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Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
MLSB-Resistant Staphylococcus aureus in Central Greece: Rate of Resistance and Molecular Characterization
Stela Sarrou1, Ergina Malli1, Katerina Tsilipounidaki1
11 Department of Microbiology, University Hospital of Larissa, Larissa, Greece.
Abstract:
The aim of the present study was to determine the rate and mechanisms of resistance to macrolides, lincosamides, and streptogramin B (MLSB) antibiotics of Staphylococcus aureus collected in Central Greece. Of the 2,893 S. aureus collected during 2012-2017, 1,161 isolates (40.2%) exhibited resistance to at least one of the MLSB agents. The rate of erythromycin resistance was statistically significantly higher in methicillin-resistant S. aureus (MRSA) (58.6%) than in methicillin-sensitive S. aureus (MSSA) isolates (20.7%) (p = 0.002). Two hundred seventy-five representative MLSB-resistant S. aureus, including 81 MSSA and 194 MRSA isolates, were further studied. Thirty-eight MSSA isolates carried ermC, 26 MSSA were positive for ermA, whereas 17 isolates carried msrA gene. Among MRSA, the ermA gene was identified in the majority of the isolates (n = 153). Thirty-seven MRSA isolates carried ermC; three isolates carried msrA, whereas the remaining MRSA was positive for two genes (ermA and ermC). Phylogenetic analysis showed that ST225, which belongs to CC5, was the most prevalent, accounting for 137 MRSA isolates. Higher genetic diversity was found in the group of MSSA isolates, which comprised of 13 sequence types. Whole-genome sequencing data showed that all ermA-positive S. aureus, with the exception of one ST398 isolate, harbored the ermA-carrying Tn554 transposon integrated into their chromosomes. Furthermore, Illumina sequencing followed by polymerase chain reaction screening identified that ermC, which was identified in a polyclonal population of MSSA and MRSA isolates, was carried by small plasmids, like pNE131. These findings highlighted the important role of high-risk clones and of mobile elements carrying resistance genes in the successful dissemination of MLSB-resistant staphylococci.
Insights
Over 40% of Staphylococcus aureus isolates in Central Greece showed resistance to macrolides, lincosamides, and streptogramin B (MLSB) antibiotics. Resistance mechanisms involved ermA, ermC, and msrA genes, often on mobile genetic elements, highlighting the spread of resistant strains.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Macrolides, lincosamides, and streptogramin B (MLSB) antibiotics are crucial for treating Staphylococcus aureus infections.
- Understanding antibiotic resistance mechanisms in S. aureus is vital for effective treatment strategies.
Purpose of the Study:
- To determine the prevalence and genetic mechanisms of MLSB resistance in S. aureus from Central Greece.
- To investigate the role of specific resistance genes and mobile genetic elements in MLSB resistance.
Main Methods:
- Analysis of 2,893 S. aureus isolates collected between 2012-2017.
- Phenotypic detection of MLSB resistance and genotypic identification of resistance genes (ermA, ermC, msrA).
- Phylogenetic analysis and whole-genome sequencing of representative resistant isolates.
Main Results:
- 40.2% of S. aureus isolates were resistant to at least one MLSB agent.
- Erythromycin resistance was significantly higher in MRSA (58.6%) than MSSA (20.7%).
- Key resistance genes identified were ermA (predominant in MRSA), ermC, and msrA, often associated with Tn554 transposon or plasmids.
Conclusions:
- High rates of MLSB resistance in S. aureus are driven by specific resistance genes and mobile genetic elements.
- High-risk clones like ST225 (CC5) and mobile elements contribute significantly to the dissemination of MLSB-resistant S. aureus.
- Effective antibiotic stewardship and surveillance are crucial to combat the spread of resistant S. aureus strains.
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