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Characterisation of fluoroquinolone-resistant clinical isolates of Streptococcus pyogenes in Barcelona, Spain
Abstract:
Resistance mechanisms and clonal relationships were determined for six Streptococcus pyogenes isolates with low- or high-level ciprofloxacin resistance. Four isolates displayed reduced susceptibility to ciprofloxacin and levofloxacin and had alterations in ParC: Ser80-->Pro (isolate emm3.1); Ser79-->Ala (two isolates emm6.0); and a double substitution Ser79-->Phe and Ala121-->Val (isolate emm12.27). Two isolates (emm12.26) displayed high-level resistance to ciprofloxacin and levofloxacin, as well as to other quinolones. These isolates had the same double substitution in ParC as isolate emm12.27, and an additional substitution (Ser81-->Tyr) in GyrA. Resistance patterns, emm typing and sequencing of the quinolone resistance-determining regions defined two clusters containing three and two isolates, respectively.
Insights
Mechanisms of ciprofloxacin resistance in Streptococcus pyogenes involve mutations in ParC and GyrA proteins. These genetic changes correlate with reduced susceptibility and define distinct bacterial clonal groups.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Streptococcus pyogenes is a significant human pathogen.
- Understanding antibiotic resistance mechanisms is crucial for effective treatment.
- Quinolone resistance in S. pyogenes is an emerging concern.
Purpose of the Study:
- To investigate the molecular basis of ciprofloxacin resistance in Streptococcus pyogenes.
- To determine the clonal relationships among resistant isolates.
Main Methods:
- Susceptibility testing for ciprofloxacin and levofloxacin.
- Sequencing of quinolone resistance-determining regions (QRDRs) in ParC and GyrA.
- emm typing for clonal analysis.
Main Results:
- Four isolates showed reduced susceptibility due to specific ParC mutations (Ser80Pro, Ser79Ala, Ser79Phe/Ala121Val).
- Two isolates exhibited high-level resistance with combined ParC and GyrA mutations (Ser79Phe/Ala121Val and Ser81Tyr).
- emm typing and QRDR sequencing identified two distinct clusters of resistant isolates.
Conclusions:
- Mutations in ParC and GyrA are key mechanisms conferring quinolone resistance in S. pyogenes.
- Specific mutation profiles correlate with resistance levels and can be used for molecular epidemiology.
- The findings highlight the need for monitoring quinolone resistance in S. pyogenes.
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