Columbia University, New York; 2006 49 Sitkiewicz I, Stockbauer

Columbia University, New York; 2006. 49. Sitkiewicz I, Stockbauer KE, Musser JM: Secreted bacterial Proteasome inhibitors in cancer therapy phospholipase A2 enzymes: better living through phospholipolysis. Trends Microbiol 2007,15(2):63–69.PubMedCrossRef 50. Pukatzki S, Kessin RH, Mekalanos JJ: The human pathogen Pseudomonas aeruginosa utilizes conserved virulence pathways to infect the social amoeba Dictyostelium discoideum . Proc Natl Acad Sci USA 2002,99(5):3159–3164.PubMedCrossRef 51. Sacks DL, Modi G, Rowton E, Späth G, Epstein L, Turco SJ, Beverley SM: The role of phosphoglycans in Leishmania -sand fly interactions. Proc Natl Acad Sci USA 2000,97(1):406–411.PubMedCrossRef

52. Woods DE: The use of animal infection models to study the pathogenesis of melioidosis and glanders. Trends Microbiol 2002,10(11):483–484. discussion 484–485PubMedCrossRef Authors’ contributions CMR and LL conducted data analyses, comparative genomics, and wrote manuscript. LB and JI participated Trichostatin A mw in bioinformatic and genomic analysis. RU and DD isolated and characterize phages and isolated phage

DNA. MS isolated RNA for transcritpome analysis. WCN and DD conceived of the study, participated in its design and coordination, and helped draft manuscript. All authors have read and approved the final manuscript.”
“Background Of the species belonging to the “”psilosis”" group, Candida parapsilosis is by far the most studied and characterised. It represents about 90% of the infection attributed these to C. parapsilosis sensu lato [1] and it seems to be better adapted to the human

host than the two relatives (C. orthopsilosis and C. metapsilosis), as also shown by the high incidence of C. parapsilosis systemic infection worldwide, assessed as the second most common candidemia in many countries [2–6]. C. parapsilosis is an opportunistic pathogen that colonises human skin and can spread nosocomially through hand carriage [7, 8]. It has been frequently associated with infections in newborns [6, 8, 9] and in catheterised patients [3]. This can be linked to the ability of C. parapsilosis to produce biofilm in the presence of plastic surfaces such as catheters or other prosthetic materials [6, 10–12]. An increasing number of studies points towards a reduced genetic variability among C. parapsilosis isolates, which has been interpreted as a predominant clonal mode of reproduction [6, 13–15]. This is in contrast to what has been recently described for C. metapsilosis and C. orthopsilosis species, in which recombination has been shown to occur by AFLP analysis [16, 17]. On the other hand, a notable variability in virulence phenotypes has been observed for C. parapsilosis, such as the ability to produce biofilm or hydrolytic enzymes [6, 18]. In this study, a selection of 62 C.

Comments are closed.