Arráiz R Nailet, Romay B Zolay, Faría M Nelba
Sección de Biología Molecular y Escuela de Bioanálisis, Centro de Investigaciones Endocrino-Metabólicas Dr. Félix Gómez, Facultad de Medicina, Universidad del Zulia, Maracaibo, Venezuela.
Rev Chilena Infectol. 2007 Apr;24(2):99-105. doi: 10.4067/s0716-10182007000200002. Epub 2007 Apr 12.
Mycobacteria that cause tuberculosis in animals and humans belong to the Mycobacterium tuberculosis complex. Techniques for conventional diagnosis are time-consuming and do not differentiate between different strains belonging to the M. tuberculosis complex. The aim of this study was to evaluate a multiplex PCR assay applicable to mycobacteria in culture with the capacity to differentiate different strains belonging to the M. tuberculosis complex in a reference laboratory. Primers based on genomics regions of difference (RD) consisting in DNA segments that are present in M. tuberculosis, but differentially deleted in several members of M. tuberculosis complex were used in a PCR assay. The test was applied to 86 clinical isolates of mycobacteria. The pattern of amplification allowed differentiating between M. tuberculosis, M. bovis and M. bovis BCG in a single PCR reaction. This PCR multiplex assay may be used in a Reference Laboratory of Tuberculosis Diagnosis as a complementary test to differentiate mycobacteria strains belonging to the M. tuberculosis complex. This test significantly reduces the time period between culture and strain identification, and thus for could favor the adoption of better strain specific antimycobacterial regimens as well as identification of zoonotic transmission of M. bovis to humans.
引起动物和人类结核病的分枝杆菌属于结核分枝杆菌复合群。传统诊断技术耗时且无法区分结核分枝杆菌复合群中的不同菌株。本研究的目的是评估一种适用于培养分枝杆菌的多重PCR检测方法,该方法能够在参考实验室中区分结核分枝杆菌复合群中的不同菌株。基于差异基因组区域(RD)的引物(由存在于结核分枝杆菌中但在结核分枝杆菌复合群的几个成员中差异缺失的DNA片段组成)用于PCR检测。该检测方法应用于86株分枝杆菌临床分离株。扩增模式允许在单个PCR反应中区分结核分枝杆菌、牛分枝杆菌和卡介苗。这种多重PCR检测方法可在结核病诊断参考实验室中用作补充检测,以区分结核分枝杆菌复合群中的分枝杆菌菌株。该检测方法显著缩短了培养和菌株鉴定之间的时间间隔,因此有利于采用更好的菌株特异性抗分枝杆菌治疗方案以及鉴定牛分枝杆菌向人类的人畜共患病传播。