)的氨基酸同一性分别为84.7%和75.2%。此外,发现16BO133的S基因含有与人类感染相关的两个关键残基的氨基酸替代(N479S和T487V)。总之,我们首次对在大韩民国发现的类SARS蝙蝠冠状病毒进行了全基因组特征分析;然而,它大概没有人类感染性。然而,由于基因突变引发人类感染的潜在风险,对来自蝙蝠的冠状病毒进行持续监测和基因组特征分析是必要的。