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Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro

Rabies is a highly fatal disease, and it is vital to find effective ways to manage and control infection. There is a need for new effective antiviral drugs that are particularly effective treatments for rabies. Deoxynivalenol (DON) is known mainly for its toxicity, but at the molecular level, it can...

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Autores principales: Liu, Qian, He, Qing, Zhu, Wuyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178062/
https://www.ncbi.nlm.nih.gov/pubmed/37175500
http://dx.doi.org/10.3390/ijms24097793
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author Liu, Qian
He, Qing
Zhu, Wuyang
author_facet Liu, Qian
He, Qing
Zhu, Wuyang
author_sort Liu, Qian
collection PubMed
description Rabies is a highly fatal disease, and it is vital to find effective ways to manage and control infection. There is a need for new effective antiviral drugs that are particularly effective treatments for rabies. Deoxynivalenol (DON) is known mainly for its toxicity, but at the molecular level, it can inhibit RNA and DNA replication, and there is increasing evidence that different doses of DON have a positive effect on inhibiting virus replication. Based on this, we evaluated the effect of DON on inhibiting the rabies virus in vitro. The inhibitory effect of DON on rabies virus activity was dose- and time-dependent, and 0.25 μg/mL of DON could inhibit 99% of rabies virus activity within 24 h. Furthermore, DON could inhibit the adsorption, entry, replication, and release of rabies virus but could not inactivate the virus. The inhibitory effect of DON on rabies virus may be achieved by promoting apoptosis. Our study provides a new perspective for the study of anti-rabies virus and expands the direction of action of mycotoxins.
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spelling pubmed-101780622023-05-13 Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro Liu, Qian He, Qing Zhu, Wuyang Int J Mol Sci Article Rabies is a highly fatal disease, and it is vital to find effective ways to manage and control infection. There is a need for new effective antiviral drugs that are particularly effective treatments for rabies. Deoxynivalenol (DON) is known mainly for its toxicity, but at the molecular level, it can inhibit RNA and DNA replication, and there is increasing evidence that different doses of DON have a positive effect on inhibiting virus replication. Based on this, we evaluated the effect of DON on inhibiting the rabies virus in vitro. The inhibitory effect of DON on rabies virus activity was dose- and time-dependent, and 0.25 μg/mL of DON could inhibit 99% of rabies virus activity within 24 h. Furthermore, DON could inhibit the adsorption, entry, replication, and release of rabies virus but could not inactivate the virus. The inhibitory effect of DON on rabies virus may be achieved by promoting apoptosis. Our study provides a new perspective for the study of anti-rabies virus and expands the direction of action of mycotoxins. MDPI 2023-04-25 /pmc/articles/PMC10178062/ /pubmed/37175500 http://dx.doi.org/10.3390/ijms24097793 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Qian
He, Qing
Zhu, Wuyang
Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title_full Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title_fullStr Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title_full_unstemmed Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title_short Deoxynivalenol Mycotoxin Inhibits Rabies Virus Replication In Vitro
title_sort deoxynivalenol mycotoxin inhibits rabies virus replication in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178062/
https://www.ncbi.nlm.nih.gov/pubmed/37175500
http://dx.doi.org/10.3390/ijms24097793
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