EFFECTS OF MANNAN OLIGOSACCHARIDES AS A DIETARY SUPPLEMENT ON PERFORMANCE AND CARCASS CHARACTERISTICS OF JAPANESE QUAILS (COTURNIX JAPONICA)

Document Type : Research article

Authors

1 Department of Nutrition and Clinical Nutrition, Faculty of Veterinary Medicine, Assiut University, Assiut, Egypt

2 Dept of Animal Production, Faculty of Agriculture, South Valley University, Qena, Egypt

Abstract

The effect of three levels of mannan oligosaccharides (MOS) as a dietarysupplement on growth performance, carcass characteristics and some blood metabolites of growing Japanese quails (Coturnix japonica) was the main objective of this experiment. A total of one hundred 1-day-old Japanese quails were randomly divided into 4 experimental groups (25 birds/ each treatment) with 3 replicates (8 birds in two replicates and 9 birds in one replicate). The experimental groups consisted of four dietary treatments: 1) a control basal diet without supplementation; 2) a basal diet with a MOS at level of 1 g/kg feed (low MOS); 3) a diet with MOS at a level of 3 g/kg feed (medium MOS); and 4) a diet with a MOS at a level of 5 g/kg feed (high MOS). The experimental period extended for 42 days. The data revealed that, birds fed diets containing medium MOS level (3 g /kg feed) recorded significant           (P < 0.05) improvements in body weight, weight gain, feed conversion efficiency, performance index, energy and protein efficiency compared with those fed the control one, low and high levels of MOS. Also medium level of MOS supplementation increased the dressing percentage and edible giblets, while the offal's percentages and carcass abdominal fat were significantly decreased. Growth performance was significantly improved at 3 g MOS/ kg diet, however high dosage of MOS have negative effects on growth rate of the birds. The triglyceride, total cholesterol and total lipids concentrations in quails blood decreased significantly in concomitant with a significant decrease in carcass fat % as a response to dietary MOS supplementation. From the results of the current study, it could be concluded that the responses of Japanese quails to MOS are influenced by the level of its supplementation in the diet. Therefore, this factor needs to be carefully considered in order to obtain maximal growth-promoting effects of MOS in Japanese quail production.

Keywords


EFFECTS OF MANNAN OLIGOSACCHARIDES AS A DIETARY SUPPLEMENT ON PERFORMANCE AND CARCASS CHARACTERISTICS OF JAPANESE QUAILS(COTURNIX JAPONICA)

 

SH.M. ABDEL-RAHEEM* and Z.S.H. ESMAIL**

 

* Department of Nutrition and Clinical Nutrition, Faculty of Veterinary Medicine, AssiutUniversity, Assiut, Egypt

** Dept of Animal Production, Faculty of Agriculture, SouthValleyUniversity, Qena, Egypt

    Corresponding author: abdelrheem@yahoo.com

 

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                                                    ABSTRACT

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Received:14/6/2012

 

 

Accepted at: 14/7/2012

The effect of three levels of mannan oligosaccharides (MOS) as a dietarysupplement on growth performance, carcass characteristics and some blood metabolites of growing Japanese quails (Coturnix japonica) was the main objective of this experiment. A total of one hundred 1-day-old Japanese quails were randomly divided into 4 experimental groups (25 birds/ each treatment) with 3 replicates (8 birds in two replicates and 9 birds in one replicate). The experimental groups consisted of four dietary treatments: 1) a control basal diet without supplementation; 2) a basal diet with a MOS at level of 1 g/kg feed (low MOS); 3) a diet with MOS at a level of 3 g/kg feed (medium MOS); and 4) a diet with a MOS at a level of 5 g/kg feed (high MOS). The experimental period extended for 42 days. The data revealed that, birds fed diets containing medium MOS level (3 g /kg feed) recorded significant           (P < 0.05) improvements in body weight, weight gain, feed conversion efficiency, performance index, energy and protein efficiency compared with those fed the control one, low and high levels of MOS. Also medium level of MOS supplementation increased the dressing percentage and edible giblets, while the offal's percentages and carcass abdominal fat were significantly decreased. Growth performance was significantly improved at 3 g MOS/ kg diet, however high dosage of MOS have negative effects on growth rate of the birds. The triglyceride, total cholesterol and total lipids concentrations in quails blood decreased significantly in concomitant with a significant decrease in carcass fat % as a response to dietary MOS supplementation. From the results of the current study, it could be concluded that the responses of Japanese quails to MOS are influenced by the level of its supplementation in the diet. Therefore, this factor needs to be carefully considered in order to obtain maximal growth-promoting effects of MOS in Japanese quail production.

