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Phenotypic variation of clinical Serratia marcescens isolates repeatedly recovered from individual patients

W H Traub1, A Eiden, B Leonhard

  • 1Institut für Medizinische Mikrobiologie und Hygiene, Universität des Saarlandes, Homburg/Saar, Germany.

Zentralblatt Fur Bakteriologie : International Journal of Medical Microbiology
|June 1, 1996
PubMed

Insights

Pulsed-field gel electrophoresis (PFGE) is superior for tracking Serratia marcescens infections compared to phenotypic methods. PFGE accurately identifies genotypic variations in bacterial strains during long-term patient infections.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genetics

Background:

  • Serratia marcescens infections can exhibit phenotypic variation over time.
  • Traditional methods like bacteriocin susceptibility, carbon source assimilation, and serotyping have limitations in accurately characterizing strain diversity.
  • Long-term infections present challenges in distinguishing between strain evolution and new infections.

Purpose of the Study:

  • To compare the discriminatory power of Pulsed-field gel electrophoresis (PFGE) with traditional phenotypic methods for analyzing Serratia marcescens isolates.
  • To investigate genotypic and phenotypic diversity of S. marcescens in patients with prolonged infections.
  • To determine the most reliable method for tracking S. marcescens strain evolution and superinfections.

Main Methods:

  • Phenotypic characterization of 129 Serratia marcescens isolates from 50 patients using bacteriocin susceptibility, carbon source assimilation, and serotyping.
  • Genomic DNA analysis of 81 selected isolates from 30 patients using PFGE with XbaI and SpeI restriction enzymes.
  • Comparative analysis of results obtained from phenotypic methods and PFGE.

Main Results:

  • PFGE analysis demonstrated genotypic identity in isolates from 22 patients, close relatedness in 3, and possible relatedness in 1.
  • Phenotypic methods revealed variations in bacteriocin susceptibility, biochemical profiles, and serotypes, but were less discriminatory than PFGE.
  • One patient was infected with two genotypically distinct S. marcescens strains exhibiting identical serotypes but different bacteriocin types and biochemical profiles.
  • PFGE identified genotypic variations missed by phenotypic methods, including superinfections and strain evolution.

Conclusions:

  • PFGE is a superior method for analyzing genotypic relatedness of Serratia marcescens isolates compared to phenotypic methods.
  • Serotyping is more reliable than bacteriocin typing, which is less reliable than biochemical profiling for detecting phenotypic variants.
  • PFGE is crucial for accurately identifying distinct strains and understanding the dynamics of S. marcescens infections in patients.

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