Effects of dietary threonine and tryptophan supplementation on growing pigs induced by porcine respiratory and reproductive syndrome vaccination

A total of 32 growing pigs were used in a 2 × 2 factorial arrangement of treatments with two different diets (conventional [CON] diet vs. threonine [Thr]- and tryptophan [Trp]-rich [TTR] diet) and two immunological challenge regimens (porcine respiratory and reproductive syndrome [PRRS] vaccine vs. phosphate buffer solution [PBS]) to study the hypothesis that dietary supplementation with Trp and Thr would benefit for growing pigs vaccinated with PRRS vaccine. After feeding the experimental diets for 21 d, the pigs were intramuscularly vaccinated with PRRS or PBS. Performance data were recorded over a period of 10 weeks and are presented for the pre-challenge period (3 weeks) and the challenge period (7 weeks, where on day 1, pigs were immunologically challenged). During the pre-challenge period, the growth performance was not different between dietary treatments. PRRS vaccination resulted in increased rectal temperature and decreased feed intake and growth rate (p < 0.05). In PRRS-vaccinated pigs, diet TTR enhanced the feed intake, especially during the first 2 weeks after the PRRS vaccination compared with diet CON (p < 0.05). PRRS vaccination also resulted in increased plasma concentration of urea nitrogen, essential and non-essential amino acids (p < 0.05) and porcine reproductive and respiratory syndrome virus specific antibodies (p < 0.05), but decreased concentration of immunoproteins including alpha-1-acylglycoprotein and immunoglobulin G (p < 0.05). The alleviation of the PRRS vaccination induced decrease in feed intake and growth rate by Thr and Trp supplementation, indicating that the PRRS-vaccinated pigs had a higher Thr and Trp requirement than non-vaccinated pigs.

[1]  X. Mao,et al.  Effects of dietary threonine supplementation on immune challenge induced by swine Pseudorabies live vaccine in weaned pigs , 2014, Archives of animal nutrition.

[2]  C. F. Hansen,et al.  An increased ratio of dietary tryptophan to lysine improves feed efficiency and elevates plasma tryptophan and kynurenine in the absence of antimicrobials and regardless of infection with enterotoxigenic Escherichia coli in weaned pigs. , 2012, Journal of animal science.

[3]  C. D. de Lange,et al.  Immune system stimulation reduces the efficiency of tryptophan utilization for body protein deposition in growing pigs. , 2012, Journal of animal science.

[4]  X. Mao,et al.  Optimal dietary true ileal digestible threonine for supporting the mucosal barrier in small intestine of weanling pigs. , 2010, The Journal of nutrition.

[5]  B. Séve,et al.  Dietary tryptophan helps to preserve tryptophan homeostasis in pigs suffering from lung inflammation. , 2008, Journal of animal science.

[6]  Peng Li,et al.  Amino acids and immune function , 2007, British Journal of Nutrition.

[7]  R. Morrison,et al.  Effect of orally administered Lactobacillus casei on porcine reproductive and respiratory syndrome (PRRS) virus vaccination in pigs. , 2007, Veterinary microbiology.

[8]  F. Ceciliani,et al.  The acute phase protein alpha1-acid glycoprotein: a model for altered glycosylation during diseases. , 2007, Current protein & peptide science.

[9]  S. Qiao,et al.  Effects of graded levels of true ileal digestible threonine on performance, serum parameters and immune function of 10–25 kg pigs , 2006 .

[10]  S. Dee,et al.  Porcine reproductive and respiratory syndrome virus. , 2006, Theriogenology.

[11]  Colin D. Johnson,et al.  Assessment of the economic impact of porcine reproductive and respiratory syndrome on swine production in the United States. , 2005, Journal of the American Veterinary Medical Association.

[12]  B. Jaber,et al.  Immune‐Modulating Effects of Melatonin, N‐Acetylserotonin, and N‐Acetyldopamine , 2005, Annals of the New York Academy of Sciences.

[13]  R. Rial,et al.  Effect of orally administered l-tryptophan on serotonin, melatonin, and the innate immune response in the rat , 2004, Molecular and Cellular Biochemistry.

