Effect of Different Dietary Lysine Regimens on Slaughter and Carcass Characteristics of Indigenous Aseel Chicken
Effect of Different Dietary Lysine Regimens on Slaughter and Carcass Characteristics of Indigenous Aseel Chicken
Tahira Batool1*, Nabila Roohi1, Athar Mahmud2
1Department of Zoology, University of the Punjab, Lahore, Pakistan
2Department of Poultry Production, University of Veterinary and Animal Sciences, Lahore, Pakistan
Abstract | This study was planned to estimate the effect of different dietary lysine regimens on slaughter and carcass traits in Lakha, Mianwali, Mushki and Peshawari varieties of indigenous Aseel chicken. A total of 240 day-old chicks, 60 from each of the variety were taken randomly and sub-divided equally into three groups (A, B and C). They were offered three lysine regimens i.e., L1 constituting 1.3% lysine from 0-6th week (1-phased) to group A and L2 containing 1.4-1.2 % lysine where 1.4% lysine was offered from 0-3rd week and 1.2% lysine from 4-6th week (2-phased) to group B, while, L3 lysine regimen having 1.5%, 1.3%, 1.1% lysine was offered from 0-2nd, 3-4th and 5-6th week, respectively (3-phased) to group C. These birds were placed in Randomized Complete Block Design (RCBD) with a factorial arrangement of 3(lysine regimens) × 4 (varieties) × 20 (replicates) with one bird in each replicate under standard conditions of house management. For slaughter and carcass characteristics at the age of eighteen weeks, 72 birds including 18 from each variety with 6 from each group were randomly selected and slaughtered. The collected data were analyzed by statistical analysis system (SAS, 9.1) software through factorial Analysis of Variance technique (ANOVA) and means were compared by Duncan’s Multiple Range (DMR) test. The findings of this study revealed L3 lysine regimen to be the best for improving the slaughter characteristics including weight of head, shanks, lungs, liver, gizzard, heart, and carcass yield comprising percent weight of breast and thigh.
Article History
Received: June 13, 2017
Revised: December 09, 2017
Accepted: October 18, 2018
Published: December 11, 2018
Authors’ Contributions
TB did the experiments, collected and analysed the data and wrote the manuscript. NR and AM supervised the experiments. NR proofread the manuscript. AM verified the processed data.
Keywords
Aseel varieties, Carcass weight, Carcass yield, Lysine regimens, Pre and post slaughter weight.
*Corresponding author: Tahira Batool
tahirabatool1111@gmail.com
To cite this article: Batool, T., Roohi, N. and Mahmud, A., 2018. Effect of different dietary lysine regimens on slaughter and carcass characteristics of indigenous aseel chicken. Punjab Univ. J. Zool., 33(2): 183-191. http://dx.doi.org/10.17582/journal.pujz/2018.33.2.183.191
Introduction
Poultry farming is renowned for its quick growth, short generation period, higher feed efficiency and biomass per unit area of the land (Mekonnen, 2007). Production rate and cost of production are highly dependent upon nutrition as it covers 75-80 % of the total expenditures. Of this cost of production, 30 % is being paid out on protein as a part of feed (Coon, 2002). The maximum budgetary return could be obtained even from the largest bird if its ration fulfills the requirement for essential amino acids (Mukhtar et al., 2007). Poultry feed mainly constitute cereals grains, which have deficiency of certain amino acids (Smith, 2001). Among these most limiting sulfur amino acids, lysine is the second one after methionine, inevitable to be used in feed formulation (Ahmad et al., 2007). Lysine is used as reference amino acid for other sulfur amino acids while creating “ideal balance” and is mainly concerned as enhancer for growth and carcass (Corzo et al., 2002). Mbajiorgu et al. (2011) reported that lysine resulted in maximum weight gain when used as supplement in protein feed. Lysine is mandatory for gaining ideal weight, feed efficiency and is also required for improving breast meat as it represents 60 percent of edible protein of broiler meat (Barboza et al., 2000; Labadan et al., 2001). Though, amino acids are the basic requirements for muscle growth and lysine part in breast muscle is generally higher than
Table 1A: Composition of experimental diets for Aseel birds
Ingredients |
Dietary lysine levels (%) |
||||
1.1 |
1.2 |
1.3 |
1.4 |
1.5 |
|
Corn |
59.08 |
59.08 |
59.08 |
59.08 |
59.08 |
Sunflower Meal (24%) |
18.9 |
18.9 |
18.9 |
18.9 |
18.9 |
Soya bean Meal (44%) |
7.04 |
7.04 |
7.04 |
7.04 |
7.04 |
Rapeseed Meal |
3 |
3 |
3 |
3 |
3 |
Fish Meal (52%) |
3 |
3 |
3 |
3 |
3 |
Poultry by-product Meal |
3 |
3 |
3 |
3 |
3 |
Molasses |
3 |
3 |
3 |
3 |
3 |
Limestone |
1.14 |
1.14 |
1.14 |
1.14 |
1.14 |
Lysine Sulphate |
0.7 |
0.9 |
1.1 |
1.3 |
1.5 |
Mono Calcium Phosphate |
0.45 |
0.45 |
0.45 |
0.45 |
0.45 |
Vitamin-Mineral Premix* |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
Sodium Chloride |
0.18 |
0.18 |
0.18 |
0.18 |
0.18 |
Alimet (Novus) |
0.17 |
0.17 |
0.17 |
0.17 |
0.17 |
Betaine HCl |
0.05 |
0.05 |
0.05 |
0.05 |
0.05 |
Threonine |
0.04 |
0.04 |
0.04 |
0.04 |
0.04 |
*Vit-Min premix supplied per 1 kg of diet: Vit. A 12000 IU; Vit. D3 2200 ICU; Vit. E 10 mg; Vit. K 32 mg; Vit. B1 1 mg; Vit. B2 4 mg Vit. B6 1.5 mg; Vit. B12 10 Ug; nicotinic acid 20 mg; folic acid 1 mg; pantothenic acid 10 mg; biotin 50 Ug; choline chloride 500 mg; copper 10 iron 30 mg; manganese 55 mg; zinc 50 mg; iodine 1 mg; selenium 0.1 m
