National Veterinary Institute, Technical University of Denmark, Copenhagen V, Denmark.
Acta Vet Scand. 2010 Feb 24;52(1):17. doi: 10.1186/1751-0147-52-17.
Porcine proliferative enteropathy in pigs is caused by the obligate, intracellular bacterium Lawsonia intracellularis. In vitro studies have shown close bacterium-cell interaction followed by cellular uptake of the bacterium within 3 h post inoculation (PI). However, knowledge of the initial in vivo interaction between porcine intestinal epithelium and the bacterium is limited. The aims of the present study were to evaluate the usefulness of a ligated small intestinal loop model to study L. intracellularis infections and to obtain information on the very early L. intracellularis-enterocyte interactions.
A ligated small intestinal loop model using three different L. intracellularis inocula was applied to 10-11-week-old pigs. The inocula were 1) wild type bacteria derived from overnight incubation of L. intracellularis bacteria from spontaneous disease, 2) crude vaccine bacteria (Enterisol Ileitis Vet), and 3) vaccine bacteria propagated in cell culture. The bacteria-enterocyte interaction was visualised using immunohistochemistry on specimens derived 1, 3 and 6 h PI respectively.
Although at a low level, close contact between bacteria and the enterocyte brush border including intracellular uptake of bacteria in mature enterocytes was seen at 3 and 6 h PI for the vaccine and the propagated vaccine inocula. Interaction between the wild-type bacteria and villus enterocytes was scarce and only seen at 6 h PI, where a few bacteria were found in close contact with the brush border.
The ligated intestinal loop model was useful with respect to maintaining an intact intestinal morphology for up to 6 h. Furthermore, the study demonstrated that L. intracellularis interacts with villus enterocytes within 3 to 6 h after inoculation into intestinal loops and that the bacterium, as shown for the vaccine bacteria, propagated as well as non-propagated, was able to invade mature enterocytes. Thus, the study demonstrates the early intestinal invasion of L. intracellularis in vivo.
猪增生性肠病是由严格的、细胞内细菌劳森氏菌引起的。体外研究表明,在接种后 3 小时内,细菌与细胞密切相互作用,随后细菌被细胞摄取。然而,关于猪肠道上皮细胞与细菌的最初体内相互作用的知识有限。本研究的目的是评估结扎小肠环模型在研究劳森氏菌感染中的有用性,并获得关于劳森氏菌-肠细胞相互作用的早期信息。
使用三种不同的劳森氏菌接种物应用于 10-11 周龄猪的结扎小肠环模型。接种物为 1)来自自发疾病的劳森氏菌过夜培养的野生型细菌,2)粗制疫苗细菌(Enterisol Ileitis Vet),和 3)在细胞培养中繁殖的疫苗细菌。分别在接种后 1、3 和 6 小时采集标本,通过免疫组织化学观察细菌-肠细胞相互作用。
尽管水平较低,但在接种疫苗和繁殖疫苗接种物后 3 和 6 小时,可见到细菌与肠细胞刷状缘的紧密接触,包括成熟肠细胞内的细菌摄取。野生型细菌与绒毛状肠细胞的相互作用很少,仅在 6 小时时观察到,此时有少数细菌与刷状缘紧密接触。
结扎肠环模型对于保持完整的肠形态长达 6 小时是有用的。此外,该研究表明,劳森氏菌在接种到肠环后 3 至 6 小时内与绒毛状肠细胞相互作用,并且该细菌,如疫苗细菌所示,繁殖和非繁殖都能够侵入成熟的肠细胞。因此,该研究证明了劳森氏菌在体内的早期肠道入侵。