کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3378179 1220068 2010 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Distribution of Genes Encoding Resistance to Macrolides, Lincosamides and Streptogramins Among Clinical Staphylococcal Isolates in a Turkish University Hospital
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
پیش نمایش صفحه اول مقاله
Distribution of Genes Encoding Resistance to Macrolides, Lincosamides and Streptogramins Among Clinical Staphylococcal Isolates in a Turkish University Hospital
چکیده انگلیسی

This study investigated the prevalence of genes encoding resistance to macrolides, lincosamides and strep-togramins (MLSB) among staphylococci in a series of 301 erythromycin-resistant clinical isolates of Staphylococcus aureus and coagulase-negative staphylococci (CoNS). Erythromycin-resistance phenotypes were determined according to Clinical and Laboratory Standards Institute guidelines and specific resistance genes erm(A), erm(B), erm(C), msr(A) and msr(B) were identified using polymerase chain reaction. Two hundred of 301 (66.5%) erythromycin-resistant staphylococcal isolates exhibited resistance to MLSB antibiotics. Of these, 127 (63.5%) exhibited a cMLSB resistance phenotype (resistant to both erythromycin and clindamycin), whereas 73 (36.5%) expressed the iMLSB resistance phenotype (resistant to erythromycin and susceptible to clindamycin). The most prevalent resistance determinants were erm(A) (62%) among S. aureus and erm(C) (30%) among CoNS isolates. Combinations of resistance mechanisms were rarely seen, and occurred most often in oxacillin-resistant isolates. The results of the present study support the idea that there are geographical differences in the prevalence of erythromycin resistance mechanisms among staphylococci, therefore local surveillance studies are important tools for guiding therapy and in the promotion of judicious use of antimicrobial agents.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Microbiology, Immunology and Infection - Volume 43, Issue 6, December 2010, Pages 524-529