661-fold. Previous reports indicated that this subfamily of ABC transporters is involved in transport of many different MK-4827 nmr substrates, such as peptides, lipids, hydrophobic drugs, polysaccharides, and proteins [40]. MsbA is a lipid flippase that transports the lipid A-core moiety from the inner to the outer leaflet of the inner membrane in E. coli [17, 41]. Imp/OstA also participates in transport of LPS to the cell surface in E. coli [17] and N. meningitidis

[20]. We proposed that MsbA might be correlated with LPS transport in H. pylori. The deficiency in a LPS biosynthesis gene could result in antibiotic susceptibility, especially for hydrophobic antibiotics [42–44]. Therefore, weregarded msbA as a suitable candidate for

investigating CUDC-907 datasheet glutaraldehyde or other hydrophobic drug transport in bacteria. Reconfirmation of msbA expression in the clinical isolates by slot blots hybridization Microarray analysis demonstrated that msbA was upregulated by glutaraldehyde treatment, and the level of msbA expression in the clinical isolates after glutaraldehyde treatment was further determined by slot blot. RNA from the 11 strains used in the imp/ostA expression experiment (numbers 1~11) was extracted before or after www.selleckchem.com/products/gdc-0068.html glutaraldehyde treatment and hybridized with probes specific for 23S rRNA or msbA. The msbA transcripts were weakly detectable in the control without glutaraldehyde treatment; therefore, the RNA ratio (msbA/23S rRNA) without glutaraldehyde treatment was defined as 1, and the RNA ratio with glutaraldehyde treatment was calculated. The results confirmed the increased expression of msbA induced by glutaraldehyde (Fig. 3A). Furthermore, the level of msbA expression induced by glutaraldehyde was higher in strains with the MICs of 4–10 μg/ml than that in strains with the MICs of 1–3 μg/ml (P = 6.63 × 10-8) (Fig. 3B). Figure 3 The expression of msbA in 11 clinical isolates. (A) Slot blots analysis of msbA expression in 11 clinical isolates. Hybridization was performed with DIG probes specific for 23S

rRNA and msbA. (+) represents Nintedanib (BIBF 1120) glutaraldehyde treatment. (-) represents no glutaraldehyde treatment. (B) Bacteria were treated or not treated with glutaraldehyde by three independent experiments. The RNA ratio (msbA/23S rRNA) without glutaraldehyde treatment was defined as 1, and the RNA ratio with glutaraldehyde treatment was calculated. Effect of imp/ostA on the transcription of msbA after glutaraldehyde treatment The expression of both imp/ostA and msbA was increased in NTUH-S1 after glutaraldehyde treatment according to the results of the microarray analysis. To determine whether imp/ostA affects msbA gene expression after glutaraldehyde treatment and vice versa, RNA levels of imp/ostA and msbA in wild-type and mutant strains after 0.5 μg/ml glutaraldehyde treatment were analyzed by slot blot.