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 />
meal was fed to pigs 0 to 4 wk <strong>of</strong> age and up to 8% for 4- to<br />
8-wk-old pigs. The current study examined four commercial<br />
feed proteases used to hydrolyze chicken feather: These are<br />
from Bacillus subtilis, B. licheniformis PWD-1, Aspergillus<br />
niger and the symbiotic bacterium Serratia proteamaculans<br />
HY-3. The degree <strong>of</strong> keratinolysis by these four proteases<br />
was monitored by measuring released NH2-groups<br />
using o-phthalaldehyde (OPA) and by Scanning Electron<br />
Microscopy. The results showed that all these four feed<br />
proteases were able to degrade feather when examined at<br />
pH 5.5 and 7.0. The degree <strong>of</strong> hydrolysis was stimulated<br />
by the addition <strong>of</strong> reducing reagents such as dithiothreitol<br />
(DTT) and sodium sulfite. In general, the protease from<br />
Bacillus subtilis was more efficient in degrading feather<br />
keratin compared to the other three feed proteases at both<br />
pH5.5 and 7.0. For commercial production, the application <strong>of</strong><br />
protease from Bacillus subtilis is even more advantageous if<br />
cost-in-use may be considered.<br />
Key words: feather keratin, feed proteases, enzymes<br />
3051 Use <strong>of</strong> COSITeC in vitro model <strong>of</strong> the pig colon<br />
to assess the effect <strong>of</strong> probiotic yeast on fermentation<br />
parameters and microbiota. E. Pinloche* 1,2 , M. Williams 1 ,<br />
R. D’Inca 2 , E. Auclair 2 , and C. J. Newbold 1 , 1 Institute <strong>of</strong><br />
Biological, Environmental and Rural Sciences, Aberystwyth,<br />
United Kingdom, 2 Lesaffre Feed Additives, Marcq-en-<br />
Baroeul, France.<br />
This study evaluated 2 doses <strong>of</strong> a commercial live yeast<br />
probiotic (Actisaf Sc47) on fermentation parameters and<br />
microbiota using an in vitro model (COSITEC) to mimic<br />
digestion in the pig colon. Digesta content from colon and<br />
cecum <strong>of</strong> 8 growing pigs (circa 100 kg; fed a commercial diet<br />
with no probiotic) was collected and used as diet (freezedried<br />
digesta) and inoculum (fresh digesta). Live yeast (LY)<br />
was added to the freeze-dried digesta at a dose <strong>of</strong> 5 g/kg<br />
(L1), 50 g/kg (L2) or none (C) and fed at a rate <strong>of</strong> 2.2 g/d (n<br />
= 4). After 8 d <strong>of</strong> adaptation, samples were collected for 2<br />
d to measure VFA, ammonia, gas and methane production<br />
together with LY counts, pH, redox potential (Eh), dry matter<br />
digestibility (DMD) and microbiota structure (T-RFLP).<br />
Statistical analyses were performed using randomized block<br />
design//repeated measures ANOVA and T-RFLP pr<strong>of</strong>iles<br />
were analyzed with MANOVA. Over a 24-h period, LY counts<br />
decreased by 2.5 log and it was estimated that 65 h (L1)<br />
and 100 h (L2) would be necessary for the LY to be totally<br />
washed-out <strong>of</strong> the fermentors. Treatments did not have an<br />
impact on pH (mean <strong>of</strong> 7.08), Eh (−253 mV), gas (550 mL/d)<br />
or methane production (0.6 mL/d). L2 (but not L1) significantly<br />
improved DMD (61%) compared with C (58%) and ammonia<br />
(+15%). VFA production increased with L2 compare with C:<br />
iso-butyrate (+14%), propionate (+8.5%), iso-valerate (+17%)<br />
and N-valerate (+25%) but only N-valerate was impacted<br />
by L1 (+13%). The analysis <strong>of</strong> the microbiota, performed<br />
on both the liquid (LAB) and solid associated bacteria<br />
(SAB), revealed that there was a significant difference in<br />
the structure <strong>of</strong> the microbiota between SAB and LAB (P<br />
< 0.01), treatments (P < 0.001) but that the interaction was<br />
also significant (P = 0.043). Indeed, for the LAB only L2 had<br />
a significant impact on the microbiota (P < 0.01) whereas<br />
