Literature DB >> 27316966

Differential Utilization of Basic Proline-Rich Glycoproteins during Growth of Oral Bacteria in Saliva.

Yuan Zhou1, Jinghua Yang1, Luxia Zhang1, Xuedong Zhou2, John O Cisar1, Robert J Palmer3.   

Abstract

UNLABELLED: Although saliva is widely recognized as a primary source of carbon and nitrogen for growth of the dental plaque biofilm community, little is known about how different oral bacteria utilize specific salivary components. To address this question, 32 strains representing 16 genera commonly isolated from early plaque biofilms were compared for growth over two transfers in stimulated (by chewing Parafilm) whole saliva that was stabilized by heat treatment and dialysis. The cell densities, measured by quantitative PCR (qPCR), ranged from ∼1 × 10(6) to 1 × 10(7)/ml for strains of Streptococcus gordonii, Streptococcus oralis, and Streptococcus mitis and one strain of Streptococcus sanguinis Strains of Streptococcus mutans, Gemella haemolysans, and Granulicatella adiacens reached ∼1 × 10(5) to 1 × 10(6)/ml. In contrast, little or no growth was noted for three other strains of S. sanguinis, as well as for strains of Streptococcus parasanguinis, Streptococcus salivarius, Streptococcus vestibularis, Streptococcus sobrinus, Actinomyces spp., Abiotrophia defectiva, and Rothia dentocariosa SDS-PAGE, lectin blotting, and two-dimensional gel electrophoresis of saliva from cultures of S. gordonii, S. oralis, and S. mitis revealed species-specific differences in the degradation of basic proline-rich glycoproteins (PRG). In contrast, saliva from cultures of other bacteria was indistinguishable from control saliva. Species-dependent differences in the utilization of individual host sugars were minor. Thus, differences in salivary glycan foraging between oral species may be important to cross-feeding and cooperation between organisms in dental plaque biofilm development. IMPORTANCE: Bacteria in the mouth use saliva for nutrition. How each of the many types of bacteria uses saliva is not clear. We show that a major protein in saliva, called PRG, is an important nutrition source for certain bacteria but not for others. PRG has many sugar molecules linked in chains, but the sugar is not available for bacteria until the chains are degraded. The bacteria that can grow by digesting this protein break the sugar chains into parts which not only support their own growth but could also be available to support the growth of those bacteria that cannot use the intact protein.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2016        PMID: 27316966      PMCID: PMC4988208          DOI: 10.1128/AEM.01111-16

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  35 in total

1.  Identification of protein components in human acquired enamel pellicle and whole saliva using novel proteomics approaches.

Authors:  Yuan Yao; Eric A Berg; Catherine E Costello; Robert F Troxler; Frank G Oppenheim
Journal:  J Biol Chem       Date:  2002-11-19       Impact factor: 5.157

Review 2.  Saliva as research material: biochemical, physicochemical and practical aspects.

Authors:  Raymond G Schipper; Erika Silletti; Monique H Vingerhoeds
Journal:  Arch Oral Biol       Date:  2007-08-10       Impact factor: 2.633

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4.  An ultrastructural quantitative study of the significance of microbial multiplication during early dental plaque growth.

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Journal:  J Periodontal Res       Date:  1983-03       Impact factor: 4.419

5.  Growth of Viridans streptococci on human serum alpha1-acid glycoprotein.

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6.  Printed covalent glycan array for ligand profiling of diverse glycan binding proteins.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-11-24       Impact factor: 11.205

7.  Structure and bacterial receptor activity of a human salivary proline-rich glycoprotein.

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8.  Characterization of binding of Gal beta 4GlcNAc-specific lectins from Erythrina cristagalli and Erythrina corallodendron to glycosphinogolipids. Detection, isolation, and characterization of a novel glycosphinglipid of bovine buttermilk.

