Mutational spectra of SARS‐CoV‐2 orf1ab polyprotein and signature mutations in the United States of America

Banerjee, Shuvam; Seal, Sohan; Dey, Riju; Mondal, Kousik Kr.; Bhattacharjee, Pritha

Pandemic COVID‐19 outbreak has been caused due to SARS‐CoV‐2 pathogen, resulting millions of infection and death worldwide, USA being on top at the present moment. The long, complex orf1ab polyproteins of SARS‐CoV‐2 play an important role in viral RNA synthesis. To assess the impact of mutations in this important domain, we analyzed 1134 complete protein sequences of orf1ab polyprotein from NCBI Virus database from affected patients across various states of USA from December 2019 to 25(th) April 2020. Multiple sequence alignment using Clustal Omega followed by statistical significance was calculated. Four significant mutations T265I (nsp 2), P4715L (nsp 12) and P5828L and Y5865C (both at nsp 13) were identified in important non‐structural proteins, which function either as replicase or helicase. A comparative analysis shows 265T→I, 5828P→L and 5865Y→C are unique to USA and not reported from Europe or Asia; while one, 4715P→L is predominant in both Europe and USA. Mutational changes in amino acids are predicted to alter structure and function of corresponding proteins, thereby it is imperative to consider the mutational spectra while designing new antiviral therapeutics targeting viral orf1ab. This article is protected by copyright. All rights reserved.