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Key words: Mannan oligosaccharides, growth performance, carcass characteristics, blood metabolites, Japanese quails

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INTRODUCTION

 

Currently, many parts of the world are experimenting alternative feed additives that may be used to alleviate the problems associated with the withdrawal of antibiotics from feed. Alternatives to antibiotics including enzymes, organic acids, probiotics, prebiotics, herbs and etheric oils, immuno-stimulants and other management practices. These alternatives promote gut health by several possible mechanisms including altering gut pH, maintaining protective gut mucins, selecting for beneficial intestinal organisms or against pathogens, enhancing fermentation acids, enhancing nutrient uptake, and increasing the humoral immune response (Inborr, 2000). One of these alternatives is prebiotics. Gibson and Roberfroid (1995) defined a prebiotic as a non-digestible food ingredient which beneficially affects the host by selectively stimulating the growth and/or activating the metabolism of one or a limited number of health-promoting bacteria in the intestinal tract, thus improving the host's microbial balance. The growth of endogenous microbial population groups such as bifidobacteria and lactobacilli is specifically stimulated and these bacteria species are perceived as beneficial to animal health (Yang et al., 2007).

 

Prebiotics are polysaccharides and oligosaccharides which cannot be digested effectively by the animal, but are readily fermented by anaerobic, colonic bacteria that are regarded as beneficial ones (Zhang  et al., 2003). Prebiotics have shown promise in controlling pathogens such as Salmonella and Escherichia coli and in stimulating the growth of bifidobacteria and lactobacilli, thus promoting health and performance of animals (Xu et al., 2003; Zhang  et al., 2003; Chung and Day, 2004; Yang et al., 2007). Some researchers hinted that prebiotics may have cholesterol-lowering properties (Liong and Shah, 2006; Li et al., 2007). Some positive changes in digestive enzymes, gut morphology, and immune system were noticed in birds given prebiotic-supplemented feed (Xu et al., 2003; Zhang et al., 2003; Huang et al., 2007). However, there are many considerations in supplementing prebiotics in animal feed. These include type of the diet (i.e., the content of non-digestible oligosaccharides) and the inclusion level of the supplements; animal characteristics (species, age, stage of production); and the hygiene status of the farm (Verdonk et al., 2005).

 

Japanese quail (Coturnix japonica) is a diversified poultry species reared for commercial egg and meat production. It is blessed with unique characteristics of fast growth, early sexual maturity, high rate of egg production, short generation interval and shorter incubation period that makes it suitable for diversified animal agriculture. The information about the effective level of MOS that optimizing growth and maximize production is lacking.

 

Therefore, the objective of the present study was to investigate the effect of different dietary levels of mannan oligosaccharides (MOS) on growth performance, carcass characteristics and on some blood metabolites of the growing Japanese quail (Coturnix japonica).

 

MATERIALS and METHODS

 

Bird and housing:

 

This study was carried out at the quail production unit, Faculty of Veterinary Medicine, South Valley University, Egypt, during the period from May to June 2011. Chemical analyses were performed in the laboratories of the Department of Nutrition and Clinical Nutrition, Faculty of Veterinary Medicine, AssiutUniversity, Assiut, Egypt. A total number of 100 one day old Japanese quail chicks were divided randomly into four treatments (25 birds each); each group was subdivided into three replicates (two of 8 birds and one of 9 birds /battery cage).

