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 />
The PCR analysis showed that the COS supplementation<br />
enriched (P < 0.05) the amounts <strong>of</strong> Lactobacillus in ileum<br />
and Bifidobacterium and Lactobacillus in cecum, while<br />
suppressed (P < 0.05) the amounts <strong>of</strong> Peptostreptococcus<br />
in ileum and Peptostreptococcus and Escherichia in<br />
cecum. Collectively, these findings suggested that the<br />
COS may improve protein metabolism marginally, and<br />
enhance intestinal health by regulating the intestinal flora in<br />
Huanjiang mini-piglets.<br />
Key words: pigs, digestion and absorption, intestinal flora<br />
1008 Soybean oligosaccharides alter short-chain<br />
fatty acid production and microbial population <strong>of</strong> colon<br />
in vitro. X. L. Zhou 1,2 , X. F. Kong 1 , and Y. L. Yin* 1 , 1 Huanjiang<br />
Observation and Research Station for Karst Ecosystems,<br />
Institute <strong>of</strong> Subtropical Agriculture, Chinese Academy<br />
<strong>of</strong> Sciences, Changsha,Hunan 410125, China, 2 Key Laboratory<br />
<strong>of</strong> Food Science and Technology, College <strong>of</strong> Life<br />
Science and Food Engineering, Nanchang University, Nanchang<br />
330047, China.<br />
This study was conducted to determine the fermentation<br />
characteristics <strong>of</strong> soybean oligosaccharides (SBOS) in an<br />
in vitro system. Colon digesta collected from Huanjiang<br />
mini-pigs was used as the inoculums, and SBOS (0.2 g per<br />
10 fermentation broth) was used as the substrate during<br />
the in vitro fermentation. At the same time, the inoculum or<br />
inoculum plus glucose (0.2 g per fermentation broth) were<br />
used as negative or positive controls, respectively. Each<br />
group was accurately weighed in 3 replicates. The slurry<br />
was fermented for 48 h in an anaerobic, gas production<br />
recording was taken after 1, 2, 4, 6, 8, 10, 12, 14, 16, 18,<br />
20, 22, 24, 28, 32, 36, 42 or 48 h <strong>of</strong> incubation by referring<br />
to the moving scale on the plunger <strong>of</strong> the glass syringes,<br />
and then fermentation kinetic parameters, pH value, NH3-N<br />
content, short chain fat acids (SCFA) levels and microbial<br />
community in the fermentation broth were determined. Our<br />
data showed that the maximum volume and gas production<br />
rate in the SBOS-supplemented group were higher (P<br />
< 0.05), and the lag time <strong>of</strong> gas production in SBOS- or<br />
glucose-supplemented groups were lower (P < 0.05) than<br />
the free-supplemented group; the pH value and NH3-N<br />
content in fermentation broth supplemented with SBOS<br />
were lower (P < 0.05) than the free-supplemented group;<br />
the SCFA contents in the SBOS- or glucose-supplemented<br />
groups were higher (P < 0.05) than that <strong>of</strong> the freesupplemented<br />
group, the maximum content <strong>of</strong> butyrate<br />
acid was found in colon supplemented with SBOS. SBOS<br />
increased (P < 0.05) the microbial diversity and population<br />
<strong>of</strong> Bifidobacterium and Lactobacillus, while decreased (P <<br />
0.05) Escherichia and Streptococcus when compared with<br />
the free-supplemented group based on real-time fluorescent<br />
quantitative PCR and terminal restriction fragment length<br />
polymorphism analysis. These findings suggested that<br />
the SBOS, as a functional dietary ingredient, can be<br />
selectively fermented by beneficial commensal bacteria in<br />
colon, improve the gut microbiota balance and modulate its<br />
metabolism.<br />
Key words: pigs, digestion and absorption, soybean<br />
oligosacch<br />
<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />
DIGESTIVE PHYSIOLOGY OF PIGS<br />
41<br />
Session I<br />
1009 Effect <strong>of</strong> a bacterial endo-1,4-β-xylanase on<br />
