Register      Login
Animal Production Science Animal Production Science Society
Food, fibre and pharmaceuticals from animals
RESEARCH ARTICLE

Spray-dried porcine plasma and yeast derived protein meal influence the adaption to weaning of primiparous and multiparous sow progeny in different ways

M. V. Edwards A G , R. G. Campbell B , T. Chapman C , H. Brouwers C , S. G. Pierzynowski D , B. R. Weström D , O. Prykhod’ko D , L. Gabor E and M. Choct F
+ Author Affiliations
- Author Affiliations

A ACE Livestock Consulting Pty Ltd, Cockatoo Valley, SA 5351, Australia.

B Pork Cooperative Research Centre, Roseworthy, SA 5118, Australia.

C IMDRU, Industry and Investment NSW, Menangle, NSW 2568, Australia.

D Department of Cell and Organism Biology, Lund University, Skåne, Sweden.

E Novartis Animal Health Australasia Pty Ltd, North Ryde, NSW 2113, Australia.

F Poultry Cooperative Research Centre, Armidale, NSW 2350, Australia.

G Corresponding author. Email: megan@acelive.com.au

Animal Production Science 53(1) 75-86 https://doi.org/10.1071/AN12151
Submitted: 3 May 2012  Accepted: 17 October 2012   Published: 29 November 2012

Abstract

Pigs from 154 litters (n = 1132, 19 ± 3 days of age, 4.9 ± 1.1 kg of bodyweight) were used in a 3 × 2 factorial design to evaluate two raw materials with nutraceutical properties being used in feeds, spray-dried porcine plasma (SDPP) and a yeast protein meal, and their effects on growth performance, immune parameters and gastrointestinal adaption of piglets to weaning. Factors included dietary treatments being (1) 5% SDPP (PLA), (2) 3.5% yeast protein meal (NUP) and (3) medicated control (TMC) and parity (primiparous versus multiparous). The treatment groups were imposed from Day 19 through to weaning at Day 27. Selected pigs (n = 720, 28 ± 3 days of age, 7.4 ± 1.0 kg of bodyweight) were weaned and remained on their respective diets from Day 28 to Day 34. From Day 35 to Day 48 all group-housed pigs were offered a commercial weaner 1 diet, and from Day 49 to Day 68 pigs were offered a commercial weaner 2 diet. Growth performance, survival, and serum immunoglobulin G were monitored throughout the nursery phase (Day 28 to Day 68). Adaptation of the gastrointestinal tract in the acute post-weaning phase (Day 28 to Day 34) was assessed in 36 individually housed male weaners, with the effects of feed on structural, digestive, microbial and immune parameters along the gastrointestinal tract determined at Day 34. Pre-weaning feed disappearance was greater (P < 0.01) in multiparous litters independent of diet. In the commercial nursery, total removals (mortality and morbidity) were highest (P < 0.01) in primiparous sow progeny, with pigs offered NUP having greater (P ≤ 0.05) total removals. Pigs offered PLA had superior average daily gain, average daily feed intake and feed conversion ratio from Day 28 to Day 34 (P < 0.05). Pigs offered NUP tended to (P = 0.07) have superior average daily gain from Day 35 to Day 49. Pigs offered NUP had higher (P < 0.05) serum immunoglobulin G concentrations at Day 68 compared with pigs offered TMC, with the effect most pronounced in primiparous sow progeny. Individually housed weaners offered PLA consumed more (P < 0.05) feed on Day 30 to Day 31, had shorter relative intestine length (P < 0.05), greater villous height in the medial jejunum (P < 0.10) and lower immuno-pathology scores along the intestine. Pigs offered PLA also tended (P < 0.10) to have increased pancreatic-specific lipase and amylase activity compared with pigs offered NUP. Pigs offered NUP had a higher ratio of E. coli : coliforms in the colon (P < 0.01) and more counts of β-haemolytic bacteria in the medial jejunum (P < 0.05) and colon (P < 0.10). Diets containing either SDPP or NUP offered pigs benefits beyond nutrition relative to the medicated control diet. The benefits of SDPP were highly effective but transient, while the yeast derived protein had a successive or accumulative effect which was more pronounced in primiparous sow progeny.


