XII - 12th International Symposium - Digestive Physiology of Pigs
XII - 12th International Symposium - Digestive Physiology of Pigs
XII - 12th International Symposium - Digestive Physiology of Pigs
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<strong>Digestive</strong><br />
<strong>Physiology</strong><br />
<strong>of</strong> <strong>Pigs</strong><br />
piglets experimentally challenged with Escherichia<br />
coli. R. Badia 1,2 , R. Lizardo 1 , P. Martinez 2 , I. Badiola 3 , and<br />
J. Brufau* 1 , 1 IRTA - Institut de Recerca i Tecnologia Agroalimentaries,<br />
Constantí, Tarragona, Spain, 2 IBB - UAB Institut<br />
de Biotecnología i Biomedicina - Universidad Autonoma de<br />
Barcelona, Bellaterra, Barcelona, Spain, 3 CReSA - Centre<br />
de Recerca en Sanitat Animal, Bellaterra, Barcelona, Spain.<br />
Gums and yeast cells are natural mannose-rich products<br />
that can be used as subtrates for adhesion <strong>of</strong> Gram-negative<br />
bacteria. Moreover, live yeast has beneficial effects in the<br />
prevention and treatment <strong>of</strong> intestinal disorders. The aim<br />
<strong>of</strong> the study was to investigate the role <strong>of</strong> dietary locust<br />
bean gum (LBG, Salmosan, ITPSA, Spain) or live yeast<br />
(Saccharomyces cerevisae SC47, Actisaf, Lesaffre, France)<br />
as immunological enhancers <strong>of</strong> the intestinal epithelium <strong>of</strong><br />
piglets. Treatments included a non-infected group fed with a<br />
control diet and 4 other groups orally challenged with 1 × 10 8<br />
cfu <strong>of</strong> Escherichia coli K99. These 4 groups corresponded<br />
to animals fed a control diet or supplemented with colistin,<br />
LBG or yeast. Twenty-five Landrace × Duroc piglets<br />
weaned at 4 wk were used. They were housed in groups<br />
and fed experimental diets for 2 wk before the challenge<br />
and euthanized 3 d later. Blood, bile, ileum and mesenteric<br />
lymph node (MLN) were sampled for analysis <strong>of</strong> C-reactive<br />
protein (CRP), secretory immunoglobulin A (sIgA) and tolllike<br />
receptors 2 (TLR2) and 4 (TLR4). C-reactive protein <strong>of</strong><br />
control fed piglets increased after the challenge (P < 0.001).<br />
However, piglets previously fed with LBG and yeast diets<br />
showed CRP levels similar to the non-challenged group.<br />
Bile sIgA levels increased for all the challenged groups<br />
and particularly for the pigs fed the yeast diet (P < 0.01).<br />
Compared with non-challenged pigs, both receptors in MLN<br />
and ileal TLR4 were upregulated in control group after the<br />
challenge (P < 0.05). <strong>Pigs</strong> fed yeast diet showed similar<br />
expression <strong>of</strong> TLR2 and TLR4 to unchallenged pigs in both<br />
tissues, whereas pigs fed LBG diets showed intermediate<br />
results. It appears that piglets fed yeast diet were protected<br />
against an E.coli infection. In conclusion, live yeast S.<br />
cerevisiae and locust bean gum may reduce the risk <strong>of</strong> E.<br />
coli infection and may be suitable alternatives to antibiotic<br />
growth promoters for the weaned piglet.<br />
Key words: piglet, immunity, E. coli challenge<br />
2006 effects <strong>of</strong> feeding capsicum oleoresin, garlicon,<br />
or turmeric oleoresin on gene expression <strong>of</strong> ileal mucosa<br />
<strong>of</strong> pigs experimentally infected with a pathogenic E.<br />
coli. Y. Liu* 1 , M. Song1 , T. M. Che1 , J. A. Soares-Almeida1 ,<br />
J. J. Lee1 , D. Bravo2 , C. W. Maddox1 , and J. E. Pettigrew1 ,<br />
1 2 University <strong>of</strong> Illinois, Urbana, IL, USA, Pancosma SA, Geneva,<br />
Switzerland.<br />
This study characterized the effects <strong>of</strong> 3 plant extracts<br />
on gene expression in ileal mucosa <strong>of</strong> weaned pigs<br />
experimentally infected with a pathogenic E. coli. Weaned<br />
pigs (n = 64, 6.3 kg BW, 21 d old) were housed in individual<br />
pens for 15 d: 4 d before and 11 d after the first inoculation<br />
(d 0). Treatments were in a 2 × 4 factorial arrangement:<br />
with or without an F-18 E. coli challenge and 4 diets (a<br />
nursery basal diet (CON), 10 ppm <strong>of</strong> capsicum oleoresin<br />
