期刊
ARCHIVES OF VIROLOGY
卷 166, 期 8, 页码 2209-2216出版社
SPRINGER WIEN
DOI: 10.1007/s00705-021-05130-x
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资金
- project of Thailand Grand Challenge of National Research Council of Thailand
- National Science and Technology Development Agency [P-15-5004]
- Center of Excellence in Clinical Virology at Chulalongkorn University, King Chulalongkorn Memorial Hospital
- Rachadapisek Sompote Fund of Chulalongkorn University
Eleven full-length genome sequences of 2019 EV-A71 C1 strains isolated from HFMD patients in Thailand from 2019 to early 2020 were described, showing the emergence of multiple lineages through recombination. Bayesian-based phylogenetic analysis indicated that the 2019 EV-A71 C1 Thai strains share a common ancestor with variants in Europe. The substitution rate for the 2019 EV-A71 C1 genome was estimated to be similar to that observed in previous outbreaks. These findings are crucial for understanding the evolution of EV-A C1 during the ongoing HFMD outbreak and its relevance to disease outcomes in children worldwide.
Enterovirus A71 (EV-A71) can cause hand, foot, and mouth disease (HFMD) in children and may be associated with severe neurological complications. There have been numerous reports of increased incidence of EV-A71 subgenogroup C1 (EV-A71 C1) infections associated with neurological diseases since the first occurrence in Germany in 2015. Here, we describe 11 full-length genome sequences of 2019 EV-A71 C1 strains isolated from HFMD patients in Thailand from 2019 to early 2020. The genetic evolution of 2019 EV-A71 C1 was traced in the outbreaks, and the emergence of multiple lineages was detected. Our results demonstrated that 2019 EV-A71 C1 from Thailand emerged through recombination between its nonstructural protein gene and those of other EV-A genotypes. Bayesian-based phylogenetic analysis showed that the 2019 EV-A71 C1 Thai strains share a common ancestor with variants in Europe (Denmark and France). The substitution rate for the 2019 EV-A71 C1 genome was estimated to be 4.38 x 10(-3) substitutions/(site center dot year(-1)) (95% highest posterior density interval: 3.84-4.94 x 10(-3) substitutions/[site center dot year(-1)]), approximating that observed between previous EV-A71 C1 outbreaks. These data are essential for understanding the evolution of EV-A C1 during the ongoing HFMD outbreak and may be relevant to disease outcomes in children worldwide.
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