Effect of Phytase Supplementation on Growth Performance in Broiler Chickens
Effect of Phytase Supplementation on Growth Performance in Broiler Chickens
Kalimullah Khan1,*, Hafsa Zaneb2, Zia Ur Rehman3, Hamza Maris4 and Habib ur Rehman1
1Department of Physiology, Faculty of Biosciences, University of Veterinary and Animal Sciences, Lahore
2Department of Anatomy and Histology, Faculty of Biosciences, University of Veterinary and Animal Sciences, Lahore
3Department of Poultry Science, Faculty of Animal Husbandry and Veterinary Sciences, The University of Agriculture, Peshawar
4Department of Livestock and Poultry Science, Faculty of Veterinary and Animal Sciences, Gomal University, Dera Ismail Khan
ABSTRACT
Day-old broiler birds (n = 96) were randomly divided into four groups, each group with four replicates and having 6 birds in each replicate. The birds were supplemented with corn-based diet. On day 35, birds were slaughtered to determine the relative weights of heart, liver, kidneys, spleen, gizzard and intestines. Results showed that supplementation of phytase enzymes affected the weight and length of small intestine and feed conversion ratio (FCR) and did not affect the other zoo technical variables like body weight, feed consumption, and weight gain during the whole experimental period. Application of phytase failed to exert any influence on the weights of gizzard, provetriculus, heart, liver, spleen and empty intestine. The weights and lengths of the small intestine were highly significant (P > 0.05) in the treatment groups. This study showed the potency of phytase to enhance the growth performance in broilers and it will lay foundation for future research on poultry feed in Pakistan.
Article Information
Received 16 April 2017
Revised 12 March 2018
Accepted 01 August 2018
Available online 01 March 2019
Authors’ Contribution
HZ designed the study. KK performed the study. ZR and HM wrote the paper. HR edited the manuscript.
Key words
Phytase, Broiler, Performance.
DOI: http://dx.doi.org/10.17582/journal.pjz/2019.51.2.531.535
* Corresponding author: [email protected]
0030-9923/2019/0002-0731 $ 9.00/0
Copyright 2019 Zoological Society of Pakistan
Introduction
Poultry feed contains plant ingredients as their major component, such as corn and soya bean meal in which there is about 67% of the total phosphorus which is present chelated form with phytate (Ravindran et al., 1999). Phytic acid is present in plant ingredients such as seeds and grains as a chelated salt which is called as phytate, which is also called as the phytic acid molecule get chelated to protein, lipid, carbohydrates or both lipid and carbohydrates and mineral cations (Selle et al., 2000). In animal feeds of plant origin the main source of phosphorus is phytate, but this phosphorus is not available for absorption in the intestine unless it hydrolyzes and the phosphate group is removed from this molecule either by intrinsic feed phytase, microbial phytase or intestinal phytase (Abd El-Hack et al., 2018). In plant seeds and grains the major storage form of phosphorus is phytic acid. The efficiency and the amount of endogenous phytase which is produced in the gastrointestinal tract (GIT) of poultry birds is not sufficient to hydrolyze the phytate present in feed stuff, so it reduces the digestibility of nutrients which are phytate chelated and therefore reduces the bioavailability of phosphorus phytate is therefore considered as an anti-nutritional factor in animal feeds. To overcome this problem, inorganic or nonphytate phosphorus is added in the feed to meet the animal body requirements which increases the cost of production (Ravindran et al., 1999). Dietary phytases are the enzymes that can produce a physiological effect on the digestion processes of proteins and carbohydrate by modifying endogenous secretions of different digestive enzymes and nutrient transportations in the gastrointestinal tract of chickens (Cowieson et al., 2007). Non-starch polysaccharides (NSP), phytate, tannins and other anti-nutritional factors in cereal grains, seeds and their by-products reduce their digestibility and nutrient availability, and therefore their feeding value too (Annison et al., 1995).
In animal bodies the second most occurring mineral is phosphorus and approximately 80 % of this mineral is found in ash, bone and teeth. Phosphorus with calcium helps in the maintenance and formation of bones in the body and 20 % of phosphorus which is not found in the skeletal muscles and tissues is widely distributed in the soft tissues and other body fluids inside the body, where it performs a variety of essential functions. Approximately, two-third of the total phosphorus is present in the form of phytate in those plants, which forms major constituents of poultry feeds and it is not available or very poorly utilized by monogastric animals and humans and (Viveros et al., 2000).
