Bonjean Marie, Hodille Elisabeth, Dumitrescu Oana, Dupieux Céline, Nkoud Mongo Christina, Allam Camille, Beghin Mathilde, Paris Mickael, Borrel Ophelie, Chardon Hubert, Laurent Fréderic, Rasigade Jean-Philippe, Lina Gerard
IAI, Hospices Civils de Lyon, Lyon, France.
CIRI, International Center for Infectiology Research, Lyon, France.
J Clin Microbiol. 2016 Dec;54(12):2905-2909. doi: 10.1128/JCM.01195-16. Epub 2016 Sep 14.
Disk diffusion testing is widely used to detect methicillin resistance in staphylococci, and cefoxitin is currently considered the best marker for mecA-mediated methicillin resistance. In low-inoculum diffusion testing (colony suspension at 10 CFU/ml), the addition of moxalactam in combination with cefoxitin has been reported to improve on cefoxitin alone for the detection of methicillin-heteroresistant staphylococci. However, moxalactam is absent from EUCAST and CLSI guidelines, which use high-inoculum diffusion testing (colony suspension at 10 CFU/ml), calling into question the potential interest of including moxalactam in their recommendations. The inhibition zone diameters of cefoxitin and moxalactam, alone and in combination, were evaluated for concordance with mecA and mecC positivity in a large collection of clinical Staphylococcus isolates (611 Staphylococcus aureus, Staphylococcus lugdunensis, and Staphylococcus saprophyticus isolates and 307 coagulase-negative staphylococci other than S. lugdunensis and S. saprophyticus isolates, of which 22% and 53% were mecA-positive, respectively) and in 25 mecC-positive S. aureus isolates using high-inoculum diffusion testing. Receiver operating characteristic, sensitivity, and specificity analyses indicated that the detection of mecA- and mecC-positive and negative isolates did not improve with moxalactam, either alone or in combination with cefoxitin, compared to cefoxitin alone. These findings were similar in both the S. aureus/S. lugdunensis/S. saprophyticus group and in the coagulase-negative staphylococci group. Our results do not support the use of moxalactam as an additional marker of methicillin resistance when testing with high-inoculum disk diffusion.
纸片扩散法广泛用于检测葡萄球菌对甲氧西林的耐药性,目前头孢西丁被认为是mecA介导的甲氧西林耐药性的最佳标志物。在低接种量扩散试验(菌落悬液浓度为10 CFU/ml)中,据报道,联合使用莫拉卡坦和头孢西丁比单独使用头孢西丁在检测甲氧西林异质性耐药葡萄球菌方面更具优势。然而,欧洲抗菌药物敏感性试验委员会(EUCAST)和美国临床和实验室标准协会(CLSI)的指南中没有莫拉卡坦,这些指南采用高接种量扩散试验(菌落悬液浓度为10 CFU/ml),这使得将莫拉卡坦纳入其推荐中的潜在意义受到质疑。在大量临床葡萄球菌分离株(611株金黄色葡萄球菌、路邓葡萄球菌和腐生葡萄球菌分离株以及307株除路邓葡萄球菌和腐生葡萄球菌分离株外的凝固酶阴性葡萄球菌,其中分别有22%和53%为mecA阳性)以及25株mecC阳性金黄色葡萄球菌分离株中,使用高接种量扩散试验评估了头孢西丁和莫拉卡坦单独及联合使用时的抑菌圈直径与mecA和mecC阳性的一致性。受试者工作特征曲线、敏感性和特异性分析表明,与单独使用头孢西丁相比,莫拉卡坦单独或与头孢西丁联合使用时,在检测mecA和mecC阳性及阴性分离株方面并无改善。在金黄色葡萄球菌/路邓葡萄球菌/腐生葡萄球菌组和凝固酶阴性葡萄球菌组中,这些结果相似。我们的结果不支持在高接种量纸片扩散试验中使用莫拉卡坦作为甲氧西林耐药性的额外标志物。