Laboratoire de Microbiologie et Génétique Moléculaires, Centre de Biologie Intégrative (CBI), Centre National de la Recherche Scientifique (CNRS), Université de Toulouse, UPS, F-31000 Toulouse, France.
Genes (Basel). 2020 Jun 20;11(6):675. doi: 10.3390/genes11060675.
Natural genetic transformation is a programmed mechanism of horizontal gene transfer in bacteria. It requires the development of competence, a specialized physiological state during which proteins involved in DNA uptake and chromosomal integration are produced. In , competence is transient. It is controlled by a secreted peptide pheromone, the competence-stimulating peptide (CSP) that triggers the sequential transcription of two sets of genes termed early and late competence genes, respectively. Here, we used a microfluidic system with fluorescence microscopy to monitor pneumococcal competence development and transformation, in live cells at the single cell level. We present the conditions to grow this microaerophilic bacterium under continuous flow, with a similar doubling time as in batch liquid culture. We show that perfusion of CSP in the microfluidic chamber results in the same reduction of the growth rate of individual cells as observed in competent pneumococcal cultures. We also describe newly designed fluorescent reporters to distinguish the expression of competence genes with temporally distinct expression profiles. Finally, we exploit the microfluidic technology to inject both CSP and transforming DNA in the microfluidic channels and perform near real time-tracking of transformation in live cells. We show that this approach is well suited to investigating the onset of pneumococcal competence together with the appearance and the fate of transformants in individual cells.
自然遗传转化是细菌中水平基因转移的一种程序性机制。它需要发展出感受态,这是一种特殊的生理状态,在此期间,涉及 DNA 摄取和染色体整合的蛋白质被产生。在肺炎链球菌中,感受态是短暂的。它由一种分泌的肽类信息素即感受态刺激肽(CSP)控制,该信息素触发分别称为早期和晚期感受态基因的两组基因的顺序转录。在这里,我们使用带有荧光显微镜的微流控系统在单细胞水平上监测活细胞中的肺炎链球菌感受态的发展和转化。我们提出了在连续流动下生长这种微需氧细菌的条件,其倍增时间与批次液体培养相似。我们表明,在微流控室中灌注 CSP 会导致单个细胞的生长速率与在有感受态的肺炎链球菌培养物中观察到的相同降低。我们还描述了新设计的荧光报告基因,以区分具有不同时间表达谱的感受态基因的表达。最后,我们利用微流控技术将 CSP 和转化 DNA 注入微流控通道,并在活细胞中进行转化的近实时跟踪。我们表明,这种方法非常适合研究肺炎链球菌感受态的发生,以及转化子在单个细胞中的出现和命运。