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Macrolide resistance genotypes and phenotypes among erythromycin-resistant clinical isolates ofStaphylococcus aureusand coagulase-negative staphylococci, Italy: Table 1
- Source :
- FEMS Immunology & Medical Microbiology. 55:62-67
- Publication Year :
- 2009
- Publisher :
- Oxford University Press (OUP), 2009.
-
Abstract
- One hundred macrolide-resistant staphylococcal isolates from clinically relevant infections in Italy during a 19-month period were studied. Four distinct resistance phenotypes were observed using the triple-disk induction test (erythromycin, clindamycin, telithromycin): the cMLS(B) phenotype (24 isolates); the iMLS(B) phenotype (41 isolates); the MS phenotype (three isolates); and the iMTS phenotype (erythromycin-induced telithromycin resistance) (32 isolates). ermC and ermA genes predominated within erythromycin-resistant Staphylococcus aureus isolates with iMLS(B) phenotype and cMLS(B) phenotype, respectively. Among erythromycin-resistant CoNS isolates, half of the strains showed the iMTS or MS/msrA association, and ermC gene predominated among isolates with MLS(B) phenotype. By pulsed-field gel electrophoresis, high genetic heterogeneity was observed among the isolates studied. Both independent acquisition of macrolide resistance genes and spread of specific resistant clones were observed. Association between certain clonal types and specific types of infection could be detected. To our knowledge, this is the first report on characterization of erythromycin-resistant staphylococci in Italy.
- Subjects :
- Microbiology (medical)
medicine.drug_class
Immunology
Telithromycin
Clindamycin
Erythromycin
General Medicine
Biology
medicine.disease_cause
Microbiology
Virology
Macrolide Antibiotics
Infectious Diseases
Staphylococcus aureus
Genotype
medicine
Pulsed-field gel electrophoresis
Immunology and Allergy
Coagulase
medicine.drug
Subjects
Details
- ISSN :
- 1574695X and 09288244
- Volume :
- 55
- Database :
- OpenAIRE
- Journal :
- FEMS Immunology & Medical Microbiology
- Accession number :
- edsair.doi...........26e7bff2acc26dacb83808b8f77b6de3