Rantakokko-Jalava K, Viljanen M K
Department of Medical Microbiology, University of Turku, Kiinamyllynkatu 13, 20520 Turku, Finland.
Clin Microbiol Infect. 2003 Oct;9(10):1051-6. doi: 10.1046/j.1469-0691.2003.00736.x.
We evaluated PCR for the detection of Bacillus anthracis DNA from simulated clinical specimens relevant for the microbiological diagnosis of anthrax or exposure to B. anthracis spores. In simulated blood specimens, the lowest limit of detection was 400 CFU per mL of blood, which may be sufficient for samples from patients with septic anthrax. Screening nasal swabs by PCR may not be sensitive enough to rule out dangerous exposure to anthrax spores, as a minimum of 2000 spores per sample was required for detectable amplification. As spores survived some standard DNA purification methods, special attention should be paid to laboratory safety when preparing samples possibly containing live spores.
我们评估了聚合酶链反应(PCR)用于从模拟临床标本中检测炭疽芽孢杆菌DNA的效果,这些标本与炭疽的微生物学诊断或接触炭疽芽孢杆菌孢子相关。在模拟血液标本中,检测下限为每毫升血液400个菌落形成单位(CFU),这对于败血症型炭疽患者的样本可能足够。通过PCR筛查鼻拭子可能不够灵敏,无法排除危险的炭疽孢子暴露,因为每个样本至少需要2000个孢子才能检测到扩增。由于孢子能在一些标准DNA纯化方法中存活,在制备可能含有活孢子的样本时,应特别注意实验室安全。