Optimal dietary zinc levels of broiler chicks fed a corn–soybean meal diet from 22 to 42 days of age
Xiudong Liao A B , Ang Li B , Lin Lu A , Songbai Liu A , Sufen Li A C , Liyang Zhang A , Guangying Wang B and Xugang Luo A DA Mineral Nutrition Research Division, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, People’s Republic of China.
B College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, People’s Republic of China.
C Hebei Normal University of Science and Technology, Qinhuangdao 066004, People’s Republic of China.
D Corresponding author. Email: wlysz@263.net
Animal Production Science 53(5) 388-394 https://doi.org/10.1071/AN12291
Submitted: 18 August 2012 Accepted: 5 October 2012 Published: 7 February 2013
Abstract
An experiment was conducted to investigate the effect of dietary zinc (Zn) level on growth performance, Zn concentration, Zn metalloenzyme activity, Zn transporter 2 (ZnT2) mRNA abundance, metallothionein (MT) mRNA abundance and MT concentration in either serum or tissues, so as to evaluate the optimal dietary Zn level of broiler chicks fed a corn–soybean meal diet from 22 to 42 days of age. At 22 days of age, 288 birds were assigned randomly by bodyweight to one of eight dietary treatments of six replicate cages each with six birds per cage, and fed a Zn-unsupplemented basal corn–soybean meal diet containing 27.66 mg of Zn/kg or the basal diet supplemented with 20, 40, 60, 80, 100, 120 or 140 mg of Zn/kg from reagent-grade ZnSO4·7H2O. Regression analysis was performed to estimate the optimal dietary Zn level in the presence of asymptotic response. The results showed that dietary Zn level had no effect (P > 0.25) on the growth performance, serum alkaline phosphatase and 5′-nucleotidase activities, and liver copper-Zn superoxide dismutase activity, but affected (P < 0.07) tibia Zn concentration, pancreas Zn concentration, ZnT2 mRNA abundance, MT mRNA abundance and MT concentration. The optimal dietary Zn requirements of broilers from 22 to 42 days of age were 62.44 mg/kg for tibia Zn, 64.30 mg/kg for ZnT2 mRNA abundance and 53.50 mg/kg for MT mRNA abundance based on asymptotic models, respectively. Accordingly, the optimal dietary Zn level for broilers from 22 to 42 days of age was 65 mg/kg in this study.
References
Bafundo KW, Baker DH, Fitzgerald PR (1984) Zinc utilization in the chick as influenced by dietary concentrations of calcium and phytate and by Eimeria acervulina infection. Poultry Science 63, 2430–2437.| Zinc utilization in the chick as influenced by dietary concentrations of calcium and phytate and by Eimeria acervulina infection.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXhtFWqtrs%3D&md5=c21f07d1387abc1a1a733ca085092063CAS |
Bao YM, Choct M (2009) Trace mineral nutrition for broiler chickens and prospects of application of organically complexed trace minerals: a review. Animal Production Science 49, 269–282.
| Trace mineral nutrition for broiler chickens and prospects of application of organically complexed trace minerals: a review.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktVGktbg%3D&md5=26f5f30ec980112de79b0231c7088527CAS |
Bartlett JR, Smith MO (2003) Effects of different levels of zinc on the performance and immunocompetence of broilers under heat stress. Poultry Science 82, 1580–1588.
Berg JM, Shi YG (1996) The galvanization of biology: a growing appreciation for the roles of zinc. Science 271, 1081–1085.
| The galvanization of biology: a growing appreciation for the roles of zinc.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28Xht1GksLk%3D&md5=b5d9383f8b36c5d0b61037cd0d32fa65CAS |
Cao J, Henry PR, Davis SR, Cousins RJ, Miles RD, Littell RC, Ammerman CB (2002) Relative bioavailability of organic zinc sources based on tissue zinc and metallothionein in chicks fed conventional dietary zinc concentrations. Animal Feed Science and Technology 101, 161–170.
| Relative bioavailability of organic zinc sources based on tissue zinc and metallothionein in chicks fed conventional dietary zinc concentrations.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XnsVSjs7g%3D&md5=37e8728550c08cd25d46a010c93f69feCAS |
Cepelak I, Barisic K, Luterotti S, Sokolic B, Rupic V (2002) Zinc-dependent enzymes as indicators of zinc status in swine. Periodicum Biologorum 104, 445–450.
Chesters JK (1992) Trace element-gene interactions. Nutrition Reviews 50, 217–223.
| Trace element-gene interactions.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s%2FisF2huw%3D%3D&md5=16b3117027191073af1672ba8e1b9a92CAS |
Corzo A, Dozier WA, Kidd MT (2006) Dietary lysine needs of late-developing heavy broilers. Poultry Science 85, 457–461.
Cousins RJ, Lee-Ambrose LM (1992) Nuclear zinc uptake and interactions and metallothionein gene expression are influenced by dietary zinc in rats. The Journal of Nutrition 122, 56–64.
