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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 />

> 0.05) on the ATTD <strong>of</strong> energy among treatments. <strong>Pigs</strong> fed<br />

the S1.0 diet had higher (P < 0.05) serum Fe concentration<br />

compared with those fed the CON and S0.5 diets at the<br />

end <strong>of</strong> the experiment. There was no difference in total<br />

iron–binding capacity among dietary treatments. Dietary<br />

application <strong>of</strong> sericite didn′t affect the ammonia, hydrogen<br />

sulfide, and total mercaptans emission on d 1, 3, 5, and 7.<br />

In conclusion, dietary supplementation with 0.5 and 1.0%<br />

sericite increased the ATTD <strong>of</strong> DM and N, whereas the<br />

inclusion <strong>of</strong> 1.0% sericite reduced serum Fe concentration<br />

in growing pigs.<br />

Key words: apparent total tract digestibility, sericite, growing<br />

pigs<br />

1078 effects <strong>of</strong> faba beans and faba bean hulls on the<br />

expression <strong>of</strong> selected genes in the small intestine <strong>of</strong><br />

piglets. A. J. M. Jansman,* J. van Baal, H. C. A. Widjaja,<br />

J. van der Meulen, and M. A. Smits, Wageningen UR Livestock<br />

Research, Lelystad, The Netherlands.<br />

In a study using the small intestinal perfusion technique<br />

in pigs, the effects were studied <strong>of</strong> intestinal perfusion<br />

<strong>of</strong> ground fava beans, fava bean hulls or saline on the<br />

intestinal net fluid absorption in intestinal segments<br />

either or not challenged with an enterotoxigenic E. coli<br />

(ETEC). After an 8 h perfusion test, the piglets were<br />

euthanized and small intestinal mucosa samples were<br />

taken for analyzing the expression <strong>of</strong> several selected<br />

genes, which were previously shown to be responsive<br />

toward an ETEC challenge. Samples <strong>of</strong> frozen <strong>of</strong> the<br />

jejunal mucosa were ground in liquid nitrogen and total<br />

RNA was extracted and purified. Real-time quantitative<br />

PCR (qPCR) was performed. Each sample was run in<br />

duplicate. The expression <strong>of</strong> the following genes coding<br />

for the following proteins was quantified relative to the<br />

quantity <strong>of</strong> 18S RNA: 1) apolipoproteine C3 (ApoC3), 2)<br />

metalloproteinase 1 inhibitor (TIMP1), 3) aquaporine 8<br />

(AQP8), 4) matrix metalloproteinase 1 (MMP1), 5) mucin<br />

13 (MUC13) and 6) pancreatitis-associated protein (PAP).<br />

There was a significant interaction between the effects <strong>of</strong><br />

perfusion treatment (saline, fava beans or fava bean hulls)<br />

and ETEC challenge on the expression <strong>of</strong> the genes in<br />

mucosal tissue, except for MUC13. Nature <strong>of</strong> the perfusion<br />

treatment had a significant effect on the expression <strong>of</strong><br />

AQP8 and MUC13, while the ETEC challenge had a<br />

significant effect on the expression <strong>of</strong> all selected genes,<br />

except for MUC13. The expression <strong>of</strong> APOC3 and<br />

AQP8 was increased by the ETEC challenge, while the<br />

expression <strong>of</strong> TIMP1, MMP and PAP was decreased as<br />

a result <strong>of</strong> the ETEC challenge. Overall, the expression <strong>of</strong><br />

