Heat-labile enterotoxin enhances small intestinal colonization wi | 53516
Journal of Clinical and Cellular Immunology

Journal of Clinical and Cellular Immunology
Open Access

ISSN: 2155-9899

+44 1223 790975

Heat-labile enterotoxin enhances small intestinal colonization with F18ac+ verotoxigenic E. coli

International Conference on Mucosal Immunology and Vaccine Development

July 28-29, 2016 Melbourne, Australia

Eric Cox

Ghent University, Belgium

Keynote: J Clin Cell Immunol

Abstract :

Enterotoxigenic E. coli (ETEC) play a major role in post-weaning diarrhea in pigs. Upon weaning, F4+ETEC rapidly colonize the small intestinal mucosa and produce LT enterotoxin which enhances fluid secretion leading to clinical signs. F18+ verotoxigenic E. coli (VTEC) mainly cause edema disease, which peaks the second week post-weaning. We postulated that exposure to LT, even in subclinical concentrations, changes the intestinal mucosa, enhancing colonization with F18+VTEC. Whereas 10 �?¼g LT (6 hours in 20 cm long small intestinal segment) was the lowest dose consistently inducing fluid secretion (56�?±70 g fluid/cm2 mucosa) and removing some mucus (76�?±7% mucus coverage), 30 �?¼g had a clearer effect (60�?±7%; control segments 89�?±5%). Inoculating the loops with 108 CFU F4ac+ETEC (LT+STa+STb+) induced a comparable fluid loss (356�?±133 mg fluid/cm2) and mucus coverage (68�?±8%). To analyze the effect of LT in vivo, the small intestinal tract of 4-week-old piglets was injected at 5 sites with different doses of LT, of which 350 �?¼g showed intermediate fluid and mucus loss and 250 �?¼g had no effect. Both latter doses were injected intraluminal in 7 and 4 pigs, respectively, to see if LT could enhance colonization of F18ab+VTEC strain (STx2e+) (1011 CFU in 10 ml PBS, 6 hours later, intragastrically) in comparison with placebo injected animals (n=7). Either 250 �?¼g or 350 �?¼g LT prolonged the duration of VTEC excretion and significantly increased the VTEC colonization between 4 and 7 days after the inoculation, supporting our hypothesis and the importance of vaccination against LT.

Biography :

Eric Cox has completed his PhD in 1991 at University of Ghent, Belgium. After completing his Post doctorate, he became Assistant Professor of Immunology at the Faculty of Veterinary Medicine, Gent University, Belgium. He is currently a full Professor and Head of the Lab of Immunology as well as Promotor of Provaxs a consortium of Gent University labs working on immunization and prophylaxis. He has published more than 200 papers in reputed journals. He has been serving as an Associated Editor of Frontiers in Mucosal Immunity.