pyrF as a Counterselectable Marker for Unmarked Genetic Manipulations in Treponema denticola

• Published in: Applied and environmental microbiology 2016-02, Vol.82 (4), p.1346-1352
• Main Authors: Kurniyati, Kurni, Li, Chunhao
• Format: Article
• Language: English
• Subjects: Drug Resistance, Bacterial; Gene expression; Gene Knockout Techniques - methods; Genetics; Genetics and Molecular Biology; Genetics, Microbial - methods; Gram-negative bacteria; Mutation; Orotic Acid - analogs & derivatives; Orotic Acid - toxicity; Orotidine-5'-Phosphate Decarboxylase - genetics; Pathogens; Selection, Genetic; Spotlight; Treponema denticola; Treponema denticola - drug effects; Treponema denticola - genetics; Treponema denticola - growth & development
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.03704-15

The pathophysiology of Treponema denticola, an oral pathogen associated with both periodontal and endodontic infections, is poorly understood due to its fastidious growth and recalcitrance to genetic manipulations. Counterselectable markers are instrumental in constructing clean and unmarked mutations in bacteria. Here, we demonstrate that pyrF, a gene encoding orotidine-5'-monophosphate decarboxylase, can be used as a counterselectable marker in T. denticola to construct marker-free mutants. T. denticola is susceptible to 5-fluoroorotic acid (5-FOA). To establish a pyrF-based counterselectable knockout system in T. denticola, the pyrF gene was deleted. The deletion conferred resistance to 5-FOA in T. denticola. Next, a single-crossover mutant was constructed by reintroducing pyrF along with a gentamicin resistance gene (aacC1) back into the chromosome of the pyrF mutant at the locus of choice. In this study, we chose flgE, a flagellar hook gene that is located within a large polycistronic motility gene operon, as our target gene. The obtained single-crossover mutant (named FlgE(in)) regained the susceptibility to 5-FOA. Finally, FlgE(in) was plated on solid agar containing 5-FOA. Numerous colonies of the 5-FOA-resistant mutant (named FlgE(out)) were obtained and characterized by PCR and Southern blotting analyses. The results showed that the flgE gene was deleted and FlgE(out) was free of selection markers (i.e., pyrF and aacC1). Compared to previously constructed flgE mutants that contain an antibiotic selection marker, the deletion of flgE in FlgE(out) has no polar effect on its downstream gene expression. The system developed here will provide us with a new tool for investigating the genetics and pathogenicity of T. denticola.