All authors read and approved the final manuscript “
“Backgr

All authors read and approved the final manuscript.”
“Background Helicobacter Tideglusib in vitro pylori was first isolated from the gastric mucosa of a patient with gastritis and peptic ulceration by Marshall and Warren in 1982 [1]. It is an important human pathogen, responsible for type B gastritis and peptic ulcers. Furthermore, infection by H. pylori is a risk factor for gastric adenocarcinoma and for lymphoma in the mucosa-associated lymphoid tissue of the BTK inhibitor libraries stomach in humans [2–5]. H. pylori is believed to be transmitted from person to person by oral-oral or oral-fecal routes [6]. However, another possible route involves transmission during endoscopic

examination of patients because contamination of endoscopy equipment by H. pylori frequently occurs after endoscopic examination of H. pylori-infected patients [7–9]. Because H. pylori is prevalent in the population [10],

it is important to prevent its transmission. In the hospital, manual pre-cleaning and soaking in glutaraldehyde click here is an important process used to disinfect endoscopes [7, 11]. However, endoscopic disinfection might not be sufficient to remove H. pylori completely [12, 13]. Some glutaraldehyde-resistant bacteria might survive and be passed to the next person undergoing endoscopic examination through unidentified mechanisms. Therefore, it is an important issue to clarify the mechanism of glutaraldehyde resistance. In our previous study, we demonstrated that the Imp/OstA protein was associated with glutaraldehyde resistance in a clinical strain of H. pylori [14]. OstA (organic solvent tolerance) [15] has also been called imp (increased membrane permeability) [16], and was recently named lptD in Escherichia coli [17]. Imp/OstA exists widely in Gram-negative bacteria and participates in biogenesis of the cell envelope. It is an essential outer membrane protein

in E. coli, depletion mutation of imp/ostA results in the formation of aberrant membranes Cediranib (AZD2171) [18]. Furthermore, Imp/OstA forms a complex with the RlpB lipoprotein and is responsible for lipopolysaccharide (LPS) assembly at the surface of the cell [17, 19]. In addition, it mediates the transport of LPS to the surface in Neisseria meningitidis [20]. To further investigate the mechanism of glutaraldehyde resistance, we monitored the minimum inhibitory concentrations (MICs) and the expression of imp/ostA and Imp/OstA protein after glutaraldehyde treatment in 11 clinical isolates. Full-genome expression was also studied by microarray analysis; 40 genes were upregulated and 31 genes were downregulated in NTUH-S1 after glutaraldehyde treatment. Among the upregulated genes, msbA, was selected for further study. MsbA is an essential inner membrane protein in E. coli and a member of the ABC transporter superfamily of proteins [21]. MsbA produced in the Gram-positive organism Lactococcus lactis is capable of conferring drug resistance to the organism [22].

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