Literature DB >> 8408879

Antigenic relationships among oral Actinomyces isolates, Actinomyces naeslundii genospecies 1 and 2, Actinomyces howellii, Actinomyces denticolens, and Actinomyces slackii.

E E Putnins1, G H Bowden.   

Abstract

Antigenic relatedness among human strains of oral Actinomyces and similar isolates from cattle has been analyzed by agglutination and immunoblotting. Whole cell agglutination placed A. viscosus serotype II, A. naeslundii serotypes II and III, Actinomyces NV, and strains from numerical taxomonic clusters C1, C2, C3, C4, and C6 into a single group. A. viscosus serotype I cross-reacted weakly with this group. A naeslundii serotype I strains and the cattle isolates Actinomyces denticolens and Actinomyces howellii were distinct. The agglutination results for A. slackii were equivocal. Immunoblots of cell wall extracts developed with non-absorbed sera showed cross-reactivity (23% to 90% antigenic similarity) among all of the strains tested, including A. israelii. The range of antigenic similarities among the group which included strains of A. viscosus serotype II, the A. naeslundii serotypes, and clusters C1, C2, C3, C4, and C6 was from 39% to 89%. Immunoblotting showed that A. howellii and A. denticolens were between 39% and 72% similar to A. naeslundii and A. viscosus. Absorption of antisera with A. israelii cell walls removed antibodies recognizing antigens common to Actinomyces and made the sera more specific. Immunoblotting with absorbed sera supported the grouping and separation of strains shown by agglutination. In some cases, serotypes could be included into a specific taxonomic cluster. A. naeslundii serotype II and Actinomyces NV most closely resembled cluster C1 strains, and A. naeslundii serotype III resembled cluster C1 strains, and A. naeslundii serotype I and A. viscosus serotype I were included into clusters C5 and C7, respectively. The results support a recent proposal that strains of A. viscosus serotype II, A. naeslundii serotypes II and III, and Actinomyces NV be included into A. naeslundii genospecies 2, that A. naeslundii serotype I should be designated A. naeslundii genospecies 1, and that A. viscosus serotype I should be retained distinct from A. naeslundii, as A. viscosus.

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Year:  1993        PMID: 8408879     DOI: 10.1177/00220345930720100601

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  10 in total

1.  Strains of Actinomyces naeslundii and Actinomyces viscosus exhibit structurally variant fimbrial subunit proteins and bind to different peptide motifs in salivary proteins.

Authors:  T Li; I Johansson; D I Hay; N Strömberg
Journal:  Infect Immun       Date:  1999-05       Impact factor: 3.441

Review 2.  Quantitative analysis of multi-species oral biofilms by TaqMan Real-Time PCR.

Authors:  Nao Suzuki; Akihiro Yoshida; Yoshio Nakano
Journal:  Clin Med Res       Date:  2005-08

3.  Phenotypic and genotypic selection of microbiota surviving under dental restorations.

Authors:  J S Paddick; S R Brailsford; E A M Kidd; D Beighton
Journal:  Appl Environ Microbiol       Date:  2005-05       Impact factor: 4.792

4.  Different type 1 fimbrial genes and tropisms of commensal and potentially pathogenic Actinomyces spp. with different salivary acidic proline-rich protein and statherin ligand specificities.

Authors:  T Li; M K Khah; S Slavnic; I Johansson; N Strömberg
Journal:  Infect Immun       Date:  2001-12       Impact factor: 3.441

5.  Humoral immunity to commensal oral bacteria in human infants: salivary antibodies reactive with Actinomyces naeslundii genospecies 1 and 2 during colonization.

Authors:  M F Cole; S Bryan; M K Evans; C L Pearce; M J Sheridan; P A Sura; R Wientzen; G H Bowden
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

6.  Study of humoral immunity to commensal oral bacteria in human infants demonstrates the presence of secretory immunoglobulin A antibodies reactive with Actinomyces naeslundii genospecies 1 and 2 ribotypes.

Authors:  Michael F Cole; Mishell K Evans; Jennifer L Kirchherr; Michael J Sheridan; G H W Bowden
Journal:  Clin Diagn Lab Immunol       Date:  2004-05

7.  Effect of the environment on genotypic diversity of Actinomyces naeslundii and Streptococcus oralis in the oral biofilm.

Authors:  James S Paddick; Susan R Brailsford; Edwina A M Kidd; Steven C Gilbert; Douglas T Clark; Sharmin Alam; Zoe J Killick; David Beighton
Journal:  Appl Environ Microbiol       Date:  2003-11       Impact factor: 4.792

8.  Role of the C terminus in antigen P1 surface localization in Streptococcus mutans and two related cocci.

Authors:  M K Homonylo-McGavin; S F Lee
Journal:  J Bacteriol       Date:  1996-02       Impact factor: 3.490

9.  Application of MLST and pilus gene sequence comparisons to investigate the population structures of Actinomyces naeslundii and Actinomyces oris.

Authors:  Uta Henssge; Thuy Do; Steven C Gilbert; Steven Cox; Douglas Clark; Claes Wickström; A J M Ligtenberg; David R Radford; David Beighton
Journal:  PLoS One       Date:  2011-06-30       Impact factor: 3.240

10.  Emended description of Actinomyces naeslundii and descriptions of Actinomyces oris sp. nov. and Actinomyces johnsonii sp. nov., previously identified as Actinomyces naeslundii genospecies 1, 2 and WVA 963.

Authors:  Uta Henssge; Thuy Do; David R Radford; Steven C Gilbert; Douglas Clark; David Beighton
Journal:  Int J Syst Evol Microbiol       Date:  2009-03       Impact factor: 2.747

  10 in total

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