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 />
subtilis C-3102 (C-3102), on health and productivity <strong>of</strong><br />
sows and their litters. The study was performed in a farrowto-finish<br />
farm with a capacity <strong>of</strong> 350 sows and its own feed<br />
mill, using an all-in-all-out batch management system.<br />
Following weaning <strong>of</strong> the previous litter, sows were housed<br />
in individual crates for 30 d, until served and pregnancy<br />
confirmed. Subsequently, weekly batches <strong>of</strong> 14-15 sows at<br />
the same gestation stage were loose-housed in a pen with<br />
individual feeders until 103-110 d <strong>of</strong> gestation, then moved<br />
to a farrowing room until weaning <strong>of</strong> piglets at approximately<br />
26 d <strong>of</strong> age. Four batches <strong>of</strong> sows were studied throughout<br />
pregnancy and lactation. Of these, two batches <strong>of</strong> sows<br />
(T2) were fed a top-dressing supplying 3 x10 5 cfu C-3102<br />
per gram complete feed, and two control batches (T1) were<br />
fed the basal top-dressing free <strong>of</strong> probiotic. The <strong>of</strong>fspring<br />
<strong>of</strong> the T1 control group were <strong>of</strong>fered T1 basal creep feed,<br />
while piglets <strong>of</strong> the T2 group were <strong>of</strong>fered basal feed<br />
supplemented with C-3102 supplying 3 x10 5 cfu C-3102 per<br />
gram complete feed. Each dam with her litter represented<br />
an experimental unit (replicate). Treatment groups (T1 and<br />
T2) were similar with respect to sow age/parity distribution.<br />
During lactation, weight loss <strong>of</strong> T2 sows was significantly<br />
lower, while mean weaning weight and growth, birth to<br />
weaning, <strong>of</strong> T2 piglets were significantly improved. The<br />
positive effect <strong>of</strong> C-3102 on sow condition during lactation,<br />
as evidenced by reduced weight loss, may improve sow<br />
milk production and conception rate. By weaning, T2 piglets<br />
were on average 0.5 kg heavier than T1 control piglets,<br />
possibly due to indirect (through the dam), or direct (through<br />
the creep feed) effects <strong>of</strong> the probiotic.<br />
Key words: sows, Bacillus subtilis C-3102, creep feed<br />
1019 G protein-coupled receptor120 (GPR120) transcription<br />
in intestinal epithelial cells are significantly<br />
affected by bacteria belonging to the Bacteroides,<br />
Proteobacteria, and Firmicutes phyla. M. Fredborg, P.<br />
K. Theil, B. B. Jensen, and S. Purup,* Aarhus University,<br />
Denmark.<br />
Free fatty acids (FFAs) are produced in the intestine by<br />
microbial fermentation. Recently, a family <strong>of</strong> G proteincoupled<br />
receptors (GPR) acting as FFA transporters has<br />
been reported; including GPR120 which is expressed by<br />
intestinal epithelial cells and has been reported to function<br />
as a control point for anti-inflammatory effects. The aim<br />
<strong>of</strong> the present study was to evaluate whether 12 selected<br />
intestinal bacteria, representing the 3 major phyla present<br />
in the intestine, affects intestinal epithelial cell GP120transcription<br />
Caco-2 intestinal epithelial cells were cultured<br />
on filter inserts for 21 d until fully differentiated. Supernatants<br />
<strong>of</strong> the 12 bacteria were added to cell culture medium at<br />
the apical side in a cell:bacteria ratio <strong>of</strong> 1:200. After 4 h<br />
incubation, changes in cellular transcription <strong>of</strong> GPR120<br />
by bacterial supernatant were examined using real time<br />
reverse transcriptase polymerase chain reaction (RT-PCR).<br />
Supernatants from 6 <strong>of</strong> the 12 bacteria analyzed influenced<br />
the mRNA level <strong>of</strong> GPR120 significantly (P < 0.05) compared<br />
with cells without added bacteria. A significant increase in<br />
cellular GPR120 mRNA was observed by E. faecium, L.<br />
reuteri, L. salivarius, E. coli K-12, B. fragilis and F. prausnitzii.<br />
