Janke B, Dobrindt U, Hacker J, Blum-Oehler G
Institut für Molekulare Infektionsbiologie, Universität Würzburg, Röntgenring 11, D-97070, Würzburg, Germany.
FEMS Microbiol Lett. 2001 May 15;199(1):61-6. doi: 10.1111/j.1574-6968.2001.tb10651.x.
Suppression subtractive hybridisation (SSH) was performed to identify genomic differences between the uropathogenic Escherichia coli strain 536 and the non-pathogenic E. coli K-12 strain MG1655. In total, 22 DNA fragments were isolated which were specific for strain 536. Five of these fragments showed homology to known virulence determinants and four fragments matched genes for lipopolysaccharide (LPS) or capsule biosynthesis and a siderophore receptor. Seven fragments did not show any homology to known genes. These fragments may represent parts of putative pathogenicity islands (PAIs). Whereas two fragments were highly specific for uropathogenic E. coli (UPEC), the other fragments could also be detected among the other tested wild-type strains.
采用抑制性消减杂交技术(SSH)来鉴定尿路致病性大肠杆菌菌株536与非致病性大肠杆菌K-12菌株MG1655之间的基因组差异。总共分离出22个对菌株536特异的DNA片段。其中5个片段与已知的毒力决定簇具有同源性,4个片段与脂多糖(LPS)或荚膜生物合成基因以及一个铁载体受体基因相匹配。7个片段与已知基因无任何同源性。这些片段可能代表推定的致病岛(PAIs)的部分。虽然有两个片段对尿路致病性大肠杆菌(UPEC)具有高度特异性,但在其他测试的野生型菌株中也能检测到其他片段。