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Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection
Salmonella Typhimurium sequence type (ST) 313 produces septicemia in infants in sub-Saharan Africa. Although there are known genetic and phenotypic differences between ST313 strains and gastroenteritis-associated ST19 strains, conflicting data about the in vivo virulence of ST313 strains have been r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559095/ https://www.ncbi.nlm.nih.gov/pubmed/28783750 http://dx.doi.org/10.1371/journal.pntd.0005697 |
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author | Ramachandran, Girish Panda, Aruna Higginson, Ellen E. Ateh, Eugene Lipsky, Michael M. Sen, Sunil Matson, Courtney A. Permala-Booth, Jasnehta DeTolla, Louis J. Tennant, Sharon M. |
author_facet | Ramachandran, Girish Panda, Aruna Higginson, Ellen E. Ateh, Eugene Lipsky, Michael M. Sen, Sunil Matson, Courtney A. Permala-Booth, Jasnehta DeTolla, Louis J. Tennant, Sharon M. |
author_sort | Ramachandran, Girish |
collection | PubMed |
description | Salmonella Typhimurium sequence type (ST) 313 produces septicemia in infants in sub-Saharan Africa. Although there are known genetic and phenotypic differences between ST313 strains and gastroenteritis-associated ST19 strains, conflicting data about the in vivo virulence of ST313 strains have been reported. To resolve these differences, we tested clinical Salmonella Typhimurium ST313 and ST19 strains in murine and rhesus macaque infection models. The 50% lethal dose (LD(50)) was determined for three Salmonella Typhimurium ST19 and ST313 strains in mice. For dissemination studies, bacterial burden in organs was determined at various time-points post-challenge. Indian rhesus macaques were infected with one ST19 and one ST313 strain. Animals were monitored for clinical signs and bacterial burden and pathology were determined. The LD(50) values for ST19 and ST313 infected mice were not significantly different. However, ST313-infected BALB/c mice had significantly higher bacterial numbers in blood at 24 h than ST19-infected mice. ST19-infected rhesus macaques exhibited moderate-to-severe diarrhea while ST313-infected monkeys showed no-to-mild diarrhea. ST19-infected monkeys had higher bacterial burden and increased inflammation in tissues. Our data suggest that Salmonella Typhimurium ST313 invasiveness may be investigated using mice. The non-human primate results are consistent with clinical data, suggesting that ST313 strains do not cause diarrhea. |
format | Online Article Text |
id | pubmed-5559095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55590952017-08-25 Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection Ramachandran, Girish Panda, Aruna Higginson, Ellen E. Ateh, Eugene Lipsky, Michael M. Sen, Sunil Matson, Courtney A. Permala-Booth, Jasnehta DeTolla, Louis J. Tennant, Sharon M. PLoS Negl Trop Dis Research Article Salmonella Typhimurium sequence type (ST) 313 produces septicemia in infants in sub-Saharan Africa. Although there are known genetic and phenotypic differences between ST313 strains and gastroenteritis-associated ST19 strains, conflicting data about the in vivo virulence of ST313 strains have been reported. To resolve these differences, we tested clinical Salmonella Typhimurium ST313 and ST19 strains in murine and rhesus macaque infection models. The 50% lethal dose (LD(50)) was determined for three Salmonella Typhimurium ST19 and ST313 strains in mice. For dissemination studies, bacterial burden in organs was determined at various time-points post-challenge. Indian rhesus macaques were infected with one ST19 and one ST313 strain. Animals were monitored for clinical signs and bacterial burden and pathology were determined. The LD(50) values for ST19 and ST313 infected mice were not significantly different. However, ST313-infected BALB/c mice had significantly higher bacterial numbers in blood at 24 h than ST19-infected mice. ST19-infected rhesus macaques exhibited moderate-to-severe diarrhea while ST313-infected monkeys showed no-to-mild diarrhea. ST19-infected monkeys had higher bacterial burden and increased inflammation in tissues. Our data suggest that Salmonella Typhimurium ST313 invasiveness may be investigated using mice. The non-human primate results are consistent with clinical data, suggesting that ST313 strains do not cause diarrhea. Public Library of Science 2017-08-04 /pmc/articles/PMC5559095/ /pubmed/28783750 http://dx.doi.org/10.1371/journal.pntd.0005697 Text en © 2017 Ramachandran et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ramachandran, Girish Panda, Aruna Higginson, Ellen E. Ateh, Eugene Lipsky, Michael M. Sen, Sunil Matson, Courtney A. Permala-Booth, Jasnehta DeTolla, Louis J. Tennant, Sharon M. Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title | Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title_full | Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title_fullStr | Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title_full_unstemmed | Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title_short | Virulence of invasive Salmonella Typhimurium ST313 in animal models of infection |
title_sort | virulence of invasive salmonella typhimurium st313 in animal models of infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559095/ https://www.ncbi.nlm.nih.gov/pubmed/28783750 http://dx.doi.org/10.1371/journal.pntd.0005697 |
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