1887

Abstract

Non-host-adapted serovars, including the common human food-borne pathogen serovar Typhimurium ( Typhimurium), are opportunistic pathogens that can colonize food-producing animals without causing overt disease. Interventions against are needed to enhance food safety, protect animal health and allow the differentiation of infected from vaccinated animals (DIVA).

An attenuated . Typhimurium DIVA vaccine (BBS 866) was characterized for the protection of pigs following challenge with virulent 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.

Vaccination significantly reduced fever and interferon-gamma (IFNγ) levels in swine challenged with virulent . Typhimurium compared to mock-vaccinated pigs. faecal shedding and gastrointestinal tissue colonization were significantly lower in vaccinated swine. RNA-Seq analysis comparing BBS 866 to its parental 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.

Evaluation of the . Typhimurium DIVA vaccine indicates that vaccination will provide both swine health and food safety benefits.

Loading

Article metrics loading...

/content/journal/jmm/10.1099/jmm.0.000482
2017-05-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/jmm/66/5/651.html?itemId=/content/journal/jmm/10.1099/jmm.0.000482&mimeType=html&fmt=ahah

References

  1. Boyen F, Haesebrouck F, Maes D, Van Immerseel F, Ducatelle R et al. Non-typhoidal Salmonella infections in pigs: a closer look at epidemiology, pathogenesis and control. Vet Microbiol 2008; 130:1–19 [View Article][PubMed]
    [Google Scholar]
  2. Andres VM, Davies RH. Biosecurity measures to control Salmonella and other infectious agents in pig farms: a review. Compr Rev Food Sci Food Saf 2015; 14:317–335 [View Article]
    [Google Scholar]
  3. Bearson BL, Bearson SMD, Kich JD, Lee IS. An rfaH mutant of Salmonella enterica serovar Typhimurium is attenuated in swine and reduces intestinal colonization, fecal shedding, and disease severity due to virulent Salmonella Typhimurium. Front Vet Sci 2014; 1: [View Article][PubMed]
    [Google Scholar]
  4. Wales AD, Davies RH. Salmonella vaccination in pigs: a review. Zoonoses Public Hlth 2017; 64:1–13 [View Article][PubMed]
    [Google Scholar]
  5. Bearson BL, Bearson SM, Kich JD. A DIVA vaccine for cross-protection against Salmonella. Vaccine 2016; 34:1241–1246 [View Article][PubMed]
    [Google Scholar]
  6. Bearson BL, Bearson SM, Lee IS, Brunelle BW. The Salmonella enterica serovar Typhimurium QseB response regulator negatively regulates bacterial motility and swine colonization in the absence of the QseC sensor kinase. Microb Pathog 2010; 48:214–219 [View Article][PubMed]
    [Google Scholar]
  7. Bearson SM, Bearson BL, Loving CL, Allen HK, Lee I et al. Prophylactic administration of vector-encoded porcine granulocyte-colony stimulating factor reduces Salmonella shedding, tonsil colonization, and microbiota alterations of the gastrointestinal tract in Salmonella-challenged swine. Front Vet Sci 2016; 3:66 [View Article][PubMed]
    [Google Scholar]
  8. Andrews S. FastQC: A Quality Control Tool for High Throughput Sequence Data 2010
    [Google Scholar]
  9. Patterson SK, Borewicz K, Johnson T, Xu W, Isaacson RE. Characterization and differential gene expression between two phenotypic phase variants in Salmonella enterica serovar Typhimurium. PLoS One 2012; 7:e43592 [View Article][PubMed]
    [Google Scholar]
  10. Brunelle BW, Bearson BL, Bearson SM. Chloramphenicol and tetracycline decrease motility and increase invasion and attachment gene expression in specific isolates of multidrug-resistant Salmonella enterica serovar Typhimurium. Front Microbiol 2014; 5:801 [View Article][PubMed]
    [Google Scholar]
  11. Choi I, Bao H, Kommadath A, Hosseini A, Sun X et al. Increasing gene discovery and coverage using RNA-seq of globin RNA reduced porcine blood samples. BMC Genomics 2014; 15:954 [View Article][PubMed]
    [Google Scholar]