Dewar WA, Downie JN (1984) The zinc requirements of broiler chicks and turkey poults fed on purified diets. The British Journal of Nutrition 51, 467–477.
| The zinc requirements of broiler chicks and turkey poults fed on purified diets.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2cXktVGrtr0%3D&md5=85dadcfab348feb6f5c6227a141d2388CAS |
Eaton DL, Toal BF (1982) Evaluation of the Cd/hemoglobin affinity assay for the rapid determination of metallothionein in biological tissues. Toxicology and Applied Pharmacology 66, 134–142.
| Evaluation of the Cd/hemoglobin affinity assay for the rapid determination of metallothionein in biological tissues.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXkvF2iug%3D%3D&md5=501edda9e6c77e12f04609a43b817ec0CAS |
Hambidge M (2003) Biomarkers of trace mineral intake and status. The Journal of Nutrition 133, 948S–955S.
Huang YL, Lu L, Luo XG, Liu B (2007) An optimal dietary zinc level of broiler chicks fed a corn–soybean meal diet. Poultry Science 86, 2582–2589.
| An optimal dietary zinc level of broiler chicks fed a corn–soybean meal diet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhsVygsbbF&md5=c318a42d318719d077ead2e21c08c058CAS |
Huang YL, Lu L, Li SF, Luo XG, Liu B (2009) Relative bioavailabilities of organic zinc sources with different chelation strengths for broilers fed a conventional corn–soybean meal diet. Journal of Animal Science 87, 2038–2046.
| Relative bioavailabilities of organic zinc sources with different chelation strengths for broilers fed a conventional corn–soybean meal diet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXms1eisr4%3D&md5=4af48262faa5bc34703c7149a34cc5baCAS |
Kambe T, Yamaguchi-Iwai Y, Sasaki R, Nagao M (2004) Overview of mammalian zinc transporters. Cellular and Molecular Life Sciences 61, 49–68.
| Overview of mammalian zinc transporters.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXjt1yhur4%3D&md5=a1c79946906e4d420ca4e22d78757f89CAS |
Lease JG (1966) Effect of autoclaving sesame meal on its phytic acid content and on availability of its zinc to chick. Poultry Science 45, 237–241.
| Effect of autoclaving sesame meal on its phytic acid content and on availability of its zinc to chick.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF28XpslWlug%3D%3D&md5=166b95780963bed1b0e0dbdf86c53ce3CAS |
Leeson S (2005) Trace mineral requirements of poultry – validity of the NRC recommendations. In ‘Redefining mineral nutrition’. (Eds JA Taylor-Pickard, LA Tucker) pp. 107–117. (Nottingham University Press: Nottingham, UK)
Lichten LA, Cousins RJ (2009) Mammalian zinc transporters: nutritional and physiologic regulation. Annual Review of Nutrition 29, 153–176.
| Mammalian zinc transporters: nutritional and physiologic regulation.Crossref | GoogleScholarGoogle Scholar |
Liuzzi JP, Blanchard RK, Cousins RJ (2001) Differential regulation of zinc transporter 1, 2, and 4 mRNA expression by dietary zinc in rats. The Journal of Nutrition 131, 46–52.
Liuzzi JP, Bobo JA, Lichten LA, Samuelson DA, Cousins RJ (2004) Responsive transporter genes within the murine intestinal-pancreatic axis form a basis of zinc homeostasis. Proceedings of the National Academy of Sciences of the United States of America 101, 14 355–14 360.
| Responsive transporter genes within the murine intestinal-pancreatic axis form a basis of zinc homeostasis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXovVertLo%3D&md5=f0ca44aa7b1c5056ac9b45d45b82ba33CAS |
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods (San Diego, Calif.) 25, 402–408.
| Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhtFelt7s%3D&md5=e7ddb0df18f96a9072b5ab8d1f12c74cCAS |
Meftah S, Prasad AS, Lee DY, Brewer GJ (1991) Ecto 5′nucleotidase (5′nt) as a sensitive indicator of human zinc-deficiency. The Journal of Laboratory and Clinical Medicine 118, 309–316.
Mohanna C, Nys Y (1999) Effect of dietary zinc content and sources on the growth, body zinc deposition and retention, zinc excretion and immune response in chickens. British Poultry Science 40, 108–114.
| Effect of dietary zinc content and sources on the growth, body zinc deposition and retention, zinc excretion and immune response in chickens.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXivFSks78%3D&md5=f7dc310f48033545f3be98457183cd83CAS |
Mondal S, Haldar S, Saha P, Ghosh TK (2010) Metabolism and tissue distribution of trace elements in broiler chickens’ fed diets containing deficient and plethoric levels of copper, manganese, and zinc. Biological Trace Element Research 137, 190–205.
| Metabolism and tissue distribution of trace elements in broiler chickens’ fed diets containing deficient and plethoric levels of copper, manganese, and zinc.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtFWhtL7N&md5=039e55b85c310baad4c857a9a34a5f28CAS |
Morrison AB, Sarett HP (1958) Studies on zinc deficiency in the chick. The Journal of Nutrition 65, 267–280.
