Detection of a Novel G2603T Mutation in cfr Harboring Linezolid-Resistant Staphylococcus haemolyticus : First Report from India

被引:3
|
作者
Khodabux, Rhea Michelle J. [1 ]
Mariappan, Shanthi [1 ]
Sekar, Uma [1 ]
机构
[1] Sri Ramachandra Inst Higher Educ & Res SRIHER, Dept Microbiol, Chennai 600116, Tamil Nadu, India
关键词
linezolid resistance; cfr gene; 23S rRNA gene; Staphylococcus haemolyticus; COAGULASE-NEGATIVE STAPHYLOCOCCI; RIBOSOMAL-RNA GENE; CLONAL DISSEMINATION; G2576T MUTATION; MECHANISMS; EMERGENCE; ISOLATE;
D O I
10.1055/s-0042-1757419
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Staphylococcus haemolyticus has emerged as an important multidrug-resistant nosocomial pathogen. Linezolid is useful in the treatment of severe infections caused by methicillin-resistant Staphylococci . Resistance to linezolid in Staphylococci is due to one or more of the following mechanisms: acquisition of the cfr (chloramphenicol florfenicol resistance) gene, mutation in the central loop of domain V of the 23S rRNA, and mutation in the rplC and rplD genes. This study was carried out to detect and characterize resistance to linezolid among the clinical isolates of Staphylococcus haemolyticus . Materials and Methods The study included 84 clinical isolates of Staphylococcus haemolyticus . Susceptibility to various antibiotics was determined by disc diffusion method. Minimum inhibitory concentration (MIC) was determined by agar dilution method for linezolid. Methicillin resistance was screened using oxacillin and cefoxitin disc. Polymerase chain reaction was done to detect mecA, cfr and mutations in the V domain of the 23S rRNA gene. Results Resistance to linezolid was exhibited by 3 of the 84 study isolates with MIC more than 128 mu g/mL. The cfr gene was detected in all the three isolates. The G2603T mutation was observed in the domain V of the 23S rRNA among two isolates, whereas one isolate lacked any mutation. Conclusion The emergence and spread of linezolid-resistant Staphylococcus haemolyticus isolates carrying G2603T mutation in the domain V of the 23S rRNA and harboring the cfr gene pose a threat in clinical practice.
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页码:207 / 211
页数:5
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