Dietary carbohydrates and swine dysentery

A total of sixty surgically castrated male pigs (Large White £ Landrace) weighing 31·2 (SD 4·3) kg were used in a randomised block experiment to examine the effect of added dietary inulin (0, 20, 40 and 80 g/kg) on the occurrence of swine dysentery (SD) and on fermentation characteristics in the large intestine after experimental challenge with the causative spirochaete Brachyspira hyodysenteriae. The pigs were allowed to adapt to the diets for 2 weeks before each pig was challenged orally four times with a broth culture containing B. hyodysenteriae on consecutive days. Increasing dietary levels of inulin linearly (P¼ 0·001) reduced the risk of pigs developing SD; however, eight out of fifteen pigs fed the diet with 80 g/kg inulin still developed the disease. The pH values in the caecum (P¼0·072) tended to decrease, and in the upper colon, the pH values did decrease (P¼0·047) linearly with increasing inulin levels in the diets, most probably due to a linear increase in the concentration of total volatile fatty acids in the caecum (P¼ 0·018), upper colon (P¼0·001) and lower colon (P¼0·013). In addition, there was a linear reduction in the proportion of the branched-chain fatty acids isobutyric acid and isovaleric acid in the caecum (P¼ 0·015 and 0·026) and upper colon (P¼ 0·011 and 0·013) with increasing levels of dietary inulin. In conclusion, the present study showed that a diet supplemented with a high level of inulin (80 g/kg) but not lower levels reduced the risk of pigs developing SD, possibly acting through a modification of the microbial fermentation patterns in the large intestine.

Sixty-three male pigs (Landrace × Large White) weighing 49.5 ± 0.40 kg were used to (1) examine the variation in DE content of Lupinus angustifolius L. in relation to variety and geographical growing region and (2) establish prediction equations for DE content from physical and chemical composition. The pigs were randomly allocated to a 4 × 2 factorial treatment design with respective factors being 4 varieties (cv. Belara, Coromup, Mandelup, and Tanjil) and 2 growing locations (northern and southern agricultural areas of Western Australia). In addition, a wheat control diet was fed as a reference for calculation of lupin DE content. The lupins were ground through a hammer mill fitted with a 4-mm screen to a mean particle size of 888 μm. Pigs were fed their respective experimental diets at 3 times maintenance energy level [3 × (0.458 × BW 0.75 )/diet DE] in the study. The DE content of lupins ranged from 13.3 to 15.7 MJ/kg with a mean value of 14.2 MJ/kg. Variety of lupins affected (P < 0.01) the DE content, and lupins grown in the northern agricultural region had a greater DE content than the same lupins grown in the southern agricultural area (P < 0.01). Although the variation in DE content of lupins was mostly caused by significantly greater DE content of cv. Coromup grown in the northern agricultural region, the results suggest that genetic and environmental conditions during the growth of lupins have a significant impact on the utilization of energy in grower pigs. Simple regression analysis showed that prediction of DE content was possible from the proportion of hulls [R 2 = 0.88, residual SD (RSD) = 1.116, P < 0.001], 1,000-seed weight (R 2 = 0.77, RSD = 1.092, P < 0.01), and soluble arabinoxylan content (R 2 = 0.64, RSD = 1.072, P < 0.05). Multiple regression analysis showed that adding total nonstarch polysaccharide (R 2 = 0.96, RSD = 1.187, P < 0.01) and soluble nonstarch polysaccharide (R 2 = 0.95, RSD = 1.200, P < 0.01) to the equation along with the proportion of hull and 1,000-seed weight significantly improved the accuracy of prediction. Results indicate that the DE content of lupins varies by up to 2.4 MJ/kg and that the DE content can be predicted with a good degree of accuracy using physical and chemical characteristics.

One hundred and sixty pigs were used to evaluate dietary copper (Cu) and zinc (Zn) supplementation on performance, fecal mineral levels, body mineral status and carcass and meat quality. Diets differed in mineral form (MF) (Cu and Zn in the form of proteinate amino acid chelate (organic) or sulfate (inorganic)) and inclusion level (IL) (27 mg/kg of total Cu and 65 mg/kg of total Zn ('low') or 156 mg/kg of total Cu and 170 mg/kg of total Zn ('high')) according to a 2 3 2 factorial arrangement of treatments. Pigs were used from 25 to 107 kg body weight (BW) and fed their respective diets ad libitum. Blood and fecal samples were collected on days 14 and 77 of the experiment. Blood was analyzed for concentration of Cu and Zn, hemoglobin (Hb), Cu content of red blood cells (RBC Cu) and alkaline phosphatase (ALP) and feces for Cu and Zn concentration. Hot carcass weight (HCW) and backfat depth were measured at slaughter and indices of meat quality were assessed on a section of longissimus thoracis. Liver, kidney and bone samples were collected immediately after slaughter and liver and kidney were tested for Cu and Zn content, while bone was only tested for Zn. Over the entire experimental period (25 to 107 kg BW) no significant treatment differences in average daily gain (ADG) or average daily feed intake (ADFI) occurred; however, feed conversion ratio (FCR) was improved by the inclusion of proteinate amino acid chelate ( P 5 0.012). Copper and Zn concentrations in feces were in direct proportion to the IL in the diet. Blood mineral levels were within normal physiological ranges in all treatments and tissue Cu and Zn concentrations increased with dietary IL ( P , 0.05). Results indicate that Cu and Zn fecal concentrations were reduced by approximately 6-fold for Cu and by 2.5-fold for Zn by feeding 27 mg/kg Cu and 65 mg/kg Zn, in either the proteinate amino acid chelate or the sulfate form, compared with a diet containing 156 mg/kg Cu and 170 mg/kg Zn. This decrease in total dietary Cu and Zn did not reduce performance or mineral status of pigs.

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