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Updated: Jun 11, 2025

Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
Molecular diversity in fusidic acid-resistant Methicillin Susceptible Staphylococcus aureus
Dalida Bivona1, Emanuele Nicitra1, Carmelo Bonomo1
1Department of Biomedical and Biotechnological Sciences, Medical Molecular Microbiology and Antibiotic Resistance Laboratory (MMARLab), University of Catania, 95123 Catania, Italy.
Objectives:
The recent emergence of fusidic acid (FA)-resistant Staphylococcus aureus has underscored the importance of active surveillance in isolating these strains. The molecular basis of fusidic acid resistance and the carriage of virulence factors in four borderline oxacillin-resistant Staphylococcus aureus (BORSA) clinical strains was assessed through phenotypical and genotypical methods.
Methods:
All S. aureus clinical strains were obtained from various hospital units in Sicily. In vitro antibiotic susceptibility testing was conducted. WGS was performed using the Illumina MiSeq Platform, and data analysis was carried out to determine ST, resistome and virulome profiles.
Results:
Genotypic characterization revealed that the strains belong to four STs: ST630, ST8, ST15, and ST1. FA resistance was associated with mutations in the fusA gene or fusB and fusC genes. Additionally, one case exhibited resistance to mupirocin, related to the presence of the mupA gene. Borderline MIC values were observed for cefoxitin in three out of four cases, leading to their categorization as BORSA. Virulence gene content was complex and diversified, with one testing positive for the lukS/F genes, coding for PVL toxin.
Conclusions:
Resistance to FA is multifactorial, involving point mutations in chromosomal genes or association with mobile genetic elements. Monitoring the resistance to these antibiotics might help to manage and eradicate mupirocin- and FA-resistant S. aureus strains, which are also known to be important carriers of virulence determinants.
Insights
Fusidic acid resistance in Staphylococcus aureus is multifactorial, linked to gene mutations or mobile elements. Surveillance of resistant strains, including BORSA, is crucial for managing infections and understanding virulence factors.
Area of Science:
- Microbiology
- Molecular Biology
- Infectious Diseases
Background:
- Emergence of fusidic acid-resistant Staphylococcus aureus necessitates active surveillance.
- Understanding the genetic basis of resistance and virulence in clinical strains is critical.
Purpose of the Study:
- To investigate the molecular mechanisms of fusidic acid resistance.
- To characterize virulence factors in borderline oxacillin-resistant Staphylococcus aureus (BORSA) clinical isolates.
Main Methods:
- Phenotypic and genotypic methods were employed.
- Whole genome sequencing (WGS) was performed on clinical S. aureus strains.
- Antibiotic susceptibility testing and analysis of resistome and virulome profiles were conducted.
Main Results:
- Four distinct sequence types (STs) were identified: ST630, ST8, ST15, and ST1.
- Fusidic acid resistance was associated with mutations in fusA, fusB, or fusC genes.
- One strain showed mupirocin resistance due to the mupA gene; three strains were classified as BORSA.
- Complex virulence gene content was observed, including the PVL toxin gene (lukS/F).
Conclusions:
- Fusidic acid resistance in S. aureus is multifactorial, involving chromosomal mutations or mobile genetic elements.
- Monitoring antibiotic resistance is key to managing and eradicating resistant S. aureus strains.
- Resistant S. aureus strains can act as significant carriers of virulence determinants.
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