National Institute of Public Health - National Institute of Hygiene, Warsaw, Poland.
Pol J Microbiol. 2012;61(4):299-303.
The capacities of differentiation of Mycobacterium bovis BCG from other members of M. tuberculosis complex species using PCR-RFLP, multiplex PCR, and PCR-based genomic deletion analysis approaches were compared. In the study, mycobacteria isolated from patients suspected of adverse events following vaccination with BCG, primarily classified according presence of RD1 marker as virulent and avirulent mycobacteria, were used. The PCR-based genomic deletion analysis was found the best option for mycobacteria diagnostics improvement, as it was capable precisely differentiate virulent and avirulent mycobacteria or virulent species of M. tuberculosis complex. The routine confirmation of mycobacteria species in the cases of adverse events following BCG vaccination is highly expected, especially in clinical practice of patients with primary immunodeficiency.
本研究比较了聚合酶链反应-限制性片段长度多态性(PCR-RFLP)、多重 PCR 和基于 PCR 的基因组缺失分析等方法,以区分牛分枝杆菌卡介苗与结核分枝杆菌复合群其他成员的分化能力。在这项研究中,使用了从疑似接种卡介苗后发生不良反应的患者中分离出的分枝杆菌,这些分枝杆菌主要根据 RD1 标记的存在分为毒力和非毒力分枝杆菌。基于 PCR 的基因组缺失分析被发现是改善分枝杆菌诊断的最佳选择,因为它能够准确地区分毒力和非毒力分枝杆菌或结核分枝杆菌复合群的毒力种。在接种卡介苗后发生不良反应的情况下,非常期望对分枝杆菌进行常规确认,特别是在原发性免疫缺陷患者的临床实践中。