Division of Internal Medicine, University Hospital of Zurich, Switzerland.
Clin Infect Dis. 2011 Dec;53(12):1245-51. doi: 10.1093/cid/cir692. Epub 2011 Oct 5.
Broad-range 16S ribosomal RNA (rRNA) gene polymerase chain reaction (PCR) is used for detection and identification of bacterial pathogens in clinical specimens from patients with a high suspicion for infection. However, prospective studies addressing the impact and clinical value of broad-range bacterial 16S rRNA gene amplification for diagnosis of acute infectious diseases in nonselected patient populations are lacking.
We first assessed the diagnostic performance of 16S rRNA gene PCR compared with routine bacterial culture. Second, we addressed prospectively the impact and clinical value of broad-range PCR for the diagnosis of acute infections using samples that tested negative by routine bacterial culture; the corresponding patients' data were evaluated by detailed medical record reviews.
Results from 394 specimens showed a high concordance of >90% for 16S rRNA gene PCR and routine bacterial culture, indicating that the diagnostic performance of PCR for acute bacterial infections is comparable to that of bacterial culture, which is currently considered the gold standard. In thisprospective study, 231 specimens with a negative result on routine bacterial culture were analyzed with PCR, and patients' clinical data were reviewed. We found that broad-range 16S rRNA gene PCR showed a sensitivity, specificity, positive predictive value, and negative predictive value of 42.9%, 100%, 100%, and 80.2% for culture-negative bacterial infections.
This study defines the role of 16S rRNA gene PCR for diagnosis of culture-negative bacterial infections. Our data show that 16S rRNA gene PCR is particularly useful for identification of bacterial pathogens in patients pretreated with antibiotics.
广谱 16S 核糖体 RNA(rRNA) 基因聚合酶链反应(PCR) 用于检测和鉴定高度怀疑感染的患者临床标本中的细菌病原体。然而,缺乏前瞻性研究来解决非选择性患者人群中广谱细菌 16S rRNA 基因扩增对急性传染病诊断的影响和临床价值。
我们首先评估了 16S rRNA 基因 PCR 与常规细菌培养的诊断性能。其次,我们前瞻性地解决了广谱 PCR 对常规细菌培养阴性的急性感染诊断的影响和临床价值;通过详细的病历回顾评估了相应患者的数据。
394 份标本的结果显示,16S rRNA 基因 PCR 和常规细菌培养的一致性>90%,表明 PCR 对急性细菌感染的诊断性能与目前被认为是金标准的细菌培养相当。在这项前瞻性研究中,对 231 份常规细菌培养阴性的标本进行了 PCR 分析,并对患者的临床数据进行了回顾。我们发现,广谱 16S rRNA 基因 PCR 对培养阴性的细菌感染的敏感性、特异性、阳性预测值和阴性预测值分别为 42.9%、100%、100%和 80.2%。
本研究确定了 16S rRNA 基因 PCR 在诊断培养阴性细菌感染中的作用。我们的数据表明,16S rRNA 基因 PCR 特别有助于鉴定抗生素预处理患者的细菌病原体。