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Direct Visualization of Horizontal Gene Transfer by Transformation in Live Pneumococcal Cells Using Microfluidics

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2020 Jun 25
PMID 32575751
Citations 4
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Abstract

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.

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References
1.
Charpentier X, Polard P, Claverys J . Induction of competence for genetic transformation by antibiotics: convergent evolution of stress responses in distant bacterial species lacking SOS?. Curr Opin Microbiol. 2012; 15(5):570-6. DOI: 10.1016/j.mib.2012.08.001. View

2.
Dubnau D, Blokesch M . Mechanisms of DNA Uptake by Naturally Competent Bacteria. Annu Rev Genet. 2019; 53:217-237. DOI: 10.1146/annurev-genet-112618-043641. View

3.
Slager J, Kjos M, Attaiech L, Veening J . Antibiotic-induced replication stress triggers bacterial competence by increasing gene dosage near the origin. Cell. 2014; 157(2):395-406. DOI: 10.1016/j.cell.2014.01.068. View

4.
Peterson S, Sung C, Cline R, Desai B, Snesrud E, Luo P . Identification of competence pheromone responsive genes in Streptococcus pneumoniae by use of DNA microarrays. Mol Microbiol. 2004; 51(4):1051-70. DOI: 10.1046/j.1365-2958.2003.03907.x. View

5.
Peterson J, Guild W . Fractionated strands of bacterial deoxyribonucleic acid. 3. Transformation efficiencies and rates of phenotypic expression. J Bacteriol. 1968; 96(6):1991-6. PMC: 252548. DOI: 10.1128/jb.96.6.1991-1996.1968. View