Literature DB >> 3882766

Actinobacillus actinomycetemcomitans in human periodontal disease.

J J Zambon.   

Abstract

Recent evidence implicates Actinobacillus actinomycetemcomitans in the etiology of localized juvenile periodontitis. This paper reviews the morphological, biochemical and serological charcteristics of A. actinomycetemcomitans, evidence incriminating it as a periodontopathogen, its importance in human nonoral infections, and virulence factors which may be involved in the pathogenesis of A. actinomycetemcomitans infections. A. actinomycetemcomitans is a non-motile, gram-negative, capnophilic, fermentative coccobacillus which closely resembles several Haemophilus species but which does not require X or V growth factors. The organism has been categorized into 10 biotypes based on the variable fermentation of dextrin, maltose, mannitol, and xylose and into 3 serotypes on the basis of heat stable, cell surface antigens. A. actinomycetemcomitans' primary human ecologic niche is the oral cavity. It is found in dental plaque, in periodontal pockets, and buccal mucosa in up to 36% of the normal population. The organism can apparently seed from these sites to cause severe infections throughout the human body such as brain abscesses and endocarditis. There is a large body of evidence which implicates A. actinomycetemcomitans as an important micro-organism in the etiology of localized juvenile periodontitis including: (1) an increased prevalence of the organism in almost all localized juvenile periodontitis patients and their families compared to other patient groups; (2) the observation that localized juvenile periodontitis patients exhibit elevated antibody levels to A. actinomycetemcomitans in serum, saliva and gingival crevicular fluid; (3) the finding that localized juvenile periodontitis can be successfully treated by eliminating A. actinomycetemcomitans from periodontal pockets; (4) histopathologic investigations showing that A. actinomycetemcomitans invades the gingival connective tissue in localized juvenile periodontitis lesions; (5) the demonstration of several pathogenic products from A. actinomycetemcomitans including factors which may: (a) facilitate its adherence to mucosal surfaces such as capsular polysaccharides; (b) inhibit host defense mechanisms including leukotoxin, a polymorphonuclear leukocyte chemotaxis inhibiting factor, and a lymphocyte suppressing factor (c) cause tissue destruction such as lipopolysaccharide endotoxin, a bone resorption-inducing toxin, acid and alkaline phosphatases, collagenase, a fibroblast inhibiting factor and an epitheliotoxin.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3882766     DOI: 10.1111/j.1600-051x.1985.tb01348.x

Source DB:  PubMed          Journal:  J Clin Periodontol        ISSN: 0303-6979            Impact factor:   8.728


  233 in total

1.  Identification of genes coding for exported proteins of Actinobacillus actinomycetemcomitans.

Authors:  K P Mintz; P M Fives-Taylor
Journal:  Infect Immun       Date:  1999-11       Impact factor: 3.441

2.  Secretion of RTX leukotoxin by Actinobacillus actinomycetemcomitans.

Authors:  S C Kachlany; D H Fine; D H Figurski
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

3.  impA, a gene coding for an inner membrane protein, influences colonial morphology of Actinobacillus actinomycetemcomitans.

Authors:  K P Mintz; P M Fives-Taylor
Journal:  Infect Immun       Date:  2000-12       Impact factor: 3.441

4.  Nonspecific adherence by Actinobacillus actinomycetemcomitans requires genes widespread in bacteria and archaea.

Authors:  S C Kachlany; P J Planet; M K Bhattacharjee; E Kollia; R DeSalle; D H Fine; D H Figurski
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

5.  A novel factor isolated from Actinobacillus actinomycetemcomitans stimulates mouse B cells and human peripheral blood mononuclear cells.

Authors:  S J Jeong; S T Yee; W S Jo; S H Yu; S H Lee; Y J Lim; Y H Yoo; J M Kim; J D Lee; M H Jeong
Journal:  Infect Immun       Date:  2000-09       Impact factor: 3.441

6.  Population structure and genetic diversity of Actinobacillus actinomycetemcomitans strains isolated from localized juvenile periodontitis patients.

Authors:  Jeffrey B Kaplan; Helen C Schreiner; David Furgang; Daniel H Fine
Journal:  J Clin Microbiol       Date:  2002-04       Impact factor: 5.948

7.  Identification and molecular analysis of rough-colony-specific outer membrane proteins of Actinobacillus actinomycetemcomitans.

Authors:  E M Haase; J L Zmuda; F A Scannapieco
Journal:  Infect Immun       Date:  1999-06       Impact factor: 3.441

8.  Production of an interleukin-1 inhibitor by cell line P388D1 murine macrophages stimulated with Haemophilus actinomycetemcomitans lipopolysaccharide.

Authors:  T Nishihara; T Koga; S Hamada
Journal:  Infect Immun       Date:  1988-11       Impact factor: 3.441

9.  Tumor necrosis factor alpha enhances Actinobacillus actinomycetemcomitans leukotoxin-induced HL-60 cell apoptosis by stimulating lymphocyte function-associated antigen 1 expression.

Authors:  Noboru Yamaguchi; Chie Kubo; Yoshikazu Masuhiro; Edward T Lally; Toshihiko Koga; Shigemasa Hanazawa
Journal:  Infect Immun       Date:  2004-01       Impact factor: 3.441

10.  Genes involved in the synthesis and degradation of matrix polysaccharide in Actinobacillus actinomycetemcomitans and Actinobacillus pleuropneumoniae biofilms.

Authors:  Jeffrey B Kaplan; Kabilan Velliyagounder; Chandran Ragunath; Holger Rohde; Dietrich Mack; Johannes K-M Knobloch; Narayanan Ramasubbu
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

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