Literature DB >> 11943318

F4 receptor-independent priming of the systemic immune system of pigs by low oral doses of F4 fimbriae.

Wim Van den Broeck1, Hilde Bouchaut, Eric Cox, Bruno M Goddeeris.   

Abstract

Oral administration of F4 fimbriae of Escherichia coli induces intestinal mucosal immune responses in F4 receptor-positive (F4R(+)) pigs, but not in F4R(-) pigs. We examined whether F4 fimbriae in F4R(-) animals behave like a food antigen and can induce oral tolerance. Therefore, F4R(+) and F4R(-) pigs were fed 2mg of F4 and challenged i.m. to evaluate the effect of oral F4 on the systemic immune system. As control antigen, two different oral doses (2 and 600 mg) of OVA were used. Thirty days after the i.m. OVA challenge, the OVA-specific serum IgG titre in 600 mg-fed pigs was lower than that in non-fed animals, indicating that tolerance was induced. Conversely, in the 2mg-fed pigs a rapid increase of OVA-specific IgG with higher titres than those in non-fed pigs was seen following challenge, indicating a priming of the systemic immune system. A similar priming was seen in both F4-fed F4R(-) and F4R(+) pigs. Upon challenge, non-fed pigs displayed a primary immune response with a slow increase of F4-specific serum IgG, whereas F4-fed F4R(-) and F4R(+) pigs showed secondary responses with a rapid increase of serum IgG. This was expected in F4R(+) pigs, as in these animals oral F4 induces F4-specific antibody-secreting cells in the spleen, suggesting a priming of the systemic immune system. However, also the F4-fed F4R(-) pigs displayed a secondary response, despite the failure to detect a response upon oral F4 administration. These findings suggest that the F4 antigen, at a dose of 2 mg, behaves like a common food antigen in F4R(-) pigs, namely it induces a systemic priming.

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Year:  2002        PMID: 11943318     DOI: 10.1016/s0165-2427(01)00429-9

Source DB:  PubMed          Journal:  Vet Immunol Immunopathol        ISSN: 0165-2427            Impact factor:   2.046


  7 in total

1.  Receptor-dependent immune responses in pigs after oral immunization with F4 fimbriae.

Authors:  W Van den Broeck; E Cox; B M Goddeeris
Journal:  Infect Immun       Date:  1999-02       Impact factor: 3.441

Review 2.  Animal Enterotoxigenic Escherichia coli.

Authors:  J Daniel Dubreuil; Richard E Isaacson; Dieter M Schifferli
Journal:  EcoSal Plus       Date:  2016-10

3.  Optimized FaeG expression and a thermolabile enterotoxin DNA adjuvant enhance priming of an intestinal immune response by an FaeG DNA vaccine in pigs.

Authors:  V Melkebeek; E Sonck; F Verdonck; B M Goddeeris; E Cox
Journal:  Clin Vaccine Immunol       Date:  2006-11-15

4.  Production of a subunit vaccine candidate against porcine post-weaning diarrhea in high-biomass transplastomic tobacco.

Authors:  Igor Kolotilin; Angelo Kaldis; Bert Devriendt; Jussi Joensuu; Eric Cox; Rima Menassa
Journal:  PLoS One       Date:  2012-08-03       Impact factor: 3.240

5.  The fecal presence of enterotoxin and F4 genes as an indicator of efficacy of treatment with colistin sulfate in pigs.

Authors:  Mohamed Rhouma; John Morris Fairbrother; William Thériault; Francis Beaudry; Nadia Bergeron; Sylvette Laurent-Lewandowski; Ann Letellier
Journal:  BMC Microbiol       Date:  2017-01-05       Impact factor: 3.605

6.  Deletion of FaeG alleviated Enterotoxigenic Escherichia coli F4ac-induced apoptosis in the intestine.

Authors:  Pengpeng Xia; Yunping Wu; Siqi Lian; Guomei Quan; Yiting Wang; Guoqiang Zhu
Journal:  AMB Express       Date:  2021-03-18       Impact factor: 3.298

7.  F4-related mutation and expression analysis of the aminopeptidase N gene in pigs.

Authors:  T Goetstouwers; M Van Poucke; V U Nguyen; V Melkebeek; A Coddens; D Deforce; E Cox; L J Peelman
Journal:  J Anim Sci       Date:  2014-03-18       Impact factor: 3.159

  7 in total

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