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Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
Burden of Rifampicin- and Methicillin-Resistant Staphylococcus aureus in Italy
Dafne Bongiorno1, Gino Mongelli1, Stefania Stefani1
1Medical Molecular Microbiology and Antibiotic Resistance Laboratory (MMAR Lab), Department of Biomedical and Biotechnological Sciences (BIOMETEC), University of Catania , Catania, Italy .
Abstract:
Rifampicin is one of the major drugs used on its own and also in combination to treat numerous infections sustained by methicillin-resistant Staphylococcus aureus (MRSA). In Italy, rifampicin resistance (RIF-R) is increasing in multidrug-resistant-MRSA isolates (16.4%), with respect to Europe (5.7%). In our study, the relationship between clones, rpoB mutations, and susceptibility profiles in 50 RIF-R MRSA isolated from hospitalized patients was evaluated. Antimicrobial susceptibility testing was performed by the broth microdilution method. Isolates were typed by MLST/SCCmec/spa-typing. The rpoB gene was analyzed by PCR and sequence analysis. RIF-R isolates were 60% heterogeneous vancomycin-intermediate S. aureus (hVISA) and 22% daptomycin nonsusceptible and belonged to the major MRSA clones: ST228-SCCmec I (44%), ST8-SCCmec IV (18%), ST239-SCCmec III (16%), ST5-SCCmec II (14%), and ST22-SCCmec IVh (4%). Thirteen diverse RpoB amino acid substitutions were identified. Half of the strains harbored the H481N substitution, conferring low-level resistance. Different single mutations at the equivalent locus (H481D; H481Y) or in other loci, and multiple mutations conferred high-level resistance. In conclusion, this study investigated the nature of RIF-R in Italy among RIF-R-MRSA strains, finding a prevalence of ST228, strongly associated with reduced susceptibility to glycopeptides (hVISA). The spread of RIF-R strains in clinical settings represents a serious threat, due to their complex resistance nature even to new anti-Gram-positive drugs, making these infections particularly difficult to treat.
Insights
Rifampicin resistance in MRSA is rising in Italy, linked to specific bacterial clones and mutations. This complex resistance poses a significant challenge for treating infections, even with newer antibiotics.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) infections are a significant healthcare concern.
- Rifampicin is a key antibiotic for MRSA treatment, but rifampicin resistance (RIF-R) is increasing globally.
- Italy shows a higher prevalence of RIF-R in multidrug-resistant MRSA (16.4%) compared to Europe (5.7%).
Purpose of the Study:
- To investigate the relationship between bacterial clones, rpoB gene mutations, and antimicrobial susceptibility profiles in RIF-R MRSA isolates from hospitalized patients in Italy.
- To understand the genetic and phenotypic characteristics of RIF-R MRSA strains.
- To assess the clinical implications of RIF-R MRSA in a healthcare setting.
Main Methods:
- Antimicrobial susceptibility testing using broth microdilution.
- Bacterial isolate characterization via MLST, SCCmec, and spa-typing.
- Analysis of the rpoB gene through PCR and sequence analysis.
Main Results:
- RIF-R MRSA isolates exhibited high rates of heterogeneous vancomycin-intermediate S. aureus (hVISA) (60%) and daptomycin nonsusceptibility (22%).
- Dominant MRSA clones included ST228-SCCmec I (44%), ST8-SCCmec IV (18%), ST239-SCCmec III (16%), ST5-SCCmec II (14%), and ST22-SCCmec IVh (4%).
- Thirteen distinct RpoB amino acid substitutions were identified, with H481N being common for low-level resistance, while other single or multiple mutations conferred high-level resistance.
Conclusions:
- The study identified ST228 as a prevalent clone in Italy, strongly associated with reduced susceptibility to glycopeptides (hVISA).
- The increasing prevalence of RIF-R MRSA strains with complex resistance mechanisms poses a serious threat to patient treatment.
- These findings highlight the difficulty in treating infections caused by these multidrug-resistant strains, even with novel antibiotics.
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