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耐甲氧西林金黄色葡萄球菌和耐万古霉素肠球菌菌株对利奈唑胺的体外敏感性

[In vitro susceptibility to linezolid in methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus strains].

作者信息

Efe Sirin, Sinirtaş Melda, Ozakin Cüneyt

机构信息

Ozel Bahar Hastanesi, Enfeksiyon Hastaliklari ve Klinik Mikrobiyoloji, Bursa.

出版信息

Mikrobiyol Bul. 2009 Oct;43(4):639-43.

PMID:20084917
Abstract

There has been a dramatic increase in the number of infections caused by methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) worldwide. Linezolid which is one of the first oxazolidinones in clinical use, has bacteriostatic activity on gram-positive bacteria including MRSA and VRE. The aim of this study was to investigate the in vitro susceptibilities of MRSA and VRE clinical isolates to linezolid. A total of 100 MRSA strains isolated from clinical specimens as infectious agents (96 blood, 2 pleural fluid, 1 peritoneal fluid, 1 joint fluid isolates), and 101 VRE (Enterococcus faecium) strains isolated from clinical specimens as colonizing or infectious agents (79 rectal swabs, 11 blood, 3 catheter, 3 peritoneal fluid, 3 urine, 2 wound isolates) in Microbiology Laboratory of Uludag University Medical Faculty Hospital, Turkey, were included to the study. In vitro linezolid activity has been searched by E-test method and all of the isolates were found susceptible to linezolid. Linezolid minimal inhibitory concentration (MIC) ranged for MRSA and VRE between 0.25-3 microg/mL and 0.25-2 microg/mL, respectively. Linezolid MIC50 and MIC90 values for MRSA were 1.5 microg/mL and 2 microg/mL, respectively, while for VRE these values were 0.75 microg/mL and 1.5 microg/mL, respectively. Our results were in parallel with the data of other national and international studies, emphasizing that linezolid is a new and effective choice in treatment of infections caused by resistant gram-positive bacteria.

摘要

全球耐甲氧西林金黄色葡萄球菌(MRSA)和耐万古霉素肠球菌(VRE)引起的感染数量急剧增加。利奈唑胺是临床使用的首批恶唑烷酮类药物之一,对包括MRSA和VRE在内的革兰氏阳性菌具有抑菌活性。本研究的目的是调查MRSA和VRE临床分离株对利奈唑胺的体外敏感性。土耳其乌鲁达大学医学院医院微生物实验室纳入了100株从临床标本中分离出的作为感染病原体的MRSA菌株(96株血液、2株胸水、1株腹水、1株关节液分离株),以及101株从临床标本中分离出的作为定植或感染病原体的VRE(粪肠球菌)菌株(79株直肠拭子、11株血液、3株导管、3株腹水、3株尿液、2株伤口分离株)。通过E-test法检测利奈唑胺的体外活性,发现所有分离株对利奈唑胺敏感。MRSA和VRE的利奈唑胺最低抑菌浓度(MIC)范围分别为0.25 - 3μg/mL和0.25 - 2μg/mL。MRSA的利奈唑胺MIC50和MIC90值分别为1.5μg/mL和2μg/mL,而VRE的这些值分别为0.75μg/mL和1.5μg/mL。我们的结果与其他国内和国际研究的数据一致,强调利奈唑胺是治疗耐甲氧西林革兰氏阳性菌引起的感染的一种新的有效选择。

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