Cargando…

Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine

PURPOSE: Non-host-adapted Salmonella serovars, including the common human food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium), are opportunistic pathogens that can colonize food-producing animals without causing overt disease. Interventions against Salmonella are needed to e...

Descripción completa

Detalles Bibliográficos
Autores principales: Bearson, Bradley L, Bearson, Shawn M. D, Brunelle, Brian W, Bayles, Darrell O, Lee, In Soo, Kich, Jalusa D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817229/
https://www.ncbi.nlm.nih.gov/pubmed/28516860
http://dx.doi.org/10.1099/jmm.0.000482
_version_ 1783300833412120576
author Bearson, Bradley L
Bearson, Shawn M. D
Brunelle, Brian W
Bayles, Darrell O
Lee, In Soo
Kich, Jalusa D
author_facet Bearson, Bradley L
Bearson, Shawn M. D
Brunelle, Brian W
Bayles, Darrell O
Lee, In Soo
Kich, Jalusa D
author_sort Bearson, Bradley L
collection PubMed
description PURPOSE: Non-host-adapted Salmonella serovars, including the common human food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium), are opportunistic pathogens that can colonize food-producing animals without causing overt disease. Interventions against Salmonella are needed to enhance food safety, protect animal health and allow the differentiation of infected from vaccinated animals (DIVA). METHODOLOGY: An attenuated S. Typhimurium DIVA vaccine (BBS 866) was characterized for the protection of pigs following challenge with virulent S. Typhimurium. The porcine transcriptional response to BBS 866 vaccination was evaluated. RNA-Seq analysis was used to compare gene expression between BBS 866 and its parent; phenotypic assays were performed to confirm transcriptional differences observed between the strains. RESULTS: Vaccination significantly reduced fever and interferon-gamma (IFNγ) levels in swine challenged with virulent S. Typhimurium compared to mock-vaccinated pigs. Salmonella faecal shedding and gastrointestinal tissue colonization were significantly lower in vaccinated swine. RNA-Seq analysis comparing BBS 866 to its parental S. Typhimurium strain demonstrated reduced expression of the genes involved in cellular invasion and bacterial motility; decreased invasion of porcine-derived IPEC-J2 cells and swimming motility for the vaccine strain was consistent with the RNA-Seq analysis. Numerous membrane proteins were differentially expressed, which was an anticipated gene expression pattern due to the targeted deletion of several regulatory genes in the vaccine strain. RNA-Seq analysis indicated that genes involved in the porcine immune and inflammatory response were differentially regulated at 2 days post-vaccination compared to pre-vaccination. CONCLUSION: Evaluation of the S. Typhimurium DIVA vaccine indicates that vaccination will provide both swine health and food safety benefits.
format Online
Article
Text
id pubmed-5817229
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-58172292018-02-20 Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine Bearson, Bradley L Bearson, Shawn M. D Brunelle, Brian W Bayles, Darrell O Lee, In Soo Kich, Jalusa D J Med Microbiol Research Article PURPOSE: Non-host-adapted Salmonella serovars, including the common human food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium), are opportunistic pathogens that can colonize food-producing animals without causing overt disease. Interventions against Salmonella are needed to enhance food safety, protect animal health and allow the differentiation of infected from vaccinated animals (DIVA). METHODOLOGY: An attenuated S. Typhimurium DIVA vaccine (BBS 866) was characterized for the protection of pigs following challenge with virulent S. Typhimurium. The porcine transcriptional response to BBS 866 vaccination was evaluated. RNA-Seq analysis was used to compare gene expression between BBS 866 and its parent; phenotypic assays were performed to confirm transcriptional differences observed between the strains. RESULTS: Vaccination significantly reduced fever and interferon-gamma (IFNγ) levels in swine challenged with virulent S. Typhimurium compared to mock-vaccinated pigs. Salmonella faecal shedding and gastrointestinal tissue colonization were significantly lower in vaccinated swine. RNA-Seq analysis comparing BBS 866 to its parental S. Typhimurium strain demonstrated reduced expression of the genes involved in cellular invasion and bacterial motility; decreased invasion of porcine-derived IPEC-J2 cells and swimming motility for the vaccine strain was consistent with the RNA-Seq analysis. Numerous membrane proteins were differentially expressed, which was an anticipated gene expression pattern due to the targeted deletion of several regulatory genes in the vaccine strain. RNA-Seq analysis indicated that genes involved in the porcine immune and inflammatory response were differentially regulated at 2 days post-vaccination compared to pre-vaccination. CONCLUSION: Evaluation of the S. Typhimurium DIVA vaccine indicates that vaccination will provide both swine health and food safety benefits. Microbiology Society 2017-05 2017-05-18 /pmc/articles/PMC5817229/ /pubmed/28516860 http://dx.doi.org/10.1099/jmm.0.000482 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International 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
Bearson, Bradley L
Bearson, Shawn M. D
Brunelle, Brian W
Bayles, Darrell O
Lee, In Soo
Kich, Jalusa D
Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title_full Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title_fullStr Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title_full_unstemmed Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title_short Salmonella DIVA vaccine reduces disease, colonization and shedding due to virulent S. Typhimurium infection in swine
title_sort salmonella diva vaccine reduces disease, colonization and shedding due to virulent s. typhimurium infection in swine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817229/
https://www.ncbi.nlm.nih.gov/pubmed/28516860
http://dx.doi.org/10.1099/jmm.0.000482
work_keys_str_mv AT bearsonbradleyl salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine
AT bearsonshawnmd salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine
AT brunellebrianw salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine
AT baylesdarrello salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine
AT leeinsoo salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine
AT kichjalusad salmonelladivavaccinereducesdiseasecolonizationandsheddingduetovirulentstyphimuriuminfectioninswine