any other amino acid. The inadequacy of lysine in feed has been found to be involved in reduced breast meat yield than other body muscles, thus its supplementation for perfect improvement of muscles and meat yield is of supreme importance (Tang et al., 2007). Under the increasing threat of socio-economic issues concerning the bird’s welfare as is caused by intensive farming, there is an emerging trend towards the diversification and versatility of poultry production systems like free range or pasture feeding (Sundrum, 2001). In spite of the fact that customers are of the will to pay low costs for poultry meat, they are progressively being attracted towards products that they see as naturally created or ecologically well supportive and well balanced with the welfare of the birds (Fanatico et al., 2007). The utilization of commercially available strains is being discouraged for welfare issues and chickens with a moderate growth rate are favored for broad production systems. They demonstrate “natural” interactive patterns with full benefit of broad rearing systems and are more adaptable, whereas the rapidly growing meat type chicken portray a very low level of adjustment and resistance towards the natural habitat (Fanatico et al., 2008). In spite of a high retail cost than traditional poultry products, these sorts of chicken have raised active attention in state markets. The local breeds of chicken are also being given attention and are being well-maintained in many countries of the world especially due to their unique carcass and meat quality traits (Zanetti et al., 2010). There is an increasing trend towards the native breeds since the last decade as the conservation of biodiversity has become the most important challenge for the international scientific community (FAO, 2009). The indigenous Aseel of Pakistan is unique in its physique and stamina to be equally adaptable in all sorts of environments (Sing, 2001) and is an excellent source of animal protein but its rearing is getting less important due to high inputs and low production potential (Batool, 2017). Keeping in view the importance of Aseel chicken and lysine amino acid, a study was planned to enhance the initial growth and the carcass quality characteristics of indigenous Aseel varieties following their supplementation with different dietary lysine regimens.
Materials and Methods
The present experiment was conducted at Indigenous Chicken Genetic Resource Center (ICGRC), Ravi Campus, Pattoki, UVAS, Lahore, by keeping in view the standard instructions for the care and welfare of the experimental birds and the ethical permission was granted by the concerned university before the conduction of this study. For this experiment, 240 day-old chicks including 60 from each of the four varieties i.e., Lakha, Mianwali, Mushki and Peshawari, were arbitrarily selected and divided into three sub-groups A, B and C, with 20 birds in each. These birds were offered three lysine regimens i.e., L1 constituting 1.3% lysine from 0-6th week in one phase to group A, and L2 containing1.4-1.2 % lysine, where 1.4% lysine was offered from 0-3rd week and 1.2% lysine from 4-6th week in two phases to group B, while, L3 lysine regimen having 1.5%, 1.3%, 1.1% lysine was offered from 0-2nd, 3-4th and 5-6th week, respectively in three phases to group C (Composition of lysine regimens is mentioned in Table 1A and B). The experimental feed was formulated and analyzed as per NRC (1996) and AOAC (2005) guidelines, respectively. These birds were placed under Randomized Complete Block Design (RCBD) with a factorial arrangement of 3(lysine regimens) × 4(varieties) × 20(replicates) with one bird in each replicate. Afterwards, all these birds were equally offered the normal broiler grower feed having 20.5% CP and 3000kcal/kg metabolizable energy. At the end of eighteenth week, 72 birds including 18 birds from each of the four varieties with 6 birds from each treatment group were randomly taken to evaluate the slaughter and carcass traits. These birds were subjected to fast for twelve hours and then were weighed to calculate the pre-slaughter weight and then slaughtered according to Halal Muslim method (Fuseini et al., 2016). These birds were then defeathered and their head and shanks were separated from the main body to measure the dressed weight, whereas, skin was kept intact for supporting the internal organs. The selected slaughter and carcass traits i.e., post slaughter weight (g), carcass weight (g), carcass yield (percent of final live body weight), head, shanks, liver, gizzard (filled with and empty from contents) and heart weight (g) were calculated. The intestinal weight (g) and intestinal length (cm) was also measured. Among carcass traits, neck weight as well as breast and thigh yields were taken as percent of carcass weight. The collected data were analyzed by SAS software through factorial ANOVA and results were expressed as means and their standard errors. The treatment means were compared by Duncan’s Multiple Range (DMR) test (Duncan, 1955) and were considered as significant at P≤0.05.
Table 1B: Calculated values of nutrients.
