Fauconnier Alan, Allaoui Abdelmounaaïm, Campos Andrés, Van Elsen Ary, Cornelis Guy R, Bollen Alex
Applied Genetics, Université Libre de Bruxelles, Rue de I'Industrie 24, B-1400 Nivelles, Belgium.
Microbial Pathogenesis Unit, International Institute of Cellular and Molecular Pathology and Faculté de Médecine, Université Catholique de Louvain, Avenue Hippocrate 74, B-1200 Bruxelles, Belgium.
Microbiology (Reading). 1997 Nov;143 ( Pt 11):3461-3471. doi: 10.1099/00221287-143-11-3461.
The inv gene of Yersinia enterocolitica codes for invasin, a member of the invasin/intimin-like protein family, which mediates the internalization of the bacterium into cultured epithelial cells. The putative inclusion of inv into a pathogenicity island was tested by investigating its flanking sequences. Indeed, the enteropathogenic Escherichia coli (EPEC) intimin, a member of the same family of proteins, is encoded by eaeA, a gene which belongs to a pathogenicity island. An ORF located upstream from inv was of particular interest since it appeared homologous both to the flagellar flhA gene and to sepA, an EPEC gene lying inside the same pathogenicity island as eaeA. A mutant in this ORF was non-motile and non-flagellated while its invasion phenotype remained unaffected. These data indicated that the ORF corresponded to the flhA gene of Y. enterocolitica. Subsequently, the flhB and flhE genes, located respectively upstream and downstream from flhA, were identified. The three flh genes appear to be transcribed from a single operon called flhB, according to the nomenclature used for Salmonella typhimurium. Intergenic sequence between flhE and inv includes a grey hole, with no recognizable function. Downstream from inv, we have detected the flagellar flgM operon as already reported. Finally, the incongruous localization of inv amidst the flagellar cluster is discussed; while transposition could explain this phenomenon, no trace of such an event was detected.
小肠结肠炎耶尔森菌的inv基因编码侵袭素,它是侵袭素/紧密黏附素样蛋白家族的成员,介导细菌内化进入培养的上皮细胞。通过研究inv侧翼序列来检测其是否可能包含在致病岛中。实际上,同一家族蛋白成员的肠致病性大肠杆菌(EPEC)紧密黏附素由eaeA编码,eaeA是一个属于致病岛的基因。位于inv上游的一个开放阅读框(ORF)特别引人关注,因为它与鞭毛flhA基因以及sepA同源,sepA是一个与eaeA位于同一致病岛内的EPEC基因。该ORF中的一个突变体无运动性且无鞭毛,但其侵袭表型未受影响。这些数据表明该ORF对应于小肠结肠炎耶尔森菌的flhA基因。随后,分别位于flhA上游和下游的flhB和flhE基因被鉴定出来。根据鼠伤寒沙门氏菌使用的命名法,这三个flh基因似乎从一个名为flhB的单一操纵子转录。flhE和inv之间的基因间序列包含一个无明显功能的“灰洞”。在inv下游,我们已检测到如先前报道的鞭毛flgM操纵子。最后,讨论了inv在鞭毛簇中的不协调定位;虽然转座可以解释这一现象,但未检测到此类事件的痕迹。