EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN

The strain of Salmonella typhimurium isolated from the subcutaneous abscess of a runted mouse and used in this study was somewhat unusual, but not unique, in that it had a high virulence for young mice, yet low infectivity. This strain could mimic many of the features, signs, and symptoms of immuno...

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Main Author: Brooke, Marcus S.
Format: Online
Language:English
Published: The Rockefeller University Press 1964
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137763/
id pubmed-2137763
recordtype oai_dc
spelling pubmed-21377632008-04-17 EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN Brooke, Marcus S. Article The strain of Salmonella typhimurium isolated from the subcutaneous abscess of a runted mouse and used in this study was somewhat unusual, but not unique, in that it had a high virulence for young mice, yet low infectivity. This strain could mimic many of the features, signs, and symptoms of immunological runting when injected into neonates, either in pure culture, or when mixed with spleen cells, or when present in infected isologous or F1 hybrid spleen cells. Thus, the incidence of Salmonella runting was dose-dependent and related to the age of the neonate. Runts failed to gain weight, were sickly, and usually died within 30 days. They had a marked splenomegaly and hepatomegaly associated with areas of necrosis. However, in marked contrast to immunological runts they did not have lymphoid atrophy. The incidence of runting was diminished when frozen-thawed spleen cell suspensions were used, but not with sonicated or heated suspensions or spleen cells from lethally irradiated mice. Runting could be prevented by immunizing breeders with S. typhimurium, and serum from mice immunized against S. typhimurium protected neonates injected with this organism. Isologous adult spleen cells did not protect against Salmonella runting. It is suggested that in studies on runting only the intravenous route be used and that heated cells serve as a control. More rigid criteria should be applied to runting than those frequently accepted and mice should be autopsied whenever possible. The Rockefeller University Press 1964-09-01 /pmc/articles/PMC2137763/ /pubmed/14207058 Text en Copyright © 1964 by The Rockefeller Institute This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Brooke, Marcus S.
spellingShingle Brooke, Marcus S.
EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
author_facet Brooke, Marcus S.
author_sort Brooke, Marcus S.
title EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
title_short EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
title_full EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
title_fullStr EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
title_full_unstemmed EXPERIMENTAL RUNT DISEASE IN MICE CAUSED BY SALMONELLA TYPHIMURIUM, VAR. COPENHAGEN
title_sort experimental runt disease in mice caused by salmonella typhimurium, var. copenhagen
description The strain of Salmonella typhimurium isolated from the subcutaneous abscess of a runted mouse and used in this study was somewhat unusual, but not unique, in that it had a high virulence for young mice, yet low infectivity. This strain could mimic many of the features, signs, and symptoms of immunological runting when injected into neonates, either in pure culture, or when mixed with spleen cells, or when present in infected isologous or F1 hybrid spleen cells. Thus, the incidence of Salmonella runting was dose-dependent and related to the age of the neonate. Runts failed to gain weight, were sickly, and usually died within 30 days. They had a marked splenomegaly and hepatomegaly associated with areas of necrosis. However, in marked contrast to immunological runts they did not have lymphoid atrophy. The incidence of runting was diminished when frozen-thawed spleen cell suspensions were used, but not with sonicated or heated suspensions or spleen cells from lethally irradiated mice. Runting could be prevented by immunizing breeders with S. typhimurium, and serum from mice immunized against S. typhimurium protected neonates injected with this organism. Isologous adult spleen cells did not protect against Salmonella runting. It is suggested that in studies on runting only the intravenous route be used and that heated cells serve as a control. More rigid criteria should be applied to runting than those frequently accepted and mice should be autopsied whenever possible.
publisher The Rockefeller University Press
publishDate 1964
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137763/
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