Dietary lysine level % |
|||||
1.1 |
1.2 |
1.3 |
1.4 |
1.5 |
|
Metabolize Energy(k calories/kg) |
2746.99 |
2753.69 |
2760.39 |
2767.09 |
2773.79 |
Dry Matter |
87.17 |
87.36 |
87.56 |
87.76 |
87.96 |
Crude Protein |
17.06 |
17.18 |
17.29 |
17.40 |
17.51 |
Crude Fiber |
6.93 |
6.93 |
6.93 |
6.93 |
6.93 |
Ash |
4.09 |
4.09 |
4.09 |
4.09 |
4.09 |
Either Extract |
3.59 |
3.59 |
3.59 |
3.59 |
3.59 |
Calcium |
0.84 |
0.84 |
0.84 |
0.84 |
0.84 |
Chloride |
0.22 |
0.22 |
0.22 |
0.22 |
0.22 |
Sodium |
0.16 |
0.16 |
0.16 |
0.16 |
0.16 |
Total phosphorus |
0.68 |
0.68 |
0.68 |
0.68 |
0.68 |
Potassium |
0.71 |
0.71 |
0.71 |
0.71 |
0.71 |
Digestible phosphorus |
0.36 |
0.36 |
0.36 |
0.36 |
0.36 |
Linoleic Acid |
1.42 |
1.42 |
1.42 |
1.42 |
1.42 |
Lysine |
1.1 |
1.2 |
1.3 |
1.4 |
1.5 |
Methionine |
0.45 |
0.45 |
0.45 |
0.45 |
0.45 |
Methionine+Cystine |
0.78 |
0.78 |
0.78 |
0.78 |
0.78 |
Digestible Arginine |
0.98 |
0.98 |
0.98 |
0.98 |
0.98 |
Digestible Tryptophan |
0.14 |
0.14 |
0.14 |
0.14 |
0.14 |
Digestible Threonine |
0.57 |
0.57 |
0.57 |
0.57 |
0.57 |
Digestible Lysine |
0.99 |
1.09 |
1.20 |
1.31 |
1.41 |
Digestible methionine |
0.42 |
0.42 |
0.42 |
0.42 |
0.42 |
Digestible Methionine + Cystine |
0.67 |
0.67 |
0.67 |
0.67 |
0.67 |
Threonine |
0.67 |
0.67 |
0.67 |
0.67 |
0.67 |
Tryptophan |
0.19 |
0.19 |
0.19 |
0.19 |
0.19 |
Arginine |
1.10 |
1.10 |
1.10 |
1.10 |
1.10 |
Cystine |
0.32 |
0.32 |
0.32 |
0.32 |
0.32 |
Digestible Cystine |
0.26 |
0.26 |
0.26 |
0.26 |
0.26 |
Valine |
0.82 |
0.82 |
0.82 |
0.82 |
0.82 |
Digestible Valine |
0.71 |
0.71 |
0.71 |
0.71 |
0.71 |
Histidine |
0.43 |
0.43 |
0.43 |
0.43 |
0.43 |
Digestible Histidine |
0.37 |
0.37 |
0.37 |
0.37 |
0.37 |
Phenylalanine |
0.78 |
0.78 |
0.78 |
0.78 |
0.78 |
Digestible Phenylalanine |
0.67 |
0.67 |
0.67 |
0.67 |
0.67 |
Leucine |
1.44 |
1.44 |
1.44 |
1.44 |
1.44 |
Digestible Leucine |
1.21 |
1.21 |
1.21 |
1.21 |
1.21 |
Isoleucine |
0.66 |
0.66 |
0.66 |
0.66 |
0.66 |
Digestible Isoleucine |
0.58 |
0.58 |
0.58 |
0.58 |
0.58 |
Table 2: Effect of lysine regimens, Aseel varieties and their interactions on selected slaughter parameters.
Parameters /Variables |
Pre- slaughter/ final Live Body weight (g) |
Post-slaughteredweight (g) |
Carcass weight (g) |
Carcass yield (% of BW) |
Head weight (g) |
Shanks weight (g) |
|
Lysine (%) /Regimens |
|||||||
1.3 (L1) |
1540.04± 40.57b |
1457.10± 42.58b |
1140.58± 28.12b |
74.32±1.00c |
52.83± 1.50b |
53.96± 1.44c |
|
1.4-1.2 (L2) |
1583.00± 45.64b |
1533.85± 43.35b |
1229.79± 27.81b |
78.11±0.96b |
58.96± 1.44a |
66.71± 1.28b |
|
1.5-1.3-1.1 (L3) |
1794.21± 57.91a |
1704.50± 55.02a |
1461.33± 48.10a |
81.50±0.72a |
60.50± 1.34a |
79.63± 2.24a |
|
Aseel Varieties |
|||||||
Lakha |
1618.28± 78.59 |
1539.45± 77.33 |
1279.06± 56.54 |
79.60±1.37 |
62.56± 0.96a |
69.56± 3.08ab |
|
Mianwali |
1616.06± 74.07 |
1539.98± 71.25 |
1244.56± 63.21 |
76.98±1.30 |
57.33± 2.21b |
70.33± 3.12a |
|
Mushki |
1669.67± 45.89 |
1596.18± 43.29 |
1297.89± 44.16 |
77.63±1.04 |
55.06± 1.95b |
64.89± 3.61bc |
|
Peshawari |
1652.33± 42.28 |
1584.99± 39.37 |
1287.44± 45.39 |
77.71±1.24 |
54.78± 1.33b |
61.94± 2.29c |
|
Lysine Levels (%)/Regimens × Aseel Varieties |
|||||||
1.3 (L1) |
Lakha |
1509.33± 129.02bc |
1410.12± 133.66bc |
1139.17± 62.67c |
76.56±2.75bcd |
60.17± 1.22abcd |
58.50± 1.28c |
Mianwali |
1450.00± 39.54c |
1361.67± 47.89c |
1046.00± 22.64c |
72.22±0.93d |
47.83± 2.37f |
61.17± 1.45bc |
|
Mushki |
1563.00± 65.14abc |
1484.85± 61.89abc |
1168.17± 25.62c |
75.06±1.60cd |
53.50± 3.70def |
45.83± 0.83d |
|
Peshawari |
1637.83± 63.24abc |
1571.78± 65.76abc |
