J Bacteriol 2010,192(12):3235–3239 PubMedCrossRef 19 Casino P, R

J Bacteriol 2010,192(12):3235–3239.PubMedCrossRef 19. Casino P, Rubio V, Marina A: Structural insight into partner specificity and phosphoryl transfer in two-component signal transduction. Cell 2009,139(2):325–336.PubMedCrossRef

20. Ratajczak E, Strozecka J, Matuszewska M, Zietkiewicz S, Kuczynska-Wisnik D, Laskowska E, Liberek K: IbpA the small heat shock protein from Escherichia coli forms fibrils in the absence of its cochaperone IbpB. FEBS Lett 2010,584(11):2253–2257.PubMedCrossRef Authors’ contributions AZD5363 mouse CVDH performed all experiments with the help of others, as indicated below, and drafted the MI-503 manuscript. CC and JW performed to the gel permeation experiment. MD participated to the construction of the plasmid used for PdhS-mCherry production in E. coli. JYM contributed to the microscopy. JJL participated in the writing of the manuscript. XDB coordinated the study and finalized the manuscript. All authors read and approved the final manuscript.”
“Background Salmonella enterica Serovar Enteritidis (S. Enteritidis) is a facultative intracellular pathogen responsible for

acute gastroenteritis and is currently the second most frequently isolated serovar in the United States – accounting for nearly 15% of total cases of human salmonellosis [1]. S. Enteritidis maintains its status as a leading cause of foodborne infections mainly due to its prevalence in poultry products and its environmental persistence despite the harsh conditions it encounters. Nutlin-3 purchase The survival of this pathogen under intense conditions has been linked to its remarkable ability to quickly respond to environmental signals

and adapt to its surroundings, as well as the induction of specific stress responses during environmental adaptation [2–6]. Throughout MTMR9 its infection cycle, S. Enteritidis encounters several distinctive environments including those rich in the short chain fatty acids (SCFAs) acetate, propionate (PA), and butyrate. PA is one of many SCFAs deemed acceptable for use in food preservation and is frequently employed to suppress bacterial growth in foods such as meat, salad dressing, and mayonnaise [7]. Also, the anaerobic environment of the mammalian ileum, cecum, and colon are rich in SCFAs and accumulate PA as a main byproduct of fermentative bacterial species [8, 9]. Although the aforementioned SCFAs are all commonly encountered by S. Enteritidis during successful infection, a previous study indicates that PA may play a more important role than other SCFAs in the induction of subsequent stress responses [5]. Food processing systems and the mammalian gut are excellent sources for long term exposure to PA.

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