References

Bailey M, Haverson K, Inman C, Harris C, Jones P, Corfield G, Miller B, Stokes C (2005) The development of the mucosal immune system pre- and post-weaning: balancing regulatory and effector function. The Proceedings of the Nutrition Society 64, 451–457.
The development of the mucosal immune system pre- and post-weaning: balancing regulatory and effector function.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2MnjvFehsg%3D%3D&md5=dac744b957681433bd286cb4b729ae77CAS |

Bauer E, Williams BA, Smidt H, Mosenthin R, Verstegen MWA (2006) Influence of dietary components on development of the microbiota in single-stomached species. Nutrition Research Reviews 19, 63–78.
Influence of dietary components on development of the microbiota in single-stomached species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XoslWls7Y%3D&md5=fad14a27f87f0b70a16a1a78f2dc1660CAS |

Bianchi ATJ, Moonen-Leusen HWM, van der Heijden PJ, Bokhout BA (1995) The use of a double antibody sandwich ELISA and monoclonal antibodies for the assessment of porcine IgM, IgG and IgA concentrations. Veterinary Immunology and Immunopathology 44, 309–317.
The use of a double antibody sandwich ELISA and monoclonal antibodies for the assessment of porcine IgM, IgG and IgA concentrations.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXltlCrs7c%3D&md5=03aa0c3dbe6442203fba1824a0128f3cCAS |

Borgström B, Erlanson C (1973) Pancreatic lipase and co-lipase. European Journal of Biochemistry 37, 60–68.
Pancreatic lipase and co-lipase.Crossref | GoogleScholarGoogle Scholar |

Bosi P, Casini L, Finamore A, Cremokolini C, Merialdi G, Trevisi P, Nobili F, Mengheri E (2004) Spray-dried plasma improves growth performance and reduces inflammatory status of weaned pigs challenged with enterotoxigenic Escherichia coli K88. Journal of Animal Science 82, 1764–1772.

Botermans JA, Pierzynowski SG (1999) Relations between body weight, feed intake, daily weight gain, and exocrine pancreatic secretion in chronically catheterized growing pigs. Journal of Animal Science 77, 450–456.

Bourne FJ (1973) The immunoglobulin system of the suckling pig. The Proceedings of the Nutrition Society 32, 205–215.
The immunoglobulin system of the suckling pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2cXkslKkuro%3D&md5=09cffd9cb43cad1dedd36ee6931e7529CAS |

Boyd RD, Castro GC, Cabrera RA (2002) Nutrition and management of the sow to maximize lifetime productivity. Advances in Pork Production 13, 47–59.

Brunser O, Espinoza J, Araya M, Cruchet S, Gil A (1994) Effect of dietary nucleotide supplementation on diarrhoeal disease in infants. Acta Paediatrica (Oslo, Norway) 83, 188–191.
Effect of dietary nucleotide supplementation on diarrhoeal disease in infants.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2c3ltFSktg%3D%3D&md5=824e29bd94d03cd1572af00861e5fc68CAS |

Chapman T (2005) Novel approaches to the analysis of pathogenic bacterial populations in neonatal and weaner porcine colibacillosis. PhD thesis, University of Wollongong, Australia.

Coffey R, Cromwell G (1995) The impact of environment and antimicrobial agents on the growth response of early-weaned pigs to spray dried porcine plasma. Journal of Animal Science 73, 2532–2539.

Corring T (1980) The adaptation of digestive enzymes to the diet: its physiological significance. Reproduction, Nutrition, Development 20, 1217–1235.
The adaptation of digestive enzymes to the diet: its physiological significance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXmtF2msbc%3D&md5=1c3f754a73507dcc25a14f312158ed96CAS |

Curtis J, Bourne FJ (1973) Half-lives of immunoglobulins IgG, IgA and IgM in the serum of new-born pigs. Immunology 24, 147–155.

Dionissopoulos L, de Lange CFM, Dewey CE, MacInnes JI, Friendship RM (2001) Effect of health management strategy during rearing on grower-finisher pig performance and selected indicators of immune system stimulation. Canadian Journal of Animal Science 81, 179–187.
Effect of health management strategy during rearing on grower-finisher pig performance and selected indicators of immune system stimulation.Crossref | GoogleScholarGoogle Scholar |

Dunshea FR, Kerton DK, Eason PJ, Pluske JR, Moyes T (2002) Diets containing high-quality animal proteins increase growth of early-weaned pigs. Australian Journal of Agricultural Research 53, 779–784.
Diets containing high-quality animal proteins increase growth of early-weaned pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xmt1GmtLo%3D&md5=19a58875904043c6215622fe1ea461f0CAS |

Erlanger BF, Kokowsky N, Cohen W (1961) The preparation and properties of two new chromogenic substrates of trypsin. Archives of Biochemistry and Biophysics 95, 271–278.
The preparation and properties of two new chromogenic substrates of trypsin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF38XkslOmtg%3D%3D&md5=87262a9a37abc83f818c39ac7ecc0aafCAS |

Garriga C, Perez-Bosque A, Amat C, Campbell JM, Russell L, Polo J, Planas JM, Moreto M (2005) Spray-dried porcine plasma reduces the effects of staphylococcal enterotoxin B on glucose transport in rat intestine. The Journal of Nutrition 135, 1653–1658.