1209.00± 81.09bc |
73.43±2.26d |
49.83± 1.78ef |
50.33± 1.89d |
|
1.4-1.2 (L2) |
Lakha |
1619.33± 120.20abc |
1568.37± 114.19abc |
1275.83± 69.57abc |
79.48±2.42abc |
63.50± 1.28ab |
65.33± 3.26bc |
Mianwali |
1544.33± 91.03abc |
1497.12± 86.48abc |
1183.17± 32.19c |
77.40±2.79abcd |
66.17± 1.45a |
65.83± 2.02bc |
|
Mushki |
1635.50± 92.29abc |
1583.73± 92.29abc |
1283.73± 87.68bc |
76.19±0.97bcd |
50.83± 0.83ef |
69.83± 3.27b |
|
Peshawari |
1532.83± 73.82abc |
1486.19± 70.13abc |
1215.50± 54.06bc |
79.39±0.91abc |
55.33± 1.89cde |
65.83± 1.45bc |
|
1.5-1.3-1.1 (L3) |
Lakha |
1726.17± 164.96abc |
1639.86± 156.71abc |
1422.17±125.81ab |
82.75±1.41a |
64.00± 2.13ab |
84.83± 3.16a |
Mianwali |
1853.83± 168.10a |
1761.14± 159.70a |
1504.50± 130.57a |
81.31±0.59ab |
58.00± 2.90bcd |
85.00± 6.42a |
|
Mushki |
1810.50± 47.32ab |
1719.98± 44.96ab |
1480.83± 64.15a |
81.63±1.62ab |
60.83± 3.69abc |
79.00± 1.97a |
|
Peshawari |
1786.33± 47.93abc |
1697.02± 45.54ab |
1437.83± 68.72ab |
80.31±2.02abc |
59.17± 1.62abcd |
69.67± 2.43b |
|
Source of Variation |
P-Value |
||||||
LR |
0.0011 |
0.0018 |
<.0001 |
<.0001 |
0.0002 |
<.0001 |
|
AV |
0.8877 |
0.8348 |
0.8250 |
0.3221 |
0.0015 |
0.0033 |
|
LR × AV |
0.1139 |
0.1250 |
0.0002 |
0.0012 |
<.0001 |
<.0001 |
Values have been mentioned as Mean±SEM and various superscripted alphabets show significant (P≤0.05) differences among them (order of significance is as: a>b>c…….)
Results
The present study showed increased (P≤0.05) pre-slaughter (1794.21±57.91g), post-slaughter (1704.50±55.02g), carcass (1461.33±48.10g) and head (60.50±1.34) weights of Aseel birds in L3 (1.5-1.3-1.1%) than L2 (1.4-1.2%) and L1 (1.3%) lysine regimens (Table 2). Whereas, significantly (P≤0.05) highest weights of shanks (79.63±2.24g), liver (41.92±1.17g), filled gizzard (55.88±1.24g), empty gizzard (44.58±0.90g) and heart (14.04±0.28g) were observed in L3 followed by L2 and L1 lysine regimen (Table 2-3). Among visceral organs, intestinal length (137.67±0.71cm) and weight (57.04±2.10g) were comparatively higher in L3 followed by L2 and L1 lysine regimen (Table 2). Carcass yield (81.50±0.72% of live body weight), Neck (5.72±0.08%), breast (34.03±0.77%) and thigh (17.15±0.25%) percent to carcass weight too showed significantly (P≤0.05) highest value in L3 followed by L2 and L1 lysine regimen (Table 4). Among varieties, Lakha showed a significantly (P≤0.05) greater head (62.56±0.96g) and intestine (61.28±2.48g) weight than Mianwali, Mushki and Peshawari varieties. Likewise, Mianwali variety depicted a significantly (P≤0.05) greater shanks (70.33±3.12g), liver (41.94±1.17g), neck (4.90±0.24% of carcass) and thigh (16.50±0.27 % of carcass) weight than other three varieties (Table 2, 3, 4).
As far as results of interactions among lysine regimens and Aseel varieties are considered, Mianwali showed higher pre-slaughter (1853.83±168.10g), post-slaughter (1761.14±159.70g), carcass (1504.50±130.57g), shanks (85.00±6.42g), weight and neck (5.99±0.09%), thigh (17.69±0.44%) yields with L3 lysine regimen. Lakha variety showed a greater carcass yield (82.75±1.41%), shanks (84.83±3.16g), filled gizzard (56.33±2.03g) and heart (15.17±0.17g) weight, while, Peshawari showed a higher liver (45.33±1.63), gizzard (58.33±1.20, 47.83±0.87 filled with and empty from contents, respectively) weight (g) and breast yield (37.02±0.58% of carcass weight) with L3 regimen (Table 2, 3, 4).
Table 3: Effect of lysine regimens, Aseel varieties and their interactions on weight (g) of Heart, Liver, Gizzard, Intestine and Intestinal length (cm).
