Literature DB >> 3965396

Surface structures (peritrichous fibrils and tufts of fibrils) found on Streptococcus sanguis strains may be related to their ability to coaggregate with other oral genera.

P S Handley, P L Carter, J E Wyatt, L M Hesketh.   

Abstract

We screened 36 strains of Streptococcus sanguis biotype I and 8 strains of S. sanguis biotype II for the presence of surface structures and for their ability to coaggregate with Actinomyces viscosus, Actinomyces naeslundii, and Fusobacterium nucleatum. Negative staining under an electron microscope revealed detectable surface structures on all S. sanguis strains. The majority of strains (38 of 44) carried peritrichous fibrils, which have an irregular profile and no distinct width. They usually appeared as a fringe with a constant width around the cell. Strains selected for measurement had a fringe with an average length of 72.4 +/- 8.5 nm on biotype I strains and 51.6 +/- 3.3 nm on biotype II strains. Some fibrillar biotype I strains carried an additional, longer (158.7 +/- 33.1 nm) type of fibril projecting through the shorter fibrils. Fibrillar density was characteristic for each strain, ranging from very dense on all cells in a population to very sparse on a few cells in a population. A small group of six strains carried tufts of fibrils in a lateral or polar position on the cell. Either one or two lengths of fibril were present in the tuft depending on the strain. One strain carried both peritrichous fibrils and fimbriae. Fimbriae are flexible structures with a constant width (4.5 to 5.0 nm) all along their length but very variable lengths (less than or equal to 0.7 micron) on each cell. S. sanguis I and II both included strains with peritrichous fibrils and tufts of fibrils, but the mixed morphotype strain was confined to biotype II. Fibrils were present on cells at all stages throughout the growth cycle for the strains tested. Freshly isolated fibrillar strains coaggregated consistently well with A. viscosus and A. naeslundii, although some fibrillar reference strains lacked the ability. In addition, all tufted strains could not coaggregate, but the strains with the mixed morphotype coaggregated well. Coaggregation with F. nucleatum was very strong for the fibrillar strains, but less strong for the tufted strains. We discuss the possible correlation between S. sanguis surface structure and ability to coaggregate.

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Year:  1985        PMID: 3965396      PMCID: PMC261499          DOI: 10.1128/iai.47.1.217-227.1985

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


  32 in total

1.  Ecology, physiology, and genetics of fimbriae and pili.

Authors:  J C Ottow
Journal:  Annu Rev Microbiol       Date:  1975       Impact factor: 15.500

2.  Use of autoclaved extracts of hemolytic streptococci for serological grouping.

Authors:  L A RANTZ; E RANDALL
Journal:  Stanford Med Bull       Date:  1955-05

3.  Effect of diphosphonates on root resorption.

Authors:  P J Robinson; I M Shapiro
Journal:  J Dent Res       Date:  1976 Jan-Feb       Impact factor: 6.116

4.  Examination of the test for compressive strength applied to zinc oxide eugenol cements.

Authors:  A D Wilson
Journal:  J Dent Res       Date:  1976 Jan-Feb       Impact factor: 6.116

5.  Aggregation of oral streptococci with Fusobacterium and Actinomyces.

Authors:  J Kelstrup; T D Funder-Nielsen
Journal:  J Biol Buccale       Date:  1974-12

6.  Interbacterial aggregation of plaque bacteria.

Authors:  R J Gibbons; M Nygaard
Journal:  Arch Oral Biol       Date:  1970-12       Impact factor: 2.633

7.  Adherence as an ecological determinant for streptococci in the human mouth.

Authors:  J Van Houte; R J Gibbons; A J Pulkkinen
Journal:  Arch Oral Biol       Date:  1971-10       Impact factor: 2.633

8.  Adherence as a determinant of the presence of Streptococcus salivarius and Streptococcus sanguis on the human tooth surface.

Authors:  J Van Houte; R J Gibbons; S B Banghart
Journal:  Arch Oral Biol       Date:  1970-11       Impact factor: 2.633

9.  Twitching motility and possession of polar fimbriae in spreading Streptococcus sanguis isolates from the human throat.

Authors:  S D Henriksen; J Henrichsen
Journal:  Acta Pathol Microbiol Scand B       Date:  1975-04

10.  Serology of Streptococcus sanguis: localization of antigens with unlabeled antisera.

Authors:  C Lai; M Listgarten; B Rosan
Journal:  Infect Immun       Date:  1973-09       Impact factor: 3.441

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  34 in total

Review 1.  Multiple adhesins of streptococci.

Authors:  D L Hasty; I Ofek; H S Courtney; R J Doyle
Journal:  Infect Immun       Date:  1992-06       Impact factor: 3.441

2.  Genome of the opportunistic pathogen Streptococcus sanguinis.

Authors:  Ping Xu; Joao M Alves; Todd Kitten; Arunsri Brown; Zhenming Chen; Luiz S Ozaki; Patricio Manque; Xiuchun Ge; Myrna G Serrano; Daniela Puiu; Stephanie Hendricks; Yingping Wang; Michael D Chaplin; Doruk Akan; Sehmi Paik; Darrell L Peterson; Francis L Macrina; Gregory A Buck
Journal:  J Bacteriol       Date:  2007-02-02       Impact factor: 3.490

3.  Localized tufts of fibrils on Staphylococcus epidermidis NCTC 11047 are comprised of the accumulation-associated protein.

Authors:  Miriam A Banner; John G Cunniffe; Robin L Macintosh; Timothy J Foster; Holger Rohde; Dietrich Mack; Emmy Hoyes; Jeremy Derrick; Mathew Upton; Pauline S Handley
Journal:  J Bacteriol       Date:  2007-02-02       Impact factor: 3.490

Review 4.  Streptococcus adherence and colonization.

Authors:  Angela H Nobbs; Richard J Lamont; Howard F Jenkinson
Journal:  Microbiol Mol Biol Rev       Date:  2009-09       Impact factor: 11.056

5.  Sialidase activity of the "Streptococcus milleri group" and other viridans group streptococci.

Authors:  D Beighton; R A Whiley
Journal:  J Clin Microbiol       Date:  1990-06       Impact factor: 5.948

6.  Cell surface components of Streptococcus sanguis: relationship to aggregation, adherence, and hydrophobicity.

Authors:  E J Morris; N Ganeshkumar; B C McBride
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

Review 7.  Subgingival biofilm formation.

Authors:  Masae Kuboniwa; Richard J Lamont
Journal:  Periodontol 2000       Date:  2010-02       Impact factor: 7.589

8.  Identification and preliminary characterization of a Streptococcus sanguis fibrillar glycoprotein.

Authors:  E J Morris; N Ganeshkumar; M Song; B C McBride
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

9.  Differentiation of salivary agglutinin-mediated adherence and aggregation of mutans streptococci by use of monoclonal antibodies against the major surface adhesin P1.

Authors:  L J Brady; D A Piacentini; P J Crowley; P C Oyston; A S Bleiweis
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

10.  Characterization of an amylase-binding component of Streptococcus gordonii G9B.

Authors:  F A Scannapieco; G G Haraszthy; M I Cho; M J Levine
Journal:  Infect Immun       Date:  1992-11       Impact factor: 3.441

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