The level of Lux induction with pBAD-aphB compared to pBAD24 in E. coli in the presence of 0.01% arabinose is given in the table. Alignment of putative AphB binding sites in tcpP, aphB, and toxR promoter region is given. (B) Gel shift assays using BKM120 datasheet purified MBP-AphB and DNA containing various lengths of the regulatory regions of the toxR promoter. Protein concentrations used in the gel shift assay (shown as shaded triangles) were 0, 20, 40, 80 ng/reaction (5 μl). The selleck effects of AphB on ToxR-regulated genes In addition to regulation

of toxT, ToxR has been previously shown to alter the porin levels in V. cholerae by activating expression of ompU and repressing ompT [26, 27]. Since we showed that AphB affects ToxR levels, we hypothesized that AphB might thus indirectly modulate the expression of ompU and ompT as well. We performed SDS-PAGE on total protein extracts of wild type V. cholerae as well as toxR and aphB mutants. As expected, DNA Damage inhibitor the toxR strain had significantly lower OmpU and higher OmpT levels than in the wild-type strain. Interestingly, the aphB mutant strain produced slightly higher levels of OmpT than wild type, though OmpU

levels did not seem to change (Fig. 6A). In addition, Provenzano et al. showed that ToxR-dependent modulation of outer membrane proteins enhances V. cholerae resistance to antimicrobial compounds such as bile salts and sodium dodecyl sulfate (SDS) [28]. We confirmed that the toxR mutant strain had a reduced minimum bactericidal concentration (MBC) Progesterone of SDS compared to wild type strains, but AphB did not affect the MBC of SDS (Fig. 6A). Thus, AphB may only subtly modulate outer membrane porin expression through its effect on toxR expression. This may be another downstream effect of AphB on the virulence capabilities of V. cholerae in addition to its better characterized influences on ToxT levels. Moreover, as both

ToxR and TcpP are required to activate toxT expression and AphB is required to activate tcpP expression (Fig. 1) [19, 29], we tested whether AphB effects on toxR expression affect toxT expression under the AKI virulence induction condition [22]. As expected, toxT expression in aphB mutants was significantly reduced as compared to that of wild type (Fig. 6B), however, bypassing the AphB regulation of tcpP by constitutively expressing tcpPH (pBAD-tcpPH induced with 0.01% arabinose) restored toxT expression in aphB mutants. These data suggest that AphB modulation of toxR expression has minor effects on virulence gene expression as compared to that of AphB regulation of tcpP under the condition we tested. Figure 6 The influence of AphB on V. cholerae outer membrane composition, SDS resistance, and toxT expression. (A). Analysis of outer membrane preparations of V. cholerae derivatives. SDS-PAGE gel stained with Coomassie blue. OmpT and OmpU are indicated at the right.