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Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin
Avian infectious bronchitis virus (IBV) was adapted to Vero cells by serial passage. No significant inhibition of IBV replication was observed when infected Vero cells were treated with α-amanitin or actinomycin D. In thin sections of infected cells, assembly of IBV was observed at the rough endopla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
1984
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134135/ https://www.ncbi.nlm.nih.gov/pubmed/6099655 http://dx.doi.org/10.1016/0168-1702(84)90070-4 |
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author | Alonso-Caplen, Firelli V. Matsuoka, Yumiko Wilcox, Graham E. Compans, Richard W. |
author_facet | Alonso-Caplen, Firelli V. Matsuoka, Yumiko Wilcox, Graham E. Compans, Richard W. |
author_sort | Alonso-Caplen, Firelli V. |
collection | PubMed |
description | Avian infectious bronchitis virus (IBV) was adapted to Vero cells by serial passage. No significant inhibition of IBV replication was observed when infected Vero cells were treated with α-amanitin or actinomycin D. In thin sections of infected cells, assembly of IBV was observed at the rough endoplasmic reticulum (RER), and mature IBV particles were located in dilated cisternae of the RER as well as in smooth cytoplasmic vesicles. In addition to typical IBV particles, enveloped particles containing numerous ribosomes were identified at later times postinfection. Monensin, a sodium ionophore which blocks glycoprotein transport to plasma membranes at the level of the Golgi complex, was found to inhibit the formation of infectious IBV. In thin sections of infected Vero cells treated with the ionophore, IBV particles were located in dilated cytoplasmic vesicles, but fewer particles were found when compared to controls. A similar pattern of virus-specific proteins was detected in control or monensin-treated IBV-infected cells, which included two glycoproteins (170000 and 24000 daltons) and a polypeptide of 52000 daltons. These results suggesl lhal the ionophore inhibits assembly of a virus which malures at intracellular membranes. |
format | Online Article Text |
id | pubmed-7134135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71341352020-04-08 Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin Alonso-Caplen, Firelli V. Matsuoka, Yumiko Wilcox, Graham E. Compans, Richard W. Virus Res Article Avian infectious bronchitis virus (IBV) was adapted to Vero cells by serial passage. No significant inhibition of IBV replication was observed when infected Vero cells were treated with α-amanitin or actinomycin D. In thin sections of infected cells, assembly of IBV was observed at the rough endoplasmic reticulum (RER), and mature IBV particles were located in dilated cisternae of the RER as well as in smooth cytoplasmic vesicles. In addition to typical IBV particles, enveloped particles containing numerous ribosomes were identified at later times postinfection. Monensin, a sodium ionophore which blocks glycoprotein transport to plasma membranes at the level of the Golgi complex, was found to inhibit the formation of infectious IBV. In thin sections of infected Vero cells treated with the ionophore, IBV particles were located in dilated cytoplasmic vesicles, but fewer particles were found when compared to controls. A similar pattern of virus-specific proteins was detected in control or monensin-treated IBV-infected cells, which included two glycoproteins (170000 and 24000 daltons) and a polypeptide of 52000 daltons. These results suggesl lhal the ionophore inhibits assembly of a virus which malures at intracellular membranes. Published by Elsevier B.V. 1984 2002-11-12 /pmc/articles/PMC7134135/ /pubmed/6099655 http://dx.doi.org/10.1016/0168-1702(84)90070-4 Text en Copyright © 1984 Published by Elsevier B.V. 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 Alonso-Caplen, Firelli V. Matsuoka, Yumiko Wilcox, Graham E. Compans, Richard W. Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title | Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title_full | Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title_fullStr | Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title_full_unstemmed | Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title_short | Replication and morphogenesis of avian coronavirus in Vero cells and their inhibition by monensin |
title_sort | replication and morphogenesis of avian coronavirus in vero cells and their inhibition by monensin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134135/ https://www.ncbi.nlm.nih.gov/pubmed/6099655 http://dx.doi.org/10.1016/0168-1702(84)90070-4 |
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