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Diagnostic PCR Analysis of the Occurrence of Methicillin and Tetracycline Resistance Genes among Staphylococcus aureus Isolates from Phase 3 Clinical Trials of Tigecycline for Complicated Skin and Skin Structure Infections

机译:Tigecycline复杂皮肤和皮肤结构感染三期临床试验中金黄色葡萄球菌分离株中甲氧西林和四环素抗性基因的诊断PCR分析

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摘要

Diagnostic PCR assays were developed to track common genetic determinants of oxacillin resistance as well as resistance to classical tetracyclines in Staphylococcus aureus isolates from the recently completed worldwide phase 3 clinical trials of tigecycline. A total of 503 unique S. aureus strains isolated from complicated skin and skin structure infections were analyzed. The mecA gene was amplified from 120 strains (23.9%) determined to be resistant to oxacillin (MICs ≥ 4 μg/ml). The prevalence of the mecA gene was found to vary regionally from 6.5% to 50.9% among isolates originating in Eastern Europe and North America, respectively. The presence of a tetracycline resistance determinant, tet(M) or tet(K), among methicillin-resistant S. aureus (MRSA) isolates also varied regionally, with a range of 11.9% to 46.2% among isolates tested from North America and Eastern Europe, respectively. The occurrence of a tetracycline resistance marker in methicillin-susceptible S. aureus (MSSA) strains varied from 2.5 to 16.1% among the isolates tested across the regions of study. The presence of tet(M) or tet(K) had no discernible effect on the tigecycline MICs for either MRSA or MSSA strains, which is consistent with the ability of the glycylcyclines to retain activity in the presence of both the ribosomal protection and efflux mechanisms of resistance to the tetracyclines.
机译:开发了诊断性PCR检测方法来追踪最近完成的全球替加环素的3期全球临床试验中金黄色葡萄球菌分离物中奥沙西林耐药性以及对经典四环素类耐药的常见遗传决定因素。分析了从复杂皮肤和皮肤结构感染中分离出的总共503株独特的金黄色葡萄球菌。从120株(23.9%)扩增出mecA基因,确定其对奥沙西林(MIC≥4μg/ ml)有抗性。发现在起源于东欧和北美的分离株中,mecA基因的流行率区域差异从6.5%到50.9%。耐甲氧西林的金黄色葡萄球菌(MRSA)分离株中四环素抗性决定子tet(M)或tet(K)的存在也因地区而异,在从北美和东部测试的分离株中,范围为11.9%至46.2%欧洲分别。在整个研究区域测试的分离物中,对甲氧西林敏感的金黄色葡萄球菌(MSSA)菌株中四环素抗性标记的发生率从2.5%到16.1%不等。 tet(M)或tet(K)的存在对MRSA或MSSA菌株的替加环素MIC没有明显影响,这与糖核环素在存在核糖体保护和外排机制的情况下保留活性的能力是一致的对四环素的抵抗力。

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