 

Chicks were individually weighed to the nearest gram at the start of experiment (the mean of the initial body weight was about 9.66 ± 0.26 g), wing-banded and randomly allotted to the dietary treatments. Chicks were raised in electrically heated batteries with raised wire mesh floors and had a free access to the mesh feed and fresh water from nipple drinkers throughout the experiment. Light was provided for 23 h/d. Room temperature on day 0 was 35ºC and decreased approximately 2.5ºC per week until 25 ºC was reached, according to standard poultry rearing practices. Batteries were placed into a room provided with continuous fans for ventilation. Heating and forced ventilation system allowed room temperature to be maintained between 25 and 35 ºC.

 

Dietary treatments:

 

The dietary treatments were: 1( a control diet without Y-MOS supplementation; 2) a diet with a prebiotic Y-MOS at a level of 1 g/kg feed; 3( a diet with Y-MOS at a level of 3 g/kg feed, and 4) a diet with a Y-MOS at a level of 5 g/kg feed. Diets were fed in mash form. A commercial prebiotic source Y-Mos® (Nutrex, Belgium) was used in this experiment, chemical composition of the Y-MOS is presented in Table 1.Basal diet was formulated to contain the ME density (2900 kcal/kg) and crude protein (24 %) concentrations recommended by NRC (1994). Physical and calculated chemical compositions of the basal experimental diet are presented in Table 2. No coccidiostats or antibiotics were used during the study. Feed and water were provided ad libitum. All birds were kept under hygienic conditions and were subjected to a prophylactic vaccination against viral diseases.

 

Growth Performance and feed conversion:

 

All birds were weighed individually (initial weight) and every week during the course of the experiment. Feed consumption was recorded weekly in the course of the whole experiment per pen basis, and calculated at days 21 and 42 of the experiment and the feed conversion rates were calculated subsequently. Feed conversion ratio was calculated as the amount of feed consumed per unit body weight gain and was adjusted to the weight of chicks at the first day. Performance Index for each group was calculated by dividing the total weight gain (g) by the feed conversion ratio (Ghosh et al., 2007). Mortality was recorded as it occurred.

 

Carcass traits:

 

Five birds randomly selected from each group were slaughtered at the end of the experiment. The birds were fasted for 10-12 h prior to determination of the final body weight at slaughtering, carcass weight (the weight of the slaughtered birds after removal of feathers, head, and feet but including the edible giblet (liver without gall bladder, heart, skinned empty gizzard and abdominal fat). The absolute organ weights were recorded. Dressing %, offal's %, and giblet % are calculated as relative weight to live body weight.

 

Meat chemical composition:

 

Different parts from the carcass as breast and thigh were sealed in polyethylene bags and frozen at -20 ºC for further analysis. The meat was removed from the bones, it was homogenized and it was analyzed for crude protein, crude fat, moisture and ash, according to the guidelines of AOAC (2005).

 

Blood Collection and Analysis:

 

At the end of the experimental period (day 42), 5 birds were randomly selected from each group and blood samples were collected from the bronchial vein during slaughter. The collected blood samples were centrifuged at 4000 rpm for 15 min and the sera were decanted into aseptically treated vials and stored at –20 ºC until further analysis. Serum samples were analyzed for total protein, albumen, glucose, total cholesterol, total lipid and triglycerides, by spectrophotometer using commercial test kits (Spectrum, Cairo, Egypt).

 

Statistical analysis:

 

The data were subjected to statistical analysis with one way AOVA using SPSS program for Windows Version 13; (SPSS GmbH, Munich, Germany) to determine if variables differed between groups. Statistical significant effects were further analyzed, and means were compared using Duncan’s multiple range test. Statistical significance was determined at   P (< 0.05).

 

RESULTS

 

Growth Performance:

 