Parameters /Variables |
Heart |
Liver |
Gizzard (filled) |
Gizzard (Empty) |
Intestine |
Intestinal length |
|||
Lysine levels (%)/Regimens |
|||||||||
1.3 (L1) |
7.08± 0.50c |
32.67± 1.31c |
38.13±0.86c |
26.75±0.54c |
50.83±1.67b |
134.71±3.53 |
|||
1.4- 1.2 (L2) |
10.00± 0.40b |
37.71± 1.42b |
46.71±1.71b |
34.67±1.22b |
56.42±2.61ab |
135.79±3.90 |
|||
1.5- 1.3- 1.1 (L3) |
14.04± 0.28a |
41.92± 1.17a |
55.88±1.24a |
44.58±0.90a |
57.04±2.10a |
137.67±0.71 |
|||
Aseel Varieties |
|
||||||||
Lakha |
10.56± 0.97 |
36.44± 2.04b |
47.89±2.46 |
36.61±2.15 |
61.28±2.48a |
137.11±2.71 |
|||
Mianwali |
10.61± 0.78 |
41.94± 1.17a |
47.11±2.02 |
34.72±1.79 |
53.39±2.86b |
137.61±3.55 |
|||
Mushki |
9.94± 0.76 |
33.78± 1.42b |
45.89±2.24 |
34.44±1.96 |
52.67±2.47b |
130.89±3.26 |
|||
Peshawari |
10.39± 0.80 |
37.56± 1.70b |
46.72±2.54 |
35.56±2.31 |
51.72±1.81b |
138.61±4.31 |
|||
Lysine level(%)/Regimens × Aseel Varieties |
|||||||||
1.3 (L1) |
Lakha |
5.50± 0.43f |
28.17± 0.83d |
37.00±1.73c |
26.33±1.17ef |
54.50±1.23bcd |
126.83±3.13cde |
||
Mianwali |
6.83± 1.14ef |
41.17± 1.47a |
37.67±1.93c |
26.00±1.03f |
41.50±3.38e |
125.00±6.23de |
|||
Mushki |
8.67± 1.05de |
28.83± 1.14cd |
39.33±0.80c |
27.50±0.89ef |
50.00±2.11cde |
137.67±2.97bcd |
|||
Peshawari |
7.33± 0.95ef |
32.50± 2.46cd |
27.17±1.35c |
27.17±1.35ef |
57.33±2.30abc |
149.33±9.82ab |
|||
1.4-1.2 (L2) |
Lakha |
11.00± 0.26c |
41.50± 2.13a |
50.33±3.93ab |
39.17±2.98bc |
67.00±1.65a |
148.50±4.15ab |
||
Mianwali |
11.50± 0.22bc |
42.50± 3.22a |
50.33±1.58ab |
36.17±1.19cd |
66.50±2.28a |
152.83±2.79a |
|||
Mushki |
7.67± 0.33e |
32.00± 1.86cd |
42.83±3.05bc |
31.67±2.19de |
46.50±4.56de |
115.33±4.99e |
|||
Peshawari |
9.83± 0.98cd |
34.83± 1.45bc |
43.33±4.00bc |
31.67±2.09de |
45.67±3.29de |
126.50±6.22cde |
|||
1.5-1.3-1.1 (L3) |
Lakha |
15.17± 0.17a |
39.67± 4.05ab |
56.33±2.03a |
44.33±1.52ab |
62.33±6.51ab |
136.00±0.73bcd |
||
Mianwali |
13.50± 0.43ab |
42.17± 1.14a |
53.33±2.79a |
42.00±1.98b |
52.17±1.99bcd |
135.00±1.53bcd |
|||
Mushki |
13.50± 0.85ab |
40.50± 1.15ab |
55.50±3.51a |
44.17±2.12ab |
61.50±3.54ab |
139.67±1.17abcd |
|||
Peshawari |
14.00± 0.37a |
45.33± 1.63a |
58.33±1.20a |
47.83±0.87a |
52.17±1.89bcd |
140.00±1.06abc |
|||
Source of Variation |
P-Value |
||||||||
LR |
<.0001 |
<.0001 |
<.0001 |
<.0001 |
0.0704 |
0.7889 |
|||
AV |
0.7433 |
0.0008 |
0.8321 |
0.4913 |
0.0220 |
0.4093 |
|||
LR × AV |
<.0001 |
<.0001 |
<.0001 |
<.0001 |
<.0001 |
<.0001 |
Values have been mentioned as Mean±SEM and various superscripted alphabets show significant (P≤0.05) differences among them (order of significance is as: a>b>c……).
Table 4: Percent effects of lysine regimens, Aseel varieties and their interactions on carcass yield (% of body weight) and weight (% of carcass weight) of Neck, Breast and Thigh.