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Journal:  J Biol Chem       Date:  1994-03-18       Impact factor: 5.157

9.  Degradation of MUC7 and MUC5B in human saliva.

Authors:  Sachiko Takehara; Masaki Yanagishita; Katarzyna Anna Podyma-Inoue; Yoko Kawaguchi
Journal:  PLoS One       Date:  2013-07-18       Impact factor: 3.240

10.  The evolution of cooperation within the gut microbiota.

Authors:  Seth Rakoff-Nahoum; Kevin R Foster; Laurie E Comstock
Journal:  Nature       Date:  2016-04-25       Impact factor: 49.962

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  13 in total

1.  Oral Microbiota Display Profound Differential Metabolic Kinetics and Community Shifts upon Incubation with Sucrose, Trehalose, Kojibiose, and Xylitol.

Authors:  Stanley O Onyango; Nele De Clercq; Koen Beerens; John Van Camp; Tom Desmet; Tom Van de Wiele
Journal:  Appl Environ Microbiol       Date:  2020-08-03       Impact factor: 4.792

2.  The Role of Glycoside Hydrolases in S. gordonii and C. albicans Interactions.

Authors:  Zhiyan Zhou; Biao Ren; Jiyao Li; Xuedong Zhou; Xin Xu; Yuan Zhou
Journal:  Appl Environ Microbiol       Date:  2022-05-04       Impact factor: 5.005

Review 3.  Glycan recognition at the saliva - oral microbiome interface.

Authors:  Benjamin W Cross; Stefan Ruhl
Journal:  Cell Immunol       Date:  2018-08-18       Impact factor: 4.868

4.  Cell Surface Glycoside Hydrolases of Streptococcus gordonii Promote Growth in Saliva.

Authors:  Jinghua Yang; Yuan Zhou; Luxia Zhang; Nehal Shah; Cheng Jin; Robert J Palmer; John O Cisar
Journal:  Appl Environ Microbiol       Date:  2016-08-15       Impact factor: 4.792

Review 5.  [Research progress on carbohydrate active enzymes of human microbiome].

Authors:  Zhi-Yan Zhou; Xin Xu; Yuan Zhou
Journal:  Hua Xi Kou Qiang Yi Xue Za Zhi       Date:  2019-12-01

6.  The Predominant Oral Microbiota Is Acquired Early in an Organized Pattern.

Authors:  Rosalyn M Sulyanto; Zachary A Thompson; Clifford J Beall; Eugene J Leys; Ann L Griffen
Journal:  Sci Rep       Date:  2019-07-22       Impact factor: 4.379

7.  Host-glycan metabolism is regulated by a species-conserved two-component system in Streptococcus pneumoniae.

Authors:  Patrick Rosendahl Andreassen; Claudia Trappetti; Vikrant Minhas; Flemming Damgaard Nielsen; Kevin Pakula; James C Paton; Mikkel Girke Jørgensen
Journal:  PLoS Pathog       Date:  2020-03-04       Impact factor: 6.823

8.  Sulfated vizantin causes detachment of biofilms composed mainly of the genus Streptococcus without affecting bacterial growth and viability.

Authors:  Taisuke Hasegawa; Shoji Takenaka; Masataka Oda; Hisanori Domon; Takumi Hiyoshi; Karin Sasagawa; Tatsuya Ohsumi; Naoki Hayashi; Yasuko Okamoto; Hirofumi Yamamoto; Hayato Ohshima; Yutaka Terao; Yuichiro Noiri
Journal:  BMC Microbiol       Date:  2020-11-25       Impact factor: 3.605

9.  Probiotics alter biofilm formation and the transcription of Porphyromonas gingivalis virulence-associated genes.

Authors:  Karin Hitomi Ishikawa; Daniela Mita; Dione Kawamoto; Jacques Robert Nicoli; Emmanuel Albuquerque-Souza; Maria Regina Lorenzetti Simionato; Marcia Pinto Alves Mayer
Journal:  J Oral Microbiol       Date:  2020-08-20       Impact factor: 5.474

10.  Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis.

Authors:  Yu-Wen Chen; Shiao-Wen Li; Chia-Der Lin; Mei-Zi Huang; Hwai-Jeng Lin; Chia-Yin Chin; Yi-Ru Lai; Cheng-Hsun Chiu; Chia-Yu Yang; Chih-Ho Lai
Journal:  Front Cell Dev Biol       Date:  2020-10-26
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