Pathophysiological mechanisms underlying gastrointestinal symptoms in patients with COVID-19
- PMID: 34040326
- PMCID: PMC8130047
- DOI: 10.3748/wjg.v27.i19.2341
Pathophysiological mechanisms underlying gastrointestinal symptoms in patients with COVID-19
Abstract
Gastrointestinal (GI) symptoms, such as diarrhea, abdominal pain, vomiting, and anorexia, are frequently observed in patients with coronavirus disease 2019 (COVID-19). However, the pathophysiological mechanisms connecting these GI symptoms to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections remain elusive. Previous studies indicate that the entry of SARS-CoV-2 into intestinal cells leads to downregulation of angiotensin converting enzyme 2 (ACE2) receptors resulting in impaired barrier function. While intestinal ACE2 functions as a chaperone for the amino acid transporter B0AT1, the B0AT1/ACE2 complex within the intestinal epithelium acts as a regulator of gut microbiota composition and function. Alternations to the B0AT1/ACE2 complex lead to microbial dysbiosis through increased local and systemic immune responses. Previous studies have also suggested that altered serotonin metabolism may be the underlying cause of GI disorders involving diarrhea. The findings of elevated plasma serotonin levels and high fecal calprotectin in COVID-19 patients with diarrhea indicate that the viral infection evokes a systemic inflammatory response that specifically involves the GI. Interestingly, the elevated proinflammatory cytokines correlate with elevated serotonin and fecal calprotectin levels further supporting the evidence of GI inflammation, a hallmark of functional GI disorders. Moreover, the finding that rectal swabs of COVID-19 patients remain positive for SARS-CoV-2 even after the nasopharynx clears the virus, suggests that viral replication and shedding from the GI tract may be more robust than that of the respiratory tract, further indicating fecal-oral transmission as another important route of viral spread. This review summarized the evidence for pathophysiological mechanisms (impaired barrier function, gut inflammation, altered serotonin metabolism and gut microbiota dysbiosis) underlying the GI symptoms in patients with COVID-19.
Keywords: Angiotensin converting enzyme 2 receptor; COVID-19; Gastrointestinal symptoms; Gut microbiota dysbiosis; Impaired barrier function; Serotonin.
©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
Conflict of interest statement
Conflict-of-interest statement: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures

Similar articles
-
Gastrointestinal Manifestations of SARS-CoV-2: Transmission, Pathogenesis, Immunomodulation, Microflora Dysbiosis, and Clinical Implications.Viruses. 2023 May 24;15(6):1231. doi: 10.3390/v15061231. Viruses. 2023. PMID: 37376531 Free PMC article. Review.
-
Gastrointestinal pathophysiology in long COVID: Exploring roles of microbiota dysbiosis and serotonin dysregulation in post-infectious bowel symptoms.Life Sci. 2024 Dec 1;358:123153. doi: 10.1016/j.lfs.2024.123153. Epub 2024 Oct 23. Life Sci. 2024. PMID: 39454992 Review.
-
COVID-19 and gut immunomodulation.World J Gastroenterol. 2021 Dec 14;27(46):7925-7942. doi: 10.3748/wjg.v27.i46.7925. World J Gastroenterol. 2021. PMID: 35046621 Free PMC article. Review.
-
COVID-19 and the gastrointestinal tract: Source of infection or merely a target of the inflammatory process following SARS-CoV-2 infection?World J Gastroenterol. 2021 Apr 14;27(14):1406-1418. doi: 10.3748/wjg.v27.i14.1406. World J Gastroenterol. 2021. PMID: 33911464 Free PMC article. Review.
-
Premises among SARS-CoV-2, dysbiosis and diarrhea: Walking through the ACE2/mTOR/autophagy route.Med Hypotheses. 2020 Nov;144:110243. doi: 10.1016/j.mehy.2020.110243. Epub 2020 Sep 2. Med Hypotheses. 2020. PMID: 33254549 Free PMC article.
Cited by
-
Faecal calprotectin in COVID-19 patients with intestinal symptoms.Prz Gastroenterol. 2022;17(4):332-337. doi: 10.5114/pg.2022.114685. Epub 2022 Mar 18. Prz Gastroenterol. 2022. PMID: 36514448 Free PMC article.
-
Farnesoid X receptor enhances epithelial ACE2 expression and inhibits virally induced IL-6 secretion: implications for intestinal symptoms of SARS-CoV-2.Am J Physiol Gastrointest Liver Physiol. 2023 Nov 1;325(5):G446-G452. doi: 10.1152/ajpgi.00099.2023. Epub 2023 Sep 12. Am J Physiol Gastrointest Liver Physiol. 2023. PMID: 37697930 Free PMC article.
-
Unravelling the gut-lung axis: insights into microbiome interactions and Traditional Indian Medicine's perspective on optimal health.FEMS Microbiol Ecol. 2023 Sep 19;99(10):fiad103. doi: 10.1093/femsec/fiad103. FEMS Microbiol Ecol. 2023. PMID: 37656879 Free PMC article. Review.
-
Reduced circulating FABP2 in patients with moderate to severe COVID-19 may indicate enterocyte functional change rather than cell death.Sci Rep. 2022 Nov 5;12(1):18792. doi: 10.1038/s41598-022-23282-x. Sci Rep. 2022. PMID: 36335131 Free PMC article.
-
Pathogenic mechanisms of post-acute sequelae of SARS-CoV-2 infection (PASC).Elife. 2023 Mar 22;12:e86002. doi: 10.7554/eLife.86002. Elife. 2023. PMID: 36947108 Free PMC article. Review.
References
-
- Hui DS, I Azhar E, Madani TA, Ntoumi F, Kock R, Dar O, Ippolito G, Mchugh TD, Memish ZA, Drosten C, Zumla A, Petersen E. The continuing 2019-nCoV epidemic threat of novel coronaviruses to global health - The latest 2019 novel coronavirus outbreak in Wuhan, China. Int J Infect Dis. 2020;91:264–266. - PMC - PubMed
-
- Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, Wang W, Song H, Huang B, Zhu N, Bi Y, Ma X, Zhan F, Wang L, Hu T, Zhou H, Hu Z, Zhou W, Zhao L, Chen J, Meng Y, Wang J, Lin Y, Yuan J, Xie Z, Ma J, Liu WJ, Wang D, Xu W, Holmes EC, Gao GF, Wu G, Chen W, Shi W, Tan W. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. 2020;395:565–574. - PMC - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous