Nilsson P, Alexandersson H, Ripa T
Department of Clinical Microbiology and Infection Control, The County Hospital of Halmstad, Sweden.
Clin Microbiol Infect. 2005 Dec;11(12):1027-34. doi: 10.1111/j.1469-0691.2005.01291.x.
A rapid and sensitive method for excluding the presence of methicillin-resistant Staphylococcus aureus (MRSA) in clinical samples was developed and evaluated. The method utilised an MRSA-selective enrichment broth for 16 h, followed by PCR quantification of the nuc gene. Samples below a quantitative PCR threshold were reported as MRSA-negative. Broths from PCR-positive samples were subcultured for MRSA isolation. Clinical samples (n = 334) in a constructed high prevalence population were analysed in parallel with a selective plating method. The new broth-PCR assay increased the number of positive samples by 35% (49 vs. 66), and 94% of negative samples were reported within 24 h. To reduce costs and workload, 665 clinical samples were grown separately in enrichment broth and then pooled in the PCR step. The broth-PCR assay increased the number of MRSA positive samples from 11 to 15 compared with selective plating. Most (89%) of the culture-negative samples were also PCR-negative and could be reported within 24 h. The growth of 25 European EMRSA strains was tested in the selective enrichment broth. On average, the MRSA strains showed a 300 000-fold increase in CFU, compared with 30-fold for the eight methicillin-sensitive Staphylococcus aureus strains tested.
开发并评估了一种用于排除临床样本中耐甲氧西林金黄色葡萄球菌(MRSA)的快速灵敏方法。该方法使用MRSA选择性增菌肉汤培养16小时,随后对nuc基因进行PCR定量。定量PCR阈值以下的样本报告为MRSA阴性。PCR阳性样本的肉汤进行传代培养以分离MRSA。在构建的高流行人群中对334份临床样本与选择性平板接种法进行平行分析。新的肉汤-PCR检测法使阳性样本数量增加了35%(49份对66份),94%的阴性样本在24小时内报告。为降低成本和工作量,665份临床样本分别在增菌肉汤中培养,然后在PCR步骤中合并。与选择性平板接种相比,肉汤-PCR检测法使MRSA阳性样本数量从11份增加到15份。大多数(89%)培养阴性样本PCR也为阴性,且可在24小时内报告。对25株欧洲EMRSA菌株在选择性增菌肉汤中的生长情况进行了测试。平均而言,MRSA菌株的菌落形成单位增加了300000倍,而所测试的8株甲氧西林敏感金黄色葡萄球菌菌株仅增加了30倍。