Phenotypic Characterization of Macrolide-Lincosamide-Streptogramin B Resistance in Staphylococcus aureus

被引:1
|
作者
Modukuru, Giridhar Kumar [1 ]
Surya, Pradeep Madala Sobhana [1 ]
Kakumanu, Vishnuvardhana Rao [1 ]
Yarava, Saritha [1 ]
机构
[1] Dr Pinnamaneni Siddhartha Inst Med Sci & Res Fdn, Dept Microbiol, Krishna 521286, Andhra Pradesh, India
关键词
Staphylococcus aureus; MRSA; MSSA; D-test; inducible clindamycin resistance; MLSB phenotypes; INDUCIBLE CLINDAMYCIN RESISTANCE; PREVALENCE; ANTIBIOTICS; COMMUNITY;
D O I
10.22207/JPAM.15.2.18
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Staphylococcus aureus (S.aureus) is a prevalent organism causing infections in the community and hospital. A variety of antibiotics are used, including the Macrolide-Lincosamide-StreptograminB (MLSB) family of antibiotics in which clindamycin is the preferred agent. Widespread use of these antibiotics leads to resistance to these MLSB antibiotics; a D-test can characterize the different MLSB phenotypes. This study was taken up with an objective to perform a double disc diffusion test for detecting different phenotypes in S.aureus with particular reference to inducible clindamycin resistance. Out of a total of 174(100%) strains of S.aureus, 98(56.32%) were MRSA, and 76(43.68%) were MSSA. All isolates were tested by D-test. A total of 47(27.01%) were of cMLSB phenotype, 31(17.82%) were of iMLSB phenotype, and 96(55.17%) were of MS phenotype. The majority of MRSA strains were cMLSB phenotype(76.60%) and iMLSB phenotype (64.52%) in comparison to MSSA isolates. Although iMLSB phenotypes are present in both MRSA and MSSA, iMLSB was more in MRSA isolates. Appropriate susceptibility data is essential for a clinician to start clindamycin therapy to prevent therapeutic failures with inducible MLSB resistance in S.aureus isolates. It will be appropriate for all the clinical laboratories to report inducible Clindamycin resistance in S.aureus strains (both MRSA and MSSA), for which D-test is a reliable testing method.
引用
收藏
页码:689 / 694
页数:6
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