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Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection

A reliable and reproducible model in vitro for swine enteric coronaviruses infection would be intestinal models that support virus replication and can be long-term cultured and manipulated experimentally. Here, we designed a robust long-term culture system for porcine intestinal organoids from the i...

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Autores principales: Zhang, Min, Lv, Lilei, Cai, Hongming, Li, Yanhua, Gao, Fei, Yu, Lingxue, Jiang, Yifeng, Tong, Wu, Li, Liwei, Li, Guoxin, Tong, Guangzhi, Liu, Changlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967161/
https://www.ncbi.nlm.nih.gov/pubmed/35369438
http://dx.doi.org/10.3389/fmicb.2022.865336
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author Zhang, Min
Lv, Lilei
Cai, Hongming
Li, Yanhua
Gao, Fei
Yu, Lingxue
Jiang, Yifeng
Tong, Wu
Li, Liwei
Li, Guoxin
Tong, Guangzhi
Liu, Changlong
author_facet Zhang, Min
Lv, Lilei
Cai, Hongming
Li, Yanhua
Gao, Fei
Yu, Lingxue
Jiang, Yifeng
Tong, Wu
Li, Liwei
Li, Guoxin
Tong, Guangzhi
Liu, Changlong
author_sort Zhang, Min
collection PubMed
description A reliable and reproducible model in vitro for swine enteric coronaviruses infection would be intestinal models that support virus replication and can be long-term cultured and manipulated experimentally. Here, we designed a robust long-term culture system for porcine intestinal organoids from the intestinal crypt or single LGR5(+) stem cell by combining previously defined insights into the growth requirements of the intestinal epithelium of humans. We showed that long-term cultured swine intestinal organoids were expanded in vitro for more than 6 months and maintained the potential to differentiate into different types of cells. These organoids were successfully infected with porcine enteric coronavirus, including porcine epidemic diarrhea virus (PEDV) and transmissible gastroenteritis virus (TGEV), and were capable of supporting virus replication and progeny release. RNA-seq analysis showed robust induction of transcripts associated with antiviral signaling in response to enteric coronavirus infection, including hundreds of interferon-stimulated genes and cytokines. Moreover, gene set enrichment analysis indicated that PEDV infection could suppress the immune response in organoids. This 3D intestinal organoid model offers a long-term, renewable resource for investigating porcine intestinal infections with various pathogens.
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spelling pubmed-89671612022-03-31 Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection Zhang, Min Lv, Lilei Cai, Hongming Li, Yanhua Gao, Fei Yu, Lingxue Jiang, Yifeng Tong, Wu Li, Liwei Li, Guoxin Tong, Guangzhi Liu, Changlong Front Microbiol Microbiology A reliable and reproducible model in vitro for swine enteric coronaviruses infection would be intestinal models that support virus replication and can be long-term cultured and manipulated experimentally. Here, we designed a robust long-term culture system for porcine intestinal organoids from the intestinal crypt or single LGR5(+) stem cell by combining previously defined insights into the growth requirements of the intestinal epithelium of humans. We showed that long-term cultured swine intestinal organoids were expanded in vitro for more than 6 months and maintained the potential to differentiate into different types of cells. These organoids were successfully infected with porcine enteric coronavirus, including porcine epidemic diarrhea virus (PEDV) and transmissible gastroenteritis virus (TGEV), and were capable of supporting virus replication and progeny release. RNA-seq analysis showed robust induction of transcripts associated with antiviral signaling in response to enteric coronavirus infection, including hundreds of interferon-stimulated genes and cytokines. Moreover, gene set enrichment analysis indicated that PEDV infection could suppress the immune response in organoids. This 3D intestinal organoid model offers a long-term, renewable resource for investigating porcine intestinal infections with various pathogens. Frontiers Media S.A. 2022-03-14 /pmc/articles/PMC8967161/ /pubmed/35369438 http://dx.doi.org/10.3389/fmicb.2022.865336 Text en Copyright © 2022 Zhang, Lv, Cai, Li, Gao, Yu, Jiang, Tong, Li, Li, Tong and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhang, Min
Lv, Lilei
Cai, Hongming
Li, Yanhua
Gao, Fei
Yu, Lingxue
Jiang, Yifeng
Tong, Wu
Li, Liwei
Li, Guoxin
Tong, Guangzhi
Liu, Changlong
Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title_full Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title_fullStr Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title_full_unstemmed Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title_short Long-Term Expansion of Porcine Intestinal Organoids Serves as an in vitro Model for Swine Enteric Coronavirus Infection
title_sort long-term expansion of porcine intestinal organoids serves as an in vitro model for swine enteric coronavirus infection
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967161/
https://www.ncbi.nlm.nih.gov/pubmed/35369438
http://dx.doi.org/10.3389/fmicb.2022.865336
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