Laboratory of Bacteriology, Instituto Butantan, Avenida Vital Brazil 1500, São Paulo, SP 05503-900, Brazil.
Infect Immun. 2011 May;79(5):1833-41. doi: 10.1128/IAI.00693-10. Epub 2011 Feb 22.
Enteropathogenic Escherichia coli (EPEC) induces a characteristic histopathology on enterocytes known as the attaching-and-effacing (A/E) lesion, which is triggered by proteins encoded by the locus of enterocyte effacement (LEE). EPEC is currently classified as typical EPEC (tEPEC) and atypical EPEC (aEPEC), based on the presence or absence of the EPEC adherence factor plasmid, respectively. Here we analyzed the LEE regions of three aEPEC strains displaying the localized adherence-like (LAL), aggregative adherence (AA), and diffuse adherence (DA) patterns on HEp-2 cells as well as one nonadherent (NA) strain. The adherence characteristics and the ability to induce A/E lesions were investigated with HeLa, Caco-2, T84, and HT29 cells. The adherence patterns and fluorescent actin staining (FAS) assay results were reproducible with all cell lines. The LEE region was structurally intact and functional in all strains regardless of their inability to cause A/E lesions. An EspF(U)-expressing plasmid (pKC471) was introduced into all strains, demonstrating no influence of this protein on either the adherence patterns or the capacity to cause A/E of the adherent strains. However, the NA strain harboring pKC471 expressed the LAL pattern and was able to induce A/E lesions on HeLa cells. Our data indicate that FAS-negative aEPEC strains are potentially able to induce A/E in vivo, emphasizing the concern about this test for the determination of aEPEC virulence. Also, the presence of EspF(U) was sufficient to provide an adherent phenotype for a nonadherent aEPEC strain via the direct or indirect activation of the LEE4 and LEE5 operons.
肠致病性大肠杆菌(EPEC)在肠细胞上诱导一种特征性的组织病理学改变,称为附着和消除(A/E)病变,这是由肠上皮细胞消除(LEE)基因座编码的蛋白质触发的。EPEC 目前根据是否存在 EPEC 粘附因子质粒,分别归类为典型 EPEC(tEPEC)和非典型 EPEC(aEPEC)。在这里,我们分析了 3 株显示局部粘附样(LAL)、聚集性粘附(AA)和弥漫性粘附(DA)模式的 aEPEC 菌株以及 1 株非粘附(NA)菌株的 LEE 区。使用 HeLa、Caco-2、T84 和 HT29 细胞研究了粘附特性和诱导 A/E 病变的能力。所有细胞系均能重现粘附模式和荧光肌动蛋白染色(FAS)试验结果。无论其是否不能引起 A/E 病变,LEE 区在所有菌株中结构完整且功能正常。将 EspF(U)表达质粒(pKC471)引入所有菌株中,证明该蛋白对粘附株的粘附模式和引起 A/E 的能力没有影响。然而,携带 pKC471 的 NA 菌株表达 LAL 模式,并能够在 HeLa 细胞上诱导 A/E 病变。我们的数据表明,FAS 阴性的 aEPEC 菌株在体内可能具有诱导 A/E 的能力,这强调了对该试验用于确定 aEPEC 毒力的关注。此外,EspF(U)的存在足以通过直接或间接激活 LEE4 和 LEE5 操纵子,为非粘附性 aEPEC 菌株提供粘附表型。