A RAGE Based Strategy for the Genome Engineering of the Human Respiratory Pathogen Mycoplasma pneumoniae.

L. Garcia Morales, Estelle Ruiz, Géraldine Gourgues, Fabien Rideau, Carlos Pinero-Lambea, Maria Lluch-Senar, Alain Blanchard, Carole Lartigue

Research output: Contribution to journalArticleAcademicpeer-review


Genome engineering of microorganisms has become a standard in microbial biotechnologies. Several efficient tools are available for the genetic manipulation of model bacteria such as Escherichia coli and Bacillus subtilis, or the yeast Saccharomyces cerevisiae. Difficulties arise when transferring these tools to nonmodel organisms. Synthetic biology strategies relying on genome transplantation (GT) aim at using yeast cells for engineering bacterial genomes cloned as artificial chromosomes. However, these strategies remain unsuccessful for many bacteria, including Mycoplasma pneumoniae (MPN), a human pathogen infecting the respiratory tract that has been extensively studied as a model for systems biology of simple unicellular organisms. Here, we have designed a novel strategy for genome engineering based on the recombinase-assisted genomic engineering (RAGE) technology for editing the MPN genome. Using this strategy, we have introduced a 15 kbp fragment at a specific locus of the MPN genome and replaced 38 kbp from its genome by engineered versions modified either in yeast or in E. coli. A strain harboring a synthetic version of this fragment cleared of 13 nonessential genes could also be built and propagated in vitro. These strains were depleted of known virulence factors aiming at creating an avirulent chassis for SynBio applications. Such a chassis and technology are a step forward to build vaccines or deliver therapeutic compounds in the lungs to prevent or cure respiratory diseases in humans.
Original languageEnglish
Pages (from-to)2737-2748
JournalACS synthetic biology
Issue number10
Publication statusPublished - 5 Oct 2020
Externally publishedYes


  • Mycoplasma pneumoniae (MPN) transformation-associated recombination-cloning (TAR-cloning) recombinase-assisted genomic engineering (RAGE) Saccharomyces cerevisiae genome editing phage recombinases

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