Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Tingfan, Qian, Jinhan, Shen, Zijun, Shao, Hongxia, Qian, Kun, Jin, Wenjie, Qin, Aijian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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
_version_ 1785076840165015552
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
work_keys_str_mv AT zhutingfan vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT qianjinhan vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT shenzijun vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT shaohongxia vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT qiankun vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT jinwenjie vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication
AT qinaijian vectordeliveredartificialmirnaeffectivelyinhibitsporcineepidemicdiarrheavirusreplication