TY - JOUR
T1 - Genetic diversity of enterovirus G detected in faecal samples of wild boars in Japan
T2 - identification of novel genotypes carrying a papain-like cysteine protease sequence
AU - Nagata, Ayaka
AU - Sekiguchi, Yuya
AU - Oi, Toru
AU - Sunaga, Fujiko
AU - Madarame, Hiroo
AU - Imai, Ryo
AU - Sano, Kaori
AU - Katayama, Yukie
AU - Omatsu, Tsutomu
AU - Oba, Mami
AU - Furuya, Tetsuya
AU - Shirai, Junsuke
AU - Okabayashi, Tamaki
AU - Misawa, Naoaki
AU - Oka, Tomoichiro
AU - Mizutani, Tetsuya
AU - Nagai, Makoto
N1 - Publisher Copyright:
© 2020 Microbiology Society. All rights reserved.
PY - 2020
Y1 - 2020
N2 - 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.
AB - 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.
KW - Enterovirus G
KW - Papain-like cysteine protease sequence
KW - Recombination
KW - Sequence diversity
KW - Wild boar
UR - https://www.scopus.com/pages/publications/85090078530
U2 - 10.1099/jgv.0.001446
DO - 10.1099/jgv.0.001446
M3 - Article
C2 - 32553066
AN - SCOPUS:85090078530
SN - 0022-1317
VL - 101
SP - 840
EP - 852
JO - Journal of General Virology
JF - Journal of General Virology
IS - 8
ER -