Transposon Mutagenesis in Chlamydia trachomatis Identifies CT339 as a ComEC Homolog Important for DNA Uptake and Lateral Gene Transfer

• Published in: mBio 2019-08, Vol.10 (4)
• Main Authors: LaBrie, Scott D, Dimond, Zoë E, Harrison, Kelly S, Baid, Srishti, Wickstrum, Jason, Suchland, Robert J, Hefty, P Scott
• Format: Article
• Language: English
• Subjects: Animals; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Chlamydia Infections - microbiology; Chlamydia trachomatis; Chlamydia trachomatis - genetics; Chlamydia trachomatis - metabolism; DNA Transposable Elements; DNA, Bacterial - genetics; DNA, Bacterial - metabolism; Female; Gene Transfer, Horizontal; genetic competence; Host-Microbe Biology; Humans; Mice; Mice, Inbred C57BL; mutagenesis; Mutagenesis, Insertional; Mutation; transposons
• ISSN: 2161-2129; 2150-7511
• DOI: 10.1128/mBio.01343-19

Transposon mutagenesis is a widely applied and powerful genetic tool for the discovery of genes associated with selected phenotypes. is a clinically significant, obligate intracellular bacterium for which many conventional genetic tools and capabilities have been developed only recently. This report describes the successful development and application of a transposon mutagenesis system for generating single-insertion mutant clones of This system was used to generate a pool of 105 transposon mutant clones that included insertions in genes encoding flavin adenine dinucleotide (FAD)-dependent monooxygenase ( [ ]), deubiquitinase ( ), and competence-associated ( ) proteins. A subset of Tn mutant clones was evaluated for growth differences under cell culture conditions, revealing that most phenocopied the parental strain; however, some strains displayed subtle and yet significant differences in infectious progeny production and inclusion sizes. Bacterial burden studies in mice also supported the idea that a FAD-dependent monooxygenase ( ) and a deubiquitinase ( ) were important for these infections. The gene encodes a hypothetical protein with limited sequence similarity to the DNA-uptake protein ComEC. A transposon insertion in rendered the mutant incapable of DNA acquisition during recombination experiments. This observation, along with structural analysis, supports the idea that this protein is playing a role in the fundamental process of lateral gene transfer similar to that of ComEC. In all, the development of the transposon system for provides an effective genetic tool for further discovery of genes that are important for basic biology and pathogenesis aspects. infections have an immense impact on public health; however, understanding the basic biology and pathogenesis of this organism has been stalled by the limited repertoire of genetic tools. This report describes the successful adaptation of an important tool that has been lacking in studies: transposon mutagenesis. This advance enabled the generation of 105 insertional mutants, demonstrating that numerous gene products are not essential for growth. Mammalian infections using these mutants revealed that several gene products are important for infections Moreover, this tool enabled the investigation and discovery of a gene critical for lateral gene transfer; a process fundamental to the evolution of bacteria and likely for as well. The development of transposon mutagenesis for has broad impact for the