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Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses
Swine enteric coronavirus (CoV) is an important group of pathogens causing diarrhea in piglets. At least four kinds of swine enteric CoVs have been identified, including transmissible gastroenteritis virus (TGEV), porcine epidemic diarrhea virus (PEDV), porcine deltacoronavirus (PDCoV), and the emer...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier B.V.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117161/ https://www.ncbi.nlm.nih.gov/pubmed/31176408 http://dx.doi.org/10.1016/j.vetmic.2019.04.014 |
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author | Wang, Xunlei Fang, Liurong Liu, Shudan Ke, Wenting Wang, Dang Peng, Guiqing Xiao, Shaobo |
author_facet | Wang, Xunlei Fang, Liurong Liu, Shudan Ke, Wenting Wang, Dang Peng, Guiqing Xiao, Shaobo |
author_sort | Wang, Xunlei |
collection | PubMed |
description | Swine enteric coronavirus (CoV) is an important group of pathogens causing diarrhea in piglets. At least four kinds of swine enteric CoVs have been identified, including transmissible gastroenteritis virus (TGEV), porcine epidemic diarrhea virus (PEDV), porcine deltacoronavirus (PDCoV), and the emerging HKU2-like porcine enteric alphacoronavirus (PEAV). The small intestines, particularly the jejunum and ileum, are the most common targets of these four CoVs in vivo, and co-infections by these CoVs are frequently observed in clinically infected pigs. This study was conducted to investigate the susceptibility of the porcine ileum epithelial cell line, IPI-2I, to different swine enteric CoVs. We found that IPI-2I cells are highly susceptible to TGEV, PDCoV, and PEAV, as demonstrated by cytopathic effect and virus multiplication. However, only a small number of cells could be infected by PEDV, possibly due to the heterogeneity of IPI-2I cells. A homogeneous cell line, designated IPI-FX, obtained from IPI-2I cells by sub-cloning with limited serial dilutions, was found to be highly susceptible to PEDV. Furthermore, IPI-FX cells were also highly susceptible to TGEV, PDCoV, as well as PEAV. Thus, this sub-cloned IPI-FX cell line is an ideal cell model to study the mechanisms of infection, particularly co-infections of swine enteric CoVs. |
format | Online Article Text |
id | pubmed-7117161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71171612020-04-02 Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses Wang, Xunlei Fang, Liurong Liu, Shudan Ke, Wenting Wang, Dang Peng, Guiqing Xiao, Shaobo Vet Microbiol Article Swine enteric coronavirus (CoV) is an important group of pathogens causing diarrhea in piglets. At least four kinds of swine enteric CoVs have been identified, including transmissible gastroenteritis virus (TGEV), porcine epidemic diarrhea virus (PEDV), porcine deltacoronavirus (PDCoV), and the emerging HKU2-like porcine enteric alphacoronavirus (PEAV). The small intestines, particularly the jejunum and ileum, are the most common targets of these four CoVs in vivo, and co-infections by these CoVs are frequently observed in clinically infected pigs. This study was conducted to investigate the susceptibility of the porcine ileum epithelial cell line, IPI-2I, to different swine enteric CoVs. We found that IPI-2I cells are highly susceptible to TGEV, PDCoV, and PEAV, as demonstrated by cytopathic effect and virus multiplication. However, only a small number of cells could be infected by PEDV, possibly due to the heterogeneity of IPI-2I cells. A homogeneous cell line, designated IPI-FX, obtained from IPI-2I cells by sub-cloning with limited serial dilutions, was found to be highly susceptible to PEDV. Furthermore, IPI-FX cells were also highly susceptible to TGEV, PDCoV, as well as PEAV. Thus, this sub-cloned IPI-FX cell line is an ideal cell model to study the mechanisms of infection, particularly co-infections of swine enteric CoVs. Elsevier B.V. 2019-06 2019-04-14 /pmc/articles/PMC7117161/ /pubmed/31176408 http://dx.doi.org/10.1016/j.vetmic.2019.04.014 Text en © 2019 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Wang, Xunlei Fang, Liurong Liu, Shudan Ke, Wenting Wang, Dang Peng, Guiqing Xiao, Shaobo Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title | Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title_full | Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title_fullStr | Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title_full_unstemmed | Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title_short | Susceptibility of porcine IPI-2I intestinal epithelial cells to infection with swine enteric coronaviruses |
title_sort | susceptibility of porcine ipi-2i intestinal epithelial cells to infection with swine enteric coronaviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7117161/ https://www.ncbi.nlm.nih.gov/pubmed/31176408 http://dx.doi.org/10.1016/j.vetmic.2019.04.014 |
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