首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >In Vitro Activities of Quinupristin-Dalfopristin and Cefepime Alone and in Combination with Various Antimicrobials against Multidrug-Resistant Staphylococci and Enterococci in an In Vitro Pharmacodynamic Model
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In Vitro Activities of Quinupristin-Dalfopristin and Cefepime Alone and in Combination with Various Antimicrobials against Multidrug-Resistant Staphylococci and Enterococci in an In Vitro Pharmacodynamic Model

机译:喹诺普林汀-达福普汀和头孢吡肟单独和与多种抗菌素联合使用在体外药代动力学模型中对多药耐药葡萄球菌和肠球菌的体外活性

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摘要

Use of combinations of antimicrobials that together achieve synergistic activities against targeted microorganisms is one potential strategy for overcoming bacterial resistance. As the incidence of infections caused by multidrug-resistant staphylococci and enterococci increases, the importance of devising additional synergistic drug combinations for these bacteria is magnified. We evaluated a number of antimicrobial combinations, with a focus on quinupristin-dalfopristin (Q-D), cefepime, and linezolid, using a previously described in vitro pharmacodynamic model. The combination of Q-D with either linezolid or vancomycin, as well as the combination of cefepime-vancomycin, resulted in enhanced killing (≥2-log10 increase in killing versus the most-active single agent) against methicillin-resistant Staphylococcus aureus (MRSA) 494. An improved effect (<2 log10 kill increase in kill) against MRSA 494 was noted for cefepime plus either Q-D or linezolid, as well as linezolid-vancomycin. Similar relationships were observed for a methicillin-susceptible S. aureus isolate (isolate 1199). Against methicillin-resistant S. epidermidis R444, enhanced killing was achieved with the combination of cefepime-linezolid, while improvement was noted for vancomycin with either cefepime or linezolid. The combination of cefepime and vancomycin also achieved enhanced killing against a glycopeptide-intermediate-susceptible S. aureus isolate (isolate 992). The combination of linezolid and doxycycline achieved an enhanced effect against vancomycin-resistant Enterococcus faecalis (VREFc) and E. faecium. Q-D plus ampicillin or linezolid resulted in similar enhancement of activity against the VREFc isolate. The results of this study suggest a number of novel antimicrobial combinations that may be useful against staphylococci and enterococci. Combination regimens including cefepime, Q-D, and/or linezolid warrant further investigation for the treatment of refractive infections due to multidrug-resistant gram-positive pathogens.
机译:共同实现针对目标微生物的协同活性的抗菌剂组合的使用是克服细菌耐药性的一种潜在策略。随着由多药耐药性葡萄球菌和肠球菌引起的感染的发生率增加,为这些细菌设计其他协同药物组合的重要性被放大。我们使用先前描述的体外药效学模型评估了多种抗菌药物组合,重点是奎奴普丁-达福普汀(Q-D),头孢吡肟和利奈唑胺。 QD与利奈唑胺或万古霉素的组合,以及头孢吡肟-万古霉素的组合导致对耐甲氧西林的金黄色葡萄球菌(MRSA)的杀灭作用增强(杀灭作用比活性最高的单药增加≥2-log10)494观察到头孢吡肟加QD或利奈唑胺以及利奈唑胺-万古霉素对MRSA 494的作用有所改善(杀伤力增加<2 log10,杀伤力增加)。对于甲氧西林敏感的金黄色葡萄球菌分离株(分离株1199)观察到相似的关系。对于耐甲氧西林的表皮葡萄球菌R444,头孢吡肟-利奈唑胺的联合使用可增强杀伤力,而万古霉素与头孢吡肟或利奈唑胺的结合也有所改善。头孢吡肟和万古霉素的组合还提高了对糖肽中间敏感金黄色葡萄球菌分离株(分离株992)的杀灭能力。利奈唑胺和强力霉素的组合对耐万古霉素的粪肠球菌(VREFc)和粪肠球菌具有增强的作用。 Q-D加氨苄西林或利奈唑胺导致类似的VREFc分离物活性增强。这项研究的结果表明,许多新的抗菌药物组合可能对葡萄球菌和肠球菌有用。包括头孢吡肟,Q-D和/或利奈唑胺在内的联合治疗方案值得进一步研究,以治疗由于多重耐药的革兰氏阳性病原体引起的屈光感染。

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