Abstract

BackgroundBovine 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.ResultsThe 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.ConclusionsWe 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.

Highlights

  • Bovine enterovirus (BEV) belongs to the species Enterovirus E or F, genus Enterovirus and family Picornaviridae

  • BEVs have been classified based on virus antigenicity determined by cross neutralization testing [13,14,15,16], the genotype based on the capsid protein amino acid sequences are used to classify BEVs [4, 10,11,12, 17, 18]

  • RNA extracted from the Kagoshima sample collected in 2014 and virus stocks of BEV IS1/Bos taurus/JPN/1990 (BEV-IS1), BEV-IS2 and BEV-Ho12 were subjected to deep sequencing

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Summary

Introduction

Bovine enterovirus (BEV) belongs to the species Enterovirus E or F, genus Enterovirus and family Picornaviridae. We identified a novel BEV in diarrheal feces collected for that survey. Bovine enterovirus (BEV) is a single positive-stranded RNA virus belonging to the genus Enterovirus within family Picornaviridae. The viral particle is composed of a small, non-enveloped and icosahedral virion and 7.5 kbase genome containing a single open reading frame (ORF) flanked by untranslated regions (UTRs) at the 5′ and 3′ ends. BEVs belong to EV-E and EV-F (formerly known as BEV-A and BEVB, respectively) and can be distinguished from other EVs by the unique secondary structure of their RNA genome: a 5′-cloverleaf and internal ribosome entry site (IRES) linked by additional nucleotide sequences at the 5′UTR [3,4,5]. BEVs are classified into 4 sero-/genotypes and 6 sero-/genotypes in EV-E (E1, E2, E3 and E4) and EV-F (F1, F2, F3, F4, F5 and F6), respectively

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