Department of Medicine, Center for Tuberculosis Research, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS One. 2010 Apr 21;5(4):e10289. doi: 10.1371/journal.pone.0010289.
It has been hypothesized that the virulence of lab-passaged Mycobacterium tuberculosis and recombinant M. tuberculosis mutants might be reduced due to multiple in vitro passages, and that virulence might be augmented by passage of these strains through mice before quantitative virulence testing in the mouse or guinea pig aerosol models.
METHODOLOGY/PRINCIPAL FINDINGS: By testing three M. tuberculosis H37Rv samples, one deletion mutant, and one recent clinical isolate for survival by the quantitative organ CFU counting method in mouse or guinea pig aerosol or intravenous infection models, we could discern no increase in bacterial fitness as a result of passaging of M. tuberculosis strains in mice prior to quantitative virulence testing in two animal models. Surface lipid expression as assessed by neutral red staining and thin-layer chromatography for PDIM analysis also failed to identify virulence correlates.
CONCLUSIONS/SIGNIFICANCE: These results indicate that animal passaging of M. tuberculosis strains prior to quantitative virulence testing in mouse or guinea pig models does not enhance or restore potency to strains that may have lost virulence due to in vitro passaging. It is critical to verify virulence of parental strains before genetic manipulations are undertaken and comparisons are made.
有人假设,由于多次体外传代,实验室传代的结核分枝杆菌和重组结核分枝杆菌突变株的毒力可能降低,并且这些菌株在进行定量毒力测试之前通过小鼠传代,可能会增强毒力在小鼠或豚鼠气溶胶模型中。
方法/主要发现:通过定量器官 CFU 计数方法在小鼠或豚鼠气溶胶或静脉内感染模型中测试三种 H37Rv 结核分枝杆菌样本、一个缺失突变体和一个最近的临床分离株的存活情况,我们无法发现由于在进行两种动物模型中的定量毒力测试之前将结核分枝杆菌菌株在小鼠中传代,细菌适应性会增加。用中性红染色和 PDIM 分析的薄层色谱法评估表面脂质表达也未能确定毒力相关性。
结论/意义:这些结果表明,在进行小鼠或豚鼠模型中的定量毒力测试之前,将结核分枝杆菌菌株在动物中传代不会增强或恢复由于体外传代而丧失毒力的菌株的效力。在进行遗传操作并进行比较之前,验证亲本菌株的毒力至关重要。