L1 also tended to change the structure <strong>of</strong> the microbiota in<br />
<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />
DIGESTIVE PHYSIOLOGY OF PIGS<br />
139<br />
Session VII<br />
the SAB (P = 0.075). Overall, this study showed that a LY<br />
probiotic could improve the fermentation pattern in a colonic<br />
simulation model but only at the higher dose used and this<br />
was probably due to a shift in the microbiota.<br />
Key words: yeast, dry matter digestibility, microbiota<br />
3052 Responses <strong>of</strong> dietary ileal amino acid digestibility<br />
to consumption <strong>of</strong> different cultivars <strong>of</strong> potatoes<br />
and conventional fibers in pigs fed a high-fat basal diet.<br />
Q. Wang* 1 , X. Yang 1 , S. Leonard 1 , T. Archbold 1 , A. Sullivan 1 ,<br />
B. Bizimungu 2 , A. Murphy 2 , A. Duncan 1 , D. Ma 1 , J. Htoo 3 ,<br />
and M. Fan 1 , 1 University <strong>of</strong> Guelph, Guelph, ON, Canada,<br />
2 Agriculture and Agri-Food Canada Potato Research<br />
Centre, Fredericton, NB, Canada, 3 Evonik Industries AG,<br />
Hanau-Wolfgang, Germany.<br />
While dietary fibers are well recognized for nutritional<br />
management <strong>of</strong> human health issues, fiber components<br />
are also known to be one <strong>of</strong> the anti-nutritional factors<br />
potentially affecting digestive utilization <strong>of</strong> dietary proteins.<br />
As a staple food, potato may be a significant dietary fiber<br />
source. The objective <strong>of</strong> this study was to examine effects<br />
<strong>of</strong> dietary supplementation <strong>of</strong> 6 potato cultivars that are<br />
different in soluble fiber contents and 2 conventional fiber<br />
components (cellulose and guar gum) on the apparent<br />
ileal amino acid (AA) digestibility in pigs fed a high-fat<br />
basal diet. The basal diet was formulated as a control<br />
to contain 41.5% poultry meal, 4% casein, 15% animal<br />
fat-oil blend, 2.8% sucrose, 31% cornstarch and the<br />
rest as trace mineral and vitamin supplements with fat<br />
contributing to 47% <strong>of</strong> dietary gross energy. The 2 fiber<br />
diets were formulated by diluting the basal diet with 10%<br />
guar gum and cellulose at the expense <strong>of</strong> cornstarch.<br />
Six other test diets were formulated by diluting the basal<br />
diet with 25.1% <strong>of</strong> 6 cultivars <strong>of</strong> dehydrated potato tuber<br />
powder to contain 10% total dietary fiber at the expense<br />
<strong>of</strong> cornstarch. Titanium oxide was included (0.30%) as a<br />
digestibility marker. A total <strong>of</strong> 81 barrows, with an average<br />
initial BW <strong>of</strong> 25 kg, were fitted with a simple T-cannula<br />
at the distal ileum and fed the 9 diets according to a<br />
completely randomized block design for 9 blocks with<br />
each block lasted 28 d. Total AA contents in samples were<br />
analyzed by gas chromatography-mass spectrometry.<br />
Compared with the control, apparent ileal digestibility <strong>of</strong><br />
Leu, Phe, Pro and Gly were decreased (P < 0.05) by 10%<br />
guar gum, while the digestibility <strong>of</strong> Leu, Phe and Gly were<br />
reduced (P < 0.05) by 10% cellulose. However, potato<br />
supplementation did not significantly affect the ileal AA<br />
digestibility compared with the 2 fiber diets. Our results<br />
suggest that 10% guar gum and cellulose supplementation<br />
may adversely affect digestive utilization <strong>of</strong> dietary protein,<br />
however, consumption <strong>of</strong> high-soluble fiber potatoes<br />
unlikely influences protein nutrition.<br />
Key words: fiber, amino acids, pigs<br />
3053 Changes in the pig small intestinal mucosal glutathione<br />
system after weaning. J. Degroote 1,2 , J. Michiels*<br />
1,2 , E. Claeys 2 , A. Ovyn 2 , and S. De Smet 2 , 1 University<br />
College Ghent, Ghent, Belgium, 2 Ghent University, Melle,<br />
Belgium.