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Microbiome-mediated incapacitation of interferon lambda production in the oral mucosa.
Rodriguez-Hernandez, Carlos J; Sokoloski, Kevin J; Stocke, Kendall S; Dukka, Himabindu; Jin, Shunying; Metzler, Melissa A; Zaitsev, Konstantin; Shpak, Boris; Shen, Daonan; Miller, Daniel P; Artyomov, Maxim N; Lamont, Richard J; Bagaitkar, Juhi.
Afiliación
  • Rodriguez-Hernandez CJ; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Sokoloski KJ; Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202.
  • Stocke KS; Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202.
  • Dukka H; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Jin S; Department of Diagnosis and Oral Health, University of Louisville, Louisville, KY 40202.
  • Metzler MA; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Zaitsev K; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Shpak B; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
  • Shen D; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
  • Miller DP; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Artyomov MN; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202.
  • Lamont RJ; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
  • Bagaitkar J; Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY 40202; juhi.bagaitkar@louisville.edu rich.lamont@louisville.edu.
Proc Natl Acad Sci U S A ; 118(51)2021 12 21.
Article en En | MEDLINE | ID: mdl-34921113
ABSTRACT
Here, we show that Porphyromonas gingivalis (Pg), an endogenous oral pathogen, dampens all aspects of interferon (IFN) signaling in a manner that is strikingly similar to IFN suppression employed by multiple viral pathogens. Pg suppressed IFN production by down-regulating several IFN regulatory factors (IRFs 1, 3, 7, and 9), proteolytically degrading STAT1 and suppressing the nuclear translocation of the ISGF3 complex, resulting in profound and systemic repression of multiple interferon-stimulated genes. Pg-induced IFN paralysis was not limited to murine models but was also observed in the oral tissues of human periodontal disease patients, where overabundance of Pg correlated with suppressed IFN generation. Mechanistically, multiple virulence factors and secreted proteases produced by Pg transcriptionally suppressed IFN promoters and also cleaved IFN receptors, making cells refractory to exogenous IFN and inducing a state of broad IFN paralysis. Thus, our data show a bacterial pathogen with equivalence to viruses in the down-regulation of host IFN signaling.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interleucinas / Interferones / Porphyromonas gingivalis / Interacciones Huésped-Patógeno / Microbiota / Encía Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interleucinas / Interferones / Porphyromonas gingivalis / Interacciones Huésped-Patógeno / Microbiota / Encía Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2021 Tipo del documento: Article