Perry John D, Davies Amie, Butterworth Lynne A, Hopley Andrew L J, Nicholson Audrey, Gould F Kate
Department of Microbiology, Freeman Hospital, Newcastle upon Tyne, Tyne and Wear, United Kingdom.
J Clin Microbiol. 2004 Oct;42(10):4519-23. doi: 10.1128/JCM.42.10.4519-4523.2004.
We describe here the development and evaluation of MRSA ID, a new chromogenic agar medium for the specific isolation and identification of methicillin-resistant Staphylococcus aureus (MRSA). We used S. aureus ID (bioMerieux, La Balme Les Grottes, France) and supplemented it with various antimicrobials, including cefoxitin, ciprofloxacin, oxacillin, and methicillin. Cefoxitin proved to be superior to the other antimicrobials for the selection of MRSA from other strains of S. aureus. MRSA ID (consisting of S. aureus ID supplemented with 4 mg of cefoxitin/liter) was evaluated by the use of 747 swabs from various clinical sites. All specimens were also cultured on CHROMagar MRSA and oxacillin resistance screening agar base (ORSAB) and in selective mannitol broth (SMB). A total of 85 MRSA strains were isolated by a combination of all methods. After 22 to 24 h of incubation, 80% of the MRSA strains were isolated as green colonies on MRSA ID, compared with 59 and 62% of the strains that were isolated as colored colonies on CHROMagar MRSA and ORSAB, respectively. After 48 h of incubation, 89, 72, and 78% of the MRSA strains were isolated on MRSA ID, CHROMagar MRSA, and ORSAB, respectively. Sixty-five percent of the strains were isolated by growth in SMB. The specificities of MRSA ID, CHROMagar MRSA, ORSAB, and SMB were 99.5, 99.3, 97.9, and 92.8%, respectively, after 22 to 24 h of incubation. We conclude that MRSA ID is a sensitive and specific medium for the isolation and identification of MRSA.
我们在此描述了MRSA ID的开发与评估,MRSA ID是一种用于特异性分离和鉴定耐甲氧西林金黄色葡萄球菌(MRSA)的新型显色琼脂培养基。我们使用了金黄色葡萄球菌ID(法国拉巴尔姆莱格罗特的生物梅里埃公司生产),并添加了各种抗菌剂,包括头孢西丁、环丙沙星、苯唑西林和甲氧西林。事实证明,在从其他金黄色葡萄球菌菌株中筛选MRSA方面,头孢西丁优于其他抗菌剂。通过使用来自不同临床部位的747份拭子对MRSA ID(由每升添加4毫克头孢西丁的金黄色葡萄球菌ID组成)进行了评估。所有标本还在CHROMagar MRSA和苯唑西林耐药性筛选琼脂基础培养基(ORSAB)上以及在选择性甘露醇肉汤(SMB)中进行培养。通过所有方法的组合共分离出85株MRSA菌株。培养22至24小时后,80%的MRSA菌株在MRSA ID上以绿色菌落形式被分离出来,相比之下,在CHROMagar MRSA和ORSAB上分别以有色菌落形式被分离出来的菌株比例为59%和62%。培养48小时后,在MRSA ID、CHROMagar MRSA和ORSAB上分别分离出89%、72%和78%的MRSA菌株。65%的菌株通过在SMB中生长而被分离出来。培养22至24小时后,MRSA ID、CHROMagar MRSA、ORSAB和SMB的特异性分别为99.5%、99.3%、97.9%和92.8%。我们得出结论,MRSA ID是一种用于分离和鉴定MRSA的灵敏且特异的培养基。