TY - JOUR
T1 - Novel intertypic recombination of Echovirus 11 in the Enterovirus species B
AU - Gong, Yu Nong
AU - Yang, Shu Li
AU - Chen, Yi Ching
AU - Liu, Yi Chun
AU - Huang, Yhu-Chering
AU - Tsao, Kuo-Chien
N1 - © 2023 Wiley Periodicals LLC.
PY - 2024/1
Y1 - 2024/1
N2 - Enteroviruses (EVs), single-stranded, positive-sense RNA viruses, can be classified into four species (A−D), which have previously been linked to a diverse range of disease manifestations and infections affecting the central nervous system. In the Enterovirus species B (EV-B), Echovirus type 11 (E11) has been observed to occasionally circulate in Taiwan, which was responsible for an epidemic of enterovirus infections in 2018. Here, 48 clinical specimens isolated in 2003, 2004, 2009, and 2018 were collected for the high-throughput sequencing. Notably, we identified 2018 Taiwanese strains having potential recombinations in the 3D gene, as well as one 2003 strain having a double recombination with E6 and Coxsackievirus B5 in the P2 and P3 regions, respectively. Additionally, one amino acid signature mutated from the Histidine (H) in throat swab specimens to the Tyrosine (Y) in cerebral spinal fluid specimens was detected at position 1496 (or 57) of the genomic coordinate (or 3A gene) to further demonstrate intra-host evolution in different organs. In conclusion, this study identifies potential intertypic recombination events and an intra-host signature mutation in E11 strains, isolated during a 2018 neurological disease outbreak in Taiwan, contributing to our understanding of its evolution and pathogenesis.
AB - Enteroviruses (EVs), single-stranded, positive-sense RNA viruses, can be classified into four species (A−D), which have previously been linked to a diverse range of disease manifestations and infections affecting the central nervous system. In the Enterovirus species B (EV-B), Echovirus type 11 (E11) has been observed to occasionally circulate in Taiwan, which was responsible for an epidemic of enterovirus infections in 2018. Here, 48 clinical specimens isolated in 2003, 2004, 2009, and 2018 were collected for the high-throughput sequencing. Notably, we identified 2018 Taiwanese strains having potential recombinations in the 3D gene, as well as one 2003 strain having a double recombination with E6 and Coxsackievirus B5 in the P2 and P3 regions, respectively. Additionally, one amino acid signature mutated from the Histidine (H) in throat swab specimens to the Tyrosine (Y) in cerebral spinal fluid specimens was detected at position 1496 (or 57) of the genomic coordinate (or 3A gene) to further demonstrate intra-host evolution in different organs. In conclusion, this study identifies potential intertypic recombination events and an intra-host signature mutation in E11 strains, isolated during a 2018 neurological disease outbreak in Taiwan, contributing to our understanding of its evolution and pathogenesis.
KW - Echovirus
KW - Enterovirus
KW - high-throughput sequencing
KW - neurological disease
KW - recombination
KW - Recombination, Genetic
KW - Humans
KW - Enterovirus Infections/epidemiology
KW - Phylogeny
KW - Enterovirus B, Human/genetics
KW - Enterovirus/genetics
UR - http://www.scopus.com/inward/record.url?scp=85181414496&partnerID=8YFLogxK
U2 - 10.1002/jmv.29323
DO - 10.1002/jmv.29323
M3 - 文章
C2 - 38164047
AN - SCOPUS:85181414496
SN - 0146-6615
VL - 96
SP - e29323
JO - Journal of Medical Virology
JF - Journal of Medical Virology
IS - 1
M1 - e29323
ER -