Literature DB >> 24002

Attachment of Bacteroides melaninogenicus subsp. asaccharolyticus to oral surfaces and its possible role in colonization of the mouth and of periodontal pockets.

J Slots, R J Gibbons.   

Abstract

This investigation examined the ability of cells of Bacteroides melaninogenicus subsp. asaccharolyticus 381 to adhere to surfaces that might be important for its initial colonization of the mouth and its subsequent colonization in periodontal pockets. Of 48 asaccharolytic strains of B. melaninogenicus, 47 agglutinated human erythrocytes, whereas none of 20 fermentative strains, which included reference cultures of the subspecies intermedius and melaninogenicus, were active. Electron microscopy indicated that both asaccharolytic and fermentative strains possessed pili; hence, the presence of pili did not correlate with the hemagglutinating activities of B. melaninogenicus strains. Both asaccharolytic and fermentative B. melaninogenicus strains suspended in phosphate-buffered saline adhered in high numbers to buccal epithelial cells and to the surfaces of several gram-positive bacteria tested, including Actinomyces viscosus, A. naeslundii, A. israelii, Streptococcus sanguis, and S. mitis. B. melaninogenicus subsp. asaccharolyticus 381 also attached, but in comparatively low numbers, to untreated and to saliva-treated hydroxyapatite. Addition of clarified whole saliva to suspensions of strain 381 almost completely eliminated adherence to buccal epithelial cells and to hydroxyapatite surfaces, but saliva had no detectable effect on attachment to gram-positive plaque bacteria. Both fermentative and nonfermentative strains of B. melaninogenicus also attached in high numbers to crevicular epithelial cells derived from human periodontal pockets, but normal human serum strongly inhibited attachment. Serum also inhibited attachment of strain 381 to saliva- and serum-treated hydroxyapatite, but it had little effect upon attachment to gram-positive bacteria. These observations suggested that salivary and serum components would strongly inhibit the attachment of B. melaninogenicus cells to several oral surfaces, but not to the surfaces of certain gram-positive bacteria commonly present in human dental plaque. This was confirmed by an in vivo experiment in which streptomycin-labeled cells of B. melaninogenicus 381-R were introduced into the mouths of two volunteers. After 10 min, several hundred-fold higher numbers of the organism were recovered from preformed bacterial plaque present on teeth than from clean tooth surfaces or from the buccal mucosa and tongue dorsum. High numbers of B. melaninogenicus cells were also recovered from preformed plaque after 150 min, but virtually no cells of the organism were recovered from the other surfaces studied. These data suggest that the presence of dental plaque containing Actinomyces and other gram-positive bacteria may be essential for the attachment and colonization of B. melaninogenicus cells after their initial introduction into the mouth. Similarly, the presence of subgingival plaque containing gram-positive bacteria may be necessary for its secondary colonization in periodontal pockets.

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Year:  1978        PMID: 24002      PMCID: PMC414075          DOI: 10.1128/iai.19.1.254-264.1978

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  22 in total

1.  Microflora in the healthy gingival sulcus in man.

Authors:  J Slots
Journal:  Scand J Dent Res       Date:  1977-05

2.  Bacterial adherence in oral microbial ecology.

Authors:  R J Gibbons; J V Houte
Journal:  Annu Rev Microbiol       Date:  1975       Impact factor: 15.500

3.  The predominant cultivable organisms in juvenile periodontitis.

Authors:  J Slots
Journal:  Scand J Dent Res       Date:  1976-01

4.  Attempts to increase viable count recovery of human supragingival dental plaque.

Authors:  A D Manganiello; S S Socransky; C Smith; D Propas; V Oram; I L Dogon
Journal:  J Periodontal Res       Date:  1977-03       Impact factor: 4.419

5.  Bacteriological studies of developing supragingival dental plaque.

Authors:  S S Socransky; A D Manganiello; D Propas; V Oram; J van Houte
Journal:  J Periodontal Res       Date:  1977-03       Impact factor: 4.419

6.  Predominant cultivable microbiota in periodontosis.

Authors:  M G Newman; S S Socransky
Journal:  J Periodontal Res       Date:  1977-03       Impact factor: 4.419

7.  The predominant cultivable microflora of advanced periodontitis.

Authors:  J Slots
Journal:  Scand J Dent Res       Date:  1977 Jan-Feb

8.  Studies of the microbiology of periodontosis.

Authors:  M G Newman; S S Socransky; E D Savitt; D A Propas; A Crawford
Journal:  J Periodontol       Date:  1976-07       Impact factor: 6.993

9.  Structure of the microbial flora associated with periodontal health and disease in man. A light and electron microscopic study.

Authors:  M A Listgarten
Journal:  J Periodontol       Date:  1976-01       Impact factor: 6.993

10.  Antigenic heterogeneity of gonococcal pili.

Authors:  T M Buchanan
Journal:  J Exp Med       Date:  1975-06-01       Impact factor: 14.307

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  109 in total

Review 1.  The pathogenic persona of community-associated oral streptococci.

Authors:  Sarah E Whitmore; Richard J Lamont
Journal:  Mol Microbiol       Date:  2011-06-03       Impact factor: 3.501

2.  Strain-specific colonization patterns and serum modulation of multi-species oral biofilm development.

Authors:  Basak Biyikoğlu; Austin Ricker; Patricia I Diaz
Journal:  Anaerobe       Date:  2012-07-05       Impact factor: 3.331

3.  Oral implantation of Bacteroides asaccharolyticus and Eikenella corrodens in conventional hamsters.

Authors:  T Nagahata; T Kiyoshige; S Tomono; R Abe; S Sasaki; I Takazoe
Journal:  Infect Immun       Date:  1982-04       Impact factor: 3.441

4.  Neuraminidase-enhanced attachment of Bacteroides intermedius to human erythrocytes and buccal epithelial cells.

Authors:  K Okuda; M Ono; T Kato
Journal:  Infect Immun       Date:  1989-05       Impact factor: 3.441

5.  Bacteroides gingivalis vesicles bind to and aggregate Actinomyces viscosus.

Authors:  R P Ellen; D A Grove
Journal:  Infect Immun       Date:  1989-05       Impact factor: 3.441

6.  Interbacterial adherence between Actinomyces viscosus and strains of Streptococcus pyogenes, Streptococcus agalactiae, and Pseudomonas aeruginosa.

Authors:  K Komiyama; R J Gibbons
Journal:  Infect Immun       Date:  1984-04       Impact factor: 3.441

7.  Fimbriae from the oral anaerobe Bacteroides gingivalis: physical, chemical, and immunological properties.

Authors:  F Yoshimura; T Takasawa; M Yoneyama; T Yamaguchi; H Shiokawa; T Suzuki
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

8.  Salivary receptors for recombinant fimbrillin of Porphyromonas gingivalis.

Authors:  A Amano; H T Sojar; J Y Lee; A Sharma; M J Levine; R J Genco
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

9.  Monoclonal antibodies against surface antigens of Bacteroides gingivalis.

Authors:  Y Naito; K Okuda; T Kato; I Takazoe
Journal:  Infect Immun       Date:  1985-10       Impact factor: 3.441

Review 10.  Microbial interactions in building of communities.

Authors:  C J Wright; L H Burns; A A Jack; C R Back; L C Dutton; A H Nobbs; R J Lamont; H F Jenkinson
Journal:  Mol Oral Microbiol       Date:  2012-12-17       Impact factor: 3.563

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