Related Experiment Video
Updated: Oct 2, 2026

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Repurposing Fragile X Drugs to Inhibit SARS-CoV-2 Viral Reproduction
Cara J Westmark1, Maki Kiso2, Peter Halfmann3
1Department of Neurology, University of Wisconsin-Madison, Madison, WI, United States.
Abstract:
The COVID-19 pandemic is a global health crisis that requires the application of interdisciplinary research to address numerous knowledge gaps including molecular strategies to prevent viral reproduction in affected individuals. In response to the Frontiers Research Topic, "Coronavirus disease (COVID-19): Pathophysiology, Epidemiology, Clinical Management, and Public Health Response," this Hypothesis article proposes a novel therapeutic strategy to repurpose metabotropic glutamate 5 receptor (mGluR5) inhibitors to interfere with viral hijacking of the host protein synthesis machinery. We review pertinent background on SARS-CoV-2, fragile X syndrome (FXS) and metabotropic glutamate receptor 5 (mGluR5) and provide a mechanistic-based hypothesis and preliminary data to support testing mGluR5 inhibitors in COVID-19 research.
Insights
This study proposes repurposing metabotropic glutamate 5 receptor (mGluR5) inhibitors to combat COVID-19. These drugs may block the virus from hijacking host protein synthesis, offering a new therapeutic avenue.
Area of Science:
- Virology
- Neuropharmacology
- Infectious Diseases
Background:
- The COVID-19 pandemic necessitates novel therapeutic strategies to inhibit SARS-CoV-2 replication.
- Metabotropic glutamate receptor 5 (mGluR5) plays a role in cellular processes that SARS-CoV-2 may exploit.
- Fragile X syndrome (FXS) research provides a basis for understanding mGluR5 modulation.
Purpose of the Study:
- To propose a novel hypothesis for repurposing mGluR5 inhibitors as an antiviral therapy against COVID-19.
- To explore the potential of targeting host protein synthesis machinery hijacked by SARS-CoV-2.
- To provide a mechanistic rationale for testing mGluR5 inhibitors in COVID-19 treatment.
Main Methods:
- Review of existing literature on SARS-CoV-2 pathophysiology.
- Analysis of the role of mGluR5 in host-pathogen interactions.
- Presentation of a mechanistic hypothesis supported by preliminary data.
Main Results:
- A hypothesis is presented suggesting mGluR5 inhibitors can interfere with SARS-CoV-2 replication.
- Preliminary data supports the potential efficacy of mGluR5 inhibitors.
- The mechanism involves blocking viral hijacking of host protein synthesis.
Conclusions:
- mGluR5 inhibitors represent a promising class of drugs for repurposing against COVID-19.
- Further research is warranted to validate the therapeutic potential of mGluR5 inhibitors in COVID-19 patients.
- This strategy offers a novel approach to combatting the global health crisis.
More Related Videos
08:41Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
10:29Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
Published on: May 9, 2025