[14]  D. Baker,et al.  Decreased protein accretion in pigs with viral and bacterial pneumonia is associated with increased myostatin expression in muscle. , 2004, The Journal of nutrition.

[15]  N. Roberts,et al.  Infection of growing swine with porcine reproductive and respiratory syndrome virus and Mycoplasma hyopneumoniae--effects on growth, serum metabolites, and insulin-like growth factor-I. , 2003, The Canadian veterinary journal = La revue veterinaire canadienne.

[16]  S. Mortensen,et al.  Risk factors for infection of sow herds with porcine reproductive and respiratory syndrome (PRRS) virus. , 2002, Preventive veterinary medicine.

[17]  A. Bailel INFLUENCE OF NUTRITIONAL DEPRIVATION ON INSULIN-LIKE GROWTH FACTOR I , SOMATOTROPIN , AND METABOLIC HORMONES IN SWINE , 2002 .

[18]  T. Stahly,et al.  The effect of dietary soy daidzein on pig growth and viral replication during a viral challenge. , 2001, Journal of animal science.

[19]  T. Stahly,et al.  Quantitative relationship of systemic virus concentration on growth and immune response in pigs. , 2000, Journal of animal science.

[20]  P. Thacker,et al.  Effects of dietary threonine on performance, plasma parameters and immune function of growing pigs , 1999 .

[21]  M. Spurlock,et al.  Effect of dietary energy source and immunological challenge on growth performance and immunological variables in growing pigs. , 1997, Journal of animal science.

[22]  S. Goyal,et al.  A Modified Serum Neutralization Test for the Detection of Antibody to Porcine Reproductive and Respiratory Syndrome Virus in Swine Sera , 1994, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[23]  P. Reeds,et al.  Do the differences between the amino acid compositions of acute-phase and muscle proteins have a bearing on nitrogen loss in traumatic states? , 1994, The Journal of nutrition.

[24]  M. J. Dauncey,et al.  Short-term regulation of plasma IGF-I concentration by food intake in young growing pigs. , 1994, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[25]  R. Grimble,et al.  Cysteine and glycine supplementation modulate the metabolic response to tumor necrosis factor alpha in rats fed a low protein diet. , 1992, The Journal of nutrition.

[26]  K. Feingold,et al.  Tumor Necrosis Factor, Interleukin, and Interferon Induced Changes in Lipid Metabolism as Part of Host Defense , 1992, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[27]  B. Séve,et al.  Interactive effects of dietary levels of tryptophan and protein on voluntary feed intake and growth performance in pigs, in relation to plasma free amino acids and hypothalamic serotonin. , 1992, Journal of animal science.

[28]  B. Séve,et al.  Impact of dietary tryptophan and behavioral type on growth performance and plasma amino acids of young pigs. , 1991, Journal of animal science.

[29]  G. Wensvoort,et al.  Experimental reproduction of porcine epidemic abortion and respiratory syndrome (mystery swine disease) by infection with Lelystad virus: Koch's postulates fulfilled. , 1991, The Veterinary quarterly.

[30]  M. Voets,et al.  Mystery swine disease in The Netherlands: the isolation of Lelystad virus. , 1991, The Veterinary quarterly.

[31]  K. Klasing Nutritional aspects of leukocytic cytokines. , 1988, The Journal of nutrition.

[32]  A. Lewis,et al.  An Evaluation of Threonine and Isoleucine as the Third and Fourth Limiting Amino Acids in Corn For Growing Swine , 1985 .

[33]  R. Easter,et al.  Effect of lysine and threonine supplementation of sorghum gestation diets on nitrogen balance and plasma constituents in first-litter gilts. , 1984, Journal of animal science.

[34]  G. Cromwell,et al.  Tryptophan, threonine, isoleucine and methionine supplementation of a 12% protein, lysine-supplemented, corn-soybean meal diet for growing pigs. , 1983, Journal of animal science.

[35]  M. Werner,et al.  Serum protein changes during the acute phase reaction. , 1969, Clinica chimica acta; international journal of clinical chemistry.

[36]  Board on Agriculture,et al.  Nutrient requirements of swine , 1964 .