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Immune response profiling of primary monocytes and oral keratinocytes to different Tannerella forsythia strains and their cell surface mutants.
Bloch, S; Zwicker, S; Bostanci, N; Sjöling, Å; Boström, E A; Belibasakis, G N; Schäffer, C.
Afiliación
  • Bloch S; Department of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Wien, Vienna, Austria.
  • Zwicker S; Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Bostanci N; Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Sjöling Å; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
  • Boström EA; Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Belibasakis GN; Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Schäffer C; Department of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Wien, Vienna, Austria.
Mol Oral Microbiol ; 33(2): 155-167, 2018 04.
Article en En | MEDLINE | ID: mdl-29235255
The oral pathogen Tannerella forsythia possesses a unique surface (S-) layer with a complex O-glycan containing a bacterial sialic acid mimic in the form of either pseudaminic acid or legionaminic acid at its terminal position. We hypothesize that different T. forsythia strains employ these stereoisomeric sugar acids for interacting with the immune system and resident host tissues in the periodontium. Here, we show how T. forsythia strains ATCC 43037 and UB4 displaying pseudaminic acid and legionaminic acid, respectively, and selected cell surface mutants of these strains modulate the immune response in monocytes and human oral keratinocytes (HOK) using a multiplex immunoassay. When challenged with T. forsythia, monocytes secrete proinflammatory cytokines, chemokines and vascular endothelial growth factor (VEGF) with the release of interleukin-1ß (IL-1ß) and IL-7 being differentially regulated by the two T. forsythia wild-type strains. Truncation of the bacteria's O-glycan leads to significant reduction of IL-1ß and regulates macrophage inflammatory protein-1. HOK infected with T. forsythia produce IL-1Ra, chemokines and VEGF. Although the two wild-type strains elicit preferential immune responses for IL-8, both truncation of the O-glycan and deletion of the S-layer result in significantly increased release of IL-8, granulocyte-macrophage colony-stimulating factor and monocyte chemoattractant protein-1. Through immunofluorescence and confocal laser scanning microscopy of infected HOK we additionally show that T. forsythia is highly invasive and tends to localize to the perinuclear region. This indicates, that the T. forsythia S-layer and attached sugars, particularly pseudaminic acid in ATCC 43037, contribute to dampening the response of epithelial tissues to initial infection and hence play a pivotal role in orchestrating the bacterium's virulence.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Periodontales / Monocitos / Queratinocitos / Membrana Celular / Tannerella forsythia Límite: Humans Idioma: En Revista: Mol Oral Microbiol Año: 2018 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Dinamarca

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Periodontales / Monocitos / Queratinocitos / Membrana Celular / Tannerella forsythia Límite: Humans Idioma: En Revista: Mol Oral Microbiol Año: 2018 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Dinamarca