Gil A, Gomez-Leon C, Rueda R (2007) Exogenous nucleic acids and nucleotides are efficiently hydrolysed and taken up as nucleosides by intestinal explants from suckling pigs. The British Journal of Nutrition 98, 285–291.
Exogenous nucleic acids and nucleotides are efficiently hydrolysed and taken up as nucleosides by intestinal explants from suckling pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpsFent7w%3D&md5=07e0195ecd5315d290252ac1270bf195CAS |

Grimble GK (1996) Why are dietary nucleotides essential nutrients? The British Journal of Nutrition 76, 475–478.
Why are dietary nucleotides essential nutrients?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28Xnt1CgtLs%3D&md5=e1a606822ccefa00cc565c0da04cc624CAS |

Hardy B (1992) Diets for young pigs. In ‘Neonatal survival and growth’. (Eds MA Varley, PEV Williams, TLJ Lawrence) pp. 99–107. (British Society of Animal Production: UK)

Hernández A, Hansen CF, Mansfield J, Mullan BP, Pluske JR (2010) The responses of light- and heavy-for-age pigs at weaning to dietary spray-dried porcine plasma. Animal Feed Science and Technology 162, 116–122.
The responses of light- and heavy-for-age pigs at weaning to dietary spray-dried porcine plasma.Crossref | GoogleScholarGoogle Scholar |

Huguet A, Savary G, Bobillier E, Lebreton Y, Le Huërou-Luron I (2006) Effects of level of feed intake on pancreatic exocrine secretions during early postweaning period in piglets. Journal of Animal Science 84, 2965–2972.
Effects of level of feed intake on pancreatic exocrine secretions during early postweaning period in piglets.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtFartr%2FK&md5=3095660c88cc8cc62e05de7aa0b8d9b9CAS |

Iji PA, Saki A, Tivey DR (2001) Body and intestinal growth of broiler chicks on a commercial starter diet. 2. Development and characteristics of intestinal enzymes. British Poultry Science 42, 514–522.
Body and intestinal growth of broiler chicks on a commercial starter diet. 2. Development and characteristics of intestinal enzymes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXnsFSis70%3D&md5=cee0b9e8251046997ef66d312162546aCAS |

Ilsley SE, Miller HM, Kamel C (2005) Effects of dietary quillaja saponin and curcumin on the performance and immune status of weaned pigs. Journal of Animal Science 83, 82–88.

Jiang R, Chang X, Stoll B, Fan MZ, Arthington J, Weaver E, Campbell J, Burrin DG (2000) Dietary plasma protein reduces small intestinal growth and lamina propria cell density in early weaned pigs. The Journal of Nutrition 130, 21–26.

Kalra E (2003) Nutraceutical – definition and introduction. AAPS PharmSci 5, 27–28.
Nutraceutical – definition and introduction.Crossref | GoogleScholarGoogle Scholar |

Kats L, Nelssen J, Tokach M, Goodband R, Hansen J, Laurin J (1994) The effect of spray-dried porcine plasma on growth performance in the early-weaned pig. Journal of Animal Science 72, 2075–2081.

Klindt J (2003) Influence of litter size and creep feeding on preweaning gain and influence of preweaning growth on growth to slaughter in barrows. Journal of Animal Science 81, 2434–2439.

Klobasa F, Butler JE, Werhahn E, Habe F (1986) Maternal-neonatal immunoregulation in swine. II. Influence of multiparity on de novo immunoglobulin synthesis by piglets. Veterinary Immunology and Immunopathology 11, 149–159.
Maternal-neonatal immunoregulation in swine. II. Influence of multiparity on de novo immunoglobulin synthesis by piglets.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaL287otFGgsw%3D%3D&md5=ae5190802b7f6b77ffde1ea4add64dfaCAS |

Lallès J, Bosi P, Smidt H, Stokes C (2007) Weaning – A challenge to gut physiologists. Livestock Science 108, 82–93.
Weaning – A challenge to gut physiologists.Crossref | GoogleScholarGoogle Scholar |

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry 193, 265–275.

Lunger AN, Craig SR, McLean E (2006) Replacement of fish meal in cobia (Rachycentron canadum) diets using an organically certified protein. Aquaculture 257, 393–399.
Replacement of fish meal in cobia (Rachycentron canadum) diets using an organically certified protein.Crossref | GoogleScholarGoogle Scholar |

McOrist S, Bowles R, Blackall P (2009) Autogenous sow vaccination for Glasser’s disease in weaner pigs in two large swine farm systems. Journal of Swine Health and Production 17, 90–96.

