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Published on: November 4, 2016
Comparison of fingerprinting methods for typing methicillin-resistant Staphylococcus aureus sequence type 398
G Rasschaert1, W Vanderhaeghen, I Dewaele
1Institute for Agricultural and Fisheries Research (ILVO), Technology and Food Science Unit, Brusselsesteenweg 370, 9090 Melle, Belgium. geertrui.rasschaert@ilvo.vlaanderen.be
This study compared multiple-locus variable-number tandem-repeat assay (MLVA) and pulsed-field gel electrophoresis (PFGE) for typing methicillin-resistant Staphylococcus aureus (MRSA) ST398. PFGE demonstrated superior discriminatory power for MRSA ST398 fingerprinting.
Area of Science:
- Microbiology
- Molecular Biology
- Epidemiology
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) sequence type 398 (ST398) is a significant pathogen.
- Accurate molecular typing methods are crucial for tracking MRSA ST398 outbreaks.
- Previous characterization included multilocus sequence typing, spa typing, and SCCmec typing.
Purpose of the Study:
- To evaluate the performance of MLVA and PFGE for fingerprinting MRSA ST398 isolates.
- To compare the typeability, discriminatory power, and concordance of MLVA and PFGE with existing typing methods.
- To determine the optimal method for MRSA ST398 strain differentiation.
Main Methods:
- Fingerprinting of MRSA ST398 isolates using MLVA.
- PFGE analysis with restriction enzymes BstZI, SacII, and ApaI.
- Comparison of MLVA and PFGE results with multilocus sequence typing, spa typing, and SCCmec typing data.
Main Results:
- Both MLVA and PFGE successfully typed all MRSA ST398 isolates.
- PFGE exhibited the highest discriminatory power, followed by MLVA, spa typing, and SCCmec typing.
- High concordance was observed between MLVA and PFGE (ApaI), and MLVA and spa typing.
Conclusions:
- Both MLVA and PFGE are effective for discriminating MRSA ST398 isolates.
- PFGE offers greater discriminatory power, particularly when using multiple restriction enzymes.
- MLVA is a faster alternative, while PFGE provides more detailed strain differentiation for MRSA ST398.
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