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A novel SARS-CoV-2 related coronavirus with complex recombination isolated from bats in Yunnan province, China.
Li, Li-Li; Wang, Jing-Lin; Ma, Xiao-Hua; Sun, Xiao-Man; Li, Jin-Song; Yang, Xiao-Fei; Shi, Wei-Feng; Duan, Zhao-Jun.
  • Li LL; National Institute for Viral Disease Control and Prevention, China CDC, Beijing, People's Republic of China.
  • Wang JL; Key Laboratory for Medical Virology and Viral Diseases, National Health Commission of the People's Republic of China, Beijing, People's Republic of China.
  • Ma XH; Yunnan Tropical and Subtropical Animal Viral Disease Laboratory, Yunnan Animal Science and Veterinary Institute, Kunming, People's Republic of China.
  • Sun XM; National Institute for Viral Disease Control and Prevention, China CDC, Beijing, People's Republic of China.
  • Li JS; School of Public Health, Gansu University of Chinese Medicine, Lanzhou, People's Republic of China.
  • Yang XF; National Institute for Viral Disease Control and Prevention, China CDC, Beijing, People's Republic of China.
  • Shi WF; Key Laboratory for Medical Virology and Viral Diseases, National Health Commission of the People's Republic of China, Beijing, People's Republic of China.
  • Duan ZJ; National Institute for Viral Disease Control and Prevention, China CDC, Beijing, People's Republic of China.
Emerg Microbes Infect ; 10(1): 1683-1690, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1341091
ABSTRACT
At the end of 2019, A new type of beta-CoV, SARS-CoV-2 emerged and triggered the COVID-19 pandemic, which spread overwhelmingly around the world in less than a year. However, the origin and direct ancestral viruses of SARS-CoV-2 remain unknown. RaTG13, a novel coronavirus found in bats in China's Yunnan Province, is the closest relative virus of the SARS-CoV-2 identified so far. In this study, a new SARS-CoV-2 related virus, provisionally named PrC31, was discovered in Yunnan province by retrospectively analyse bat next generation sequencing (NGS) data of intestinal samples collected in 2018. PrC31 shared 90.7% and 92.0% nucleotide identities to the genomes of SARS-CoV-2 and the bat SARSr-CoV ZC45, respectively. Sequence alignment of PrC31 showed that several genomic regions, especially orf1a and orf8 had the highest homology with those corresponding genomic regions of SARS-CoV-2 than any other related viruses. Phylogenetic analysis indicated that PrC31 shared a common ancestor with SARS-CoV-2 in evolutionary history. The differences between the PrC31 and SARS-CoV-2 genomes were mainly manifested in the spike genes. The amino acid homology between the receptor binding domains of PrC31 and SARS-CoV-2 was only 64.2%. Importantly, recombination analysis revealed that PrC31 underwent multiple complex recombination events (including three recombination breakpoints) involving the SARS-CoV and SARS-CoV-2 sub-lineages, indicating that PrC31 evolved from yet-to-be-identified intermediate recombination strains. Combined with previous studies, it is revealed that the beta-CoVs may possess a more complex recombination mechanism than we thought.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Recombination, Genetic / Chiroptera / SARS-CoV-2 Type of study: Prognostic study / Randomized controlled trials Limits: Animals Country/Region as subject: Asia Language: English Journal: Emerg Microbes Infect Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Recombination, Genetic / Chiroptera / SARS-CoV-2 Type of study: Prognostic study / Randomized controlled trials Limits: Animals Country/Region as subject: Asia Language: English Journal: Emerg Microbes Infect Year: 2021 Document Type: Article