APOC3 and AQP8 was negatively correlated with net fluid<br />

absorption, while the expression <strong>of</strong> TIMP1, MMP1 and PAP<br />

was positively correlated with net fluid absorption. It was<br />

concluded that the expression <strong>of</strong> ETEC responsive genes<br />

in the small intestinal mucosa is affected by perfusion with<br />

fava beans and fava bean hulls and challenge with ETEC.<br />

The expression <strong>of</strong> several genes (APOC3, AQP8, TIMP1,<br />

MMP and PAP) was correlated with the net fluid absorption<br />

in the small intestine <strong>of</strong> pigs.<br />

Key words: intestinal gene expression, faba beans<br />

<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />

DIGESTIVE PHYSIOLOGY OF PIGS<br />

69<br />

Session II<br />

1079 Improved nutrient digestibility and retention<br />

partially explains feed efficiency gains in pigs selected<br />

for low residual feed intake. A. J. Harris,* J. F. Patience,<br />

S. M. Lonergan, J. C. M. Dekkers, and N. K. Gabler, Iowa<br />

State University, Ames, IA 50011, USA.<br />

Residual feed intake (RFI) is a unique measure <strong>of</strong> feed<br />

efficiency (FE) and an alternative to traditional measures<br />

<strong>of</strong> gain:feed or feed:gain. It is defined as the difference<br />

between the actual feed intake <strong>of</strong> a pig and its expected feed<br />

intake based on its level <strong>of</strong> growth and backfat. Therefore,<br />

selecting for a pig with low RFI results in a more feed<br />

efficient animal for a given rate <strong>of</strong> growth. Our objective was<br />

to determine the extent to which apparent total tract nutrient<br />

digestibility (ATTD), energy utilization and retention explain<br />

FE differences between pigs divergently selected for low or<br />

high RFI. After 7 generations <strong>of</strong> selection, 12 high (HRFI)<br />

and 12 low RFI (LRFI) pigs (62 ± 3 kg BW), were randomly<br />

assigned to metabolism crates. <strong>Pigs</strong> were fed ad libitum<br />

a standard corn-soy diet containing 0.4% titanium oxide,<br />

an exogenous digestibility marker. After a 7 d acclimation<br />

period, total urine and feces collection was undertaken for<br />

72 h. Nutrient and energy digestibility, P digestibility and N<br />

balance were then measured and calculated to determine<br />

differences between the RFI lines. As expected, ADFI was<br />

significantly lower in the LRFI pigs (2.0 vs 2.6 kg/d, P <<br />

0.01), ADG did not differ, and FE was significantly higher<br />

in the LRFI (P = 0.0003) compared with the HRFI pigs. The<br />

digestibility coefficients for DM (87.3 vs 85.9%), N (88.3 vs<br />

86.1%), and GE (86.9 vs 85.4%) were higher (P ≤ 0.003)<br />

in the LRFI versus HRFI pigs, respectively. DE (16.59 vs<br />

16.32 MJ/kg DM) and ME (15.98 vs 15.72 MJ/kg DM)<br />

values were also significantly greater (P = 0.0006) in the<br />

LRFI pigs. When correcting for ADFI, P digestibility did not<br />

differ between the lines. However, the LRFI pigs tended to<br />

have improved N retention compared with HRFI pigs (36.91<br />

vs 32.12 g/d, P = 0.08). These data suggest that differences<br />

in energy and nutrient digestibility, utilization, and retention<br />

may partially explain the superior FE seen in pigs selected<br />

for LRFI.<br />

Key words: residual feed intake, feed efficiency, nutrient<br />

digestibility<br />

1080 Dietary protein content does not influence calcium<br />

and phosphorus absorption and retention in the<br />

Iberian pig growing from 50 to 100 kg body-weight. R.<br />

Nieto,* A. Haro, C. Delgado-Andrade, I. Seiquer, and J. F.<br />

Aguilera, Institute <strong>of</strong> Animal Nutrition, Estación Experimental<br />

del Zaidín, CSIC, Granada, Spain.<br />

The comparatively slower growth rate <strong>of</strong> the Iberian<br />

pig suggests lower Ca and P requirements than those<br />

reported for conventional or high-performing porcine<br />

breeds. The effects <strong>of</strong> dietary apparent-digestible protein<br />

content (ApDP) from excessive to marginally deficient<br />

(113, 93, 74 and 53 g/kg DM) and level <strong>of</strong> feeding (FL;<br />

0.80 and 0.95 x ad libitum) upon whole-body retention <strong>of</strong><br />

Ca and P was studied in 48 purebred Iberian barrows in<br />

the finishing stage from 50 to 100 kg BW. The diets were<br />

prepared by diluting a high-protein diet (HPC), formulated<br />

according to the ideal protein concept, with a protein-free

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