首页> 外文期刊>Journal of microbiology, immunology, and infection: Wei mian yu gan ran za zhi >In vitro activity of tigecycline against clinical isolates of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae, Serratia marcescens and Enterobacter cloacae.
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In vitro activity of tigecycline against clinical isolates of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae, Serratia marcescens and Enterobacter cloacae.

机译:替加环素对产生广谱β-内酰胺酶的肺炎克雷伯菌,粘质沙雷氏菌和阴沟肠杆菌临床分离株的体外活性。

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BACKGROUND AND PURPOSE: Strains of extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae have spread widely in Taiwan hospitals. In this study, we evaluated the in vitro antimicrobial activity of tigecycline against ESBL-producing Enterobacteriaceae, including Klebsiella pneumoniae, Serratia marcescens and Enterobacter cloacae. METHODS: 104 confirmed ESBL-producing bacteria were isolated from 4 hospitals in mid- and southern Taiwan between 2000 and 2006. The in vitro activity of tigecycline against these ESBL producers was tested by use of Etest strips. RESULTS: The minimal tigecycline concentration at which 50% of isolates were inhibited and minimal concentration at which 90% of isolates were inhibited for ESBL-producing isolates ranged from 0.38 to 0.75 microg/mL and 0.5 to 1.5 microg/mL, respectively. CONCLUSIONS: Tigecycline, a new semisynthetic glycylcycline, may be considered an alternative drug of choice for patients infected with ESBL-producing bacteria.
机译:背景与目的:产超光谱β-内酰胺酶(ESBL)的肠杆菌科细菌已在台湾医院广泛传播。在这项研究中,我们评估了替加环素对产生ESBL的肠杆菌科细菌的体外抗菌活性,其中包括肺炎克雷伯菌,粘质沙雷氏菌和阴沟肠杆菌。方法:从2000年至2006年,从台湾中南部地区的4家医院中分离出104例确诊的ESBL产生细菌。使用Etest试纸条检测了替加环素对这些ESBL产生者的体外活性。结果:对于产生ESBL的分离物,抑制50%分离物的最小替加环素浓度和抑制90%分离物的最小浓度分别为0.38至0.75 microg / mL和0.5至1.5 microg / mL。结论:替吉环素是一种新型的半合成的糖基环素,可以被感染ESBL的细菌患者替代治疗。

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