| Literature DB >> 32553066 |
Ayaka Nagata1, Yuya Sekiguchi1, Toru Oi2, Fujiko Sunaga1, Hiroo Madarame1, Ryo Imai3, Kaori Sano4, Yukie Katayama3, Tsutomu Omatsu3, Mami Oba3, Tetsuya Furuya5, Junsuke Shirai5, Tamaki Okabayashi6, Naoaki Misawa6, Tomoichiro Oka7, Tetsuya Mizutani3, Makoto Nagai3,1.
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.Entities:
Keywords: Enterovirus G; papain-like cysteine protease sequence; recombination; sequence diversity; wild boar
Year: 2020 PMID: 32553066 DOI: 10.1099/jgv.0.001446
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891