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Human and Animal Isolates of Yersinia enterocolitica Show Significant Serotype-Specific Colonization and Host-Specific Immune Defense Properties
Authors:Julia Schaake  Malte Kronshage  Frank Uliczka  Manfred Rohde  Tobias Knuuti  Eckhard Strauch  Angelika Fruth  Melissa Wos-Oxley  Petra Dersch
Affiliation:Department of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germanya;Department of Medical Microbiology, Helmholtz Centre for Infection Research, Braunschweig, Germanyb;Federal Institute for Risk Assessment, Berlin, Germanyc;Robert Koch Institute, Wernigerode, Germanyd;Department of Microbial Interactions and Processes, Helmholtz Centre for Infection Research, Braunschweig, Germanye
Abstract:
Yersinia enterocolitica is a human pathogen that is ubiquitous in livestock, especially pigs. The bacteria are able to colonize the intestinal tract of a variety of mammalian hosts, but the severity of induced gut-associated diseases (yersiniosis) differs significantly between hosts. To gain more information about the individual virulence determinants that contribute to colonization and induction of immune responses in different hosts, we analyzed and compared the interactions of different human- and animal-derived isolates of serotypes O:3, O:5,27, O:8, and O:9 with murine, porcine, and human intestinal cells and macrophages. The examined strains exhibited significant serotype-specific cell binding and entry characteristics, but adhesion and uptake into different host cells were not host specific and were independent of the source of the isolate. In contrast, survival and replication within macrophages and the induced proinflammatory response differed between murine, porcine, and human macrophages, suggesting a host-specific immune response. In fact, similar levels of the proinflammatory cytokine macrophage inflammatory protein 2 (MIP-2) were secreted by murine bone marrow-derived macrophages with all tested isolates, but the equivalent interleukin-8 (IL-8) response of porcine bone marrow-derived macrophages was strongly serotype specific and considerably lower in O:3 than in O:8 strains. In addition, all tested Y. enterocolitica strains caused a considerably higher level of secretion of the anti-inflammatory cytokine IL-10 by porcine than by murine macrophages. This could contribute to limiting the severity of the infection (in particular of serotype O:3 strains) in pigs, which are the primary reservoir of Y. enterocolitica strains pathogenic to humans.
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