Oral Methioninase for Covid-19 Methionine-restriction Therapy

In Vivo. 2020 Jun;34(3 Suppl):1593-1596. doi: 10.21873/invivo.11948.

Abstract

The Covid-19 pandemic is a world-wide crisis without an effective therapy. While most approaches to therapy are using repurposed drugs that were developed for other diseases, it is thought that targeting the biology of the SARS-CoV-2 virus, which causes Covid-19, can result in an effective therapeutic treatment. The coronavirus RNA cap structure is methylated by two viral methyltransferases that transfer methyl groups from S-adenosylmethionine (SAM). The proper methylation of the virus depends on the level of methionine in the host to form SAM. Herein, we propose to restrict methionine availability by treating the patient with oral recombinant methioninase, aiming to treat Covid-19. By restricting methionine we not only interdict viral replication, which depends on the viral RNA cap methyaltion, but also inhibit the proliferation of the infected cells, which have an increased requirement for methionine. Most importantly, the virally-induced T-cell- and macrophage-mediated cytokine storm, which seems to be a significant cause for Covid-19 deaths, can also be inhibited by restricting methionine, since T-cell and macrophrage activation greatly increases the methionine requirement for these cells. The evidence reviewed here suggests that oral recombinant methioninase could be a promising treatment for coronavirus patients.

Keywords: Coronavirus; Covid-19; RNA genome; S-adenosylmethionine; SARs-CoV-2; methioninase; methionine restriction; methylation; methyltransferase.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / therapeutic use*
  • Bacterial Proteins / administration & dosage
  • Bacterial Proteins / therapeutic use
  • Betacoronavirus / drug effects*
  • Betacoronavirus / physiology
  • COVID-19
  • Carbon-Sulfur Lyases / administration & dosage
  • Carbon-Sulfur Lyases / therapeutic use*
  • Clinical Trials as Topic
  • Coronavirus Infections / complications
  • Coronavirus Infections / drug therapy*
  • Coronavirus Infections / immunology
  • Cytokine Release Syndrome / prevention & control
  • Humans
  • Lymphocyte Activation / drug effects
  • Macrophage Activation / drug effects
  • Meta-Analysis as Topic
  • Methionine / metabolism*
  • Methylation / drug effects
  • Pandemics
  • Pneumonia, Viral / complications
  • Pneumonia, Viral / drug therapy*
  • Pneumonia, Viral / immunology
  • Pseudomonas putida / enzymology
  • RNA Caps / drug effects*
  • RNA Processing, Post-Transcriptional / drug effects*
  • RNA, Viral / drug effects*
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / therapeutic use
  • S-Adenosylmethionine / metabolism
  • SARS-CoV-2
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Bacterial Proteins
  • RNA Caps
  • RNA, Viral
  • Recombinant Proteins
  • S-Adenosylmethionine
  • Methionine
  • Carbon-Sulfur Lyases
  • L-methionine gamma-lyase