Genetic diversity of enterovirus G detected in faecal samples of wild boars in Japan: identification of novel genotypes carrying a papain-like cysteine protease sequence

Author:

Nagata Ayaka1,Sekiguchi Yuya1,Oi Toru2,Sunaga Fujiko1,Madarame Hiroo1,Imai Ryo3,Sano Kaori4,Katayama Yukie3,Omatsu Tsutomu3,Oba Mami3,Furuya Tetsuya5,Shirai Junsuke5,Okabayashi Tamaki6,Misawa Naoaki6,Oka Tomoichiro7,Mizutani Tetsuya3,Nagai Makoto31

Affiliation:

1. School of Veterinary Medicine, Azabu University, Sagamihara, Kanagawa 252-5201, Japan

2. Faculty of Bioresources and Environmental Science, Ishikawa Prefectural University, Nonoichi, Ishikawa 921-8836, Japan

3. Research and Education Center for Prevention of Global Infectious Diseases of Animals, Tokyo University of Agriculture and Technology, Fuchu, Tokyo 183-8509, Japan

4. Department of Pathology, National Institute of Infectious Diseases, Shinjuku, Tokyo 162-8640, Japan

5. Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Fuchu, Tokyo 183-8509, Japan

6. Center for Animal Disease Control, University of Miyazaki, Miyazaki 889-2192, Japan

7. Department of Virology II, National Institute of Infectious Diseases, Musashimurayama, Tokyo 208-0011, Japan

Abstract

The genetic diversity of enterovirus G (EV-G) was investigated in the wild-boar population in Japan. EV-G-specific reverse transcription PCR demonstrated 30 (37.5 %) positives out of 80 faecal samples. Of these, viral protein 1 (VP1) fragments of 20 samples were classified into G1 (3 samples), G4 (1 sample), G6 (2 samples), G8 (4 samples), G11 (1 sample), G12 (7 samples), G14 (1 sample) and G17 (1 sample), among which 11 samples had a papain-like cysteine protease (PL-CP) sequence, believed to be the first discoveries in G1 (2 samples) or G17 (1 sample) wild-boar EV-Gs, and in G8 (2 samples) or G12 (6 samples) EV-Gs from any animals. Sequences of the non-structural protein regions were similar among EV-Gs possessing the PL-CP sequence (PL-CP EV-Gs) regardless of genotype or origin, suggesting the existence of a common ancestor for these strains. Interestingly, for the two G8 and two G12 samples, the genome sequences contained two versions, with or without the PL-CP sequence, together with the homologous 2C/PL-CP and PL-CP/3A junction sequences, which may explain how the recombination and deletion of the PL-CP sequences occured in the PL-CP EV-G genomes. These findings shed light on the genetic plasticity and evolution of EV-G.

Funder

Japan Society for the Promotion of Science

Publisher

Microbiology Society

Subject

Virology

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