Mol Microbiol 2010, 77:1416–1428 PubMedCrossRef 46 Ohtani

Mol Microbiol 2010, 77:1416–1428.PubMedCrossRef 46. Ohtani

K, Bhowmik SK, Hayashi H, Shimizu T: Identification of a novel locus that regulates expression of toxin genes in Clostridium perfringens . FEMS Microbiol Lett 2002, 209:113–118.PubMedCrossRef 47. Hiscox TJ, Chakravorty A, Choo JM, Ohtani K, Shimizu T, Cheung JK: Regulation of virulence by the RevR response regulator in Clostridium perfringens . Infect Immun 2011, 79:2145–2153.PubMedCrossRef 48. Obana N, Nakamura K: A novel toxin regulator, the CPE1446-CPE1447 protein heteromeric complex, controls toxin genes in Clostridium perfringens . J Bacteriol 2011, 193:4417–4424.PubMedCrossRef 49. Brinsmade SR, Sonenshein AL: Dissecting complex metabolic integration provides direct genetic evidence for CodY activation by guanine nucleotides. J Bacteriol 2011, 193:5637–5648.PubMedCrossRef 50. SNS-032 price Dineen SS, McBride SM, Sonenshein AL: Integration of metabolism and virulence by Clostridium difficile CodY. J Bacteriol 2010, 192:5350–5362.PubMedCrossRef 51. Ohtani

K, Yuan Y, Hassan S, Wang R, Wang Y, Shimizu T: Virulence gene regulation by the agr system in Clostridium perfringens . J Bacteriol 2009, 191:3919–3927.PubMedCrossRef 52. Myers GS, Rasko DA, Cheung JK, Ravel J, Seshadri R, DeBoy RT: Skewed genomic variability in strains of the toxigenic bacterial pathogen, Clostridium perfringens . Genome Res 2006, 16:1031–1040.PubMedCrossRef 53. Deshpande A, Pant C, Jain A, Fraser TG, Rolston DD: Do fluoroquinolones predispose patients to Clostridium difficile associated disease? A review of the evidence. Curr Med Res Opin 2008, 24:329–333.PubMedCrossRef Selleckchem SU5416 Competing interests The authors declare that they have no competing interests. Obeticholic Acid solubility dmso Authors’ contributions Technical experiments and statistical analysis were performed by MP and SP. SP performed those on RT-PCR and cytotoxicity, morphological analysis and MP performed the rest of the experiments. SP wrote the first draft of the manuscript sections on RT-PCR analysis, Lonafarnib purchase cytotoxicity and cell morphology. FR planned the experiments, analyzed the data, and wrote the

manuscript. All authors have read and approved the final manuscript.”
“Background The genus Legionella includes approximately 53 species [1], with Legionella pneumophila being the most common human pathogenic species and causing 90% of all outbreaks of Legionnaires’ disease (LD) in Europe [2]. Legionella species are ubiquitous microorganisms, occurring predominantly in aquatic environments, freshwaters and hot water systems [2], soils, potting soils [3], and composts [4]. Cooling towers, whirlpool spas and shower faucets could be the sources of contaminated bioaerosols, the inhalation of which is generally considered to cause LD outbreaks [2]. A variety of culture methods to detect Legionella species are used to analyze environmental samples [5].

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