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

Front Cell Infect Microbiol. 2022 Jun 16:12:887800. doi: 10.3389/fcimb.2022.887800. eCollection 2022.

Abstract

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.

Keywords: Alzheimer’s disease; COVID-19; SARS-CoV-2; hsa-miRNA-146a-5p; hsa-miRNA-15b-5p; messenger RNA (mRNA); microRNA (miRNA); single-stranded viral RNA (ssvRNA).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19*
  • Humans
  • Immune System
  • MicroRNAs* / genetics
  • SARS-CoV-2 / genetics

Substances

  • MicroRNAs