» Articles » PMID: 20181246

Application of a Pig Ligated Intestinal Loop Model for Early Lawsonia Intracellularis Infection

Overview
Journal Acta Vet Scand
Publisher Biomed Central
Date 2010 Feb 26
PMID 20181246
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

Citing Articles

In Vitro Screening of Non-Antibiotic Components to Mitigate Intestinal Lesions Caused by , and Serovar Typhimurium.

de Groot N, Meneguzzi M, de Souza B, Costa M Animals (Basel). 2022; 12(18).

PMID: 36139216 PMC: 9494979. DOI: 10.3390/ani12182356.


Development of a vivo rabbit ligated intestinal Loop Model for HCMV infection.

Tang J, Wu Q, Tang X, Shi R, Suo J, Huang G J Anim Sci Biotechnol. 2016; 7:69.

PMID: 27999668 PMC: 5154130. DOI: 10.1186/s40104-016-0129-1.


The rabbit as an infection model for equine proliferative enteropathy.

Sampieri F, Allen A, Pusterla N, Vannucci F, Antonopoulos A, Ball K Can J Vet Res. 2013; 77(2):110-9.

PMID: 24082402 PMC: 3605926.

References
1.
Molbak L, Johnsen K, Boye M, Jensen T, Johansen M, Moller K . The microbiota of pigs influenced by diet texture and severity of Lawsonia intracellularis infection. Vet Microbiol. 2007; 128(1-2):96-107. DOI: 10.1016/j.vetmic.2007.09.012. View

2.
Hughes R, OLANDER H, Williams C . Swine dysentery: pathogenicity of Treponema hyodysenteriae. Am J Vet Res. 1975; 36(7):971-7. View

3.
McOrist S, Gebhart C, Bosworth B . Evaluation of porcine ileum models of enterocyte infection by Lawsonia intracellularis. Can J Vet Res. 2006; 70(2):155-9. PMC: 1410719. View

4.
Boesen H, Jensen T, Moller K, Nielsen L, Jungersen G . Evaluation of a novel enzyme-linked immunosorbent assay for serological diagnosis of porcine proliferative enteropathy. Vet Microbiol. 2005; 109(1-2):105-12. DOI: 10.1016/j.vetmic.2005.05.004. View

5.
Lawson G, Gebhart C . Proliferative enteropathy. J Comp Pathol. 2000; 122(2-3):77-100. DOI: 10.1053/jcpa.1999.0347. View