DOI QR코드

DOI QR Code

Toxicity of Mycotoxins from Contaminated Corn with or without Yeast Cell Wall Adsorbent on Broiler Chickens

  • Shang, Q.H. (Department of Animal Sciences and Technology, Shandong Agricultural University) ;
  • Yang, Z.B. (Department of Animal Sciences and Technology, Shandong Agricultural University) ;
  • Yang, W.R. (Department of Animal Sciences and Technology, Shandong Agricultural University) ;
  • Li, Z. (Department of Animal Sciences and Technology, Shandong Agricultural University) ;
  • Zhang, G.G. (Department of Animal Sciences and Technology, Shandong Agricultural University) ;
  • Jiang, S.Z. (Department of Animal Sciences and Technology, Shandong Agricultural University)
  • Received : 2015.05.01
  • Accepted : 2015.08.29
  • Published : 2016.05.01

Abstract

This study investigated the effects of feeds naturally contaminated with mycotoxins on growth performance, serum biochemical parameters, carcass traits, and splenic heat shock protein 70 (Hsp70) mRNA expression levels in broiler chickens. The efficacy of yeast cell wall (YCW) adsorbent in preventing mycotoxicosis was also evaluated. Three hundred 1-d-old Arbor Acres broiler chicks were randomly allotted to 3 treatments in completely randomized design for 42 d. Each treatment group had 5 replicate pens with 20 birds. The treatments were as follows: i) basal diet (control), ii) naturally contaminated diet (NCD), and iii) NCD+0.2% YCW adsorbent (NCDD). The NCD decreased average daily gain (ADG) (p<0.01) of 0 to 21 d, 22 to 42 d, and 0 to 42 d, and increased feed conversion ratio (p<0.01) of 22 to 42 d and 0 to 42 d. Both the breast meat percentage and thigh meat percentage of the NCD group were significantly higher (p<0.01) than that of the control group on d 21. The NCD group showed significantly increased levels of triglycerides (p<0.05) and cholesterol (p<0.05) on both d 21 and d 42 compared to the control group. However, the NCD significantly reduced (p<0.01) the high-density lipoprotein (HDL) on d 42 compared to controls. Compared with the NCD, supplementation with YCW significantly improved (p<0.01) the ADG of 0 to 21 d and 0 to 42 d, and increased (p<0.01) concentrations of HDL on d 42, and on d 21, and triglycerides (p<0.05) on d 21 and d 42. Supplementation with YCW reduced (p<0.01) the breast meat percentage, the thigh meat percentage, the concentrations of cholesterol (p<0.01) and the low-density lipoprotein (p<0.05) on d 21, and improved (p<0.01) the splenic Hsp70 mRNA expression levels compared with the NCD group. The results of this study indicated that feeding NCD for 42 d had adverse effects on broiler chickens, and that YCW might be beneficial in counteracting the effects of mycotoxins.

