Microbiology Laboratory, Indiana University Health Pathology Laboratory, Indianapolis, Indiana, USA.
J Clin Microbiol. 2013 Jan;51(1):202-5. doi: 10.1128/JCM.02022-12. Epub 2012 Nov 7.
Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of hospital-acquired and life-threatening infections. Active surveillance programs for MRSA utilize either molecular or culture-based methods. A prospective study was performed to compare the performance of selective and differential chromogenic media, BBL CHROMagar MRSA II (CMRSA II; BD Diagnostics, Sparks, MD), MRSASelect (Bio-Rad Laboratories, Redmond, WA), and Spectra MRSA (Remel, Lenexa, KS), for the detection of MRSA in nasal swab specimens. A total of 515 compliant remnant nasal swab specimens were sequentially used to inoculate BBL Trypticase soy agar with 5% sheep blood (TSA II) and each chromogenic medium. After 24 h of incubation, colony color reactions and morphology on chromogenic media were compared to suspicious colonies on nonselective TSA II. MRSA on TSA II was confirmed by Gram staining, a coagulase test, and a cefoxitin disk test. The overall prevalence of MRSA and methicillin-susceptible S. aureus (MSSA) on TSA II was 12.4% (64/515) and 9.7% (50/515), respectively. When each chromogenic medium was compared to the standard culture method, the sensitivity and specificity, respectively, were as follows: CMRSA II, 87.7% and 98.6%; MRSASelect, 89.0% and 93.4%; and Spectra MRSA, 83.6% and 92.1%. The positive predictive values were highest for CMRSA II (91.4%), followed by MRSASelect (69.1%) and Spectra MRSA (63.5%). False-positive results on chromogenic media were mainly due to color interpretation. The negative predictive values for all three media were greater than 97%. In conclusion, CMRSA II gave the best overall results for detecting MRSA from nasal specimens.
耐甲氧西林金黄色葡萄球菌(MRSA)是医院获得性和危及生命感染的主要原因。MRSA 的主动监测计划采用分子或基于培养的方法。进行了一项前瞻性研究,以比较选择性和差异显色培养基、BBL CHROMagar MRSA II(CMRSA II;BD 诊断公司,斯帕克斯,马里兰州)、MRSASelect(Bio-Rad 实验室,雷蒙德,华盛顿州)和 Spectra MRSA(雷梅尔,利纳萨,堪萨斯州)检测鼻拭子标本中 MRSA 的性能。总共连续使用 515 个符合要求的残余鼻拭子标本接种 BBL 胰蛋白酶大豆琼脂加 5%绵羊血(TSA II)和每种显色培养基。孵育 24 小时后,将显色培养基上的菌落颜色反应和形态与非选择性 TSA II 上的可疑菌落进行比较。TSA II 上的 MRSA 通过革兰氏染色、凝固酶试验和头孢西丁纸片试验进行确认。TSA II 上 MRSA 和甲氧西林敏感金黄色葡萄球菌(MSSA)的总体流行率分别为 12.4%(64/515)和 9.7%(50/515)。当将每种显色培养基与标准培养方法进行比较时,其灵敏度和特异性分别为:CMRSA II,87.7%和 98.6%;MRSASelect,89.0%和 93.4%;Spectra MRSA,83.6%和 92.1%。CMRSA II 的阳性预测值最高(91.4%),其次是 MRSASelect(69.1%)和 Spectra MRSA(63.5%)。显色培养基上的假阳性结果主要归因于颜色解释。三种培养基的阴性预测值均大于 97%。总之,CMRSA II 是从鼻标本中检测 MRSA 的最佳综合结果。