Materials and methods
Experimental design
A total of 96 commercial day-old broiler chicks were procured from the local market and transferred to poultry shed at University of Veterinary and Animal Sciences, Lahore. The shed was fumigated and white washed before arrival of the chicks. Chicks were weighed and all birds were randomly divided into 4 groups (A, B, C and D), with four replicates in each (n=6 in each replicate). Chicks were raised in electrically heated battery brooders for 7 days. The chicks were raised as per standard managemental conditions and provided feed and water ad libitum up to 35 days of their age without supplementation of coccidiostats or antibiotics.
Ingredients |
Volume (gm/kg) |
Wheat bran |
250.0 |
Yellow corn |
375.0 |
Soybean meal (48% protein) |
285.0 |
Canola oil |
50.0 |
Dicalcium phosphatea |
6.0 |
Limestone |
17.0 |
Vitamins and minerals premixb |
5.0 |
Sodium chloride |
2.2 |
Choline chloride 70% |
1.0 |
DL- Methionine |
2.0 |
L- Lysine HCl |
0.3 |
Coccidiostat |
1.0 |
Growth promotant |
0.5 |
Chromic oxide |
5.0 |
ME (Kcal/kg) |
2910 |
aDicalcium phosphate 220 g/kg Ca and 187 g/kg phosphorous. bSupplied per kg of diet: vitamin A (retinyl palmitate + retinyl acetate), 11000 IU; vitamin D, 2200 IU; vitamin E, 30 IU; riboflavin, 6.0 mg; thiamine, 1.5 mg; menadione, 2.0 mg; pyridoxine, 4.0 mg; niacin, 60.0 mg; vitamin B12, 0.02 mg; folic acid, 0.6 mg; pantothenic acid, 10.0 mg; biotin, 0.15 mg; iron, 80.0 mg; zinc, 80.0 mg; copper, 10.0 mg; manganese, 80.0 mg; iodine, 0.8 mg; selenium, 0.3 mg.
Dietary treatments
A corn-soybean meal based diet contained 250g wheat bran/kg (Table I) offered to control group (group D), and the treatment groups, A, B, and C were offered with same diet supplemented with various level phytase enzyme. Group D served as control group which was offered feed without phytase enzyme supplementation. Groups A, B and C were treatment groups and offered feed with phytase enzyme at the levels of 500FTU, 1000FTU, and 1500FTU per kg of feed respectively.
Growth performance
Birds were weighed on very first day of experiment and then on weekly basis up to the end of the experiment to determine body weight gain. Daily feed offered and refused, of each replicate was also being recorded on daily basis. Data thus recorded regarding body weight and feed consumption was used to calculate feed conversion ratio (FCR) on weekly basis and then at the end of the experiment. Two birds from each replicate were slaughtered on day 35 to collect visceral organs. The weights of spleen, proventiculus, empty gizzard, heart, liver, and empty intestines were measured and presented as a percentage of the total body weight (ratio of weight of organ to body weight). Moreover, the length of intestinal tract was also measured.
Statistical analysis
Statistical analysis was conducted with the Statistical Package for Social Science (SPSS for Windows version 12, SPSS Inc., Chicago, IL, USA). Data is presented as mean ± S.E.M. The Kolmogorov Smirnov test was employed to test the normal distribution of the data. The data is analyzed using one-way analysis of variance (ANOVA, completely randomized design) and body weight and feed conversion ratio is analyzed using repeated measure ANOVA. The group differences are compared by the Duncan’s Multiple Range Test (Duncan, 1955). Differences are considered significant at P < 0.05.
