Journal
PATHOGENS
Volume 12, Issue 4, Pages -Publisher
MDPI
DOI: 10.3390/pathogens12040556
Keywords
mecC; mecA; MRSA; OS-CoNS; PCR; VITEK2
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Methicillin-resistant Staphylococci, primarily encoded by the mecA gene, is a significant public health concern. The mecC gene, a new mecA analog, is responsible for methicillin resistance in certain clinical Staphylococcal isolates, but its prevalence in Egypt is still underestimated. The aim of this study was to detect the mecA and mecC genes in clinical Staphylococci isolates from a tertiary care university hospital in Egypt, comparing different phenotypic methods.
Methicillin-resistant in Staphylococci is a serious public health issue. It is mostly encoded by the mecA gene. The mecC gene is a new mecA analog responsible for resistance to methicillin in some Staphylococcal clinical isolates. This mecC gene is still underestimated in Egypt. The aim of the current study was to detect mecA and mecC genes in clinical Staphylococci isolates from a tertiary care university hospital in Egypt compared to the different phenotypic methods. A total of 118 Staphylococcus aureus (S. aureus) and 43 coagulase-negative Staphylococci (CoNS) were identified from various hospital-acquired infections. Methicillin resistance was identified genotypically using the PCR technique and phenotypically using the cefoxitin disc diffusion test, oxacillin broth microdilution and the VITEK2 system in all Staphylococcal isolates. The mecA gene was detected in 82.2% of S. aureus and 95.3% of CoNS isolates, while all of the isolates tested negative for the mecC gene. Interestingly, 30.2% of CoNS isolates showed the unique character of inducible oxacillin resistance, being mecA-positive but oxacillin-susceptible (OS-CoNS). The dual use of genotypic and phenotypic methods is highly recommended to avoid missing any genetically divergent strains.
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