<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />
DIGESTIVE PHYSIOLOGY OF PIGS<br />
94<br />
Session III<br />
(CAP), garlicon (GAR), or turmeric oleoresin (TUR)). Total<br />
RNA (4 pigs/treatment) was extracted from ileal mucosa <strong>of</strong><br />
pigs at d 5. Double-stranded cDNA was amplified, labeled,<br />
and further hybridized to the Affymetrix GeneChip Genome<br />
Array. Microarray data were analyzed in R using packages<br />
from the Bioconductor project. Bioinformatics analysis was<br />
conducted by DAVID Bioinformatics Resources. Pairwise<br />
comparisons tested 4 different effects <strong>of</strong> interest. The E. coli<br />
infection altered the expression <strong>of</strong> 240 genes <strong>of</strong> pigs fed the<br />
CON. Compared with the infected CON, feeding CAP, GAR,<br />
and TUR affected the expression <strong>of</strong> 52 (18 up, 34 down),<br />
117 (34 up, 83 down), and 84 (16 up, 68 down) genes,<br />
respectively. The E. coli infection upregulated (P < 0.05)<br />
the expression <strong>of</strong> genes related to the activation <strong>of</strong> immune<br />
response, but downregulated (P < 0.05) the expression <strong>of</strong><br />
genes involved in protein synthesis and accumulation; in<br />
most <strong>of</strong> cases the plant extracts counteracted these effects<br />
<strong>of</strong> E. coli. Compared with the infected CON, feeding CAP<br />
and GAR increased (P < 0.05) the expression <strong>of</strong> genes<br />
related to membrane, suggesting enhanced gut mucosa<br />
health. Moreover, feeding all 3 plant extracts reduced (P<br />
< 0.05) the expression <strong>of</strong> genes associated with antigen<br />
presentation or other biological processes <strong>of</strong> immune<br />
responses, indicating attenuation <strong>of</strong> overstimulation <strong>of</strong><br />
immune responses caused by E. coli. In conclusion,<br />
plant extracts regulated the expression <strong>of</strong> genes in ileal<br />
mucosa <strong>of</strong> E. coli-infected pigs, perhaps providing benefits<br />
by enhancing the gut mucosa health and attenuating the<br />
overstimulation <strong>of</strong> the immune system.<br />
Key words: Escherichia coli, pigs, plant extracts<br />
2007 Butyrate relieves weaning diarrhea by promoting<br />
repair <strong>of</strong> pig intestinal barrier. X. Ma,* S. Hu, and D.<br />
Li, State Key Laboratory <strong>of</strong> Animal Nutrition, China Agricultural<br />
University, No.2 Yuanmingyuan West Road, Beijing,<br />
P. R. China.<br />
Post-weaning diarrhea is one <strong>of</strong> the most common causes<br />
<strong>of</strong> morbidity and mortality for weanling piglets. Our previous<br />
research suggested that feeding butyrate to weanling<br />
piglets decreased the incidence <strong>of</strong> post-weaning diarrhea.<br />
However, the mechanism through which this is achieved<br />
has not been fully elucidated. The present study was<br />
carried out to evaluate the effect <strong>of</strong> butyrate on diarrhea in<br />
relation to intestinal mucosal barrier function using IPEC-J2<br />
porcine intestinal epithelial cells. Cultured IPEC-J2 cells<br />
were scratched to serve as an intestinal damage model.<br />
Supplementation <strong>of</strong> the cells in vitro with butyrate caused<br />
significant repair <strong>of</strong> the mucosal barrier, accompanied<br />
by enhanced expression <strong>of</strong> laminin and fibronectin (P<br />
< 0.05). In addition, butyrate increased the mRNA and<br />
protein expression <strong>of</strong> the intestinal mucosal tight junction<br />
proteins occludin and zonula occluden protein-1 (P <<br />
0.05), which suggests protective effects <strong>of</strong> butyrate on<br />
the intestinal barrier. Furthermore, in the butyrate treated<br />
group, intestinal tSOD (P < 0.05) and GSH-Px (P < 0.05),<br />
2 <strong>of</strong> the main antioxidant enzymes, as well as GSH (P <<br />
0.01), one <strong>of</strong> the non-enzymatic anti-oxidant components,<br />
were enhanced, whereas the MDA level, a marker <strong>of</strong> free<br />
radical mediated lipid peroxidation injury, was decreased (P<br />
< 0.01) compared with the control group. Collectively, these