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• W1644750267 abstract "A lack of relevant disease models for Campylobacter jejuni has long been an obstacle to research into this common enteric pathogen. We recently published that mice deficient in Single IgG Interleukin-1 related receptor (SIGIRR), a repressor of MyD88-dependent innate immune signaling, were highly susceptible to enteric infection by murine bacterial pathogens. Subsequently, we successfully employed these mice as an animal model for the human pathogen C. jejuni and gained substantial new insights into infection by this pathogen. The infected mice developed significant intestinal inflammation, primarily via TLR4 stimulation. Furthermore, the resulting gastroenteritis was dependent on C. jejuni pathogenesis as bacterial strains suffering mutations in key virulence factors were attenuated in causing disease. The ability to infect SIGIRR-deficient mice with C. jejuni sheds new light onto how these bacteria colonize the mucus layer of the intestinal tract, invade epithelial cells, and raises new prospects for studying the virulence strategies and pathogenesis of C. jejuni." @default.
• W1644750267 created "2016-06-24" @default.
• W1644750267 creator A5038360456 @default.
• W1644750267 creator A5074020921 @default.
• W1644750267 date "2015-03-04" @default.
• W1644750267 modified "2023-10-18" @default.
• W1644750267 title "Insights into<i>Campylobacter jejuni</i>colonization of the mammalian intestinal tract using a novel mouse model of infection" @default.
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• W1644750267 doi "https://doi.org/10.1080/19490976.2015.1016691" @default.
• W1644750267 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4615362" @default.
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