Gut probiotic Lactobacillus rhamnosus attenuates PDE4B-mediated interleukin-6 induced by SARS-CoV-2 membrane glycoprotein

J Nutr Biochem. 2021 Dec:98:108821. doi: 10.1016/j.jnutbio.2021.108821. Epub 2021 Jul 14.

Abstract

Membrane glycoprotein is the most abundant protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), but its role in coronavirus disease 2019 (COVID-19) has not been fully characterized. Mice intranasally inoculated with membrane glycoprotein substantially increased the interleukin (IL)-6, a hallmark of the cytokine storm, in bronchoalveolar lavage fluid (BALF), compared to mice inoculated with green fluorescent protein (GFP). The high level of IL-6 induced by membrane glycoprotein was significantly diminished in phosphodiesterase 4 (PDE4B) knockout mice, demonstrating the essential role of PDE4B in IL-6 signaling. Mycelium fermentation of Lactobacillus rhamnosus (L. rhamnosus) EH8 strain yielded butyric acid, which can down-regulate the PDE4B expression and IL-6 secretion in macrophages. Feeding mice with mycelia increased the relative abundance of commensal L. rhamnosus. Two-week supplementation of mice with L. rhamnosus plus mycelia considerably decreased membrane glycoprotein-induced PDE4B expression and IL-6 secretion. The probiotic activity of L. rhamnosus plus mycelia against membrane glycoprotein was abolished in mice treated with GLPG-0974, an antagonist of free fatty acid receptor 2 (Ffar2). Activation of Ffar2 in the gut-lung axis for down-regulation of the PDE4B-IL-6 signalling may provide targets for development of modalities including probiotics for treatment of the cytokine storm in COVID-19.

Keywords: Cytokine storm; IL-6; Lactobacillus rhamnosus; PDE4B; SARS-CoV-2 membrane glycoprotein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Butyric Acid
  • Cell Line
  • Cloning, Molecular
  • Coronavirus M Proteins / pharmacology*
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / genetics
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / metabolism*
  • Female
  • Fermentation
  • Gene Expression Regulation / drug effects
  • Humans
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Lacticaseibacillus rhamnosus / physiology*
  • Mice
  • Mice, Inbred ICR
  • Probiotics / pharmacology*
  • Receptors, G-Protein-Coupled / metabolism
  • SARS-CoV-2 / metabolism*

Substances

  • Coronavirus M Proteins
  • Ffar2 protein, mouse
  • Interleukin-6
  • Receptors, G-Protein-Coupled
  • Butyric Acid
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • PDE4B protein, mouse