Keywords

References

  1. Akande, K. E., M. M. Abubakar, T. A. Adegbola, and S. E. Bogoro. 2006. Nutritional and health implications of mycotoxins in animal feeds: A review. Pakistan J. Nutr. 5:398-403. https://doi.org/10.3923/pjn.2006.398.403
  2. Aravind, K. L., V. S. Patil, G. Devegowda, B. Umakantha, and S. P. Ganpule. 2003. Efficacy of esterified glucomannan to counteract mycotoxicosis in naturally contaminated feed on performance and serum biochemical and hematological parameters in broilers. Poult. Sci. 82:571-576. https://doi.org/10.1093/ps/82.4.571
  3. Awad, W. A., J. Bohm, E. Razzazi-Fazeli, and J. Zentek. 2006. Effects of feeding deoxynivalenol contaminated wheat on growth performance, organ weights and histological parameters of the intestine of broiler chickens. J. Anim. Physiol. Anim. Nutr. 90:32-37. https://doi.org/10.1111/j.1439-0396.2005.00616.x
  4. Bryden, W. L. 2012. Mycotoxin contamination of the feed supply chain: Implications for animal productivity and feed security. Anim. Feed. Sci. Technol. 173:134-158. https://doi.org/10.1016/j.anifeedsci.2011.12.014
  5. Carnevali, O. and F. Maradonna. 2003. Exposure to xenobiotic compounds: Looking for new biomarkers. Gen. Comp. Endocrinol. 131:203-208. https://doi.org/10.1016/S0016-6480(03)00105-9
  6. Che, Z., Y. Liu, H. Wang, H. Zhu, Y. Hou, and B. Ding. 2011. The protective effects of different mycotoxin adsorbents against blood and liver pathological changes induced by moldcontaminated feed in broilers. Asian Australas. J. Anim. Sci. 24:250-257.
  7. Chowdhury, S. R. and T. K. Smith. 2004. Effects of feeding blends of grains naturally contaminated with Fusarium mycotoxins on performance and metabolism of laying hens. Poult. Sci. 83:1849-1856. https://doi.org/10.1093/ps/83.11.1849
  8. Chowdhury, S. R. and T. K. Smith. 2007. Effects of feed-borne Fusarium mycotoxins on performance, plasma chemistry and hepatic fractional protein synthesis rates of turkeys. Can. J. Anim. Sci. 87:543-551. https://doi.org/10.4141/CJAS07038
  9. Conkova, E., A. Laciakova, G. Kovac, and H. Seidel. 2003. Fusarial toxins and their role in animal diseases. Vet. J. 165:214-220. https://doi.org/10.1016/S1090-0233(02)00127-2
  10. El Golli, E., W. Hassen, A. Bouslimi, C. Bouaziz, M. M. Ladjimi, and H. Bacha. 2006. Induction of Hsp 70 in Vero cells in response to mycotoxins: Cytoprotection by sub-lethal heat shock and by Vitamin E. Toxicol. Lett. 166:122-130. https://doi.org/10.1016/j.toxlet.2006.06.004
  11. Food and Agriculture Organization of the United Nations (FAO). 2006. Worldwide regulations for mycotoxins in food and feed in 2003. FAO Food and Nutrition Paper No. 81. Rome, Italy.
  12. Hassen, W., I. Ayed-Boussema, A. A. Oscoz, A. De Cerain Lopez, and H. Bacha. 2007. The role of oxidative stress in zearalenone-mediated toxicity in Hep G2 cells: Oxidative DNA damage, gluthatione depletion and stress proteins induction. Toxicology 232:294-302. https://doi.org/10.1016/j.tox.2007.01.015
  13. Hedayati, M., M. Manafi, M. Yari, and S. V. Mousavipour. 2014. Commercial broilers exposed to aflatoxin b1: Efficacy of a commercial mycotoxin binder on internal organ weights, biochemical traits and mortality. Int. J. Agric. For. 4:351-358.
  14. Huff, W. E., R. B. Harvey, L. F. Kubena, and G. E. Rottinghaus. 1988. Toxic synergism between aflatoxin and t-2 toxin in broiler chickens. Poult. Sci. 67:1418-1423. https://doi.org/10.3382/ps.0671418
  15. Huwig, A., S. Freimund, O. Kappeli, and H. Dutler. 2001. Mycotoxin detoxication of animal feed by different adsorbents. Toxicol. Lett. 122:179-188. https://doi.org/10.1016/S0378-4274(01)00360-5
  16. Kececi, T., H. Oguz, V. Kurtoglu, and O. Demet. 1998. Effects of polyvinylpolypyrrolidone, synthetic zeolite and bentonite on serum biochemical and haematological characters of broiler chickens during aflatoxicosis. Br. Poult. Sci. 39:452-458. https://doi.org/10.1080/00071669889051
  17. Klasing, K. C. and D. M. Barnes. 1988. Decreased amino acid requirements of growing chicks due to immunologic stress. J. Nutr. 118:1158-1164. https://doi.org/10.1093/jn/118.9.1158
  18. Kogan, G. and A. Kocher. 2007. Role of yeast cell wall polysaccharides in pig nutrition and health protection. Livest. Sci. 109:161-165. https://doi.org/10.1016/j.livsci.2007.01.134
  19. Li, Z., Z. B. Yang, W. R. Yang, S. J. Wang, S. Z. Jiang, and Y. B. Wu. 2012. Effects of feed-borne Fusarium mycotoxins with or without yeast cell wall adsorbent on organ weight, serum biochemistry, and immunological parameters of broiler chickens. Poult. Sci. 91:2487-2495. https://doi.org/10.3382/ps.2012-02437
  20. Maresca, M., R. Mahfoud, N. Garmy, and J. Fantini. 2002. The mycotoxin deoxynivalenol affects nutrient absorption in human intestinal epithelial cells. J. Nutr. 132:2723-2731. https://doi.org/10.1093/jn/132.9.2723
  21. Ministry of Agriculture of China. 2004. Feeding standard of Chicken of the People's Republic of China. NY/T 33-2004. Ministry of Agriculture, Beijing, China.
  22. Rosa, C. A. R., R. Miazzo, C. Magnoli, M. Salvano, S. M. Chiacchiera, S. Ferrero, M. Saenz, E. C. Q. Carvalho, and A. Dalcero. 2001. Evaluation of the efficacy of bentonite from the south of Argentina to ameliorate the toxic effects of aflatoxin in broilers. Poult. Sci. 80:139-144. https://doi.org/10.1093/ps/80.2.139
  23. Schatzmayr, G. and E. Streit. 2013. Global occurrence of mycotoxins in the food and feed chain: Facts and figures. World Mycotoxin J. 6:213-222. https://doi.org/10.3920/WMJ2013.1572
  24. Swamy, H. V. L. N., T. K. Smith, E. J. MacDonald, N. A. Karrow, B. Woodward, and H. J. Boermans. 2003. Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on growth and immunological measurements of starter pigs, and the efficacy of a polymeric glucomannan mycotoxin adsorbent. J. Anim. Sci. 81:2792-2803. https://doi.org/10.2527/2003.81112792x
  25. Swamy, H. V., T. K. Smith, E. J. MacDonald, H. J. Boermans, and E. J. Squires. 2002a. Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on swine performance, brain regional neurochemistry, and serum chemistry and the efficacy of a polymeric glucomannan mycotoxin adsorbent. J. Anim. Sci. 80:3257-3267. https://doi.org/10.2527/2002.80123257x
  26. Swamy, H. V., T. K. Smith, P. F. Cotter, H. J. Boermans, and A. E. Sefton. 2002b. Effects of feeding blends of grains naturally contaminated with Fusarium mycotoxins on production and metabolism in broilers. Poult. Sci. 81:966-975. https://doi.org/10.1093/ps/81.7.966
  27. Wang, W. 2013. Phytoestrogen ${\alpha}$-Zearalanol in an Animal Model of Menopause. In: Nutrition and Diet in Menopause (Eds. C. H. Martin, R. R. Watson, and V. R. Preedy). Humana Press, New York, NY, USA. pp. 407-417.
  28. Xu, L., S. D. Eicher, and T. J. Applegate. 2011. Effects of increasing dietary concentrations of corn naturally contaminated with deoxynivalenol on broiler and turkey poult performance and response to lipopolysaccharide. Poult. Sci. 90:2766-2774. https://doi.org/10.3382/ps.2011-01654
  29. Yiannikouris, A., J. Francois, L. Poughon, C. G. Dussap, G. Bertin, G. Jeminet, and J. P. Jouany. 2004. Alkali extraction of ${\beta}$-Dglucans from Saccharomyces cerevisiae cell wall and study of their adsorptive properties toward zearalenone. J. Agric. Food Chem. 52:3666-3673. https://doi.org/10.1021/jf035127x
  30. Young, L. G., H. Ping, and G. J. King. 1990. Effects of feeding zearalenone to sows on rebreeding and pregnancy. J. Anim. Sci. 68:15-20. https://doi.org/10.2527/1990.68115x

