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The Effects of Dietary Biotite V Supplementation as an Alternative Substance to Antibiotics in Growing Pigs

  • Chen, Y.J. (Department of Animal Resource & Science, Dankook University) ;
  • Kwon, O.S. (Department of Animal Resource & Science, Dankook University) ;
  • Min, B.J. (Department of Animal Resource & Science, Dankook University) ;
  • Son, K.S. (Department of Animal Resource & Science, Dankook University) ;
  • Cho, J.H. (Department of Animal Resource & Science, Dankook University) ;
  • Hong, J.W. (Department of Animal Resource & Science, Dankook University) ;
  • Kim, I.H. (Department of Animal Resource & Science, Dankook University)
  • Received : 2005.02.01
  • Accepted : 2005.05.18
  • Published : 2005.11.01

Abstract

This study was conducted to investigate the effects of Biotite V supplementation on growth performance, nutrients digestibility and blood constituents and to evaluate whether Biotite V could replace an antibiotics in growing pigs diet. One hundred twenty pigs with initial body weight of 18.35${\pm}$0.15 kg were used in a 28 days growth trial. Pigs were allotted to four treatments by sex and body weight in a randomized complete block design. There were six replicate pens per treatment and five pigs per pen. Four dietary treatments were: 1) NC (basal diet without antibiotics), 2) PC (basal diet+0.1% CTC), 3) NCBV (NC diet+0.5% 200 mesh Biotite V) and 4) PCBV (PC diet+0.5% 200 mesh Biotite V). Through the entire experimental period, ADG tented to increase in NCBV and PCBV treatments compared to NC and PC treatments respectively, but no significant differences were observed (p>0.05). ADFI was slightly lower in NCBV and PCBV treatments than that in NC and PC treatments without significant differences (p>0.05). Gain/feed in PC and PCBV treatments was improved significantly compared to NC treatment (p<0.05). N and Ca digestibilities were higher in PCBV treatments than those in PC treatment (p<0.05). DM and P digestibilities were not affected by the addition of Biotite V (p>0.05). RBC, HCT, Hb, lymphocyte and monocyte were increased numerically in NCBV and PCBV treatments compared to NC and PC treatments (p>0.05). WBC was lower in treatment groups than that in NC treatment, but no significant differences were observed (p>0.05). In conclusion, dietary supplementation of Biotite V can better the gain/feed and some of the nutrients digestibilities in growing pigs. It has a possibility to replace antibiotics in swine diet.

Keywords

References

  1. AOAC. 1995. Official method of analysis. 16th Edition. Association of Official Analytical Chemists, Washington, DC.
  2. Barton, M. D. 2000. Antibiotics use in animal feed and its impact on human health. Nut. Res. Rev. 13:1-22. https://doi.org/10.1079/095442200108728972
  3. Castro, M. and M. Iglesias. 1989. Effect of zeolite on traditional diets for fattening pigs. Cuban J. Agric. Sci. 23:289-291.
  4. Chen, Y. J., O. S. Kwon, B. J. Min, K. S. Shon, J. H. Cho and I. H. Kim. 2005. The effects of dietary Biotite V supplementation on growth performance, nutrients digestibility and fecal noxious gas content in finishing pigs. Asian-Aust. J. Anim. Sci. 18:1147-1152.
  5. Corpet, D. E. 2000. Mechanism of antimicrobial growth promoters used in animal feed (French). Rev. Med. Vet. 151:99-104.
  6. Dupont, D. P., G. E. Duhamel, M. P. Carlson and M. R. Mathiesen. 1994. Effect of divalent cations on hemolysin synthesis by Serpulina (Treponema) hyodysenteriae: Inhibition induced by zinc and copper. Vet. Microbiol. 41:63-73.
  7. Hays, V. W. 1981. The Hays Report: Effectiveness of Feed Additive Usage of Antibacterial Agents in Swine and Poultry Production. Office of Technology Assessment, US Congress, Washington DC, and Rachelle Laboratories, Long Beach, CA.
  8. Hill, G. M., G. L. Cromwell, T. D. Crenshaw, C. R. Dove, R. C. Dove, R. C. Ewan, D. A. Knabe, A. J. Lewis, G. W. Libal, D. C. Mahan, G. C. Shurosn, L. L. Southern and T. L. Venum. 2000. Growth promotion effects and plasma changes from feeding high dietary concentrations of zinc and copper to weanling pigs (regional study). J. Anim. Sci. 78:1010-1016.
  9. Kiser, J. S. 1976. A perspective on the use of antibiotics in animal feeds. J. Anim. Sci. 42:1058-1072. https://doi.org/10.2527/jas1976.4241058x
  10. Kwon, O. S., I. H. Kim, J. W. Hong, S. H. Lee, Y. K. Jung, B. J. Min and W. B. Lee. 2003. Effects of dietary germanium biotite in weaned, growing and finishing pigs. Korea J. Anim. Sci. Technol. 45:355-368.
  11. Mumpton, F. A. and P. H. Fishman. 1977. The application of natural zeolites in animal science and aquaculture. J. Anim. Sci. 45:1188-1203.
  12. NRC. 1998. Nutrient requirement of pigs. 10th Edition. National Research Council, Academy Press. Washington, DC.
  13. Pearson, G., W. C. Smith and J. M. Fox. 1985. Influence of dietary zeolite in pig performance over the weight range 25-78 kg. New Zealand J. Exp. Agric. 13:151-154.
  14. Pond, W. G. and J. T. Yen. 1983. Protection by clinoptilolite or zeolite NrA against cadmium-induced anemia in growing swine. Proc. Soc. Exp. Biol. Mad. 173:332.
  15. Poulsen, H. D. and N. Oksbjerg. 1995. Effects of dietary inclusion of a zeolite (clinoptilolite) on performance and protein metabolism of young growing pigs. Anim. Feed Sci. Technol. 53:297-303.
  16. Roof, M. D. and D. C. Mahan. 1982. Effect of carbadox and various dietary copper levels for weanling swine. J. Anim. Sci. 55:1109-1117.
  17. SAS. 1996. SAS user’s guide. Release 6.12 edition. SAS Institude. Inc Cary NC.
  18. Shurson, G. C., P. K. Ku, E. R. Miller and M. T. Yokoyama. 1984. Effects of zeolite or clinoptilolite in diets of growing swine. J. Anim. Sci. 59:1536-1545.
  19. Stahly, T. S., G. L. Cromwell and H. J. Monegue. 1980. Effects of the dietary inclusion of copper and (or) antibiotics on the performance of weanling pigs. J. Anim. Sci. 51:1347-1351.
  20. Taylor, D. J. 1997. A realistic assessment of the risks of antimicrobial use in animals and its effects on feed safety. Pig J. 40:46-59.
  21. Thacker, P. A. 2003. Performance of growing-finishing pigs fed diets containing graded levels of biotite, an alumninosilicate clay. Asian-Aust. J. Anim. Sci. 16:1666-1672. https://doi.org/10.5713/ajas.2003.1666
  22. Watkins, K. L., D. B. Vagnoni and L. L. Southm. 1989. Effect of dietary sodium zeolite A and excess calcium on growth and tibia calcium and phosphorus in uninfected and Eimeria acervulina-infected chicks. Poult. Sci. 68:1236.
  23. Yuan, S. L., X. S. Piao, D. F. Li, Y. H. He and X. H. Guo. 2004. Effects of Biotite V on Growth Performance and Serum Lymphocyte Proliferation in Weaned Piglets. National Feed Engineering Technology Research Center, China Agricultural University (Unpublished).

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