Efficacy of a reduced protein diet on clinical expression of post-weaning diarrhoea and life-time performance after experimental challenge with an enterotoxigenic strain of Escherichia coli
Previous experiments have shown that feeding a reduced protein diet within the first 2 weeks post-weaning reduces gastrointestinal protein fermentation and clinical expression of post-weaning diarrhoea (PWD). However, growth of young pigs receiving a reduced protein diet without crystalline essential amino acids (CEAA) supplementation is depressed after weaning. It has been argued that the short-term performance reduction caused by feeding a reduced protein diet would be compensated and the lifetime performance of pigs would not be affected. An experiment was therefore conducted to examine PWD and lifetime growth of pigs after feeding a reduced protein diet without and with CEAA supplementation for 2 weeks after weaning. Two hundred individually housed pigs weaned at 21 d of age (Large White×Landrace, castrate:female ratio of 1:1, mean±SEM body weight of 5.5±0.05kg) were stratified to one of four dietary treatments (n=50): High protein+antimicrobial compound diet (HP+AMC, 230g crude protein (CP) with 2.5g lincospectin and 3g zinc oxide per kg feed), High protein diet (HP, 230gCP/kg), Reduced protein+amino acid supplemented diet (RP+AA, 185gCP/kg with added CEAA up to HP level), and Reduced protein diet (RP, 185g CP/kg without CEAA supplementation). Pigs were fed the experimental diet for 2 weeks and then all pigs were fed the same series of commercial diets until slaughter. All pigs were experimentally infected with an enterotoxigenic strain of E. coli (6 and 10mL of 1.9×109cfu/mL, serotype O149:K91:K88) at 72, and 96h after weaning. Infection increased plasma haptoglobin levels (P0.05). Carcass characteristics were not affected (P>0.05) by the treatments. The results indicate that although feeding a RP diet without CEAA supplementation decreased performance after weaning, it did not influence lifetime performance or carcass characteristics and reduced the clinical expression of PWD
