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Susceptibility Profile ofStaphylococcus epidermidisandStaphylococcus haemolyticusIsolated from Blood Cultures to Vancomycin and Novel Antimicrobial Drugs over a Period of 12 Years
- Source :
- Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP
- Publication Year :
- 2016
- Publisher :
- Mary Ann Liebert Inc, 2016.
-
Abstract
- Made available in DSpace on 2018-12-11T17:03:21Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-06-01 The aim of this study was to evaluate the antimicrobial susceptibility profile of 85 Staphylococcus epidermidis and 84 Staphylococcus haemolyticus strains isolated from blood cultures to oxacillin, vancomycin, tigecycline, linezolid, daptomycin, and quinupristin/dalfopristin over a period of 12 years. S. epidermidis and S. haemolyticus isolated from blood cultures of inpatients, attended at a teaching hospital, were analyzed for the presence of the mecA gene and by SCCmec typing. The minimum inhibitory concentration (MIC) values of tigecycline, linezolid, daptomycin, quinupristin/dalfopristin, and vancomycin were determined. Isolates exhibiting vancomycin MICs of ≥2 μg/ml were typed by pulsed-field gel electrophoresis (PFGE). The rate of mecA positivity was 92.9% and 100% in S. epidermidis and S. haemolyticus, respectively. The most frequent SCCmec types were type III (53.2%) in S. epidermidis and type I (32.1%) in S. haemolyticus. All isolates were susceptible to linezolid and daptomycin, but 7.1% of S. haemolyticus and 2.3% of S. epidermidis isolates were resistant to tigecycline, and 1.2% each of S. haemolyticus and S. epidermidis were resistant and intermediately resistant to quinupristin/dalfopristin, respectively. S. epidermidis exhibited higher vancomycin MICs (40% with MIC of ≥2 μg/ml). Clonal typing of strains with vancomycin MIC of ≥2 μg/ml revealed the presence of different PFGE types of S. epidermidis and S. haemolyticus over a period of up to 4 years (2002-2004, 2005-2008, 2006-2009, 2010-2011). Despite the observation of a high prevalence of mecA, the clinical strains were fully susceptible to vancomycin and to the new drugs linezolid, daptomycin, tigecycline, and quinupristin/dalfopristin. The PFGE types with vancomycin MIC of ≥2 μg/ml exhibited a great diversity of SCCmec cassettes, demonstrating that S. epidermidis and S. haemolyticus may easily acquire these resistance-conferring genetic elements. Departamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Distrito de Rubião Jr. s/n Nucleo de Doencas Entericas e Infeccoes Por Patogenos Especiais Centro de Bacteriologia Instituto Adolfo Lutz São Paulo Departamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Distrito de Rubião Jr. s/n
- Subjects :
- 0301 basic medicine
medicine.medical_treatment
Gene Expression
Dalfopristin
Minocycline
Tigecycline
Virginiamycin
chemistry.chemical_compound
Staphylococcus epidermidis
Drug Resistance, Multiple, Bacterial
Prevalence
polycyclic compounds
Oxacillin
biology
Staphylococcal Infections
Anti-Bacterial Agents
Bacterial Typing Techniques
Electrophoresis, Gel, Pulsed-Field
Staphylococcus haemolyticus
Vancomycin
Brazil
medicine.drug
Microbiology (medical)
030106 microbiology
Immunology
Microbiology
03 medical and health sciences
Bacterial Proteins
Daptomycin
medicine
Humans
Hospitals, Teaching
Pharmacology
Quinupristin
SCCmec
Linezolid
biochemical phenomena, metabolism, and nutrition
bacterial infections and mycoses
biology.organism_classification
030104 developmental biology
chemistry
Blood Culture
Mutation
bacteria
Subjects
Details
- ISSN :
- 19318448 and 10766294
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Microbial Drug Resistance
- Accession number :
- edsair.doi.dedup.....6829878353b16f85415763305b5162f2
- Full Text :
- https://doi.org/10.1089/mdr.2015.0064