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Phenotypic variation of Staphylococcus epidermidis slime production in vitro and in vivo

G D Christensen1, L M Baddour, W A Simpson

  • 1Veterans Administration Medical Center, Memphis, Tennessee 38104.

Infection and Immunity
|December 1, 1987
PubMed

Insights

Slime production in Staphylococcus epidermidis is linked to medical device infections. A non-adherent strain showed reduced infectivity, suggesting slime

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Biotechnology

Background:

  • Coagulase-negative staphylococci, particularly Staphylococcus epidermidis, are significant pathogens associated with indwelling medical device infections.
  • Slime production, an extracellular polysaccharide matrix, is a key virulence factor in these staphylococcal infections.
  • Understanding the role of slime and bacterial adherence is crucial for developing strategies to prevent and treat device-related infections.

Purpose of the Study:

  • To investigate the role of slime production and bacterial adherence in the pathogenesis of Staphylococcus epidermidis infections.
  • To compare the infectivity of slime-producing and non-slime-producing strains in animal models of foreign body infection and infective endocarditis.

Main Methods:

  • Isolation of distinct Staphylococcus epidermidis strains with varying adherence and slime production capabilities (RP62A, RP62A-NA, RP62A-NAR) through serial centrifugation and subculture.
  • Characterization of strains using biochemical tests, antimicrobial susceptibility, plasmid analysis, and transmission electron microscopy with Alcian blue staining.
  • Evaluation of infectivity in a mouse foreign body infection model and a rat catheter-induced infective endocarditis model.

Main Results:

  • Adherent, slime-producing strains (RP62A, RP62A-NAR) exhibited an extracellular coat of polysaccharide material, while the non-adherent strain (RP62A-NA) lacked this coat.
  • In both animal models, the non-adherent, non-slime-producing strain (RP62A-NA) demonstrated significantly lower infectivity (threefold greater 50% infective dose) compared to the slime-producing strain (RP62A).
  • Bacterial adherence characteristics showed some variation in vivo, but the general trend of reduced infectivity for the non-adherent strain was consistent.

Conclusions:

  • The phenotypic expression of slime production in Staphylococcus epidermidis is variable both in vitro and in vivo.
  • Reduced bacterial adherence and lack of slime production significantly decrease the infectivity of Staphylococcus epidermidis in foreign body infection and infective endocarditis models.
  • Slime production is a critical factor in the pathogenesis of staphylococcal infections associated with indwelling medical devices.

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