Wieler L H, Vieler E, Erpenstein C, Schlapp T, Steinrück H, Bauerfeind R, Byomi A, Baljer G
Institut für Hygiene und Infektionskrankheiten, Tiere der Universität Giessen, Germany.
J Clin Microbiol. 1996 Dec;34(12):2980-4. doi: 10.1128/jcm.34.12.2980-2984.1996.
Out of 174 bovine Shiga toxin-producing Escherichia coli (STEC) strains isolated from diarrheic calves in Germany and Belgium, 122 strains (70.1%) were selected because of their reactivity with the eae (E. coli attaching and effacing gene) probe ECW1-ECW2. One hundred seven of these eae-positive strains (87.7%) harbored stx1 genes, 13 strains (10.7%) had stx2 genes, and 2 strains (1.6%) had both stx genes. The strains displayed 17 different O types, the majority (97 strains) [79.5%]) belonging to O5 (5 strains), O26 (21 strains), O111 (13 strains) O118 (36 strains), O145 (9 strains), and O157 (13 strains). In the HEp-2 cell adhesion assay, 99 strains (81.1%) showed a localized adhesion, and 80 strains (65.6%) stimulated actin accumulation, as determined in the fluorescence actin staining test. None of the strains harbored genes coding for bundle-forming pili (bfpA), clearly differentiating them from enteropathogenic. E. cole. espB gene sequences were only detectable in 23 (18.9%) of the eae-positive bovine STEC strains. Three different PCRs were established, differentiating between eae sequences of enteropathogenic E. coli strain E2348/69 (O127:H6) and STEC strain EDL933 (O157: H7). Primers matching in the more heterologous downstream eae sequences gave amplicons in only 8 of the 17 O types (O84:H-, O103:H2, O111:H-, O111:H2, O119:H25, O128:H-, O145:H28, and O157:H-). Only 15 STEC strains, belonging to serotypes O111H:-, O111H:2, O145:H28, and O157:H-, gave amplicons in all three eae-specific PCRs. These data demonstrate that bovine STEC strains are a heterogeneous group of pathogenic bacteria, a lot of which share virulence markers with STEC strains causing infections in humans. However, in contrast to human STEC strains, bovine eae-positive STEC strains are mainly restricted to the stx1 genotype. The observation that espB sequences are not highly conserved might have consequences for the serological recognition of the ESPB protein in patients. Like in human STEC strains, eae-related sequences are closely associated with certain E. coli O groups; however, they are not serotype specific.
在从德国和比利时腹泻犊牛中分离出的174株产志贺毒素大肠杆菌(STEC)中,有122株(70.1%)因与eae(大肠杆菌黏附和损伤基因)探针ECW1 - ECW2反应而被选取。这些eae阳性菌株中,107株(87.7%)携带stx1基因,13株(10.7%)有stx2基因,2株(1.6%)同时有两种stx基因。这些菌株呈现出17种不同的O型,大多数(97株,占79.5%)属于O5(5株)、O26(21株)、O111(13株)、O118(36株)、O145(9株)和O157(13株)。在HEp - 2细胞黏附试验中,99株(81.1%)表现出局部黏附,并且如荧光肌动蛋白染色试验所确定的,80株(65.6%)刺激了肌动蛋白积累。没有菌株携带编码束状菌毛(bfpA)的基因,这明显将它们与肠致病性大肠杆菌区分开来。espB基因序列仅在23株(18.9%)eae阳性牛源STEC菌株中可检测到。建立了三种不同的PCR方法,以区分肠致病性大肠杆菌菌株E2348/69(O127:H6)和STEC菌株EDL933(O157:H7)的eae序列。与更多异源下游eae序列匹配的引物仅在17种O型中的8种(O84:H - 、O103:H2、O111:H - 、O111:H2、O119:H25、O128:H - 、O145:H28和O157:H - )中产生扩增产物。仅15株属于血清型O111H: - 、O111H:2、O145:H28和O157:H - 的STEC菌株在所有三种eae特异性PCR中都产生了扩增产物。这些数据表明,牛源STEC菌株是一组异质性病原菌,其中许多与导致人类感染的STEC菌株共享毒力标记。然而,与人类STEC菌株不同,牛源eae阳性STEC菌株主要局限于stx1基因型。espB序列不高度保守这一观察结果可能对患者中ESPB蛋白的血清学识别产生影响。与人类STEC菌株一样,eae相关序列与某些大肠杆菌O群密切相关;然而,它们不是血清型特异性的。