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Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
Biotyping coagulase-negative staphylococci
G A Hébert1, R C Cooksey, N C Clark
1Hospital Infections Program, Centers for Disease Control, Atlanta, Georgia 30333.
Journal of Clinical Microbiology
|October 1, 1988
Summary
This study defines coagulase-negative staphylococci biotypes using biochemical profiles, adherence, and hemolysis tests. Biotyping helps assess the clinical significance of these common bacteria, aiding in infection control.
Area of Science:
- Clinical Microbiology
- Bacteriology
- Molecular Typing
Background:
- Coagulase-negative staphylococci (CoNS) are significant opportunistic pathogens.
- Accurate biotyping is crucial for understanding CoNS pathogenicity and clinical relevance.
- Current methods may not fully differentiate CoNS species and strains.
Purpose of the Study:
- To establish a biotyping scheme for 1,064 clinical isolates of eight CoNS species.
- To evaluate the utility of biochemical profiles, adherence, and synergistic hemolysis tests for CoNS biotyping.
- To correlate biotyping results with antimicrobial susceptibility and plasmid profiles for Staphylococcus epidermidis.
Main Methods:
- Utilized Staph-Ident panels for biochemical profiling.
- Incorporated adherence and synergistic hemolysis assays.
- Analyzed antimicrobial susceptibility and plasmid profiles for selected S. epidermidis clusters.
Main Results:
- Defined 69 biotypes among 672 Staphylococcus epidermidis isolates.
- Other CoNS species exhibited fewer biotypes due to more uniform test results.
- Biotyping, antimicrobial, and plasmid profiles showed varying discriminatory power across S. epidermidis clusters.
Conclusions:
- Biochemical profiles combined with adherence and hemolysis tests provide a robust biotyping scheme for CoNS.
- Adherence and synergistic hemolysis may serve as indices for clinical significance.
- Integrated typing methods (biochemical, antimicrobial, plasmid) offer complementary insights into CoNS epidemiology and pathogenicity.
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