Frontiers in Cellular and Infection Microbiology (Jun 2022)

microRNA, the Innate-Immune System and SARS-CoV-2

  • James M. Hill,
  • James M. Hill,
  • James M. Hill,
  • James M. Hill,
  • Walter J. Lukiw,
  • Walter J. Lukiw,
  • Walter J. Lukiw

DOI
https://doi.org/10.3389/fcimb.2022.887800
Journal volume & issue
Vol. 12

Abstract

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The single-stranded viral RNA (ssvRNA) known as the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes COVID-19 can be effectively inactivated by a number of natural ribonucleic acid-based host cell defenses. One of the most important of these defenses includes the actions of a class of small non-coding RNAs (sncRNAs) known as microRNAs (miRNAs). Via base-pair complementarity miRNAs are capable of specifically targeting ssvRNA sequences such as SARS-CoV-2 promoting its inactivation and neutralization. RNA-sequencing and bioinformatics analysis indicate that multiple naturally-occurring human miRNAs have extensive complementarity to the SARS-CoV-2 ssvRNA genome. Since miRNA abundance, speciation, and complexity vary significantly amongst human individuals, this may in part explain the variability in the innate-immune and pathophysiological response of different individuals to SARS-CoV-2 and overall susceptibility to ssvRNA-mediated viral infection.

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