4.7 Article

Decoding SARS-CoV-2 Transmission and Evolution and Ramifications for COVID-19 Diagnosis, Vaccine, and Medicine

Journal

JOURNAL OF CHEMICAL INFORMATION AND MODELING
Volume 60, Issue 12, Pages 5853-5865

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jcim.0c00501

Keywords

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Funding

  1. NIH [GM126189]
  2. NSF [DMS-1721024, DMS-1761320, IIS1900473]
  3. Michigan Economic Development Corporation
  4. Bristol-Myers Squibb
  5. Pfizer

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Tremendous effort has been given to the development of diagnostic tests, preventive vaccines, and therapeutic medicines for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Much of this development has been based on the reference genome collected on January 5, 2020. Based on the genotyping of 15 140 genome samples collected up to June 1, 2020, we report that SARS-CoV-2 has undergone 8309 single mutations which can be clustered into six subtypes. We introduce mutation ratio and mutation h-index to characterize the protein conservativeness and unveil that SARS-CoV-2 envelope protein, main protease, and endoribonuclease protein are relatively conservative, while SARS-CoV-2 nucleocapsid protein, spike protein, and papain-like protease are relatively nonconservative. In particular, we have identified mutations on 40% of nucleotides in the nucleocapsid gene in the population level, signaling potential impacts on the ongoing development of COVID-19 diagnosis, vaccines, and antibody and small-molecular drugs.

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