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Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions

Norovirus is a major cause of acute gastroenteritis globally, resulting in enormous health and societal costs. In this study, the antiviral activities of Mori Cortex Radicis (MCR) extract and its bioactive flavonoids, morusin and kuwanon G, were tested against murine norovirus (MNV), a human norovir...

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Autores principales: Lim, Chae Yeon, Kim, Hyojin, Chung, Mi Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403467/
https://www.ncbi.nlm.nih.gov/pubmed/34483697
http://dx.doi.org/10.1007/s10068-021-00958-0
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author Lim, Chae Yeon
Kim, Hyojin
Chung, Mi Sook
author_facet Lim, Chae Yeon
Kim, Hyojin
Chung, Mi Sook
author_sort Lim, Chae Yeon
collection PubMed
description Norovirus is a major cause of acute gastroenteritis globally, resulting in enormous health and societal costs. In this study, the antiviral activities of Mori Cortex Radicis (MCR) extract and its bioactive flavonoids, morusin and kuwanon G, were tested against murine norovirus (MNV), a human norovirus surrogate, using plaque assay. The antiviral activity was confirmed in simulated digestive conditions, including simulated saliva fluid (SSF), simulated gastric fluid (SGF), and simulated intestinal fluid (SIF). Pre-treatment of MNV with MCR extract at 1000 µg/mL showed antiviral activity with a 1.1-log reduction. Morusin and kuwanon G also demonstrated a 1.0-log and 0.6-log reductions of MNV titers, respectively, at 100 µM. MCR extract at a concentration of 2 mg/mL in SSF, SGF, and SIF markedly reduced MNV titers by 1.8, 1.9, and 1.5 logs, respectively. Therefore, these data suggest that MCR extract can be used to control norovirus infectivity.
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spelling pubmed-84034672021-08-30 Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions Lim, Chae Yeon Kim, Hyojin Chung, Mi Sook Food Sci Biotechnol Research Article Norovirus is a major cause of acute gastroenteritis globally, resulting in enormous health and societal costs. In this study, the antiviral activities of Mori Cortex Radicis (MCR) extract and its bioactive flavonoids, morusin and kuwanon G, were tested against murine norovirus (MNV), a human norovirus surrogate, using plaque assay. The antiviral activity was confirmed in simulated digestive conditions, including simulated saliva fluid (SSF), simulated gastric fluid (SGF), and simulated intestinal fluid (SIF). Pre-treatment of MNV with MCR extract at 1000 µg/mL showed antiviral activity with a 1.1-log reduction. Morusin and kuwanon G also demonstrated a 1.0-log and 0.6-log reductions of MNV titers, respectively, at 100 µM. MCR extract at a concentration of 2 mg/mL in SSF, SGF, and SIF markedly reduced MNV titers by 1.8, 1.9, and 1.5 logs, respectively. Therefore, these data suggest that MCR extract can be used to control norovirus infectivity. Springer Singapore 2021-08-29 /pmc/articles/PMC8403467/ /pubmed/34483697 http://dx.doi.org/10.1007/s10068-021-00958-0 Text en © The Korean Society of Food Science and Technology 2021
spellingShingle Research Article
Lim, Chae Yeon
Kim, Hyojin
Chung, Mi Sook
Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title_full Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title_fullStr Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title_full_unstemmed Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title_short Mori Cortex Radicis extract inhibits human norovirus surrogate in simulated digestive conditions
title_sort mori cortex radicis extract inhibits human norovirus surrogate in simulated digestive conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403467/
https://www.ncbi.nlm.nih.gov/pubmed/34483697
http://dx.doi.org/10.1007/s10068-021-00958-0
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