Cited by

  1. Method Development for Determination of Multi-Mycotoxins in Chicken Liver and Kidney Tissues by LC-MS/MS vol.43, pp.2, 2016, https://doi.org/10.5536/KJPS.2016.43.2.111
  2. The Effect of Hydrated Sodium Calcium Aluminosilicate on Fatty Liver and the Composition of the Intestinal Microbiota in Overfed Landes Geese vol.20, pp.2, 2018, https://doi.org/10.1590/1806-9061-2017-0499
  3. Effect of plant extracts derived from thyme and chamomile on the growth performance, gut morphology and immune system of broilers fed aflatoxin B1 and ochratoxin A contaminated diets vol.18, pp.1, 2019, https://doi.org/10.1080/1828051x.2019.1615851
  4. Detoxification Strategies for Zearalenone Using Microorganisms: A Review vol.7, pp.7, 2016, https://doi.org/10.3390/microorganisms7070208
  5. Effect of a probiotic (Lactobacillus sp.), yeast (Saccharomyces cerevisiae) and mycotoxin detoxifier alone or in combination on performance, immune response and serum biochemical parameters in broiler vol.61, pp.15, 2016, https://doi.org/10.1071/an19728
  6. Recent advances in detoxification strategies for zearalenone contamination in food and feed vol.30, pp.None, 2016, https://doi.org/10.1016/j.cjche.2020.11.011
  7. Effect of Clostridium on proliferating cell nuclear antigen and ghrelin in the small intestine of fattening pigs fed with deoxynivalenol vol.14, pp.1, 2016, https://doi.org/10.3920/wmj2020.2569
  8. Effects of Deoxynivalenol and Fumonisins on Broiler Gut Cytoprotective Capacity vol.13, pp.10, 2016, https://doi.org/10.3390/toxins13100729