Table I.
Strains used in this study.
Strain | Description | Source or reference |
---|---|---|
TEA028 | Derivative of EHEC serotype O157:H7 strain EDL933, ΔgalETKM::tetA | Ho and Waldor (2007) |
TEA028-rne | Derivative of TEA028 into which the IPTG-inducible, HA- and His6-tagged rne gene from E. coli RNE102 has been transduced. This strain also produces the LacIQ repressor from a plasmid | This study |
EDL933 ΔgalU | Derivative of EDL933 in which a kanamycin resistance marker has been inserted into the galU gene | This study |
EDL933ΔLEE | Derivative of EDL933 in which the LEE pathogenicity island encoding the T3SS has been deleted | Pósfai et al. (1997) |
RNE102 | Derivative of E. coli Keio BW25113. The rne gene is HA- and His6-tagged and transcribed from a Plac promoter. Thus, IPTG is required for rne transcription. An ampicillin resistance marker is located upstream Plac | This study |
RNE100 | Derivative of E. coli Keio BW25113. The rne gene is HA- and His6-tagged and transcribed from the rne promoter | This study |
MC4100 | Non-pathogenic E. coli K-12 strain used as a positive control for P1 transduction experiments | Casadaban (1976) |