Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-26T22:53:13.415Z Has data issue: false hasContentIssue false

Associations of acute phase protein levels with growth performance and with selection for growth performance in Large White pigs

Published online by Cambridge University Press:  09 March 2007

M. Clapperton*
Affiliation:
Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK
S. C. Bishop
Affiliation:
Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK
N. D. Cameron
Affiliation:
Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK
E. J. Glass
Affiliation:
Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK
Get access

Abstract

Abstract Acute phase proteins (APP) are released into the circulation in mammals upon infection and may be used to diagnose the health status of managed populations of animals such as pigs. The current study determines APP levels in a population of apparently healthy Large White pigs from a single farm, to address two questions: (1) whether phenotypic associations can be observed between productivity and APP, indicating the effects of possible subclinical infections and (2) whether previous selection for either food intake or ‘lean growth under restricted feeding’ influences APP levels. The APP investigated were alpha1- acid glycoprotein (AGP) and haptoglobin. The APP were measured at 18 and 24 weeks of age in pigs previously selected for high lean growth (no. = 31), low lean growth (no. = 38), high daily food intake (no. = 24) and low daily food intake (no. = 26), but performing under ad libitum feeding conditions. Performance traits and APP levels were constant over the experimental period, indicating that the farm health status did not vary over time. Performance traits and APP were recorded on 119 pigs, of which 80 had both APP and performance measurements. Multiple regression analyses were used to investigate phenotypic relationships between performance traits and APP levels. Plasma concentrations of AGP were higher in 18-week-old pigs compared with 24-week-old pigs (P < 0·01) whereas haptoglobin levels did not vary according to age. Significant sex differences in APP levels were observed. Females had higher circulating levels of AGP than males at both 18 weeks and 24 weeks. Females also had higher levels of haptoglobin at 18 weeks. Levels of AGP had significant negative correlations with daily weight gain (−0·59, P < 0·01 and −0·48, P < 0·05 at 18 and 24 weeks respectively) and with daily food intake (−0·53, P < 0·01 and −0·38, P < 0·05 at 18 and 24 weeks respectively). At age 24 weeks, haptoglobin was negatively correlated with both daily weight gain (−0·35, P < 0·05) and food efficiency (−0·34, P < 0·05). Pigs selected for high lean growth under restricted feeding had higher AGP levels than pigs selected for low lean growth under restricted feeding at 18 (593 v. 332 μg/ml, P < 0·01) and 24 weeks of age (313 v. 219 μg/ml, P < 0·05). Selection for daily food intake did not consistently affect AGP levels, and neither selection criteria influenced plasma haptoglobin concentrations. To conclude, we have demonstrated that amongst contemporaneous pigs of the same genotype, higher systemic AGP levels and, to a lesser extent, higher haptoglobin levels are associated with decreased performance, and that genetic selection for ‘efficient lean growth under restricted feeding’ can increase serum AGP levels.