Results
Zootechnical parameters
The results showed that weekly based feed intake and overall feed consumption did not change (p<0.05) in control and other treatment groups (Tables I, II). The results showed that weekly body weight gain of broilers were significant (p<0.05) in all weeks except in 2nd week and 5th week in which weight gain was not significant (p<0.05) in the control and phytase supplemented groups throughout the experimental period (Tables I, II). The results revealed that weekly and overall feed conversion ratio (FCR) was significant in the control and phytase supplemented groups (Tables I, II). Results revealed that the body weights of the phytase supplemented chicks were significantly different compared to the control group (Tables I, II). Absolute weights of visceral organs of chicks have been presented in Table III. The results revealed that dietary supplementation of phytase enzyme have significant (p<0.05) effect on weights of small intestine without digesta and increased weight of liver in group C as compared to control group. Greater increase was observed in group C when compared to control. Similarly absolute weight of spleen was tended to be higher in group C when compared to control of phytase enzyme have significant (p<0.05) effect on weight of proventiculus in group C where i have given its maximum dose as compared to control group. However no significant effect on weight of gizzard and relative live weights was observed in treated groups when compared to control. The absolute length of small intestine without digesta of broilers has been presented in Table III. The results revealed that dietary supplementation of phytase showed significant effect on lengths of small intestine. Significant (p<0.05) increase in length of small intestine in Group C as compared to control group.
Table II.- Effect of supplementation of different doses of phytase on growth performance in broilers on first five weeks.
Parameters |
Group A |
Group B |
Group C |
Group D |
P - value |
1st week |
|||||
LBW (g) |
144ab±0.8 |
147a±2.4 |
149a±2.6 |
140.5b±0.5 |
0.03 |
WG (g) |
106ab±0.8 |
109a±2.4 |
111a±2.6 |
102.5b±0.5 |
0.03 |
FI (g) |
129.7ab±0.6 |
129.08ab±0.9 |
128b±0.2 |
131.5a±1.2 |
0.05 |
FCR |
1.2ab ±0.01 |
1.2b ±0.03 |
1.2b ±0.03 |
1.3a±0.01 |
0.00 |
2nd week |
|||||
LBW (g) |
334bc±3 |
341ab±1.3 |
348a±3.1 |
330c±323.1 |
0.00 |
WG (g) |
349.2a±1.4 |
349.3a±1.4 |
349.1a±1.4 |
350.3a±0.8 |
0.91 |
FI (g) |
190a±3.3 |
194a±3.4 |
199a±2.9 |
189.5a±2.5 |
0.15 |
FCR |
1.8a±0.03 |
1.8a±0.03 |
1.8a±0.02 |
1.8a±1.8 |
0.15 |
3rd week |
|||||
LBW (g) |
739b±2.1 |
750a±3.2 |
752.5a±3 |
715.3c±2.1 |
0.00 |
WG (g) |
405a±2.7 |
409a±2.4 |
404.5a±4.5 |
385.3b±2.1 |
0.00 |
FI (g) |
579.1±1a |
575.5±1a |
576±1.8a |
575.7±1.7a |
0.27 |
FCR |
1.4b±0.00 |
1.4b±0.00 |
1.42b±0.01 |
1.5a±0.00 |
0.00 |
4th week |
|||||
LBW (g) |
1169b±4.5 |
1172b±5.6 |
1188a±2.2 |
1143c±3.2 |
0.000 |
WG (g) |
430a±5.7 |
422a±7.7 |
435.5a±5 |
427.8a±3.3 |
0.435 |
FI (g) |
736.5a±2.3 |
735.6a±1.6 |
734.8a±2.1 |
737.7a±0.4 |
0.690 |
FCR |
1.7a±0.03 |
1.7a±0.03 |
1.7a±0.02 |
1.7a±0.01 |
0.393 |
5th week |
|||||
LBW (g) |
1700b±3.9 |
1712b±4.5 |
1729a±5.3 |
1680c±7.3 |
0.000 |
WG (g) |
531a±6.7 |
540a±10.2 |
541a±4.8 |
537a±6.2 |
0.767 |
FI (g) |
1009.1a±1.2 |
1010.8a±1.9 |
1009.2a±1.8 |
1003.1b±1.3 |
0.024 |
FCR |
1.9a±0.02 |
1.9a±.03 |
1.9a±0.01 |
1.9a±0.02 |
0.745 |
LBW, live body weight; WG, weight gain; FI, feed intake; FCR, feed conversion ratio. Group A, 500FT/kg feed; Group B, 1000FTU/kg feed; Group C, 1500FTU/kg feed; Group D, Control. Data was presented as Mean± S.E.M. Different superscripts a-b represent significant difference between the groups in a rows at P<0.05.
Table III.- Effect of supplementation of different doses of phytase on relative body and organ weights in broilers.