The greatest increase was observed by the latter 2, which<br />
<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />
DIGESTIVE PHYSIOLOGY OF PIGS<br />
45<br />
Session I<br />
was observed to increase cellular GPR120 mRNA level by<br />
>2.1 fold. Intriguingly, these bacteria are categorized as<br />
either probiotics or bacteria capable <strong>of</strong> introducing an antiinflammatory<br />
effect. The beneficial effect <strong>of</strong> these bacteria<br />
may very well be mediated by regulation <strong>of</strong> GPR120. The<br />
regulation <strong>of</strong> GPR120 by intestinal microbiota represents<br />
a direct signaling pathway for gut bacteria to affect host<br />
health and metabolism.<br />
Key words: bacteria, GPR120, intestinal epithelial cells<br />
1020 Intestinal delivery <strong>of</strong> probiotics bacteria protected<br />
with succinylated β-lactoglobulin tablets and<br />
their effects on pig intestinal microbiota. I. Paquette* 1,2 ,<br />
J.-P. Brousseau 2 , G. Talbot 2 , M. Lessard 2 , R. Caillard 1 , and<br />
M. Subirade 1 , 1 Université Laval, Département des sciences<br />
et technologie des aliments, Québec, Québec, Canada,<br />
2 Dairy and Swine R & D Centre, Agriculture and Agri-Food<br />
Canada, Sherbrooke, Québec, Canada.<br />
This study was performed to evaluate the potential <strong>of</strong><br />
succinylated β-lactoglobulin (β-lg) tablets to protect 2<br />
probiotics, Lactobacillus helveticus (Lh) and Bifidobacterium<br />
longum (Bl) from in vitro gastric condition and to determine,<br />
in vivo, the influence <strong>of</strong> delivering protected probiotics in<br />
succinylated β-lg tablets on intestinal microbiota. To realize<br />
in vivo study, 48 weaned piglets <strong>of</strong> 28 d-old, were divided<br />
into 3 groups and received one <strong>of</strong> the following tablets<br />
daily: Group 1) succinylated β-lg tablets without probiotics,<br />
Group 2) non-succinylated β-lg tablets with 10 9 cfu <strong>of</strong> Lh<br />
and Bl, Group 3) succinylated β-lg tablets with 10 9 cfu <strong>of</strong><br />
Lh and Bl. After 14 and 28 d <strong>of</strong> treatment, 8 piglets per<br />
group were euthanized and colon contents were sampled<br />
to characterize bacterial population (selective medium<br />
and T-RFLP) and confirm the presence <strong>of</strong> Bl by qPCR. In<br />
vitro study showed that after 1 h incubation in simulated<br />
gastric condition, more than 10 9 cfu <strong>of</strong> each strain were<br />
still viable when incorporated in succinylated β-lg tablets.<br />
In vivo, piglets receiving protected probiotics had higher (P<br />
≤ 0.05) bifidobacteria counts in colon content than groups<br />
1 and 2 after 28 d. These results suggest that the use <strong>of</strong><br />
succinylated β-lg tablets helped maintain the viability <strong>of</strong><br />
the probiotics as they were delivered into the intestine.<br />
Analysis <strong>of</strong> colonic microbiota T-RFLP pr<strong>of</strong>iles showed that<br />
the relative abundance <strong>of</strong> bacterial population belonging<br />
to Ruminococcaceae was significantly different between<br />
treatments (P ≤ 0.05), with a higher abundance for group<br />
3. However, diversity indices (Evenness and Shannon)<br />
calculated from T-RFLP pr<strong>of</strong>iles revealed no major influence<br />
<strong>of</strong> our treatments on the colonic microbiota. Using specific<br />
primers for Bl, qPCR assays showed its presence in the<br />
colon <strong>of</strong> animals receiving tablets containing probiotics<br />
(groups 2 and 3). In conclusion, these results suggest that<br />
the protected probiotics were delivered alive in the intestine<br />
and their daily administration can modulate specific bacterial<br />
populations without affecting the overall microbiota.<br />
Key words: probiotics, microbiota, encapsulation<br />
1021 Dietary supplementation with alkaline phosphatase<br />
affects intestinal microbial populations <strong>of</strong> nursery<br />
pigs. M. H. Rostagno* 1 , J. Ferrel 2 , J. S. Radcliffe 3 , and B. T.