Miller Y, Collins A, Emery D, Begg D, Smits R, Holyoake P (2013) Piglet performance and immunity is determined by the parity of both the birth dam and rearing dam. Animal Production Science 53, 46–51.
Piglet performance and immunity is determined by the parity of both the birth dam and rearing dam.Crossref | GoogleScholarGoogle Scholar |

Moore C (2005) Parity segregation. In ‘Proceedings of the 5th London swine conference’. (Ed. JM Murphy) pp. 61–67. (London Swine Conference: Ontario, Canada)

Moore KL, Mullan BP, Pluske JR, Kim J-C, D’Souza DN (2011) The use of nucleotides, vitamins and functional amino acids to enhance the structure of the small intestine and circulating measures of immune function in the post-weaned piglet. Animal Feed Science and Technology 165, 184–190.
The use of nucleotides, vitamins and functional amino acids to enhance the structure of the small intestine and circulating measures of immune function in the post-weaned piglet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXlsFGmtLw%3D&md5=2199997d265274f29a454b210926a968CAS |

Niewold TA (2007) The nonantibiotic anti-inflammatory effect of antimicrobial growth promoters, the real mode of action? A hypothesis. Poultry Science 86, 605–609.

Nofrarias M, Manzanilla EG, Pujols J, Gibert X, Majo N, Segales J, Gasa J (2006) Effects of spray-dried porcine plasma and plant extracts on intestinal morphology and on leukocyte cell subsets of weaned pigs. Journal of Animal Science 84, 2735–2742.
Effects of spray-dried porcine plasma and plant extracts on intestinal morphology and on leukocyte cell subsets of weaned pigs.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD28rkslWgtA%3D%3D&md5=9499d615d185c0497ecc4efd0436fd69CAS |

Owusu-Asiedu A, Baidoo S, Nyachoti C, Marquardt R (2002) Response of early-weaned pigs to spray-dried porcine or animal plasma-based diets supplemented with egg-yolk antibodies against enterotoxigenic Escherichia coli. Journal of Animal Science 80, 2895–2903.

Owusu-Asiedu A, Nyachoti C, Marquardt R (2003) Response of early weaned pigs to an enterotoxigenic Escherichia coli (K88) challenge when fed diets containing spray-dried porcine plasma or pea protein isolate plus egg yolk antibody, zinc oxide, fumaric acid, or antibiotic. Journal of Animal Science 81, 1790–1798.

Perez-Bosque A, Miro L, Polo J, Russell L, Campbell J, Weaver E, Crenshaw J, Moreto M (2010) Dietary plasma protein supplements prevent the release of mucosal proinflammatory mediators in intestinal inflammation in rats. The Journal of Nutrition 140, 25–30.
Dietary plasma protein supplements prevent the release of mucosal proinflammatory mediators in intestinal inflammation in rats.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXltFSlsrw%3D&md5=fb3b8bad9dae4925f34c2c5dd21d0352CAS |

Pierzynowski SG, Weström BR, Erlanson-Albertsson C, Ahre’n B, Svendsen J, Karlsson BW (1993) Induction of exocrine pancreas maturation at weaning in young developing pigs. Journal of Pediatric Gastroenterology and Nutrition 16, 287–293.
Induction of exocrine pancreas maturation at weaning in young developing pigs.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s3mtVKhug%3D%3D&md5=9e0ebd9cca4a131d470b3d47b000bd03CAS |

Plikaytis BD, Turner SH, Gheesling LL, Carlone GM (1991) Comparisons of standard curve-fitting methods to quantitate Neisseria meningitidis group A polysaccharide antibody levels by enzyme-linked immunosorbent assay. Journal of Clinical Microbiology 29, 1439–1446.

Pluske JR (2001) Morphological and functional changes in the small intestine of the newly weaned pig. In ‘Gut environment of pigs’. (Eds A Piva, K Bach Knudsen, J Lindberg) pp. 1–27. (Nottingham University Press: Nottingham, UK)

Prykhod’ko O, Fed’kiv O, Linderoth A, Pierzynowski SG, Weström BR (2009) Precocious gut maturation and immune cell expansion by single dose feeding the lectin phytohaemagglutinin to suckling rats. The British Journal of Nutrition 101, 735–742.
Precocious gut maturation and immune cell expansion by single dose feeding the lectin phytohaemagglutinin to suckling rats.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjs1ynsLs%3D&md5=fc0e28d38b44654513003a88753a90b5CAS |

Rantzer D, Kiela P, Thaela MJ, Svendsen J, Ahren B, Karlsson S, Pierzynowski SG (1997) Pancreatic exocrine secretion during first days after weaning in pigs. Journal of Animal Science 75, 1324–1331.