  12. Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 2014; 30:2114–2120 [View Article][PubMed]
    [Google Scholar]
  13. Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 2009; 10:R25 [View Article][PubMed]
    [Google Scholar]
  14. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J et al. The sequence alignment/Map format and SAMtools. Bioinformatics 2009; 25:2078–2079 [View Article][PubMed]
    [Google Scholar]
  15. Anders S, Pyl PT, Huber W. HTSeqa Python framework to work with high-throughput sequencing data. Bioinformatics 2015; 31:166–169 [View Article][PubMed]
    [Google Scholar]
  16. Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol 2014; 15:550 [View Article][PubMed]
    [Google Scholar]
  17. Alexa A, Rahnenfuhrer J. topGO: Enrichment Analysis for Gene Ontology R package version 2.24.0 2016
    [Google Scholar]
  18. Bearson BL, Bearson SM. The role of the QseC quorum-sensing sensor kinase in colonization and norepinephrine-enhanced motility of Salmonella enterica serovar Typhimurium. Microb Pathog 2008; 44:271–278 [View Article][PubMed]
    [Google Scholar]
  19. Lippolis JD, Brunelle BW, Reinhardt TA, Sacco RE, Nonnecke BJ et al. Proteomic analysis reveals protein expression differences in Escherichia coli strains associated with persistent versus transient mastitis. J Proteomics 2014; 108:373–381 [View Article][PubMed]
    [Google Scholar]
  20. Uthe JJ, Wang Y, Qu L, Nettleton D, Tuggle CK et al. Correlating blood immune parameters and a CCT7 genetic variant with the shedding of Salmonella enterica serovar Typhimurium in swine. Vet Microbiol 2009; 135:384–388 [View Article][PubMed]
    [Google Scholar]
  21. Knetter SM, Bearson SM, Huang TH, Kurkiewicz D, Schroyen M et al. Salmonella enterica serovar Typhimurium-infected pigs with different shedding levels exhibit distinct clinical, peripheral cytokine and transcriptomic immune response phenotypes. Innate Immun 2015; 21:227–241 [View Article][PubMed]
    [Google Scholar]
  22. Snary EL, Swart AN, Simons RR, Domingues AR, Vigre H et al. A quantitative microbiological risk assessment for Salmonella in pigs for the European Union. Risk Anal 2016; 36:437–449 [View Article][PubMed]
    [Google Scholar]
  23. Althouse C, Patterson S, Fedorka-Cray P, Isaacson RE. Type 1 fimbriae of Salmonella enterica serovar Typhimurium bind to enterocytes and contribute to colonization of swine in vivo. Infect Immun 2003; 71:6446–6452 [View Article][PubMed]
    [Google Scholar]
  24. De La Cruz MA, Calva E. The complexities of porin genetic regulation. J Mol Microbiol Biotechnol 2010; 18:24–36 [View Article][PubMed]
    [Google Scholar]
  25. Vogel J. A rough guide to the non-coding RNA world of Salmonella. Mol Microbiol 2009; 71:1–11 [View Article][PubMed]
    [Google Scholar]
  26. Huang TH, Uthe JJ, Bearson SM, Demirkale CY, Nettleton D et al. Distinct peripheral blood RNA responses to Salmonella in pigs differing in Salmonella shedding levels: intersection of IFNG, TLR and miRNA pathways. PLoS One 2011; 6:e28768 [View Article][PubMed]
    [Google Scholar]
  27. Liu M, Guo S, Hibbert JM, Jain V, Singh N et al. CXCL10/IP-10 in infectious diseases pathogenesis and potential therapeutic implications. Cytokine Growth Factor Rev 2011; 22:121–130 [View Article][PubMed]
    [Google Scholar]
  28. Jain V, Armah HB, Tongren JE, Ned RM, Wilson NO et al. Plasma IP-10, apoptotic and angiogenic factors associated with fatal cerebral malaria in India. Malar J 2008; 7:83 [View Article][PubMed]
    [Google Scholar]
  29. Vasquez RE, Xin L, Soong L. Effects of CXCL10 on dendritic cell and CD4+ T-cell functions during Leishmania amazonensis infection. Infect Immun 2008; 76:161–169 [View Article][PubMed]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jmm/10.1099/jmm.0.000482
Loading
/content/journal/jmm/10.1099/jmm.0.000482
Loading

Data & Media loading...

Supplements

Supplementary File 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error