Transposon Mutagenesis of Mycoplasma gallisepticum by Conjugation with Enterococcus faecalis and Determination of Insertion Site by Direct Genomic Sequencing

• Published in: Plasmid Vol. 44; no. 2; pp. 191 - 195
• Main Authors: Ruffin, Debra C., van Santen, Vicky L., Zhang, Yijing, Voelker, LeRoy L., Panangala, Victor S., Dybvig, Kevin
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2000
• Subjects: Animals; Base Sequence; Birds - microbiology; Blotting, Southern; Conjugation, Genetic; DNA Primers; DNA Transposable Elements - genetics; Enterococcus faecalis; Enterococcus faecalis - genetics; insertional mutagenesis; Mutagenesis, Insertional - methods; Mycoplasma - genetics; Mycoplasma gallisepticum; Polymerase Chain Reaction; transposon Tn916
• ISSN: 0147-619X; 1095-9890
• DOI: 10.1006/plas.2000.1485

Few genetic systems for studying mycoplasmas exist, but transposon Tn916 has been shown to transpose into the genomes of some species and can be used as an insertional mutagen. In the current study, the ability of Enterococcus faecalis to serve as a donor for the conjugative transfer of transposon Tn916 into the genome of the avian pathogen Mycoplasma gallisepticum strain PG31 was examined. Transconjugants were obtained at a frequency of ≥6 × 10−8 per recipient CFU. To determine the transposon insertion site, an oligonucleotide primer corresponding to the 3′ end of Tn916 was designed for the purpose of directly sequencing genomic DNA without PCR amplification. Using the direct sequencing approach, Tn916 was shown to insert into any of numerous sites in the M. gallisepticum genome. This is the first report of conjugal transposition of Tn916 into the M. gallisepticum genome. The ability to determine transposon insertion sites in mycoplasmas by genomic sequencing has not been previously described and allows rapid sequence analysis of transposon-generated mutants.