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Can Salivary Innate Immune Molecules Provide Clue on Taste Dysfunction in COVID-19?

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2021 Oct 28
PMID 34707585
Citations 1
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Abstract

Emerging concerns following the severe acute respiratory syndrome coronavirus-2 (SARS-CoV2) pandemic are the long-term effects of coronavirus disease (COVID)-19. Dysgeusia in COVID-19 is supported by the abundant expression of the entry receptor, angiotensin-converting enzyme-2 (ACE2), in the oral mucosa. The invading virus perturbs the commensal biofilm and regulates the host responses that permit or suppress viral infection. We correlated the microbial recognition receptors and soluble ACE2 (sACE2) with the SARS-CoV2 measures in the saliva of COVID-19 patients. Data indicate that the toll-like receptor-4, peptidoglycan recognition protein, and sACE2 are elevated in COVID-19 saliva and correlate moderately with the viral load.

Citing Articles

Reduced Salivary Gustin and Statherin in Long-COVID Cohort with Impaired Bitter Taste.

Chowdary H, Riley N, Patel P, Gossweiler A, Running C, Srinivasan M J Clin Med. 2024; 13(22).

PMID: 39597960 PMC: 11594764. DOI: 10.3390/jcm13226816.

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