Servicio de Dermatología, Hospital Universitario 'JoséE. González', Monterrey NL, Mexico.
División de Biología Celular y Molecular,Centro de Investigación Biomédica del Noreste, IMSS, MonterreyNL, Mexico.
J Med Microbiol. 2010 Apr;59(Pt 4):384-391. doi: 10.1099/jmm.0.015966-0. Epub 2010 Jan 7.
Continuous subculture has been observed to produce changes in the virulence of micro-organisms, e.g. rabies virus, poliovirus and Mycobacterium bovis BCG. The latter has been used as a vaccine for tuberculosis for the last 100 years; however, in some instances its efficacy has been observed to be very low. In order to determine whether similar changes can be produced in Mycobacterium tuberculosis, we selected four isolates, M. tuberculosis H37Rv, a Beijing strain (DR-689), and two more isolates with deletion of the phospholipase C locus (plcA-plcB-plcC ), and subjected them to serial culturing on Middlebrook 7H9 medium, with or without ox bile. After 100 passages, we performed RFLP-IS6110 analysis to determine whether genomic changes were produced. We also checked their genomic composition by microarray analysis. Changes in virulence were studied by measuring the cytotoxic effect of parental and subcultured isolates on a THP-1 macrophage monolayer. The most visible change was the change of position of an IS6110 band of approximately 1400 bp to approximately 1600 bp in the Beijing isolate subcultured in the ox bile medium. Analysis by microarray and PCR confirmation did not reveal any genomic changes. Cytotoxic activity was decreased in the isolates at levels close to that of BCG, and more consistently in those subcultured in the presence of ox bile.
连续传代会导致微生物毒力发生变化,例如狂犬病病毒、脊髓灰质炎病毒和牛分枝杆菌 BCG。后者在过去 100 年中一直被用作结核病疫苗;然而,在某些情况下,其疗效被观察到非常低。为了确定结核分枝杆菌是否会发生类似的变化,我们选择了四个分离株,即结核分枝杆菌 H37Rv、北京株(DR-689)以及两个缺失磷脂酶 C 基因座(plcA-plcB-plcC)的分离株,并在含有或不含有牛胆盐的 Middlebrook 7H9 培养基上进行连续培养。经过 100 代后,我们进行 RFLP-IS6110 分析以确定是否产生了基因组变化。我们还通过微阵列分析检查了它们的基因组组成。通过测量亲本和传代分离株对 THP-1 巨噬细胞单层的细胞毒性作用来研究毒力变化。最明显的变化是在北京株在牛胆盐培养基中传代培养时,大约 1400bp 的 IS6110 带的位置发生了变化,变为大约 1600bp。微阵列分析和 PCR 确认分析没有发现任何基因组变化。分离株的细胞毒性活性降低,接近卡介苗的水平,并且在含有牛胆盐的情况下传代培养时更为一致。