Bailo Nathalie, Kanaan Hussein, Kay Elisabeth, Charpentier Xavier, Doublet Patricia, Gilbert Christophe
CIRI, International Center for Infectiology Research, CNRS, UMR5308, Inserm, U1111, Université Lyon 1, Université de Lyon, Lyon, France.
Methods Mol Biol. 2019;1921:93-105. doi: 10.1007/978-1-4939-9048-1_6.
Studying bacterial physiology and pathogenesis often requires isolation of targeted mutants. From the early days of bacterial genetics, many genetic tools have been developed to achieve this goal in a lot of bacteria species, and a major key is to be able to manipulate the targeted genome region with a minimum impact on the rest of the genome. Here, we described a two-step protocol relevant in Legionella pneumophila. This efficient two-step protocol uses the natural transformability of L. pneumophila and linear DNA fragments as substrates for recombination without the necessity of intermediate hosts to amplify targeted DNA. Based on a suicide cassette strategy, this genetic toolbox enables to generate clean scar-free deletions, single-nucleotide mutation, transcriptional or translational fusions, as well as insertion at any chosen place in L. pneumophila chromosome, therefore enabling multiple mutations with no need of multiple selection markers.
研究细菌生理学和发病机制通常需要分离靶向突变体。从细菌遗传学早期开始,人们就开发了许多遗传工具来在多种细菌物种中实现这一目标,而一个关键要点是能够对靶向基因组区域进行操作,同时对基因组的其余部分影响最小。在此,我们描述了一种与嗜肺军团菌相关的两步法方案。这种高效的两步法方案利用嗜肺军团菌的天然转化能力,并以线性DNA片段作为重组底物,无需中间宿主来扩增靶向DNA。基于自杀盒策略,这个遗传工具箱能够产生无痕的干净缺失、单核苷酸突变、转录或翻译融合,以及在嗜肺军团菌染色体的任何选定位置进行插入,因此无需多个选择标记就能实现多重突变。