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Published on: December 23, 2020
The Role of Molecular Chaperones in Virus Infection and Implications for Understanding and Treating COVID-19
Letizia Paladino1,2, Alessandra Maria Vitale1,2, Celeste Caruso Bavisotto1,2
1Department of Biomedicine, Neuroscience and Advances Diagnosis (BIND), Section of Human Anatomy, University of Palermo, 90127 Palermo, Italy.
Abstract:
The COVID-19 pandemic made imperative the search for means to end it, which requires a knowledge of the mechanisms underpinning the multiplication and spread of its cause, the coronavirus SARS-CoV-2. Many viruses use members of the hosts' chaperoning system to infect the target cells, replicate, and spread, and here we present illustrative examples. Unfortunately, the role of chaperones in the SARS-CoV-2 cycle is still poorly understood. In this review, we examine the interactions of various coronaviruses during their infectious cycle with chaperones in search of information useful for future research on SARS-CoV-2. We also call attention to the possible role of molecular mimicry in the development of autoimmunity and its widespread pathogenic impact in COVID-19 patients. Viral proteins share highly antigenic epitopes with human chaperones, eliciting anti-viral antibodies that crossreact with the chaperones. Both, the critical functions of chaperones in the infectious cycle of viruses and the possible role of these molecules in COVID-19 autoimmune phenomena, make clear that molecular chaperones are promising candidates for the development of antiviral strategies. These could consist of inhibiting-blocking those chaperones that are necessary for the infectious viral cycle, or those that act as autoantigens in the autoimmune reactions causing generalized destructive effects on human tissues.
Insights
Molecular chaperones are crucial for SARS-CoV-2 replication and spread. Targeting these host proteins offers a promising antiviral strategy against COVID-19 and related autoimmune complications.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- The COVID-19 pandemic necessitates understanding SARS-CoV-2 mechanisms.
- Viruses often exploit host chaperones for infection and replication.
- The role of chaperones in the SARS-CoV-2 lifecycle is not well-defined.
Purpose of the Study:
- To review coronavirus-chaperone interactions for insights into SARS-CoV-2.
- To explore the potential role of molecular mimicry in COVID-19 autoimmunity.
- To identify molecular chaperones as targets for antiviral therapies.
Main Methods:
- Literature review of coronavirus-chaperone interactions.
- Analysis of viral protein epitopes and host chaperone homology.
- Examination of autoimmune phenomena linked to chaperone cross-reactivity.
Main Results:
- Coronaviruses interact with host chaperones during their infectious cycle.
- Viral proteins can share antigenic epitopes with human chaperones, leading to cross-reactivity.
- Molecular mimicry may contribute to autoimmune conditions observed in COVID-19 patients.
Conclusions:
- Molecular chaperones are vital for viral replication and spread.
- Chaperones are implicated in COVID-19-associated autoimmunity.
- Inhibiting essential chaperones or blocking autoantigenic sites presents a viable antiviral strategy.
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