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利奈唑胺、奎奴普丁/达福普汀和泰利霉素对基因明确的高水平氟喹诺酮耐药耐甲氧西林金黄色葡萄球菌的体外活性。

In vitro activity of linezolid, synercid and telithromycin against genetically defined high level fluoroquinolone-resistant methicillin-resistant Staphylococcus aureus.

作者信息

Muñoz Bellido J L, Gutiérrez Zufiaurre M N, Sánchez Hernández F J, Yagüe Guirao G, Segovia Hernández M, García-Rodríguez J A

机构信息

Departamento de Medicina Preventiva, Salud Pública y Microbiología Médica, Universidad de Salamanca, Salamanca, Spain.

出版信息

Int J Antimicrob Agents. 2002 Jul;20(1):61-4. doi: 10.1016/s0924-8579(02)00107-3.

Abstract

The in vitro activity of levofloxacin, moxifloxacin, gatifloxacin, erythromycin, telithromycin, linezolid, synercid and vancomycin was measured against 36 genetically defined, gyrA/grlA double mutant MRSA clinical strains with an MIC to ciprofloxacin > or = 8 mg/l. The three newer fluoroquinolones tested were more active than ciprofloxacin. Resistance rates for levofloxacin and gatifloxacin were high (44.5 and 36.1%, respectively). All the strains were moxifloxacin-susceptible, though most of them had MICs close to the break point. All the strains were intermediate or resistant to erythromycin and most were also resistant to telithromycin. No strains were resistant to linezolid, synercid or vancomycin (MIC(90): 2, 1 and 2 mg/l, respectively).

摘要

测定了左氧氟沙星、莫西沙星、加替沙星、红霉素、泰利霉素、利奈唑胺、奎奴普丁/达福普汀和万古霉素对36株经基因鉴定的gyrA/grlA双突变耐甲氧西林金黄色葡萄球菌(MRSA)临床菌株的体外活性,这些菌株对环丙沙星的最低抑菌浓度(MIC)≥8mg/L。所测试的三种新型氟喹诺酮类药物比环丙沙星活性更强。左氧氟沙星和加替沙星的耐药率较高(分别为44.5%和36.1%)。所有菌株对莫西沙星敏感,不过大多数菌株的MIC接近折点。所有菌株对红霉素呈中介或耐药,且大多数对泰利霉素也耐药。没有菌株对利奈唑胺、奎奴普丁/达福普汀或万古霉素耐药(MIC90分别为2mg/L、1mg/L和2mg/L)。

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