Tauch Andreas, Trost Eva, Tilker Alexandra, Ludewig Ulrike, Schneiker Susanne, Goesmann Alexander, Arnold Walter, Bekel Thomas, Brinkrolf Karina, Brune Iris, Götker Susanne, Kalinowski Jörn, Kamp Paul-Bertram, Lobo Francisco Pereira, Viehoever Prisca, Weisshaar Bernd, Soriano Francisco, Dröge Marcus, Pühler Alfred
Institut für Genomforschung und Systembiologie, Centrum für Biotechnologie, Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany.
J Biotechnol. 2008 Aug 31;136(1-2):11-21. doi: 10.1016/j.jbiotec.2008.02.009. Epub 2008 Mar 10.
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.
解脲棒杆菌是人类皮肤菌群中一种需要脂质、能分解尿素的细菌,已被确认为尿路感染的病原体。我们报告了对解脲棒杆菌DSM7109完整基因组序列的分析,该菌株最初从一名患有碱性结痂性膀胱炎的患者中分离得到。基因组序列通过焦磷酸测序和桑格技术相结合的方法测定。解脲棒杆菌DSM7109的染色体大小为2,369,219bp,包含2024个预测的编码序列,其中78%被认为与杰氏棒杆菌K411基因组中的基因直系同源。对其需要脂质表型的代谢分析表明,该菌缺乏脂肪酸合酶基因,但存在β-氧化途径以及大量用于降解外源脂肪酸的辅助基因。一个具有ureABCEFGD基因顺序的脲酶基因座可能通过使人尿液碱化和形成鸟粪石结石,在解脲棒杆菌的毒力中发挥关键作用。解脲棒杆菌DSM7109的多重耐药性由转座元件介导,使其对大环内酯类、林可酰胺类、酮内酯类、氨基糖苷类、氯霉素和四环素产生耐药性。解脲棒杆菌的完整基因组序列揭示了这种机会性人类病原体的生活方式的详细情况。