Parameters/Variables |
Carcass |
Neck |
Breast |
Thigh |
||||
Lysine (%)/Regimens |
||||||||
1.3 (L1) |
74.32±1.00c |
3.17±0.15c |
24.03±0.41c |
14.87±0.15c |
||||
1.4-1.2 (L2) |
78.11±0.96b |
5.05±0.11b |
29.67±0.75b |
15.66±0.19b |
||||
1.5- 1.3- 1.1 (L3) |
81.50±0.72a |
5.72±0.08a |
34.03±0.77a |
17.15±0.25a |
||||
Aseel Varieties |
||||||||
Lakha |
79.60±1.37 |
4.57±0.30ab |
29.17±1.05 |
15.42±0.35c |
||||
Mianwali |
76.98±1.30 |
4.90±0.24a |
28.62±1.18 |
16.50±0.27a |
||||
Mushki |
77.63±1.04 |
4.68±0.30ab |
29.81±1.34 |
15.61±0.25bc |
||||
Peshawari |
77.71±1.24 |
4.43±0.32b |
29.38±1.42 |
16.05±0.36ab |
||||
Lysine (%)/Regimens × Aseel Varieties |
||||||||
1.3 (L1) |
Lakha |
76.56±2.75bcd |
2.91±0.21f |
25.01±1.10fg |
14.45±0.17f |
|||
Mianwali |
72.22±0.93d |
3.69±0.06e |
23.33±0.53g |
15.62±0.19cde |
||||
Mushki |
75.06±1.60cd |
3.30±0.43ef |
24.33±0.73fg |
14.79±0.26def |
||||
Peshawari |
73.43±2.26d |
2.79±0.23f |
23.47±0.84g |
14.61±0.33ef |
||||
1.4-1.2 (L2) |
Lakha |
79.48±2.42abc |
5.32±0.18abcd |
32.39±1.98bcd |
14.52±0.04f |
|||
Mianwali |
77.40±2.79abcd |
5.02±0.13cd |
29.24±1.02de |
16.17±0.26c |
||||
Mushki |
76.19±0.97bcd |
5.11±0.29bcd |
29.38±1.67de |
15.74±0.15cd |
||||
Peshawari |
79.39±0.91abc |
4.75±0.23d |
27.65±0.60ef |
16.21±0.44c |
||||
1.5-1.3-1.1 (L3) |
Lakha |
82.75±1.41a |
5.49±0.18abc |
30.11±0.55cde |
17.28±0.41ab |
|||
Mianwali |
81.31±0.59ab |
5.99±0.09a |
33.27±1.68bc |
17.69±0.44a |
||||
Mushki |
81.63±1.62ab |
5.64±0.17abc |
35.73±1.39ab |
16.31±0.55bc |
||||
Peshawari |
80.31±2.02abc |
5.75±0.09ab |
37.02±0.58a |
17.32±0.51ab |
||||
Source of Variation |
P-Value |
|||||||
LR |
<.0001 |
<.0001 |
<.0001 |
<.0001 |
||||
AV |
0.3221 |
0.0769 |
0.7473 |
0.0031 |
||||
LR × AV |
0.0012 |
<.0001 |
<.0001 |
<.0001 |
Values have been mentioned as Mean±SEM and various superscripted alphabets show significant (P≤0.05) differences among them (order of significance is as: a>b>c…….).
Discussion
The findings of present study revealed a considerable influence of dietary lysine regimens amongst Aseel birds as a significantly higher pre-slaughter/live body weight and post-slaughter weight was observed in L3 lysine regimen. The results of this study are in close lines with the findings of Pirzado et al. (2016) where, broilers showed a higher live body weight when fed with lysine level of 12g/kg in their feed. The same trend of increased live body weight was also observed in another study, where, broilers gained a maximum increase in live body weight when fed with ration supplemented with lysine (Eits et al., 2003). Abbas (2014) also found maximum increase in live body weight and post-slaughter weight among Japanese quails when they were fed with 3-phase feeding lysine regimen, wherein protein/lysine as a growth enhancer was provided as per time of growth requirements. In the present study, significantly higher carcass weight and carcass yield has been shown by L3 lysine regimen. While, Mushki and Lakha showed an increased carcass weight and carcass yield, respectively, than the other varieties (Table 2, 3, 4). These findings are also in accordance with the results of Pirzado et al. (2016), where, highest carcass weight (1457.1±15.72g/bird) was depicted by broiler’s group offered with feed containing 12g/kg lysine level than those provided with 13, 14 and 10g/kg lysine levels. The increase in carcass weight was also observed in another study where broiler chicken were fed with ration having 0.62 or 0.67 % lysine (Li et al., 2013). A significantly higher live body weight and carcass weight was also reported amongst Aseel and other indigenous breeds without any treatment effect (Singh and Pathak, 2017). The present study also revealed significantly highest (P≤0.05) neck, breast and thigh percentages relative to carcass weight in L3 lysine regimen (Table 4). Rezaei et al. (2004) too found a significant (P<0.05) increase in carcass weight and breast meat yield % when feed containing 1.5g L-Lys.HCl/kg was offered to Ross broiler chicken in starter and grower periods. Melaku et al. (2015) found a significant (P<0.05) increase in breast meat yield and drumstick weight, when rations deficient in lysine were supplemented with high synthetic lysine content (150%) and then were offered to broiler chicks. The present results are also in close lines with the findings of Hussain (2018) where, he reported a significant increase in carcass weight (p=0.0001) and carcass meat yields (p<.0001) among Aseel varieties fed with medium lysine levels. The authors further pointed out that regimen with medium lysine supplementation had a significant impact on slaughter weight, breast and thigh weights (p<.0001) as well as their yields in Mianwali variety of Aseel. However, Olivera et al. (2000) reported a significant impact of four-phased feeding on breast meat yield than three-phased feeding regimen. Significantly (P≤0.05) increased breast and thigh yields in the present study are endorsed to the fact of lysine availability rightly as per growth requirements of birds in L3 lysine regimen. Significantly improved giblets weight was observed in present study i.e., liver (41.92±1.17g), gizzard (44.58±0.90g) and heart (14.04±0.28g) relative to live weight in L3 followed by L2 and L1 lysine regimen. As nutrient requirement of Aseel vary in different phases of growth, improvement in giblets weight in our study might be attributed to the fact that the Aseel birds got maximum nutrients and lysine needed at various stages of their growth. Similarly, in another study, increase in liver, heart and gizzard weight was also reported, where high lysine content in feed influenced a more efficient conversion of amino acid resulting in increased giblets weight (Nasr and Kheiri, 2011). As far as, the visceral organs are concerned, the present study revealed an increased intestinal length and significantly (P≤0.05) improved intestinal weight in L3 lysine regimen. Abbas (2014) also found a significantly greater mean intestinal length (cm) and weight (g) among both male and female as well as in close-bred stocks of Japanese quails in 3-phased lysine regimen. Ullah et al. (2012) as well as Sklan and Noy (2000) reported in two separate studies the positive effect 1.4% lysine supplementation in starter diets to increase the intestinal length and digestive tract weight by increasing its digestion, absorption and enzymatic activity of pancreas, respectively. The inconsistent increase in intestinal length and weight was reported in a study, where, different dietary protein contents (20 to 40% with balanced or unbalanced amino acid supplementation) were offered to broiler chicks at the age of 10-24th day (Swatson et al., 2002). The findings of present study revealed that L3 lysine regimen had a positive impact on observed slaughter and carcass parameters, the reason for this was probably the in time availability of lysine as per growth requirements of birds for protein as was proved by Batool et al. (2018). Although, growth stage, sex, strain and genetics might also had a prominent effect on these parameters (Dozier et al., 2008). Aseel varieties showed non-significant variations for most of the observed slaughter and carcass characteristics which might be considered due to the genetic effect of slow growing birds.
