Differential cytokine expression in avian cells in response to invasion by Salmonella typhimurium, Salmonella enteritidis and Salmonella gallinarum The GenBank accession numbers for the sequences reported in this paper are AI982185 for chicken IL-6 cDNA and AJ250838 for the partial chicken IL-6 genomic sequence, respectively.
Top Cited Papers
- 1 December 2000
- journal article
- research article
- Published by Microbiology Society in Microbiology
- Vol. 146 (12), 3217-3226
- https://doi.org/10.1099/00221287-146-12-3217
Abstract
Salmonella enterica is a facultative intracellular pathogen that is capable of causing disease in a range of hosts. Although human salmonellosis is frequently associated with consumption of contaminated poultry and eggs, and the serotypes Salmonella gallinarum and Salmonella pullorum are important world-wide pathogens of poultry, little is understood of the mechanisms of pathogenesis of Salmonella in the chicken. Type III secretion systems play a key role in host cell invasiveness and trigger the production of pro-inflammatory cytokines during invasion of mammalian hosts. This results in a polymorphonuclear cell influx that contributes to the resulting enteritis. In this study, a chicken primary cell culture model was used to investigate the cytokine responses to entry by the broad host range serotypes S. enteritidis and S. typhimurium, and the host specific serotype S. gallinarum, which rarely causes disease outside its main host, the chicken. The cytokines interleukin (IL)-1β, IL-2, IL-6 and interferon (IFN)-γ were measured by quantitative RT-PCR, and production of IL-6 and IFN-γ was also determined through bioassays. All serotypes were invasive and had little effect on the production of IFN-γ compared with non-infected cells; S. enteritidis invasion caused a slight down-regulation of IL-2 production. For IL-1β production, infection with S. typhimurium had little effect, whilst infection with S. gallinarum or S. enteritidis caused a reduction in IL-1β mRNA levels. Invasion of S. typhimurium and S. enteritidis caused an eight- to tenfold increase in production of the pro-inflammatory cytokine IL-6, whilst invasion by S. gallinarum caused no increase. These findings correlate with the pathogenesis of Salmonella in poultry. S. typhimurium and S. enteritidis invasion produces a strong inflammatory response, that may limit the spread of Salmonella largely to the gut, whilst S. gallinarum does not induce an inflammatory response and may not be limited by the immune system, leading to the severe systemic disease fowl typhoid.Keywords
This publication has 33 references indexed in Scilit:
- Production of antibodies against chicken interferon-γ: demonstration of neutralizing activity and development of a quantitative ELISAVeterinary Immunology and Immunopathology, 2000
- Salmonella efficiently enter and survive within cultured CD11c+ dendritic cells initiating cytokine expressionEuropean Journal of Immunology, 1999
- Structure of the chicken interferon-γ gene, and comparison to mammalian homologuesGene, 1998
- Cloning and Expression of the Chicken Interferon-γ GeneJournal of Interferon & Cytokine Research, 1995
- Production of Interferon-γ by Chicken T CellsJournal of Interferon & Cytokine Research, 1995
- Heterophils are decisive components in the early responses of chickens to Salmonella enteritidis infectionsMicrobial Pathogenesis, 1994
- Experimental infection of egg‐laying hens withSalmonella enteritidisphage type 4Avian Pathology, 1991
- Invasion of Vero cells by Salmonella speciesJournal of Medical Microbiology, 1989
- Chicken hematopoietic cells transformed by seven strains of defective avian leukemia viruses display three distinct phenotypes of differentiationCell, 1979
- Observations on Experimental Fowl TyphoidJournal of Comparative Pathology and Therapeutics, 1955