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First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus

The outbreak of white spot syndrome (WSS) is a looming challenge, due to dramatic losses to the crustacean aquaculture industry. However, at present, there are no prophylactic or therapeutic means to control this infectious viral disease. Here, we screened fifteen medicinal plants for their inhibito...

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Autores principales: Chen, Cheng, Shen, Jing-Lei, Liang, Chang-Shuai, Sun, Zhong-Chen, Jiang, Hai-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499679/
https://www.ncbi.nlm.nih.gov/pubmed/36142360
http://dx.doi.org/10.3390/ijms231810448
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author Chen, Cheng
Shen, Jing-Lei
Liang, Chang-Shuai
Sun, Zhong-Chen
Jiang, Hai-Feng
author_facet Chen, Cheng
Shen, Jing-Lei
Liang, Chang-Shuai
Sun, Zhong-Chen
Jiang, Hai-Feng
author_sort Chen, Cheng
collection PubMed
description The outbreak of white spot syndrome (WSS) is a looming challenge, due to dramatic losses to the crustacean aquaculture industry. However, at present, there are no prophylactic or therapeutic means to control this infectious viral disease. Here, we screened fifteen medicinal plants for their inhibitory activity on the white spot syndrome virus (WSSV), using red swamp crayfish (Procambarus clarkii) as a model species. The results showed that the crude extracts of Pinellia ternata (Thunb.) Breit. had the highest inhibitory effect (91.59%, 100 mg/kg) on WSSV proliferation, and its main component, beta-sitosterol, showed a much higher activity (95.79%, 50 mg/kg). Further, beta-sitosterol potently reduced (p < 0.01) viral loads and viral gene transcription levels in a concentration-dependent fashion, and significantly promoted the survival rate of WSSV-challenged crayfish (57.14%, 50 mg/kg). The co-incubation assay indicated that beta-sitosterol did not influence the infectivity of WSSV particles. Both pre- and post-treatment of beta-sitosterol exerted a significant inhibitory effect (p < 0.01) on the viral load in vivo. Mechanistically, beta-sitosterol not only interfered with the expression of viral genes (immediate early gene 1, ie1; DNA polymerase, DNApol) that are important in initiating WSSV transcription, but it also attenuated the hijacking of innate immune signaling pathways (Toll, IMD, and JAK/STAT pathways) by viral genes to block WSSV replication. Moreover, the expression of several antiviral immune, antioxidant, pro-inflammatory, and apoptosis-related genes changed significantly in beta-sitosterol-treated crayfish. Beta-sitosterol is a potent WSSV inhibitor and has the potential to be developed as an effective anti-WSSV agent against a WSS outbreak in crustacean aquaculture.
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spelling pubmed-94996792022-09-23 First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus Chen, Cheng Shen, Jing-Lei Liang, Chang-Shuai Sun, Zhong-Chen Jiang, Hai-Feng Int J Mol Sci Article The outbreak of white spot syndrome (WSS) is a looming challenge, due to dramatic losses to the crustacean aquaculture industry. However, at present, there are no prophylactic or therapeutic means to control this infectious viral disease. Here, we screened fifteen medicinal plants for their inhibitory activity on the white spot syndrome virus (WSSV), using red swamp crayfish (Procambarus clarkii) as a model species. The results showed that the crude extracts of Pinellia ternata (Thunb.) Breit. had the highest inhibitory effect (91.59%, 100 mg/kg) on WSSV proliferation, and its main component, beta-sitosterol, showed a much higher activity (95.79%, 50 mg/kg). Further, beta-sitosterol potently reduced (p < 0.01) viral loads and viral gene transcription levels in a concentration-dependent fashion, and significantly promoted the survival rate of WSSV-challenged crayfish (57.14%, 50 mg/kg). The co-incubation assay indicated that beta-sitosterol did not influence the infectivity of WSSV particles. Both pre- and post-treatment of beta-sitosterol exerted a significant inhibitory effect (p < 0.01) on the viral load in vivo. Mechanistically, beta-sitosterol not only interfered with the expression of viral genes (immediate early gene 1, ie1; DNA polymerase, DNApol) that are important in initiating WSSV transcription, but it also attenuated the hijacking of innate immune signaling pathways (Toll, IMD, and JAK/STAT pathways) by viral genes to block WSSV replication. Moreover, the expression of several antiviral immune, antioxidant, pro-inflammatory, and apoptosis-related genes changed significantly in beta-sitosterol-treated crayfish. Beta-sitosterol is a potent WSSV inhibitor and has the potential to be developed as an effective anti-WSSV agent against a WSS outbreak in crustacean aquaculture. MDPI 2022-09-09 /pmc/articles/PMC9499679/ /pubmed/36142360 http://dx.doi.org/10.3390/ijms231810448 Text en © 2022 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
Chen, Cheng
Shen, Jing-Lei
Liang, Chang-Shuai
Sun, Zhong-Chen
Jiang, Hai-Feng
First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title_full First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title_fullStr First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title_full_unstemmed First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title_short First Discovery of Beta-Sitosterol as a Novel Antiviral Agent against White Spot Syndrome Virus
title_sort first discovery of beta-sitosterol as a novel antiviral agent against white spot syndrome virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499679/
https://www.ncbi.nlm.nih.gov/pubmed/36142360
http://dx.doi.org/10.3390/ijms231810448
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