ammonia emission in pigs. R. Mombaerts 1 , A. Goderis* 1 ,<br />
and R. Geers 2 , 1 NUTREX NV, Lille, Belgium, 2 Catholic University<br />
<strong>of</strong> Leuven, Leuven, Belgium.<br />
Ammonia emission from pig husbandry originates mainly<br />
from urea which is converted by bacterial urease into NH 3<br />
and CO 2 . It was hypothized that bacterial endo-1,4-βxylanase<br />
(Nutrase Xyla) can reduce NH 3 emission. These<br />
xylanases have a superior ability to breakdown both WE-<br />
and WU-AX into AXOS thereby stimulating fermentation<br />
which increases the content <strong>of</strong> N fixed in bacterial protein.<br />
Some ureum may enter the colon to meet the higher<br />
bacterial N-demand. This may partly shift excretion <strong>of</strong> N via<br />
urine to feces which may decrease NH3 emission. Seventy<br />
pigs (21.5 ± 2.1 kg) were allocated to 12 pens and each<br />
<strong>of</strong> 6 pens received a control diet or the contro diet + 100<br />
ppm Nutrase Xyla. Body weight and FI were recorded and<br />
analyzed with a linear model, based on the R 2 value, root<br />
MSE and the distribution <strong>of</strong> residuals. On d 27, 4 barrows<br />
<strong>of</strong> each group (42 ± 3.02 kg) were housed individually<br />
during 2 consecutive periods <strong>of</strong> 14 d. During the last 4 d <strong>of</strong><br />
each period, feces and urine were collected and quantified<br />
individually. Those 4 barrows that received the control diet<br />
during the 1st period, changed to the xylanase-diet during<br />
the 2nd period and vice versa. After each period, urine and<br />
feces were mixed to measure NH 3 . A fixed volume <strong>of</strong> slurry<br />
was transferred into a flowunit. Air was blown over the slurry<br />
surface. A fixed volume <strong>of</strong> the NH 3 -containing outgoing<br />
air was passed through a solution <strong>of</strong> H 2 SO 4 to measure<br />
NH 3 using a photospectrometer. The xylanase group had<br />
a higher daily gain (718 g/d vs 706 g/d) and lower FCR<br />
(2.78 vs 2.82) compared with the control pigs (P > 0.05).<br />
In both periods, excretion <strong>of</strong> fecal-N/kg FI was higher for<br />
the xylanase group compared with the control group (5674<br />
vs 5340 and 4602 vs 4317 mg N/kg FI resp.; P > 0.05).<br />
Nutrase Xyla decreased NH3 emission by 9% compared<br />
with the control group (3.95 vs 3.60 ppmv; P > 0.05). The<br />
higher fecal N-excretion in the xylanase group is unlikely to<br />
be caused by the lower fecal protein digestibility, because<br />
Nutrase Xyla improved ADG and FCR compared with<br />
the control group. It is concluded that the higher fecal-N<br />
excretion, and consequently the lower NH3 emission, is<br />
caused by a shift in urinary-N to fecal-N excretion.<br />
Key words: endo-1,4-β-xylanase, ammonia, AXOS<br />
1010 The influence <strong>of</strong> grinding intensity and compaction<br />
<strong>of</strong> diets on the microbial community in the gastrointestinal<br />
tract <strong>of</strong> young pigs. J. Bullermann 1 , S. J.<br />
Sander* 1 , M. Arlinghaus 1 , J. Verspohl 2 , and J. Kamphues 1 ,<br />
1 Institute for Animal Nutrition, University <strong>of</strong> Veterinary Medicine,<br />
Hannover, Germany, 2 Institute for Microbiology, University<br />
<strong>of</strong> Veterinary Medicine, Hannover, Germany.<br />
The aim <strong>of</strong> this study was to evaluate potential effects <strong>of</strong><br />
grinding intensity (coarse, fine) and compaction (meal,<br />
pellet, extrudate) on the counts <strong>of</strong> lactobacilli, streptococci/<br />
enterococci and coliform bacteria as selected microbial<br />
groups in the content <strong>of</strong> the gastrointestinal tract (GIT) <strong>of</strong><br />
young pigs. A total <strong>of</strong> 60 weaned piglets (33 d, 8.0 ± 1.0<br />
kg body weight) were divided into 4 groups with 15 animals