Sakai M, Taniguchi K, Mamoto K, Ogawa H, Tabata M (2001) Immunostimulant effects of nucleotide isolated from yeast RNA on carp, Cyprinus carpio L. Journal of Fish Diseases 24, 433–438.
Immunostimulant effects of nucleotide isolated from yeast RNA on carp, Cyprinus carpio L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXot1Gmu78%3D&md5=a36a74c36aa9235b54add031bd65c2a8CAS |

Sangild PT, Weström B, Fowden AL, Silver M (1994) Developmental regulation of the porcine exocrine pancreas by glucocorticoids. Journal of Pediatric Gastroenterology and Nutrition 19, 204–212.
Developmental regulation of the porcine exocrine pancreas by glucocorticoids.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXmslanu7s%3D&md5=60b1b827f1ef114810232c620f0c51dfCAS |

Schrama JW, Schouten JM, Swinkels JW, Gentry JL, de Vries Reilingh G, Parmentier K (1997) Effect of hemoglobin status on humoral immune response of weanling pigs differing in coping styles. Journal of Animal Science 75, 2588–2596.

Singhal A, Macfarlane G, Macfarlane S, Lanigan J, Kennedy K, Elias-Jones A, Stephenson T, Dudek P, Lucas A (2008) Dietary nucleotides and fecal microbiota in formula-fed infants: a randomized controlled trial. The American Journal of Clinical Nutrition 87, 1785–1792.

Sutherland MA, Rodriguez-Zas SL, Ellis M, Salak-Johnson JL (2005) Breed and age affect baseline immune traits, cortisol, and performance in growing pigs. Journal of Animal Science 83, 2087–2095.

Torrallardona D (2010) Spray dried animal plasma as an alternative to antibiotics in weanling pigs: a review. Asian-Australasian Journal of Animal Sciences 23, 131–148.

Torrallardona D, Conde MR, Badiola I, Polo J, Brufau J (2003) Effect of fishmeal replacement with spray-dried animal plasma and colistin on intestinal structure, intestinal microbiology, and performance of weanling pigs challenged with Escherichia coli K99. Journal of Animal Science 81, 1220–1226.

Uauy R, Quan R, Gil A (1994) Role of nucleotides in intestinal development and repair: implications for infant nutrition. The Journal of Nutrition 124, 1436S–1441S.

Wichers H (2009) Immunomodulation by food: promising concept for mitigating allergic disease. Analytical and Bioanalytical Chemistry 395, 37–45.
Immunomodulation by food: promising concept for mitigating allergic disease.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmtVOqs70%3D&md5=06a76c0efc63f7f2d0fe727398c98c69CAS |

Xu RJ, Sangild PT, Zhang YQ, Zhang SH (2002) Bioactive compounds in porcine colostrum and milk and their effects on intestinal development in neonatal pigs. In ‘Biology of the intestine in growing animals’. (Eds R Zabielski, PC Gregory, B Weström) pp. 169–192. (Elsevier Science: Amsterdam)

Yi GF, Carroll JA, Allee GL, Gaines AM, Kendall DC, Usry JL, Torides Y, Izuru S (2005) Effect of glutamine and spray-dried plasma on growth performance, small intestinal morphology, and immune responses of Escherichia coli K88+-challenged weaned pigs. Journal of Animal Science 83, 634–643.

Zhao J, Harper AF, Estienne MJ, Webb KEJ, McElroy AP, Denbow DM (2007) Growth performance and intestinal morphology responses in early weaned pigs to supplementation of antibiotic-free diets with an organic copper complex and spray-dried plasma protein in sanitary and nonsanitary environments. Journal of Animal Science 85, 1302–1310.
Growth performance and intestinal morphology responses in early weaned pigs to supplementation of antibiotic-free diets with an organic copper complex and spray-dried plasma protein in sanitary and nonsanitary environments.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXksF2hur0%3D&md5=2cb1df7ade02dd2e7328fd2adc7c7ffaCAS |

Zhao J, Harper AF, Perkins BK, Southern LL, Shelton JL, Bidner TD, Webb KEJ, Estienne MJ, Kuehn LA (2008) Assessment of a marine-based hydrolyzed protein source and spray-dried plasma protein as supplements in the diet of early weaned pigs. The Professional Animal Scientist 24, 604–613.