Parameters |
Group A |
Group B |
Group C |
Group D |
P - value |
LBW |
1754.4a±61.3 |
1776.3a±55.0 |
1834.5a±20.7 |
1745.6a±72.4 |
0.676 |
Liver |
45b±2.8 |
44.8b±2.01 |
52.1a±1.6 |
48.6ab±1.9 |
0.066 |
Heart |
9.1ab±1.2 |
7.3b±0.5 |
9.8a±0.5 |
8.8ab±0.4 |
0.161 |
Spleen |
2.1a±0.1 |
2.1a±0.2 |
2.6a±0.9 |
1.5a±0.1 |
0.518 |
EPT Int. Wt |
48.9b±3.06 |
44.7b±1.7 |
58.8a±3.1 |
57.1a±3 |
0.003 |
Empty Provnentri culus Wt |
6.4a±0.4 |
7.4a±0.6 |
7.6a±0.5 |
6.3a±0.2 |
0.069 |
Empty Gizzard Wt |
28.6a±1.5 |
25.3a±0.6 |
28a±2.01 |
24.9a±0.9 |
0.159 |
Intestinal lenght |
63.9b±1.5 |
68.9a±1.5 |
72.1a±0.7 |
71.5a±0.8 |
0.000 |
Group A, 500FT/kg feed; Group B, 1000FTU/kg feed; Group C, 1500FTU/kg feed; Group D, Control. Data was presented as Mean± S.E.M. Different superscriptsa-b represent significant difference between the groups in a rows at P<0.05.
Discussion
Supplementation of phytase enzyme has become an effective tool to bring improvements in the bioavailability of phosphorus present in feed stuffs and also to minimize the environmental pollution of phosphorus which animals excrete to the environment. Soybean meal (Glycine max) acts as a major food item for humans and animals because of its high beneficial health and nutritional values. It is an important dietary source of protein, fat, vitamins, minerals and fiber. Soybean also is a source of many other valuable biologically active compounds such as phyto estrogens which has potentially high benefits for the health of human beings (Messina, 1999). Apart from this, there are other compounds which are present in soybean like phytate (anti nutritional factor) and inhibitors of trypsin that can act as negative nutritional factors and produces hindrance in protein digestibility and these chelated with other essential nutritional elements including Ca, Fe, and Zn hence reducing their availability in gut (Liener, 1994; Hurrell, 2003).
Phytases are the phosphor hydrolytic enzymes that are capable to start the stepwise removal of phosphate from the phytate. Due to soyabean high protein quality it is extensively used as protein supplement in poultry feeds (Stahl et al., 2003; Lei et al., 1993; Boling et al., 2000). Different techniques and strategies have been employed to bring useful improvements in its nutritional value which normally includes mixing with corn, and supplementing it with limiting amino acids (Liu et al., 1997), supplementing with some enzymes or treating with some organic acids (Ravindram and Kornegay, 1993). Supplementations of exogenous phytases and carbohydrases increases the dietary utilization of all essential nutrients inside the body which on other way would be lost to the animals and wasted to environment.
Furthermore, it is also well documented that benefits of phytase action are not restricted only to Ca and phosphorus release, but also include a better absorption of trace minerals also.
The results of our study revealed significantly higher differences (P < 0.05) in FCR, live body weight and no overall significant differences in, weight gain and feed consumption in experimental groups treated by phytase enzyme compared to the control group. In our study gradually increase in the body weight gain was observed in all groups but significantly no difference (P < 0.05) in the body weight gain of broilers was observed among control and phytase supplemented groups and feed conversion ratio was significant (P < 0.05) in phytase supplemented groups as compared to control. Similar findings were observed by Narasimha et al. (2013) and they reported that the body weight gain in broiler chickens fed with BD supplemented with NSP enzymes, synbiotics and phytase was significantly (P < 0.01) higher. Supplementation of NSP enzymes, synbiotics and phytase alone or in combination had significant effect on feed intake. Feed conversion ratio (1.86), which improved (P < 0.05) in comparison to basal diet (BD) (2.06) and standard diet (SD) (2.02), respectively. The cost of feeding was lower (P < 0.01) in BD. Addition of these feed additives to BD did not increase the feeding cost and was comparable to unsupplemented ones and lower (P < 0.01) than SD.
In our study the effect of supplementation of phytase on relative weights and lengths of visceral organs were observed. The results revealed that dietary supplementation of phytase have significant (P < 0.05) effect on the weight and length of empty small intestine in treatment groups when compared to control. There are no significant effects on relative weights of spleen, liver; heart, gizzard, and proventriculus were observed in treated groups when compared to control.
