| Literature DB >> 18367281 |
Andreas Tauch1, Eva Trost, Alexandra Tilker, Ulrike Ludewig, Susanne Schneiker, Alexander Goesmann, Walter Arnold, Thomas Bekel, Karina Brinkrolf, Iris Brune, Susanne Götker, Jörn Kalinowski, Paul-Bertram Kamp, Francisco Pereira Lobo, Prisca Viehoever, Bernd Weisshaar, Francisco Soriano, Marcus Dröge, Alfred Pühler.
Abstract
Corynebacterium urealyticum is a lipid-requiring, urealytic bacterium of the human skin flora that has been recognized as causative agent of urinary tract infections. We report the analysis of the complete genome sequence of C. urealyticum DSM7109, which was initially recovered from a patient with alkaline-encrusted cystitis. The genome sequence was determined by a combination of pyrosequencing and Sanger technology. The chromosome of C. urealyticum DSM7109 has a size of 2,369,219bp and contains 2024 predicted coding sequences, of which 78% were considered as orthologous with genes in the Corynebacterium jeikeium K411 genome. Metabolic analysis of the lipid-requiring phenotype revealed the absence of a fatty acid synthase gene and the presence of a beta-oxidation pathway along with a large repertoire of auxillary genes for the degradation of exogenous fatty acids. A urease locus with the gene order ureABCEFGD may play a pivotal role in virulence of C. urealyticum by the alkalinization of human urine and the formation of struvite stones. Multidrug resistance of C. urealyticum DSM7109 is mediated by transposable elements, conferring resistances to macrolides, lincosamides, ketolides, aminoglycosides, chloramphenicol, and tetracycline. The complete genome sequence of C. urealyticum revealed a detailed picture of the lifestyle of this opportunistic human pathogen.Entities:
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Year: 2008 PMID: 18367281 DOI: 10.1016/j.jbiotec.2008.02.009
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307