Mathews Anila A, Thomas Marina, Appalaraju B, Jayalakshmi J
Department of Microbiology, PSG Institute of Medical Science and Research, Coimbatore 641 004, India.
Indian J Pathol Microbiol. 2010 Jan-Mar;53(1):79-82. doi: 10.4103/0377-4929.59189.
Phenotypic methods for detection of methicillin resistant Staphylococcus aureus (MRSA) have been compared with the gold standard which, as of now, is by the detection of mecA gene and femA gene by polymerase chain reaction (PCR). Discrepancies in detection have an adverse effect on patient management, thereby highlighting the importance of accuracy in detection. Our study aims to evaluate the efficacy of cefoxitin disk diffusion test to detect MRSA and compare it with other phenotypic and molecular methods.
The study was conducted from June 2006 to December 2007 and included 610 Staphylococcus aureus (S. aureus) isolates obtained from clinical samples. All isolates were tested for MRSA using oxacillin screen agar plates with 6 microg/ml of oxacillin, cefoxitin disk diffusion using 30 microg disk and MIC of oxacillin. Selected isolates (55) were tested for presence of mecA gene and Fem A gene by PCR.
Out of 610 isolates, MRSA was identified in 34.09% by cefoxitin disk diffusion, 34.9% by oxacillin screen agar, 34.4% by MIC and 37.3% by oxacillin disk diffusion. When selected isolates were tested with molecular methods, the cefoxitin disk diffusion and PCR tests were comparable.
Prevalence of MRSA (34.09%) is quite high as in other studies. The oxacillin disk diffusion test which was used routinely earlier is showing low specificity (56%). Among all phenotypic methods, cefoxitin disk diffusion and PCR alone have similar sensitivity and specificity.
Results of cefoxitin disk diffusion test are in concordance with the PCR for mecA gene. Thus, the test can be an alternative to PCR for detection of MRSA in resource constraint settings.
已将检测耐甲氧西林金黄色葡萄球菌(MRSA)的表型方法与目前的金标准进行了比较,金标准是通过聚合酶链反应(PCR)检测mecA基因和femA基因。检测结果的差异对患者管理有不利影响,从而凸显了检测准确性的重要性。我们的研究旨在评估头孢西丁纸片扩散试验检测MRSA的效果,并将其与其他表型和分子方法进行比较。
该研究于2006年6月至2007年12月进行,纳入了从临床样本中分离出的610株金黄色葡萄球菌(S. aureus)。所有分离株均使用含6μg/ml苯唑西林的苯唑西林筛选琼脂平板检测MRSA,使用30μg纸片进行头孢西丁纸片扩散试验,并检测苯唑西林的最低抑菌浓度(MIC)。对选定的55株分离株进行PCR检测mecA基因和Fem A基因的存在情况。
在610株分离株中,通过头孢西丁纸片扩散试验鉴定出MRSA的比例为34.09%,通过苯唑西林筛选琼脂为34.9%,通过MIC为34.4%,通过苯唑西林纸片扩散为37.3%。当用分子方法检测选定的分离株时,头孢西丁纸片扩散试验和PCR试验具有可比性。
MRSA的流行率(34.09%)与其他研究一样相当高。以前常规使用的苯唑西林纸片扩散试验显示特异性较低(56%)。在所有表型方法中,仅头孢西丁纸片扩散试验和PCR具有相似的敏感性和特异性。
头孢西丁纸片扩散试验的结果与mecA基因的PCR结果一致。因此,在资源有限的情况下,该试验可作为检测MRSA的PCR替代方法。