Identification and complete genome analysis of a novel bovine picornavirus in Japan

• Published in: Virus research Vol. 210; pp. 205 - 212
• Main Authors: Nagai, Makoto, Omatsu, Tsutomu, Aoki, Hiroshi, Kaku, Yoshihiro, Belsham, Graham J., Haga, Kei, Naoi, Yuki, Sano, Kaori, Umetsu, Moeko, Shiokawa, Mai, Tsuchiaka, Shinobu, Furuya, Tetsuya, Okazaki, Sachiko, Katayama, Yukie, Oba, Mami, Shirai, Junsuke, Katayama, Kazuhiko, Mizutani, Tetsuya
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 02.12.2015
• Subjects: 3' untranslated regions; 5' untranslated regions; amino acids; Animals; Bovine; Cattle; Cattle Diseases - epidemiology; Cattle Diseases - virology; Chiroptera; Cluster Analysis; diarrhea; Diarrhea - epidemiology; Diarrhea - veterinary; Diarrhea - virology; dogs; etiology; Feces; Feces - virology; Feline calicivirus; Gene Order; Genes, Viral; genome; Genome, Viral; Japan; Japan - epidemiology; Metagenomics; Molecular Sequence Data; Novel picornavirus; pathogenicity; Phylogeny; Picornaviridae; Picornaviridae - classification; Picornaviridae - genetics; Picornaviridae - isolation & purification; Picornaviridae Infections - veterinary; Picornaviridae Infections - virology; Picornavirus; Prevalence; Reverse Transcriptase Polymerase Chain Reaction; RNA, Viral - genetics; sequence analysis; Sequence Analysis, DNA; Sequence Homology; Japan; Metagenomics; Novel picornavirus; Feces; Bovine; Japan
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/j.virusres.2015.08.001

•Novel viruses were identified in feces from cattle by metagenomics approach.•These viruses had a standard picornavirus genome organization.•They are related to unclassified Chinese picornaviruses from bat, cat and dog.•These viruses were detected in 23% (20/87) feces from cattle in Hokkaido in Japan. We identified novel viruses in feces from cattle with diarrhea collected in 2009 in Hokkaido Prefecture, Japan, by using a metagenomics approach and determined the (near) complete sequences of the virus. Sequence analyses revealed that they had a standard picornavirus genome organization, i.e. 5′ untranslated region (UTR) - L- P1 (VP4- VP3- VP2- VP1) - P2 (2A- 2B- 2C) - P3 (3A- 3B- 3C-3D) - 3′UTR- poly(A). They are closely related to other unclassified Chinese picornaviruses; bat picornaviruses group 1–3, feline picornavirus, and canine picornavirus, sharing 45.4–51.4% (P1), 38.0–44.9% (P2), and 49.6–53.3% (P3) amino acid identities, respectively. The phylogenetic analyses and detailed genome characterization showed that they, together with the unclassified Chinese picornaviruses, grouped as a cluster for the P1, 2C, 3CD and VP1 coding regions. These viruses had conserved features (e.g. predicted protein cleavage sites, presence of a leader protein, 2A, 2C, 3C, and 3D functional domains), suggesting they have a common ancestor. Reverse-transcription-PCR assays, using specific primers designed from the 5′UTR sequence of these viruses, showed that 23.0% (20/87) of fecal samples from cattle with diarrhea were positive, indicating the prevalence of these picornavirus in the Japanese cattle population in Hokkaido Prefecture. However, further studies are needed to investigate the pathogenic potential and etiological role of these viruses in cattle.