Piglet performance and immunity is determined by the parity of both the birth dam and the rearing dam
Y. J. Miller A F , A. M. Collins B , D. Emery C , D. J. Begg C , R. J. Smits D and P. K. Holyoake EA Portec Veterinary Services Australia, Welshpool, WA 6106, Australia.
B NSW Department of Primary Industries, Elizabeth Macarthur Agricultural Institute, Menangle, NSW 2570, Australia.
C The University of Sydney, Camden, NSW 2570, Australia.
D Rivalea Australia Pty Ltd, Corowa, NSW 2646, Australia.
E Department of Primary Industries, Bendigo, Vic. 3550, Australia.
F Corresponding author. Email: yvette@portec.com.au
Animal Production Science 53(1) 46-51 https://doi.org/10.1071/AN12063
Submitted: 20 February 2012 Accepted: 16 August 2012 Published: 30 October 2012
Abstract
Gilt progeny have lower weaning weights and higher post-weaning medication and mortality rates, indicating greater disease susceptibility, than do sow progeny. The present study aimed to identify explanatory innate or adaptive immunity differences between gilt and sow progeny and potential pre- or post-natal influences. Sixty-four dams were vaccinated twice pre-farrowing with tetanus toxoid (TT). Serum (pre-vaccination) and colostrum and/or milk samples were collected to determine concentrations of TT-specific immunoglobulin G (IgG), by using an enzyme-linked immunosorbent assay (ELISA). Piglets were removed from their birth dam before suckling and fostered (not to their birth dam) to form 16 gilt and 16 sow litters, with five gilt-born and five sow-born piglets per litter. Piglets were vaccinated at weaning (4 weeks old) with either TT or saline (control). Sera and whole blood were collected from three gilt-born and three sow-born piglets per litter at 2, 4 and 7 weeks of age. Innate immunity was assessed indirectly on whole blood using an interferon gamma (IFN-γ) immune cell stimulation assay and a phagocytic assay. Piglets were weighed at birth, 4, 10, 17 and 22 weeks of age. There was no difference (P > 0.05) in the concentration of TT-specific IgG in colostrum and milk from gilts and older-parity sows, suggesting a similar ability to transfer IgG antibodies to a novel antigen. Birth dam parity did not affect piglets’ TT-specific IgG concentrations pre-weaning (P > 0.05) suggesting similar ability to absorb passively acquired IgG. Sow-reared piglets, however, had lower (P < 0.05) concentrations of TT-specific IgG than did gilt-reared piglets, possibly due to haemodilution in the faster-growing sow progeny. Gilt-born progeny had a reduced IgG response post-weaning to TT vaccination relative to sow-born progeny (P < 0.05), indicating adaptive immunity differences. Birth dam parity did not affect (P > 0.05) innate immunity (number/responsiveness of cells). Rearing dam parity influenced phagocytic activity pre- and post-weaning (gilt-reared > sow-reared; P < 0.05), possibly due to increased pathogen challenge. Birthweight was affected by birth dam parity (sow-born > gilt-born; P < 0.05) while rearing dam parity determined weaning weight (sow-reared > gilt-reared; P < 0.05), with no difference evident at 22 weeks. The results of the present study suggest that gilt-born progeny may be more susceptible to disease post-weaning than sow-born progeny due to their lower birthweight and reduced humoral immune responsiveness. The rearing dam may also affect disease susceptibility in progeny due to slower pre-weaning growth, lower weaning weights and increased pathogen challenge, both pre- and post-weaning.
Additional keywords: foster, pig, vaccination.
References
Alonso-Spilsbury M, Ramirez-Necoechea R, Gonzalez-Lozano M, Mota-Rojas D, Trujillo-Ortega ME (2007) Piglet survival in early lactation: a review. Journal of Animal and Veterinary Advances 6, 76–86.Bassey EOE, Collins MT (1997) Study of T-lymphocyte subsets of healthy and Mycobacterium avium subsp. paratuberculosis-infected cattle. Infection and Immunity 65, 4869–4872.
Begg DJ, de Silva K, Bosward K, Di Fiore L, Taylor DL, Jungersen G, Whittington RJ (2009) Enzyme-linked immunospot: an alternative method for the detection of interferon gamma in Johne’s disease. Journal of Veterinary Diagnostic Investigation 21, 187–196.
| Enzyme-linked immunospot: an alternative method for the detection of interferon gamma in Johne’s disease.Crossref | GoogleScholarGoogle Scholar |
Burkey TE, Miller PS, Johnson RK, Reese DE, Moreno R (2008) Does dam parity affect progeny health status? Nebraska swine report. University of Nebraska, Lincoln, NE.
