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Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication
BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is an α-coronavirus that causes highly contagious intestinal infectious disease, involving clinically characterized by diarrhea, dehydration, vomiting, and high mortality to suckling piglets. As a strategy for antiviral therapy, artificial microRNA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364413/ https://www.ncbi.nlm.nih.gov/pubmed/37488599 http://dx.doi.org/10.1186/s12985-023-02129-5 |
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author | Zhu, Tingfan Qian, Jinhan Shen, Zijun Shao, Hongxia Qian, Kun Jin, Wenjie Qin, Aijian |
author_facet | Zhu, Tingfan Qian, Jinhan Shen, Zijun Shao, Hongxia Qian, Kun Jin, Wenjie Qin, Aijian |
author_sort | Zhu, Tingfan |
collection | PubMed |
description | BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is an α-coronavirus that causes highly contagious intestinal infectious disease, involving clinically characterized by diarrhea, dehydration, vomiting, and high mortality to suckling piglets. As a strategy for antiviral therapy, artificial microRNA (amiRNA) mediated suppression of viral replication has recently become increasingly important. In this study, we evaluated the advantages of using an amiRNA vector against PEDV. METHODS: In this study, we evaluated the advantages of using an amiRNA vector against PEDV. We designed two single amiRNA sequences for different conserved sequences of the PEDV S and N genes, and tested their inhibitory effects on PEDV in Vero cells. RESULTS: It was obvious from the CCK-8 results that the transient transfection of amiRNA was non-toxic to the cells. In addition, our results showed that the transient expression of two amiRNAs (amiRNA-349 and amiRNA-1447) significantly reduced the expression of viral RNA and protein in the cells. The TCID(50) results showed that the release of virus particles into the culture supernatant was significantly reduced, with an effect as high as 90%. To avoid virus mutation escape, the above two single amiRNA sequences were tandem in this study (amiRNA-349 + 1447), enabling a single microRNA to be expressed simultaneously. The real-time PCR and Western blot results showed that the inhibitory effect was significantly enhanced in each of the different time periods. The TCID(50) results showed that the release of virus particles in the culture supernatant was significantly reduced at the different time periods. CONCLUSIONS: In summary, these results suggest that an RNAi based on amiRNA targeting the conserved region of the virus is an effective method to improve PEDV nucleic acid inhibitors and provide a novel treatment strategy for PEDV infection. |
format | Online Article Text |
id | pubmed-10364413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103644132023-07-25 Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication Zhu, Tingfan Qian, Jinhan Shen, Zijun Shao, Hongxia Qian, Kun Jin, Wenjie Qin, Aijian Virol J Research BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is an α-coronavirus that causes highly contagious intestinal infectious disease, involving clinically characterized by diarrhea, dehydration, vomiting, and high mortality to suckling piglets. As a strategy for antiviral therapy, artificial microRNA (amiRNA) mediated suppression of viral replication has recently become increasingly important. In this study, we evaluated the advantages of using an amiRNA vector against PEDV. METHODS: In this study, we evaluated the advantages of using an amiRNA vector against PEDV. We designed two single amiRNA sequences for different conserved sequences of the PEDV S and N genes, and tested their inhibitory effects on PEDV in Vero cells. RESULTS: It was obvious from the CCK-8 results that the transient transfection of amiRNA was non-toxic to the cells. In addition, our results showed that the transient expression of two amiRNAs (amiRNA-349 and amiRNA-1447) significantly reduced the expression of viral RNA and protein in the cells. The TCID(50) results showed that the release of virus particles into the culture supernatant was significantly reduced, with an effect as high as 90%. To avoid virus mutation escape, the above two single amiRNA sequences were tandem in this study (amiRNA-349 + 1447), enabling a single microRNA to be expressed simultaneously. The real-time PCR and Western blot results showed that the inhibitory effect was significantly enhanced in each of the different time periods. The TCID(50) results showed that the release of virus particles in the culture supernatant was significantly reduced at the different time periods. CONCLUSIONS: In summary, these results suggest that an RNAi based on amiRNA targeting the conserved region of the virus is an effective method to improve PEDV nucleic acid inhibitors and provide a novel treatment strategy for PEDV infection. BioMed Central 2023-07-24 /pmc/articles/PMC10364413/ /pubmed/37488599 http://dx.doi.org/10.1186/s12985-023-02129-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhu, Tingfan Qian, Jinhan Shen, Zijun Shao, Hongxia Qian, Kun Jin, Wenjie Qin, Aijian Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title | Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title_full | Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title_fullStr | Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title_full_unstemmed | Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title_short | Vector-delivered artificial miRNA effectively inhibits Porcine epidemic diarrhea virus replication |
title_sort | vector-delivered artificial mirna effectively inhibits porcine epidemic diarrhea virus replication |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10364413/ https://www.ncbi.nlm.nih.gov/pubmed/37488599 http://dx.doi.org/10.1186/s12985-023-02129-5 |
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