Author:

Keywords:

Animals, Antigens, CD11b, Bacterial Outer Membrane Proteins, Cells, Cultured, Female, Gene Expression Profiling, Gene Expression Regulation, Immunity, Innate, Interferon-gamma, Interleukin-6, Mice, Mice, Inbred C57BL, Protein Tyrosine Phosphatases, Spleen, Yersinia Infections, Yersinia enterocolitica, Science & Technology, Life Sciences & Biomedicine, Microbiology, IMPORTANT VIRULENCE MECHANISM, PROTEIN-TYROSINE-PHOSPHATASE, FOCAL ADHESIONS, YOPH, PSEUDOTUBERCULOSIS, INFECTION, RECEPTOR, MACROPHAGES, CELLS, ACTIVATION, CD11b Antigen, 06 Biological Sciences, 07 Agricultural and Veterinary Sciences, 11 Medical and Health Sciences, 3107 Microbiology, 3207 Medical microbiology

Abstract:

BACKGROUND: Yersinia outer protein (Yop) H is a secreted virulence factor of Yersinia enterocolitica (Ye), which inhibits phagocytosis of Ye and contributes to the virulence of Ye in mice. The aim of this study was to address whether and how YopH affects the innate immune response to Ye in mice. RESULTS: For this purpose, mice were infected with wild type Ye (pYV+) or a YopH-deficient Ye mutant strain (DeltayopH). CD11b+ cells were isolated from the infected spleen and subjected to gene expression analysis using microarrays. Despite the attenuation of DeltayopH in vivo, by variation of infection doses we were able to achieve conditions that allow comparison of gene expression in pYV+ and DeltayopH infection, using either comparable infection courses or splenic bacterial burden. Gene expression analysis provided evidence that expression levels of several immune response genes, including IFN-gamma and IL-6, are high after pYV+ infection but low after sublethal DeltayopH infection. In line with these findings, infection of IFN-gammaR-/- and IL-6-/- mice with pYV+ or DeltayopH revealed that these cytokines are not necessarily required for control of DeltayopH, but are essential for defense against infection with the more virulent pYV+. Consistently, IFN-gamma pretreatment of bone marrow derived macrophages (BMDM) strongly enhanced their ability in killing intracellular Ye bacteria. CONCLUSION: In conclusion, this data suggests that IFN-gamma-mediated effector mechanisms can partially compensate virulence exerted by YopH. These results shed new light on the protective role of IFN-gamma in Ye wild type infections.