National Research Council (1994) ‘Nutrient requirements of poultry.’ 9th edn. (National Academy Press: Washington, DC)
O’Dell BL, Newberne PM, Savage JE (1958) Significance of dietary zinc for the growing chicken. The Journal of Nutrition 65, 503–523.
O’Dell BL, Yohe JM, Savage JE (1964) Zinc availability in the chick as affected by phytate, calcium and ethylenediaminetetraacetate. Poultry Science 43, 415–419.
| Zinc availability in the chick as affected by phytate, calcium and ethylenediaminetetraacetate.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF2cXksVamt7k%3D&md5=84c61e23a8bddc3b5805e70385ce6d14CAS |
Pimentel JL, Cook ME, Greger JL (1991) Research note: bioavailability of zinc-methionine for chicks. Poultry Science 70, 1637–1639.
| Research note: bioavailability of zinc-methionine for chicks.Crossref | GoogleScholarGoogle Scholar |
Robbins KR, Norton HW, Baker DH (1979) Estimation of nutrient requirements from growth data. The Journal of Nutrition 109, 1710–1714.
Roberson RH, Schaible PJ (1958) The zinc requirement of the chick. Poultry Science 37, 1321–1323.
| The zinc requirement of the chick.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaG1MXhtVSkt7k%3D&md5=35c65b96155be64c961e62c0b09c907eCAS |
Sandoval M, Henry PR, Luo XG, Littell RC, Miles RD, Ammerman CB (1998) Performance and tissue zinc and metallothionein accumulation in chicks fed a high dietary level of zinc. Poultry Science 77, 1354–1363.
Song Y, Elias V, Wong CP, Scrimgeour AG, Ho E (2010) Zinc transporter expression profiles in the rat prostate following alterations in dietary zinc. Biometals 23, 51–58.
| Zinc transporter expression profiles in the rat prostate following alterations in dietary zinc.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXisFWiuw%3D%3D&md5=c587870c6fefc94e7f3a64743f8ef5c4CAS |
Sunder GS, Panda AK, Gopinath NCS, Rao SVR, Raju MVLN, Reddy MR, Kumar CV (2008) Effects of higher levels of zinc supplementation on performance, mineral availability, and immune competence in broiler chickens. Journal of Applied Poultry Research 17, 79–86.
| Effects of higher levels of zinc supplementation on performance, mineral availability, and immune competence in broiler chickens.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXos1yqu7k%3D&md5=ebc82beacaa9ee70033e9e825220fbdeCAS |
Uauy R, Hertrampf E (2001) Food-based dietary recommendations: possibilities and limitations. In ‘Present knowledge in nutrition’. (Eds B Bowman, R Russell) pp. 636–649. (ILSI Press: Washington, DC)
Vallee BL, Auld DS (1990) Zinc coordination, function, and structure of zinc enzymes and other proteins. Biochemistry 29, 5647–5659.
| Zinc coordination, function, and structure of zinc enzymes and other proteins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3cXktF2ku70%3D&md5=20910017a99d544c33bb299c34ad052dCAS |
Vallee BL, Falchuk KH (1993) The biochemical basis of zinc physiology. Physiological Reviews 73, 79–118.
Viarengo A (1989) Heavy metals in marine invertebrates: mechanisms of regulation and toxicity at cellular level. Reviews in Aquatic Sciences 1, 295–317.
Watkins KL, Southern LL (1993) Effect of dietary sodium zeolite A on zinc utilization by chicks. Poultry Science 72, 296–305.
| Effect of dietary sodium zeolite A on zinc utilization by chicks.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXhvFSmsLw%3D&md5=79366f89d7aad32ff7fde90fea15be54CAS |
Wedekind KJ, Hortin AE, Baker DH (1992) Methodology for assessing zinc bioavailability: efficacy estimates for zinc-methionine, zinc sulfate, and zinc oxide. Journal of Animal Science 70, 178–187.
Wedekind KJ, Yu S, Combs GF (2004) The selenium requirement of the puppy. Journal of Animal Physiology and Animal Nutrition 88, 340–347.
| The selenium requirement of the puppy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVeqtrnM&md5=63ed59a51d1356635ec5cb3fd394cb90CAS |
Yang QM, Diao YX (2003) ‘The handbook for raising of broilers.’ (China Agriculture University Press: Beijing)
Zeigler TR, Leach RM, Norris LC, Scott ML (1961) Zinc requirement of the chick: factors affecting requirement. Poultry Science 40, 1584–1593.
| Zinc requirement of the chick: factors affecting requirement.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF38XkvVegsA%3D%3D&md5=0ed135ef3db3de55886dcde14ca318ebCAS |