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Genomic Surveillance of SARS-CoV-2: Distribution of Clades in the Republic of Korea in 2020. | LitMetric

Genomic Surveillance of SARS-CoV-2: Distribution of Clades in the Republic of Korea in 2020.

Osong Public Health Res Perspect

Division of Emerging Infectious Diseases, Bureau of Infectious Diseases Diagnosis Control, Korea Disease Control and Prevention Agency, Cheongju, Korea.

Published: February 2021

AI Article Synopsis

  • - A novel beta-coronavirus, SARS-CoV-2, emerged in December 2019, leading to a global outbreak and prompting genomic surveillance in South Korea.
  • - The Korea Disease Control and Prevention Agency sequenced 2,488 SARS-CoV-2 samples over a year, noting a shift in dominant virus clades from S and V to GH by March 2020.
  • - The study found that quarantining international travelers effectively limited the spread of multiple SARS-CoV-2 variants within Korea.

Article Abstract

Since a novel beta-coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in December 2019, there has been a rapid global spread of the virus. Genomic surveillance was conducted on samples isolated from infected individuals to monitor the spread of genetic variants of SARS-CoV-2 in Korea. The Korea Disease Control and Prevention Agency performed whole genome sequencing of SARS-CoV-2 in Korea for 1 year (January 2020 to January 2021). A total of 2,488 SARS-CoV-2 cases were sequenced (including 648 cases from abroad). Initially, the prevalent clades of SARS-CoV-2 were the S and V clades, however, by March 2020, GH clade was the most dominant. Only international travelers were identified as having G or GR clades, and since the first variant 501Y.V1 was identified (from a traveler from the United Kingdom on December 22, 2020), a total of 27 variants of 501Y.V1, 501Y.V2, and 484K.V2 have been classified (as of January 25, 2021). The results in this study indicated that quarantining of travelers entering Korea successfully prevented dissemination of the SARS-CoV-2 variants in Korea.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7899228PMC
http://dx.doi.org/10.24171/j.phrp.2021.12.1.06DOI Listing

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