Bleich Andre, Sundberg John P, Smoczek Anna, von Wasielewski Reinhard, de Buhr Maike F, Janus Lydia M, Julga Gwen, Ukena Sya N, Hedrich Hans-J, Gunzer Florian
Institute for Laboratory Animal Science and Central Animal Facility, Hannover Medical School, Hannover, Germany.
Int J Exp Pathol. 2008 Feb;89(1):45-54. doi: 10.1111/j.1365-2613.2007.00560.x. Epub 2007 Nov 13.
Escherichia coli Nissle 1917 (EcN) is a well-characterized probiotic bacterium. Although genomic comparisons of EcN with the uropathogenic E. coli strain CFT073 revealed high degrees of similarity, EcN is generally considered a non-pathogenic organism. However, as recent evidence suggests that EcN is capable of inducing inflammatory responses in host intestinal epithelial cells, we aimed to investigate potential pathogenic properties of EcN in an in vivo model using various germ-free (GF) mouse strains. With the exception of C3H/HeJZtm mice, which carry a defective toll-like receptor (TLR)4-allele, no lesions were obvious in mice of different strains orally inoculated with EcN for 1 week, although organ cultures (blood, lung, mesenteric lymph node, pancreas, spleen, liver and kidney) tested positive to various degrees. C3H/HeJZtm mice inoculated with EcN became clinically ill and the majority died or had to be euthanized. Organs of all gnotobiotic C3H/HeJZtm mice were positive for EcN by culture; major histological findings were moderate to severe pyogranulomatous serositis, typhlitis and pancreatitis. Histological findings were corroborated by highly elevated tumour necrosis factor (TNF) serum levels. Lesions were not detected in specified pathogen free maintained C3H/HeJZtm mice, GF C3H/HeJ mice lacking the interleukin-10 gene, or GF C3H/HeJZtm mice that were inoculated with E. coli K12 strain MG1655 as a control. In addition, mild histological lesions were detected in Ztm:NMRI mice 3 months after oral inoculation with EcN. This study shows that EcN is capable of displaying a virulent phenotype in GF C3H/HeJZtm mice. Whether this phenotype is linked to the bacterium's probiotic nature should be the focus of further studies.
大肠杆菌Nissle 1917(EcN)是一种特征明确的益生菌。尽管EcN与尿路致病性大肠杆菌菌株CFT073的基因组比较显示出高度相似性,但EcN通常被认为是一种非致病生物体。然而,由于最近有证据表明EcN能够在宿主肠道上皮细胞中诱导炎症反应,我们旨在使用各种无菌(GF)小鼠品系在体内模型中研究EcN的潜在致病特性。除了携带缺陷型Toll样受体(TLR)4等位基因的C3H/HeJZtm小鼠外,用EcN口服接种1周的不同品系小鼠均未出现明显病变,尽管器官培养物(血液、肺、肠系膜淋巴结、胰腺、脾脏、肝脏和肾脏)在不同程度上检测呈阳性。接种EcN的C3H/HeJZtm小鼠出现临床疾病,大多数死亡或不得不实施安乐死。所有悉生C3H/HeJZtm小鼠的器官经培养对EcN呈阳性;主要组织学发现为中度至重度脓性肉芽肿性浆膜炎、盲肠炎和胰腺炎。肿瘤坏死因子(TNF)血清水平大幅升高证实了组织学发现。在特定病原体-free饲养的C3H/HeJZtm小鼠、缺乏白细胞介素-10基因的GF C3H/HeJ小鼠或接种大肠杆菌K12菌株MG1655作为对照的GF C3H/HeJZtm小鼠中均未检测到病变。此外,在口服接种EcN 3个月后的Ztm:NMRI小鼠中检测到轻度组织学病变。本研究表明,EcN能够在GF C3H/HeJZtm小鼠中表现出毒性表型。这种表型是否与该细菌的益生菌性质有关应是进一步研究的重点。