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PubMedCrossRef 42. Yu J-H, Butchko RAE, Fernandes M, Keller NP, Leonard TJ, Adams TH: Conservation of structure and function of the BIX 1294 in vitro aflatoxin regulatory gene aflR from Aspergillus nidulans and A. flavus . Curr Genet 1996, 29:549–555.PubMedCrossRef 43. Brakhage A: Regulation of fungal secondary metabolism. Nat Rev Microbiol 2013, 11:21–32.PubMedCrossRef 44. Inderbitzin P, Asvarak T, Turgeon BG: S ix new genes required for production of T-toxin, a polyketide determinant of high virulence of Cochliobolus heterostrophus to maize . Mol Plant Microbe Interact 2010, 23:458–472.PubMedCrossRef 45. Hammock LG, Hammock BD, Casida JE: Detection and analysis

of epoxides with 4-(p-Nitrobenzyl)-pyridine. FHPI ic50 Bull Environ Contam Toxicol 1974, 12:759–764.PubMedCrossRef 46. Wight WD, Kim KH, Lawrence CB, Walton JD: Biosynthesis and role in virulence of the histone deacetylase inhibitor depudecin from Alternaria brassicicola . Mol Plant Microbe Interact 2009, 22:1258–1267.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions WW did most of the experimental work and wrote the first draft of the manuscript. RL discovered that A. jesenskae makes HC-toxin. JW did some of the bioinformatics analysis and wrote the

final draft of the manuscript. All authors read and approved the final manuscript.”
“Background Accurate identification of fastidious Gram-negative rods (GNR) Mocetinostat is a challenge for clinical microbiology laboratories. Fastidious GNR are slow-growing organisms, which generally require supplemented media or CO2 enriched atmosphere and fail to grow on enteric media such as MacConkey agar [1]. They are isolated infrequently and consist of different taxa including Actinobacillus, Capnocytophaga, Farnesyltransferase Cardiobacterium, Eikenella, Kingella, Moraxella, Neisseria, and Pasteurella. Most of them are colonizers of the human oral cavity but they have been demonstrated to cause severe systemic infections like endocarditis, septicemia and abscesses, particularly in immunocompromised patients [1, 2]. Accurate identification of fastidious GNR is of concern when isolated from normally sterile body sites regarding guidance of appropriate

antimicrobial therapy and patient management [1]. Identification of fastidious GNR by conventional methods is difficult and time-consuming because phenotypic characteristics such as growth factor requirements, fermentation and assimilation of carbohydrates, morphology, and staining behaviour are subject to variation and dependent on individual interpretation and expertise [1, 3]. Commercially available identification systems such as VITEK 2 NH (bioMérieux, Marcy L’Etoile, France) only partially allow for accurate identification of this group of microorganisms, e.g., Eikenella corrodens, Kingella kingae and Cardiobacterium hominis[4–6]. Most studies relied only on a subset of taxa of fastidious GNR or did not include clinical isolates under routine conditions [4–6].

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