Literature DB >> 10411260

Phenotypic variation in Actinobacillus actinomycetemcomitans during laboratory growth: implications for virulence.

D H Fine1, D Furgang, H C Schreiner, P Goncharoff, J Charlesworth, G Ghazwan, P Fitzgerald-Bocarsly, D H Figurski.   

Abstract

This study examined alteration of specific virulence traits associated with phenotypic changes seen when a low-passage disease-associated and well maintained parent strain of Actinobacillus actinomycetemcomitans was compared to a laboratory-grown spontaneous variant/mutant. Clinical isolates of A. actinomycetemcomitans recovered from periodontitis patients typically grow as rough, adherent colonies on primary culture but undergo transformation to smooth, non-adherent colonies following repeated passage in vitro. The relationship of these phenotypic changes to the virulence of the organism or to the processes that underlie this transformation are not understood. A fresh clinical isolate, designated strain CU1000, was obtained from the first molar site of a patient with classical signs of localized juvenile periodontitis and used as the parent strain to study virulence-related phenotypes. Following several passages of CU1000 on selective agar, a spontaneous variant that demonstrated smooth, opaque, non-adherent colonies was isolated and designated strain CU1060. This study compared the properties of these two strains with respect to colony morphology, autoaggregation, surface appendages, adherence to saliva-coated hydroxyapatite (SHA), LPS chemotype and activity, induction of fibroblast proteinase activity and antigenic properties. CU1000 demonstrated rough, raised, star-positive colonies which upon electron microscopic examination revealed the presence of large, flexible, bundled fibrils. In addition, CU1000 showed adherence to SHA, several unique protein antigens and elevated endotoxin and fibroblast proteinase activity. CU1060, on the other hand, showed minimal adherence to SHA and fewer reactive proteins compared to the fresh clinical isolates. This strain formed smooth, opaque colonies on agar, showed minimal fibril formation and limited endotoxin and fibroblast-proteinase-inducing activity. These findings demonstrate that clinical isolates of A. actinomycetemcomitans undergo significant virulence-reducing phenotypic alterations during in vitro passage and support the need to study this organism in its clinical form.

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Year:  1999        PMID: 10411260     DOI: 10.1099/13500872-145-6-1335

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  73 in total

1.  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

2.  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

3.  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

4.  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

5.  Detachment of Actinobacillus actinomycetemcomitans biofilm cells by an endogenous beta-hexosaminidase activity.

Authors:  Jeffrey B Kaplan; Chandran Ragunath; Narayanan Ramasubbu; Daniel H Fine
Journal:  J Bacteriol       Date:  2003-08       Impact factor: 3.490

Review 6.  Oral multispecies biofilm development and the key role of cell-cell distance.

Authors:  Paul E Kolenbrander; Robert J Palmer; Saravanan Periasamy; Nicholas S Jakubovics
Journal:  Nat Rev Microbiol       Date:  2010-07       Impact factor: 60.633

7.  Aggregatibacter actinomycetemcomitans leukotoxin cytotoxicity occurs through bilayer destabilization.

Authors:  Angela C Brown; Kathleen Boesze-Battaglia; Yurong Du; Frank P Stefano; Irene R Kieba; Raquel F Epand; Lazaros Kakalis; Philip L Yeagle; Richard M Epand; Edward T Lally
Journal:  Cell Microbiol       Date:  2012-03-28       Impact factor: 3.715

8.  TdeA, a TolC-like protein required for toxin and drug export in Aggregatibacter (Actinobacillus) actinomycetemcomitans.

Authors:  Juan A Crosby; Scott C Kachlany
Journal:  Gene       Date:  2006-10-17       Impact factor: 3.688

9.  Genetic analysis of the requirement for flp-2, tadV, and rcpB in Actinobacillus actinomycetemcomitans biofilm formation.

Authors:  B A Perez; P J Planet; S C Kachlany; M Tomich; D H Fine; D H Figurski
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

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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