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Updated: Jun 24, 2026

Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
StaphVar-DNA microarray analysis of accessory genome elements of community-acquired methicillin-resistant
F El Garch1, M Hallin, R De Mendonça
1Université Libre de Bruxelles, Hôpital Erasme, Belgium.
Objectives:
Approximately 75% of the genome of Staphylococcus aureus (the 'core' genome) is highly conserved between strains, whereas the remaining 25% (the 'accessory' genome) is composed of mobile genetic elements (MGEs), containing virulence and resistance genes. We developed a composite microarray focused on resistance and virulence genes located on the accessory or core-variable genome to characterize a collection of Belgian community-acquired methicillin-resistant S. aureus (CA-MRSA) strains.
Methods:
Oligonucleotide probes targeting 403 genes encoding antimicrobial resistance (35%), virulence (28%) and adhesion (31%) factors were designed among eight S. aureus sequenced genomes. The StaphVar Array was validated by testing five of the strains used for the design and utilized to characterize 13 CA-MRSA strains representative of the multilocus sequence typing (MLST) sequence types circulating in Belgium.
Results:
Analysis of the gene content of the five reference strains by the StaphVar Array matched 90% to 97% of the theoretical results. Analysis of CA-MRSA strains showed that 54.4% of the genes tested were strain-dependent. Strains presented specific exotoxin, enterotoxin, cytolysin and adhesin gene profiles by MLST lineage. One exception to these 'lineage-specific' profiles was the variable presence of the arginine catabolic mobile element (characteristic of the USA300 clone) within ST8 strains.
Conclusions:
The StaphVar Array enables the characterization of approximately 400 variable resistance and virulence determinants in S. aureus. CA-MRSA strains displayed extensive diversity in virulence and resistance profiles. The presence of the USA300 clone in Belgium was confirmed. Although mainly located on MGEs, associations of virulence genes were highly conserved within strains of the same MLST lineage.
Insights
A new microarray, StaphVar Array, effectively characterizes virulence and resistance genes in Staphylococcus aureus strains. Belgian community-acquired MRSA strains show significant genetic diversity, with some profiles linked to specific lineages.
Area of Science:
- Microbiology
- Genomics
- Molecular Epidemiology
Background:
- Staphylococcus aureus harbors a core genome and an accessory genome containing mobile genetic elements (MGEs).
- MGEs are crucial for the dissemination of virulence and antimicrobial resistance genes in S. aureus.
- Community-acquired methicillin-resistant S. aureus (CA-MRSA) presents a significant public health challenge.
Purpose of the Study:
- To develop and validate a composite microarray, the StaphVar Array, for characterizing variable resistance and virulence genes in S. aureus.
- To analyze the genetic profiles of Belgian CA-MRSA strains using the developed microarray.
Main Methods:
- Design of oligonucleotide probes targeting 403 genes (antimicrobial resistance, virulence, adhesion) from eight S. aureus genomes.
- Validation of the StaphVar Array using reference strains.
- Characterization of 13 Belgian CA-MRSA strains representing diverse multilocus sequence typing (MLST) lineages.
Main Results:
- The StaphVar Array demonstrated high accuracy (90-97%) in analyzing reference strains.
- Significant strain-dependent gene content variation (54.4%) was observed in CA-MRSA strains.
- Distinct exotoxin, enterotoxin, cytolysin, and adhesin gene profiles were associated with specific MLST lineages, with the USA300 arginine catabolic mobile element as a notable exception.
Conclusions:
- The StaphVar Array is a valuable tool for profiling approximately 400 variable determinants in S. aureus.
- Belgian CA-MRSA strains exhibit substantial diversity in virulence and resistance gene content.
- The study confirmed the presence of the USA300 clone in Belgium and highlighted conserved virulence gene associations within MLST lineages.
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