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Streptococcus gordonii Poised for Glycan Feeding through a MUC5B-Discriminating, Lipoteichoic Acid-Mediated Outside-In Signaling Circuit
Univ Minnesota, Sch Dent, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA..ORCID-id: 0000-0003-4619-4712
Malmö universitet, Odontologiska fakulteten (OD).ORCID-id: 0000-0001-5888-664X
Malmö universitet, Odontologiska fakulteten (OD).ORCID-id: 0000-0002-8183-8846
Univ Minnesota, Sch Dent, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA..
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2022 (Engelska)Ingår i: Journal of Bacteriology, ISSN 0021-9193, E-ISSN 1098-5530, Vol. 204, nr 6, artikel-id e00118-22Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Many oral bacteria employ cell wall-anchored adhesins to bind to the salivary films coating the teeth and mucosal surfaces. Surface binding prevents clearance and facilitates catabolism of salivary film glycoproteins. We asked whether Streptococcus gordonii adhesin expression changes in response to surface salivary cues using a eukaryote-like, outside-in recognition and signaling circuit. To determine whether the cues were discriminated, S. gordonii was tested during cell adhesion and biofilm formation on a MUC5B-rich or lower-molecular-mass salivary fraction or an uncoated abiotic surface. Cells were recovered and analyzed for differences in gene expression and proteins in cell wall fractions. In salivary-free conditions, planktonic S. gordonii presented three prominent cell wall LPXTG-motif proteins, SGO_1487, SGO_0890, and MbpA (mucin-binding protein A; SGO_0707). During biofilm formation on MUC5B-coated surfaces, MbpA, a MUC5B-binding protein, and key genes in the tagatose and quorum-sensing pathways were strongly promoted. The response to MUC5B required the two-component system (TCS), streptococcal regulator of adhesins sensor and regulator (SraSR, SGO_1180/81), lipoteichoic acid (LTA), and the homologous paired adhesins, SspA and SspB (SspAB). LTA appears to link the outside signal (MUC5B) to intramembrane SraSR. Tagatose pathway gene expression may poise cells to metabolize MUC5B glycans and, with a quorum-sensing gene (luxS), may direct formation of a consortium to facilitate glycan cross-feeding by S. gordonii. We now show that a Gram-positive bacterium discriminates specific surface environmental cues using an outside-in signaling mechanism to apparently optimize colonization of saliva-coated surfaces. IMPORTANCE All organisms throughout the tree of life sense and respond to their surface environments. To discriminate among mucosal surface environmental cues, we report that Streptococcus gordonii recognizes a high-molecular-weight mucin glycoprotein, MUC5B, using the paired adhesins SspAB and lipoteichoic acid; the latter bridges the outside signal to an intramembrane two-component system to transcriptionally regulate a MUC5B-specific adhesin and genes that may facilitate glycan catabolism. All organisms throughout the tree of life sense and respond to their surface environments. To discriminate among mucosal surface environmental cues, we report that Streptococcus gordonii recognizes a high-molecular-weight mucin glycoprotein, MUC5B, using the paired adhesins SspAB and lipoteichoic acid; the latter bridges the outside signal to an intramembrane two-component system to transcriptionally regulate a MUC5B-specific adhesin and genes that may facilitate glycan catabolism.

Ort, förlag, år, upplaga, sidor
ASM International, 2022. Vol. 204, nr 6, artikel-id e00118-22
Nyckelord [en]
Streptococcus gordonii, signaling circuit, glycan feeding, MUC5B, adhesins, lipoteichoic acid, two-component system
Nationell ämneskategori
Odontologi
Identifikatorer
URN: urn:nbn:se:mau:diva-53384DOI: 10.1128/jb.00118-22ISI: 000809024700001PubMedID: 35652671Scopus ID: 2-s2.0-85132455432OAI: oai:DiVA.org:mau-53384DiVA, id: diva2:1675043
Tillgänglig från: 2022-06-22 Skapad: 2022-06-22 Senast uppdaterad: 2024-02-05Bibliografiskt granskad

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Davies, Julia RWickström, ClaesSvensäter, Gunnel

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Lima, Bruno P.Davies, Julia RWickström, ClaesSvensäter, Gunnel
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Journal of Bacteriology
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Totalt: 213 träffar
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