Dufresne L (2006) Did parity segregation fulfil its promises? Seminar #11. In ‘37th American Association of Swine Veterinarians Annual Meeting’. pp. 1–6. (American Association of Swine Veterinarians: Perry, IA)
Farmer C, Quesnel H (2009) Nutritional, hormonal and environmental effects on colostrum in sows. Journal of Animal Science 87, 56–65.
| Nutritional, hormonal and environmental effects on colostrum in sows.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1M3mtVSqsw%3D%3D&md5=9cca61d9b59e0a177f895f0cbb51d1aeCAS |
Gardner IA, Hird DW, Franti CE (1989) Neonatal survival in swine: effects of low birth weight and clinical disease. American Journal of Veterinary Research 50, 792–797.
Harding J (2006) New approaches for controlling nursery diseases…or back to the basics? In ‘Proceedings of the 6th London Swine Conference’. (Eds JM Murphy, TM Kane) pp. 109–112. Available at http://www.londonswineconference.ca/proceedings/2006/2006.pdf [Verified 25 September 2012]
Holyoake PK, Dial GD, Trigg T, King VL (1995) Reducing piglet mortality through supervision during the perinatal period. Journal of Animal Science 73, 3543–3551.
Kitching RP, Salt JS (1995) The interference by maternally-derived antibody with active immunization of farm animals against foot-and-mouth disease. The British Veterinary Journal 151, 379–389.
| The interference by maternally-derived antibody with active immunization of farm animals against foot-and-mouth disease.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK28%2Fls1alug%3D%3D&md5=a5612b54ffbfc42e95b0306efa5e2e71CAS |
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 |
Mabry JW, Coffey MT, Seerley RW (1983) A comparison of an 8 vs 16 hour photoperiod during lactation on suckling frequency of the baby pig and maternal performance of the sow. Journal of Animal Science 57, 292–295.
Miller YJ (2008) Investigating the poor growth performance and survival of the progeny of gilts. PhD Thesis, University of Sydney.
Moore C (2001) Segregated production: How far can we go? In ‘Allen D. Leman Swine Conference Proceedings’. (Eds WC Scruton, S Claas) pp. 203–206. (Veterinary Outreach Programs, University of Minnesota: Minneapolis, MN)
Morales J, Mateos GG, Manteca X (2006) Effect of parity and rearing segregation at birth on productive performance and health status of pigs. Journal of Animal Science 84, 292
Payne RW, Harding SA, Murray DA, Soutar DM, Baird DB, Welham SJ, Kane AF, Gilmour AR, Thompson R, Webster R, Tunnicliffe Wilson R (2006) ‘Genstat release 9 reference manual.’ (VSN International: Hemel Hempstead, UK)
Smits R, Collins C (2009) Measurement and comparison of feed intake and growth performance during lactation and wean-finish of gilt progeny pigs cross-fostered onto multiparous sows. Final report 2D-111. The Pork Cooperative Research Centre, Australia.
Spencer JD, Boyd RD, Cabrera R, Allee GL (2003) Early weaning to reduce tissue mobilisation in lactating sows and milk supplementation to enhance pig weaning weight during extreme heat stress. Journal of Animal Science 81, 2041–2052.
Stokes CR, Bailey M, Haverson K, Harris C, Jones P, Inman C, Pié S, Oswald IP, Williams BA, Akkermans ADL, Sowa E, Rothkötter H-J, Miller BG (2004) Postnatal development of intestinal immune system in piglets: implications for the process of weaning. Animal Research 53, 325–334.
| Postnatal development of intestinal immune system in piglets: implications for the process of weaning.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXmtVejug%3D%3D&md5=e1a65ef726dac748123a3a058a4d5e3cCAS |
Thacker EL (2004) Lymphocyte development and maturation (part 2). The Pig Journal 53, 75–91.
Vesseur PC, Kemp B, Den Hartog LA, Noordhuizen JPTM (1997) Effect of split weaning in first and second parity sows on sow and piglet performance. Livestock Production Science 49, 277–285.
| Effect of split weaning in first and second parity sows on sow and piglet performance.Crossref | GoogleScholarGoogle Scholar |