Conclusions
This study indicated that when regimens containing various levels of lysine % were offered to Aseel birds in the form of phase-feeding, a significantly improved slaughter characteristics and carcass traits including breast and thigh % could be obtained. Furthermore, 3-phase feeding lysine regimen (L3) was found to be the best for providing the nutrients rightly as per growth requirements thus depositing the lysine and protein in body muscles to increase the lean meat in native Aseel chicken varieties.
Acknowledgements
The authors pay their gratitude to Prof. Dr. Muhammad Akram (late) for the planning of this research project and cooperation extended by the administration of UVAS, Pakistan to complete the present research work at ICGRC.
References
Abbas, Y., 2014. Effect of different dietary lysine levels and feed restriction regimes on growth performance and slaughtering characteristics in Japanese quail (Coturnix Coturnix japonica) maintained during hot season. (Doctoral dissertation), Department of poultry production, UVAS, Lahore.
Ahmad, G., Mushtaq, T., Mirza, M.A. and Ahmed, Z., 2007. Comparative bio efficacy of lysine from L-lysine hydrochloride or L-lysine sulfate in basal diets containing graded levels of canola meal for female broiler chickens. Poult. sci., 86:525-30. https://doi.org/10.1093/ps/86.3.525
Barboza, W.A., Rostagno, H.S., Albino, L.F.T. and Rodrigues, P.B., 2000. Lysine levels for broiler chickens from 1 to 21 and 15 to 40 days of age. Rev. Bras. Zootec., 29:1082-1090. https://doi.org/10.1590/S1516-35982000000400019
Batool, T., 2017. Effect of different lysine regimens on growth, productive and reproductive performance of indigenous Aseel varieties. (Doctoral dissertation). Department of Zoology, PU., Lahore.
Batool, T., Roohi, N. and Mahmud, A., 2018. Comparative growth performance and economic efficiency of indigenous Aseel varieties fed on different dietary lysine regimens. J. Anim. Plant Scis., 28:1247-1255.
Coon, C.N., 2002. Feeding egg-type replacement pullets. In Commercial chicken meat and egg production. Springer US, pp. 267-285.
Corzo, A., Moran, E.T. and Hoehler, D., 2002. Lysine need of heavy broiler males applying the ideal protein concept. Poult. Sci., 81:1863-1868. https://doi.org/10.1093/ps/81.12.1863
Dozier, W.A., Corzo, A., Kidd, M.T. and Schilling, M.W., 2008. Dietary digestible lysine requirements of male and female broilers from forty-nine to sixty-three days of age. Poult. Sci., 87:1385-1391. https://doi.org/10.3382/ps.2007-00529
Duncan, D.B., 1955. Multiple range and multiple F tests. Biometrics., 11:1-42. https://doi.org/10.2307/3001478
Eits, R., Kwakkel, R., Verstegen, M. and Emmans, G., 2003. Responses of broiler chickens to dietary protein: effects of early life protein nutrition on later responses. Bri. Poult Sci., 44:398-409. https://doi.org/10.1080/0007166031000035544
Fanatico, A.C., Pillai, P.B., Emmert, J.L. and Owens, C.M., 2007. Meat quality of slow-and fast-growing chicken genotypes fed low-nutrient or standard diets and raised indoors or with outdoor access. Poult. Sci., 86:2245-2255. https://doi.org/10.3382/ps.2007-00092
Fanatico, A.C., Pillai, P.B., Hester, P.Y., Falcone, C., Mench, J.A., Owens, C.M. and Emmert, J.L., 2008. Performance, livability, and carcass yield of slow-and fast-growing chicken genotypes fed low-nutrient or standard diets and raised indoors or with outdoor access. Poult sci., 87:1012-21. https://doi.org/10.3382/ps.2006-00424
FAO, 2009. Food and Agriculture Organization of the United Nations. The state of food and agriculture. Available on: http://www.fao.org/docrep/012/i0680e/i0680e.pdf.
