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Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells
The CPK cells derived from swine kidney were infected with the attenuated TO-163 strain of transmissible gastroenteritis (TGE) virus, and fused with uninfected Vero cells in the presence of polyethylene glycol. Repeated cocultivation of the fused cells with uninfected Vero cells rendered the virus t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087219/ https://www.ncbi.nlm.nih.gov/pubmed/1309640 http://dx.doi.org/10.1007/BF01321128 |
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author | Ishii, H. Watanabe, I. Mukamoto, M. Kobayashi, Y. Kodama, Y. |
author_facet | Ishii, H. Watanabe, I. Mukamoto, M. Kobayashi, Y. Kodama, Y. |
author_sort | Ishii, H. |
collection | PubMed |
description | The CPK cells derived from swine kidney were infected with the attenuated TO-163 strain of transmissible gastroenteritis (TGE) virus, and fused with uninfected Vero cells in the presence of polyethylene glycol. Repeated cocultivation of the fused cells with uninfected Vero cells rendered the virus to grow in Vero cells. The Vero cell-adapted virus acquired the ability to infect and produce cytopathic effects in several other non-permissive cell lines of non-porcine origin. No major differences in viral polypeptides were shown between the Vero cell-adapted TO-163 strain and its parent strain by indirect immunofluorescence and Western blotting using monoclonal and polyclonal antibodies to TGE virus. |
format | Online Article Text |
id | pubmed-7087219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-70872192020-03-23 Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells Ishii, H. Watanabe, I. Mukamoto, M. Kobayashi, Y. Kodama, Y. Arch Virol Brief Report The CPK cells derived from swine kidney were infected with the attenuated TO-163 strain of transmissible gastroenteritis (TGE) virus, and fused with uninfected Vero cells in the presence of polyethylene glycol. Repeated cocultivation of the fused cells with uninfected Vero cells rendered the virus to grow in Vero cells. The Vero cell-adapted virus acquired the ability to infect and produce cytopathic effects in several other non-permissive cell lines of non-porcine origin. No major differences in viral polypeptides were shown between the Vero cell-adapted TO-163 strain and its parent strain by indirect immunofluorescence and Western blotting using monoclonal and polyclonal antibodies to TGE virus. Springer-Verlag 1992 /pmc/articles/PMC7087219/ /pubmed/1309640 http://dx.doi.org/10.1007/BF01321128 Text en © Springer-Verlag 1992 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Brief Report Ishii, H. Watanabe, I. Mukamoto, M. Kobayashi, Y. Kodama, Y. Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title | Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title_full | Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title_fullStr | Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title_full_unstemmed | Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title_short | Adaptation of transmissible gastroenteritis virus to growth in non-permissive Vero cells |
title_sort | adaptation of transmissible gastroenteritis virus to growth in non-permissive vero cells |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087219/ https://www.ncbi.nlm.nih.gov/pubmed/1309640 http://dx.doi.org/10.1007/BF01321128 |
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