Lack of serotype antigen in A. actinomycetemcomitans

J Dent Res. 2010 Mar;89(3):292-6. doi: 10.1177/0022034509358865. Epub 2010 Feb 5.

Abstract

Aggregatibacter actinomycetemcomitans is divided into 6 serotypes. Occurrence of non-serotypeable strains is known, but background reasons are unclear. We hypothesized that non-serotypeable strains represent new serotypes or have altered expression of serotype-specific polysaccharide antigen (S-PA). We first characterized 311 strains from 189 individuals using both immunoassay- and PCR-based serotyping. Next, using natural human infection and rabbit immunization approaches, we clarified whether the phenotypically non-serotypeable strains expressed S-PA. Immunoassay identified serotypes a-f among 216 strains from 159 individuals. The remaining 95 strains from 30 individuals were phenotypically non-serotypeable. Yet, all these strains were identified by PCR-typing as serotype a-, b-, c-, or f. Non-serotypeability was confirmed by Western immunoblot with respective rabbit antisera. Patient sera remained non-reactive with autologous non-serotypeable strains at the serotype-specific region. Rabbit immunization with a phenotypically non-serotypeable strain induced no antibody production against S-PA. Thus, phenotypically non-serotypeable strains did not include novel serotypes, but lacked S-PA expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggregatibacter actinomycetemcomitans / classification*
  • Aggregatibacter actinomycetemcomitans / metabolism
  • Antigens, Bacterial / analysis
  • Antigens, Bacterial / classification
  • Antigens, Bacterial / metabolism*
  • Case-Control Studies
  • Chi-Square Distribution
  • Humans
  • Lipopolysaccharides / classification*
  • Lipopolysaccharides / metabolism
  • O Antigens / classification
  • O Antigens / metabolism
  • Periodontitis / microbiology*
  • Polysaccharides, Bacterial / analysis
  • Polysaccharides, Bacterial / classification
  • Polysaccharides, Bacterial / metabolism*
  • Serotyping / methods*
  • Species Specificity

Substances

  • Antigens, Bacterial
  • Lipopolysaccharides
  • O Antigens
  • Polysaccharides, Bacterial