Tanya M. Parsons, V. Cox, Angela E. Essex-Lopresti, M. G. Hartley, R. Lukaszewski, P. A. Rachwal, H. Stapleton, S. Weller
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引用次数: 10
摘要
三种实时PCR检测炭疽芽孢杆菌基因靶点(pXO1;pXO2和染色体)发育。两种PCR检测方法(pXO1-MGB和Ba hr- mgb)与从复制炭疽芽孢杆菌感染小鼠模型的全血样本中提取的DNA提取物进行了测试。在所有三种模型中,总共测试了45个样本,其中41个样本的一个子集通过PCR或微生物培养显示含有炭疽芽孢杆菌。将微生物培养作为常规血培养的模拟物(用于临床环境),比较PCR和血培养的检出率。在两种小鼠模型中,血培养的检出率显著高于PCR (BA1, p=0.004;BA3, p = 0.013)。在BA2模型中,PCR与血培养的检出率无显著差异。
Development of three real-time PCR assays to detect Bacillus anthracis and assessment of diagnostic utility.
Three real-time PCR assays to detect Bacillus anthracis genetic targets (pXO1; pXO2 and chromosome) were developed. Two of the PCR assays (pXO1-MGB and Ba chr-MGB) were tested against DNA extracts produced from whole blood samples obtained from a replicated B. anthracis murine infection model. Across all three models 45 samples were tested in total, within which a subset of 41 samples were shown to contain B. anthracis by either PCR or microbiological culture. Using microbiological culture as an analogue of conventional blood culture (as used in clinical settings) the detection rates of PCR and blood culture were compared. In two of the murine models blood culture had a significantly higher detection rate than PCR (BA1, p=0.004; BA3, p=0.013). In the BA2 model there was no significant difference between the detection rates of PCR and blood culture.