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論文
タイトル
タイトル(英)
Identification of a novel bovine enterovirus possessing highly divergent amino acid sequences in capsid protein
参照URL
https://researchmap.jp/kaorisano/published_papers/22564864
著者
著者(英)
Shinobu Tsuchiaka,Sayed Samim Rahpaya,Konosuke Otomaru,Hiroshi Aoki,Mai Kishimoto,Yuki Naoi,Tsutomu Omatsu,Kaori Sano,Sachiko Okazaki-Terashima,Yukie Katayama,Mami Oba,Makoto Nagai,Tetsuya Mizutani
担当区分
概要
概要(英)
Background: Bovine enterovirus (BEV) belongs to the species Enterovirus E or F, genus Enterovirus and family Picornaviridae. Although numerous studies have identified BEVs in the feces of cattle with diarrhea, the pathogenicity of BEVs remains unclear. Previously, we reported the detection of novel kobu-like virus in calf feces, by metagenomics analysis. In the present study, we identified a novel BEV in diarrheal feces collected for that survey. Complete genome sequences were determined by deep sequencing in feces. Secondary RNA structure analysis of the 5' untranslated region (UTR), phylogenetic tree construction and pairwise identity analysis were conducted. Results: The complete genome sequences of BEV were genetically distant from other EVs and the VP1 coding region contained novel and unique amino acid sequences. We named this strain as BEV AN12/Bos taurus/JPN/2014 (referred to as BEV-AN12). According to genome analysis, the genome length of this virus is 7414 nucleotides excluding the poly (A) tail and its genome consists of a 5' UTR, open reading frame encoding a single polyprotein, and 3'UTR. The results of secondary RNA structure analysis showed that in the 5' UTR, BEV-AN12 had an additional clover leaf structure and small stem loop structure, similarly to other BEVs. In pairwise identity analysis, BEV-AN12 showed high amino acid (aa) identities to Enterovirus F in the polyprotein, P2 and P3 regions (aa identity >= 82.4%). Therefore, BEV-AN12 is closely related to Enterovirus F. However, aa sequences in the capsid protein regions, particularly the VP1 encoding region, showed significantly low aa identity to other viruses in genus Enterovirus (VP1 aa identity <= 58.6%). In addition, BEV-AN12 branched separately from Enterovirus E and F in phylogenetic trees based on the aa sequences of P1 and VP1, although it clustered with Enterovirus F in trees based on sequences in the P2 and P3 genome region. Conclusions: We identified novel BEV possessing highly divergent aa sequences in the VP1 coding region in Japan. According to species definition, we proposed naming this strain as "Enterovirus K", which is a novel species within genus Enterovirus. Further genomic studies are needed to understand the pathogenicity of BEVs.
出版者・発行元
出版者・発行元(英)
BIOMED CENTRAL LTD
誌名
誌名(英)
BMC MICROBIOLOGY
17
1
開始ページ
18
終了ページ
出版年月
2017年1月
査読の有無
査読有り
招待の有無
掲載種別
研究論文(学術雑誌)
ISSN
1471-2180
DOI URL
https://doi.org/10.1186/s12866-016-0923-0
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