Cytokine response of porcine cell lines to Salmonella enterica serovar typhimurium and its hilA and ssrA mutants
Language English Country Germany Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17894638
DOI
10.1111/j.1863-2378.2007.01064.x
PII: JVB1064
Knihovny.cz E-resources
- MeSH
- Bacterial Adhesion MeSH
- Bacterial Proteins genetics MeSH
- Cytokines biosynthesis MeSH
- Epithelial Cells metabolism MeSH
- Granulocyte-Macrophage Colony-Stimulating Factor biosynthesis MeSH
- Interleukin-8 biosynthesis MeSH
- Cells, Cultured MeSH
- Macrophages metabolism MeSH
- RNA, Messenger analysis MeSH
- Mutation MeSH
- Swine Diseases microbiology MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Swine MeSH
- Salmonella enterica genetics immunology pathogenicity MeSH
- Salmonella Infections, Animal microbiology MeSH
- Tumor Necrosis Factor-alpha biosynthesis MeSH
- Trans-Activators genetics MeSH
- Virulence MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- Cytokines MeSH
- Granulocyte-Macrophage Colony-Stimulating Factor MeSH
- HilA protein, Salmonella MeSH Browser
- Interleukin-8 MeSH
- RNA, Messenger MeSH
- Tumor Necrosis Factor-alpha MeSH
- Trans-Activators MeSH
Salmonella enterica serovar Typhimurium (S. Typhimurium) is a facultative intracellular bacterium which can infect and colonize pigs. After contact with enterocytes and macrophages, S. Typhimurium induces production of cytokines thus triggering the innate immune response. In this study we evaluated the cytokine response of two porcine cell lines, IPI-2I and 3D4/31, of epithelial or macrophage origins, respectively, to the wild-type S. Typhimurium and its hilA and ssrA mutants. We observed that the 3D4/31 cell line essentially did not respond to S. Typhimurium infection when a medium with foetal calf serum was used. However when the 3D4 cell line was incubated overnight in the presence of porcine serum, it efficiently responded to the wild-type strain and the ssrA mutant but not to the noninvasive hilA mutant as measured by mRNA quantification of TNF-alpha, IL-8 and GM-CSF by the real-time RT-PCR. In IPI-2I, all the cytokines were also induced by the wild-type S. Typhimurium and the ssrA mutant although the induction of TNF-alpha was lower than that induced by the wild-type strain. The hilA mutant was unable to induce any of the cytokines tested. The ssrA mutant can therefore be considered as more suitable for further vaccine development as the stimulation of innate immune response is important for animal protection against a challenge with virulent strains.
References provided by Crossref.org
Characterization of Porcine Monocyte-Derived Macrophages Cultured in Serum-Reduced Medium