Type
Research Article
Copyright
Copyright © British Society of Animal Science 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amory, J. R., MacKenzie, A. M., Pearce, G. P., Eckersall, P. D., Lampreave, F. and Alava, M. A. 2000. The effect of respiratory disease on serum haptoglobin and major acute phase protein levels in the slaughter pigs. First European colloquium report http: //www. gla.ac.uk/faculties/vet/research/protein/01_glasgow/03_titles_abstracts. htmlGoogle Scholar
Asai, T., Mori, M., Okada, M., Urumo, K., Yazawa, S. and Shibata, I. 1999. Elevated serum haptoglobin in pigs infected with porcine reproductive syndrome virus. Veterinary Immunology and Immunopathology 70: 143148.CrossRefGoogle Scholar
Baumann, H. and Gauldie, J. 1994. The acute phase response. Immunology Today 15: 7480.CrossRefGoogle ScholarPubMed
Cameron, N. D. 1994. Selection for components of efficient lean growth rate in pigs. 1. Selection pressure applied and direct responses in a Large White herd. Animal Production 59: 251262.Google Scholar
Cameron, N. D., McCullough, E., Troup, K. and Penman, J. C. 2003. Physiological responses to divergent selection for daily food intake or lean growth rate in pigs. Animal Science 76: 2734.CrossRefGoogle Scholar
Clapperton, M., Bishop, S. C., Cameron, N. D. and Glass, E. J. 2005a. Associations of weight gain and food intake with leucocyte sub-sets in Large White pigs. Livestock Production Science In press.CrossRefGoogle Scholar
Clapperton, M., Bishop, S. C. and Glass, E. J. 2005b. Innate immune traits differ between Meishan and Large White pigs. Veterinary Immunology and Immunopathology 104: 131144.CrossRefGoogle ScholarPubMed
Colditz, I. G. 2002. Effects of the immune system on metabolism: implications for production and disease resistance in livestock. Livestock Production Science 75: 257268.CrossRefGoogle Scholar
Eckersall, P. D. 2000. Recent advances and future prospects for the use of acute phase proteins as markers of disease in animals. Revue de Médecine Vétérinaire 151: 577584.Google Scholar
Eckersall, P. D., Saini, P. K. and McComb, C. 1996. The acute phase response of acid soluble glycoprotein, alpha-1- acid glycoprotein, ceruloplasmin, haptoglobin and C-reactive protein in the pig. Veterinary Immunology and Immunopathology 51: 377385.CrossRefGoogle ScholarPubMed
Eurell, T. E., Bane, D. P., Hall, W. F. and Schaeffer, D. J. 1992. Serum haptoglobin concentration as an indicator of weight gain in pigs. Canadian Journal of Veterinary Research 56: 69.Google ScholarPubMed
Greiner, L. L., Stahly, T. S. and Stabel, T. J. 2000. Quantitative relationship of systemic virus concentration on growth and immune response in pigs. Journal of Animal Science 78: 26902695.CrossRefGoogle ScholarPubMed
Greiner, L. L., Stahly, T. S. and Stabel, T. J. 2001. The effect of dietary soy genistein on pig growth and viral replication during a viral challenge. Journal of Animal Science 79: 12721279.CrossRefGoogle ScholarPubMed
Grellner, G. F., Fangman, T. J., Carroll, J. A. and Wiedmeyer, C. E. 2002. Using serology in combination with acute phase proteins and cortisol to determine stress and immune function of early-weaned pigs. Journal of Swine Health and Production 10: 199204.Google Scholar
Haverson, K., Bailey, M., Stokes, C. R., Simon, A., LeFlufy, L., Banfield, G., Chen, Z., Hollemweguer, E. and Ledbetter, J. A. 2001. Monoclonal antibodies raised to human cells - specificity for pig leukocytes. Veterinary Immunology and Immunopathology 80: 175186.CrossRefGoogle ScholarPubMed
Heegaard, P. M. H., Klausen, J., Nielsen, J. P., Gonzalez-Ramon, N., Pineiro, M., Lampreave, F. and Alava, M. A. 1998. The porcine acute phase response to infection with Actinobacillus pleuropneumoniae. Haptoglobin, C-reactive protein (CRP) and major acute phase protein and serum amyloid A protein are sensitive indicators of infection. Comparative Biochemistry and Physiology 119B: 365373.CrossRefGoogle ScholarPubMed
Hochepied, T., Berger, F. G., Baumann, H. and Libert, C. 2003 Alpha1-acid glycoprotein: an acute phase protein with inflammatory and immunomodulating properties. Cytokine Growth Factor Reviews 14: 2534.CrossRefGoogle Scholar
Itoh, H., Tamura, K., Motoi, Y., Kidoguchi, K. and Funagamam, Y. 1992. The influence of age and health status on the serum alpha1- acid glycoprotein level of conventional and specific pathogen-free pigs. Canadian Journal of Veterinary Research 57: 7478.Google Scholar
Johnson, R. W. 1997. Inhibition of growth by pro-inflammatory cytokines. Journal of Animal Science 75: 12441255.CrossRefGoogle ScholarPubMed
Johnson, R. W. 1998. Immune and endocrine regulation of food intake in sick animals. Domestic Animal Endocrinology 15: 309319.CrossRefGoogle ScholarPubMed
Knapp, P. W. and Bishop, S. C. 2000. Relationship between genetic change and infectious disease in domestic livestock. British Society of Animal Science occasional publication no. 27, pp. 6580. http: //www. bsas. org. uk/publs/genchng/contents. pdfCrossRefGoogle Scholar
Lawes Agricultural Trust. 1983. GENSTAT a general statistical program. Numerical Algorithms Group.Google Scholar
Lipperheide, C., Diepers, N., Lampreave, F., Alava, M. and Petersen, B. 1998. Nephelometric determination of haptoglobin plasma concentrations in fattening pigs. Journal of Veterinary Medicine 45: 543550.CrossRefGoogle ScholarPubMed
Magnusson, U., Wilkie, B., Artursson, K. and Mallard, B. 1999. Interferon alpha and haptoglobin in pigs selectively bred for high and low immune response and infected with Mycoplasma hyorhinis. Veterinary Immunology and Immunopathology 68: 131137.CrossRefGoogle ScholarPubMed
Petersen, H. H., Ersboll, A. K., Jensen, C. S. and Nielsen, J. P. 2002. Serum-haptoglobin concentration in Danish slaughter pigs of different health status. Preventive Veterinary Medicine 54: 325335.CrossRefGoogle ScholarPubMed
Pukhal'skii, A. L., Shmarina, G. V., Lyutov, A. G., Novikova, L. I., Shemyakin, I. G. and Aleshkin, V. A. 2001. Alpha1-acid glycoprotein possesses in vitro pro- and anti-inflammatory activities. Bulletin of Experimental Biology and Medicine 131: 479481.CrossRefGoogle Scholar
Richter, H. 1974. Haptoglobin in domestic mammals. III. Haptoglobin content in blood plasma and serum in ruminants and pigs under various physiological conditions. Archiv für Experimentelle Veterinarmedizin 28: 205219.Google ScholarPubMed
Skinner, J. G. 2001. International standardization of acute phase proteins. Veterinary Clinical Pathology 30: 27.CrossRefGoogle ScholarPubMed
Stark, K. D. C. 2000. Epidemiological investigation of the influence of environmental risk factors on respiratory diseases in swine– a literature review. The Veterinary Journal 159: 3756.CrossRefGoogle ScholarPubMed
Szalai, A. J., Ginkel, F. W. van, Dalrymple, S. A., Murray, R., McGhee, J. R. and Volanakis, J. E. 1998. Testosterone and IL-6 requirements for human C-reactive protein gene expression in transgenic mice. Journal of Immunology 160: 52945299.CrossRefGoogle ScholarPubMed
Williams, N. H., Stahly, T. S. and Zimmerman, D. R. 1997. Effect of level of chronic immune system activation on the growth and dietary lysine needs of pigs fed from 6 to 112 kg. Journal of Animal Science 75: 24812496.CrossRefGoogle ScholarPubMed