Journal Article Review Ppublish 1 citation
PubMed: 40074704 DOI: 10.1002/rmv.70029
Oral SARS-CoV-2 Infection and Risk for Long Covid.
Rev Med Virol 35(2):e70029
Authors: Joel Schwartz, Kristelle Capistrano, Heba Hussein, Avin Hafedi, Deepak Shukla, Afsar Naqvi
Affiliations
- Department of Oral Medicine and Diagnostic Sciences, University of Illinois Chicago, Chicago, Illinois, USA.
- Department of Periodontics, University of Illinois Chicago, Chicago, Illinois, USA.
- Department of Oral Medicine, Faculty of Dentistry, Cairo University, Cairo, Egypt.
- Department of Microbiology and Immunology, University of Illinois Chicago, Chicago, Illinois, USA.
- Department of Ophthalmology and Visual Sciences, University of Illinois Chicago, Chicago, Illinois, USA.
Abstract
SARS-CoV-2 is an oral pathogen that infects and replicates in mucosal and salivary epithelial cells, contributing to oral post-acute sequelae COVID-19 (PASC) and other oral and non-oral pathologies. While pre-existing inflammatory oral diseases provides a conducive environment for the virus, acute infection and persistence of SARS-CoV-2 can also results in oral microbiome dysbiosis that further worsens poor oral mucosal health. Indeed, oral PASC includes periodontal diseases, dysgeusia, xerostomia, pharyngitis, oral keratoses, and pulpitis suggesting significant bacterial contributions to SARS-CoV-2 and oral tissue tropism. Dysbiotic microbiome-induced inflammation can promote viral entry via angiotensin-converting enzyme receptor-2 (ACE2), serine transmembrane TMPRSS2 and possibly other non-canonical pathways. Additionally, metabolites derived from a dysbiotic microbiome can alter the physiological and biochemical pathways related to the metabolism of lipids, carbohydrates, and amino acids. This may promote a pro-inflammatory microenvironment, leading to immune exhaustion, loss of tolerance, and susceptibility to a variety of oral pathogens, causing acute and later chronic inflammation. Microbial release of mimics of host metallopeptidases related to furin, ADAM17 (A disintegrin and metalloproteinase 17), and glycoprotein metabolites can further aid viral attachment to T cell immunoglobulin-like (TIMs), enhancing viral entry while simultaneously depressing oral mucosal immune resistance and clearance. Membrane reorganization characterised by neuroproteins, such as neuropilins, also functionally assists with SARS-CoV-2 entry and extends the pathogenesis of PASC from the oral cavity to the brain, gut, or other non-oral tissues. Thus, poor oral health, characterised by disrupted oral microbiomes can promote viral tropism, weaken antiviral resistance, and heightens susceptibility to SARS-CoV-2 infection. This immune dysfunction also increases the risk of additional viral infections, exacerbating oral conditions like periodontal and endodontic diseases. These persistent oral health issues can contribute to systemic inflammation, creating bidirectional effects between oral and non-oral tissues, potentially leading to Post-Acute Sequelae of COVID-19 (PASC).
MeSH
Tropism, Cells, Oral Health, Sars-Cov-2, Covid-19, Viruses, Metalloproteases, Severe Acute Respiratory Syndrome-Related Coronavirus, Tissues, Environment, Infections, Virus Internalization, Virus Diseases, Post-Acute Covid-19 Syndrome, Oral Microbiome