Fuseini, A., Knowles, T.G., Hadley, P.J. and Wotton, S., 2016. Halal stunning and slaughter: Criteria for the assessment of dead animals. Meat Sci., 119:132-137. https://doi.org/10.1016/j.meatsci.2016.04.033
Hussain, M., Mahmud, A., Hussain, J., Qaisrani, S.N., Mehmood, S. and Rehman, A.I., 2018. Subsequent Effect of Dietary Lysine Regimens Fed in the Starter Phase on the Growth Performance, Carcass Traits and Meat Chemical Composition of Aseel Chicken in the Grower Phase. Braz. J. Poult. Sci., 20:455-462. https://doi.org/10.1590/1806-9061-2017-0584
Labadan, M.C., Hsu, K.N. and Austic, R.E., 2001. Lysine and arginine requirements of broiler chickens at two-to three-week intervals to eight weeks of age. Poult. Sci., 80:599-606. https://doi.org/10.1093/ps/80.5.599
Li, J., Zhao, X.L., Yuan, Y.C., Gilbert, E.R., Wang, Y., Liu, Y.P., Zhang, Y., Zhu, Q., 2013. Dietary lysine affects chickens from local Chinese pure lines and their reciprocal crosses. Poult. Sci., 92:1683-1689. https://doi.org/10.3382/ps.2012-02865
Mbajiorgu, C.A., Ngambi, J.W., Norris, D. and Alabi, O.J., 2011. Effect of dietary lysine to energy to ratio on performance of unsexed indigenous Venda chickens. A. J. Anim. Vet. Adv., 6:517-524. https://doi.org/10.3923/ajava.2011.517.524
Mekonnen, G., 2007. Characterization of small holder poultry production and marketing system of dale, Wonsho and Loka Abaya Weredas of SNNPs. (M.Sc. Thesis), Hawassa University.
Melaku, M., Urge, M., Animut, G. and Getu, A., 2015. Effect of supplementation with synthetic lysine on the performance of finisher broiler chicks. Ir. J. Appl. Ani. Sci., 5:179-187.
Mukhtar, A.M., Mekkawi, A. and Eltigani, M., 2007. The effect of feeding increasing levels of synthetic lysine and methionine in broiler chicks. Res. J. Ani. Vet. Scis., 2:18-20.
Nasr, J. and Kheiri, F., 2011. Increasing amino acids density improves broiler live weight. Int. J. Poult. Sci., 10:523-526. https://doi.org/10.3923/ijps.2011.523.526
Oliveira, J.E.D., Sakomura, N.K., Figueiredo, A.N., Lucas Júnior, J.D. and Santos, T.M.B.D., 2000. Effect of thermal insulation under the roof on performance of broiler chickens stocked in different densities. Rev. Bras. Zootec., 29:1427-1434. https://doi.org/10.1590/S1516-35982000000500021
Pirzado, S.A., Mangsi, A.S., Mughal, G.A., Tariq, M., Kalhoro, D.H., Khaskheli, G.B. and Barham, G.S., 2016. Effect of lysine supplementation on growth and carcass yield of broilers. Sci. Int. (Lahore), 28:3861-3864.
Sing, D.P., 2001. Aseel in India. In: Proceeding of seminar on “Appropriate Poultry for Adverse Environments”. Hyderabad, India, pp. 96-100.
Sklan, D. and Noy, Y., 2000. Hydrolysis and absorption in the small intestines of post hatch chicks. Poult. Sci., 79:1306-1310. https://doi.org/10.1093/ps/79.9.1306
Rezaei, M., Moghaddam, H.N., Reza, J.P. and Kermanshahi, H., 2004. The effects of dietary protein and lysine levels on broiler performance, carcass characteristics and N excretion. Int. J. Poult. Sci., 3:148-152. https://doi.org/10.3923/ijps.2004.148.152
Singh, V.P. and Pathak, V., 2017. Quality characterization of giblets of indigenous Indian chicken breeds. Int. J. Curr. Microbiol. Appl. Sci., 6:784-797. https://doi.org/10.20546/ijcmas.2017.601.093
Smith, A.J., 2001. Poultry: The Tropical Agriculturalist series (CTA). Rev. Ed. Macmillan Education LTD, Oxford. London.
Sundrum, A., 2001. Organic livestock farming: a critical review. Livestock Pro. Sci., 67:207-215. https://doi.org/10.1016/S0301-6226(00)00188-3
Swatson, H.K., Gous, R., Iji, P.A. and Zarrinkalam, R., 2002. Effect of dietary protein level, amino acid balance and feeding level on growth, gastrointestinal tract, and mucosal structure of the small intestine in broiler chickens. Ani. Res., 51:501-515. https://doi.org/10.1051/animres:2002038
Tang, M.Y., Ma, Q.G., Chen, X.D. and Ji, C., 2007. Effects of dietary metabolizable energy and lysine on carcass characteristics and meat quality in arbor acres broilers. Asian-Aus. J. Anim. Sci., 20:1865-1873.
Ullah, M.S., Pasha, T.N., Ali, Z., Saima, Z., Khattak, F.M. and Hayat, Z., 2012. Effects of different pre-starter diets on broiler performance, gastro intestinal tract morphometry and carcass yield. J. Anim. Plant Scis., 22:570-575.
Zanetti, E., De Marchi, M., Dalvit, C., Molette, C., Remignon, H. and Cassandro, M., 2010. Carcass characteristics and qualitative meat traits of three Italian local chicken breeds. Bri. Poult. Sci., 51:629-634. https://doi.org/10.1080/00071668.2010.521142
To share on other social networks, click on any share button. What are these?