Statement of conflict of interest
Authors have declared no conflict of interest.
References
Abd El-Hack, M., Alagawany, M., Arif, M., Emam, M., Saeed, M., Arain, M.A., Siyal, F.A., Patra, A., Elnesr, S.S. and R.U. Khan. 2018. The uses of microbial phytase as a feed additive in poultry nutrition – a review. Annal. Anim. Sci., 18: 639-658.
Annison, G., Moughan, P.J. and Thomas, D.V., 1995. Nutritive activity of soluble rice bran arabinoxylanase in broiler diets. Br. Poult. Sci., 36: 479-488. https://doi.org/10.1080/00071669508417793
Boling, S.D., Webel, D.M., Mavromichalis, I., Parsons, C.M. and Baker, D.H., 2000. The effects of citric acid on phytate-phosphorus utilization in young chicks and pigs. J. Anim. Sci., 78: 682-689. https://doi.org/10.2527/2000.783682x
Cowieson, A.J. and Ravindran, V., 2007. Effect of Phytic acid and microbial phytase on the flow and amino acid composition of endogenous protein at the terminal ileum in growing broiler chickens. Br. J. Nutr., 98: 745-752. https://doi.org/10.1017/S0007114507750894
Duncan, D.B., 1955. Multiple range and multiple F-test. Biometries, 11:1–42.
Hurrell, R.F., 2003. Influence of vegetable protein sources on trace element and mineral bioavailability. J. Nutr., 133: 2973S-2977S. https://doi.org/10.1093/jn/133.9.2973S
Lei, X.G., Ku, P.K., Miller, E.R. and Yokoyama, M.T., 1993. Supplementing corn-soybean meal diets with microbial phytase linearly improves phytate phosphorus utilization by weanling pigs. J. Anim. Sci., 71: 3359-3367. https://doi.org/10.2527/1993.71123368x
Liener, I.E., 1994. Implications of antinutritional components in soybean foods. Crit. Rev. Fd. Sci. Nutr., 3: 31-67. https://doi.org/10.1080/10408399409527649
Liu, J., Bollinger, D.W., Ledoux, D.R., Ellersieck, M.R. and Veum, T.L., 1997. Soaking increases the efficacy of supplemental microbial phytase in a low-phosphorus cornsoybean meal diet for growing pigs. J. Anim. Sci., 75: 1292-1298. https://doi.org/10.2527/1997.7551292x
Messina, M.J., 1999. Legumes and soybeans: overview of their nutritional profiles and health effects. Am. J. clin. Nutr., 70: 439S-450S. https://doi.org/10.1093/ajcn/70.3.439s
Narasimha, J., Nagalakshmi, D., Reddy, Y.R. and Rao, S.T.V., 2013. Synergistic effect of non-starch polysaccharide enzymes, synbiotics and phytase on performance, nutrient utilization and gut health in broilers fed with sub-optimal energy diets. Vet. World, 6: 754-760. https://doi.org/10.14202/vetworld.2013.754-760
Ravindram, V. and Kornegay, E.T., 1993. Acidification of weaner pig diets: A review. J. Sci. Fd. Agri., 62: 313-322. https://doi.org/10.1002/jsfa.2740620402
Ravindran, V., Cabahug, S. and Ravindran, G., 1999. Influence of microbial phytase on apparent ileal amino acid digestibility of food stuffs for broilers. Poult. Sci., 78: 699-706. https://doi.org/10.1093/ps/78.5.699
Selle, P.H., Ravindran, V. and Caldwell, R.A., 2000. Phytate and phytase; consequences for protein utilisation. Nutr. Res. Rev., 13: 255-278. https://doi.org/10.1079/095442200108729098
Stahl, C.H., Wilson, D.B. and Lei, X.G., 2003. Comparison of extracellular Escherichia coli AppA phyases expressed in Streptomyces lividans and Pichia pastoris. Biotechnol. Lett., 25: 827-831. https://doi.org/10.1023/A:1023568826461
Viveros-Centeno, A.C., Brenes, A., Canales, R. and Lozano, A., 2000. Phytase and acid phosphatase activities in plant feedstuffs. J. Agric. Fd. Chem., 48: 4009-4013. https://doi.org/10.1021/jf991126m
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