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Replication of sialodacryoadenitis virus in mouse L-2 cells

Sialodacryoadenitis (SDA) is a naturally-occurring infection of the laboratory rat raused by the coronavirus, sialodacryoadenitis virus (SDAV). The study of SDAV has been limited because there is no widely available continuous cell line for the propagation of high titers of the virus. The purpose of...

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Autores principales: Percy, D., Bond, S., MacInnes, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086637/
https://www.ncbi.nlm.nih.gov/pubmed/2539798
http://dx.doi.org/10.1007/BF01315553
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author Percy, D.
Bond, S.
MacInnes, J.
author_facet Percy, D.
Bond, S.
MacInnes, J.
author_sort Percy, D.
collection PubMed
description Sialodacryoadenitis (SDA) is a naturally-occurring infection of the laboratory rat raused by the coronavirus, sialodacryoadenitis virus (SDAV). The study of SDAV has been limited because there is no widely available continuous cell line for the propagation of high titers of the virus. The purpose of this study, therefore, was to compare the ability of SDAV to replicate in the permanent cell lines, LBC, of rat origin, and the mouse cell lines. L-929 and L-2. Following 2 to 6 repeated passages of SDAV in LBC cells, the virus could be readily propagated in LBC and L-2 cells, but not in L-929 cells. Similarly, SDAV adapted to replicate directly in L-2 cells could be readily propagated in LBC, but not L-929 cells. In LBC and L-2 cells, cytopathic effect (CPE), viral antigen, viral particles, and virus infectivity could be demonstrated. Titers of up to 10(8.0) infectious viral particles/0.25 ml of culture fluid were obtained at 48 hours in L-2 cells. Titers in LBC cells were one to two logs lower. When susceptible rats were inoculated with eighth passage L-2 cell-adapted virus, they developed typical lesions of SDA. Virus could be recovered from infected tissues and propagated in L-2 cells on first passage. The ability to propagate SDAV to high titers in the widely available L-2 cell line should promote the study of this virus and facilitate its comparison with other murine coronaviruses.
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spelling pubmed-70866372020-03-23 Replication of sialodacryoadenitis virus in mouse L-2 cells Percy, D. Bond, S. MacInnes, J. Arch Virol Original Papers Sialodacryoadenitis (SDA) is a naturally-occurring infection of the laboratory rat raused by the coronavirus, sialodacryoadenitis virus (SDAV). The study of SDAV has been limited because there is no widely available continuous cell line for the propagation of high titers of the virus. The purpose of this study, therefore, was to compare the ability of SDAV to replicate in the permanent cell lines, LBC, of rat origin, and the mouse cell lines. L-929 and L-2. Following 2 to 6 repeated passages of SDAV in LBC cells, the virus could be readily propagated in LBC and L-2 cells, but not in L-929 cells. Similarly, SDAV adapted to replicate directly in L-2 cells could be readily propagated in LBC, but not L-929 cells. In LBC and L-2 cells, cytopathic effect (CPE), viral antigen, viral particles, and virus infectivity could be demonstrated. Titers of up to 10(8.0) infectious viral particles/0.25 ml of culture fluid were obtained at 48 hours in L-2 cells. Titers in LBC cells were one to two logs lower. When susceptible rats were inoculated with eighth passage L-2 cell-adapted virus, they developed typical lesions of SDA. Virus could be recovered from infected tissues and propagated in L-2 cells on first passage. The ability to propagate SDAV to high titers in the widely available L-2 cell line should promote the study of this virus and facilitate its comparison with other murine coronaviruses. Springer-Verlag 1989 /pmc/articles/PMC7086637/ /pubmed/2539798 http://dx.doi.org/10.1007/BF01315553 Text en © Springer-Verlag 1989 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 Original Papers
Percy, D.
Bond, S.
MacInnes, J.
Replication of sialodacryoadenitis virus in mouse L-2 cells
title Replication of sialodacryoadenitis virus in mouse L-2 cells
title_full Replication of sialodacryoadenitis virus in mouse L-2 cells
title_fullStr Replication of sialodacryoadenitis virus in mouse L-2 cells
title_full_unstemmed Replication of sialodacryoadenitis virus in mouse L-2 cells
title_short Replication of sialodacryoadenitis virus in mouse L-2 cells
title_sort replication of sialodacryoadenitis virus in mouse l-2 cells
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086637/
https://www.ncbi.nlm.nih.gov/pubmed/2539798
http://dx.doi.org/10.1007/BF01315553
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