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Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids
The involvement of the gastrointestinal (GI) tract in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection has been reported in multiple studies. Since it has been demonstrated that human intestinal epithelial cells support productive viral replication and that a substantial portio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941299/ https://www.ncbi.nlm.nih.gov/pubmed/35320506 http://dx.doi.org/10.1007/s12560-022-09520-5 |
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author | Harlow, Jennifer Dallner, Matthew Nasheri, Neda |
author_facet | Harlow, Jennifer Dallner, Matthew Nasheri, Neda |
author_sort | Harlow, Jennifer |
collection | PubMed |
description | The involvement of the gastrointestinal (GI) tract in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection has been reported in multiple studies. Since it has been demonstrated that human intestinal epithelial cells support productive viral replication and that a substantial portion of infected individuals shed the virus in feces, the possibility of fecal–oral and fecal-respiratory modes of transmission have been proposed for SARS-CoV-2. In order to establish viral replication in the intestine, enteric viruses need to retain their infectivity in often low pH gastric fluids, and in intestinal fluids, which contain digestive enzymes and bile salts. In this study, we examined whether human coronaviruses OC43 (HCoV-OC43) can remain infectious in simulated GI fluids that models human fasting-state and fed-state, in the presence or absence of food. We demonstrated that except for fasting-state gastric fluid (pH 1.6), the virus can remain infectious in all other gastrointestinal fluids for 1 h. Furthermore, we demonstrated that presence of food could significantly improve viral survival in gastric fluids. Therefore, this study provides evidence that ingestion with food could protect the virus against inactivation by the GI fluids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12560-022-09520-5. |
format | Online Article Text |
id | pubmed-8941299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-89412992022-03-23 Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids Harlow, Jennifer Dallner, Matthew Nasheri, Neda Food Environ Virol Brief Communication The involvement of the gastrointestinal (GI) tract in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection has been reported in multiple studies. Since it has been demonstrated that human intestinal epithelial cells support productive viral replication and that a substantial portion of infected individuals shed the virus in feces, the possibility of fecal–oral and fecal-respiratory modes of transmission have been proposed for SARS-CoV-2. In order to establish viral replication in the intestine, enteric viruses need to retain their infectivity in often low pH gastric fluids, and in intestinal fluids, which contain digestive enzymes and bile salts. In this study, we examined whether human coronaviruses OC43 (HCoV-OC43) can remain infectious in simulated GI fluids that models human fasting-state and fed-state, in the presence or absence of food. We demonstrated that except for fasting-state gastric fluid (pH 1.6), the virus can remain infectious in all other gastrointestinal fluids for 1 h. Furthermore, we demonstrated that presence of food could significantly improve viral survival in gastric fluids. Therefore, this study provides evidence that ingestion with food could protect the virus against inactivation by the GI fluids. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12560-022-09520-5. Springer US 2022-03-23 2022 /pmc/articles/PMC8941299/ /pubmed/35320506 http://dx.doi.org/10.1007/s12560-022-09520-5 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Harlow, Jennifer Dallner, Matthew Nasheri, Neda Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title | Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title_full | Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title_fullStr | Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title_full_unstemmed | Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title_short | Protective Effect of Food Against Inactivation of Human Coronavirus OC43 by Gastrointestinal Fluids |
title_sort | protective effect of food against inactivation of human coronavirus oc43 by gastrointestinal fluids |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941299/ https://www.ncbi.nlm.nih.gov/pubmed/35320506 http://dx.doi.org/10.1007/s12560-022-09520-5 |
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