The effects of MOS supplementation on BWG, FI and FCR, performance index of the quail are presented in Table 3. Growth performance of the Japanese quail was affected by dietary addition of MOS. As shown in Table 3, there were no significant differences            (P >0.05) in the initial BW of chicks between the dietary treatments. The average feed intake was not significantly differed (p>0.05) among treatments at the first 3 weeks. Medium MOS group showed the highest body weight gain (g) and performance index (98.25, 53.43) followed by low MOS group (94.8, 43.04), control (92.24, 44.56) and high MOS group (84.9, 37.21), respectively in the first 3 weeks. At the same time (4-6 weeks) quails fed diet supplemented with medium MOS had significant increases in body weight gain, performance index beside improving feed conversion rate in comparison with the other dietary groups. Also, the feed conversion was significantly (p < 0.05) improved in medium MOS supplemented group at the last 3 weeks compared to those of the low and high ones. At the last 3 weeks the feed intake was significantly higher (p < 0.05) for birds fed the diet supplemented with high MOS. The cumulative feed consumption per quail during the whole experimental period (0-6 weeks) was significantly higher in both low and high MOS supplemented birds in comparison with the control group, however medium MOS supplemented group showed an intermediate values. Quails fed diet supplemented with medium MOS had significant increases in the  cumulative (from 0 to 6 week) body weight gain, performance index and improved feed conversion rate compared to the other dietary groups. Mortality % was relatively low numerically for birds supplemented with MOS in comparison with control group and it was ranged from 8 % to 12 %. Generally, Medium MOS had improved quails performance and feed conversion efficiency.

 

Energy and protein efficiency:

 

Energy and protein efficiency of growing quails fed the experimental diets are exhibited in Table 4.  The results showed that energy efficiency (ME intake, kcal/g weight gain) and protein efficiency (protein intake, g/g weight gain) were significantly (p<0.05) improved in medium MOS supplemented group compared to low and high MOS supplemented groups, a matter which mean that birds fed low and high MOS levels consumed more energy and protein per unit gain than those fed on medium MOS level.

 

Carcass traits, absolute organ weights and meat chemical composition:

MOS supplementation significantly altered (p<0.05) carcass characteristics of growing Japanese quails. The data in Table 5 indicated that, carcass weight, and dressing % of medium MOS supplemented quails were significantly (p<0.05) higher than those supplemented with low and high MOS levels. Moreover, carcass of medium MOS supplemented quails had lower offal's weight and lower abdominal fat than other groups. In addition, the absolute liver and gizzard weight were significantly higher in medium MOS supplemented quails. Table 6 revealed that, the meat chemical composition of quails fed diet supplemented with medium MOS had a lower fat and ash %.

 

Blood metabolites:

The mean serum concentrations of the total protein and glucose increased significantly in all MOS supplemented birds and being highest in low MOS level supplemented group (Table 7). Serum total cholesterol, total lipids and triglyceride significantly decreased (p<0.05) in MOS supplemented groups.

 

 

 

Table 1: Chemical composition (%) of mannan oligosaccharide product (Y-MOS).

 

Y-MOS

Ingredients

95

DM

25

Protein /DM%

6

Ash

 

Polysaccharides

28

Β-Glucanes

28

Mannan oligosaccharides (MOS)

 

 

Table 2:  Physical and calculated chemicalcomposition of basal diet fed for Japanese quails (%, as fed-basis)

%

Ingredients

55.95

Yellow corn

39.6

Soybean meal (48)

1.00

Sunflower oil

1

Dicalcium phosphate

1.5

Ground limestone

0.4

Iodized salt

0.25

Premix*

0.1

L-lysine

0.2

DL-methionine

100

Total

 

Calculated composition

2937.16

Energy ME kcal /Kg

24.04

CP (%)

2.36

EE (%)

3.22

CF (%)

0.91

Ca (%)

0.31

Av. P (%)

1.41

Lysine (%)

0.75

Meth.+Cys. (%)

*Mineral and vitamin premix, Heromix broilers  (Heropharma Co., Egypt)

Each 2.5 kg contain: 12,000000 IU Vit. A, 2,000000 Vit D3, 10 g vit. E, 2g Vit K3, 1g Vit. B1, 5g vit B2, 1.5 g Vit. B6, 10 mg Vit B12, 30 g nicotinic acid, 10 g pantothenic acid, 1g folic acid, 50 g biotin, 250 g choline chloride 50 %, 30g iron, 10 g copper, 50g zinc, 60 g manganese, 1g iodine, 0.1 g selenium, 0.1 g cobalt and carrier Caco3 to 2.5 kg

 

Table 3: Body weight gain (BWG), feed intake (FI), feed conversion efficiency (FC), performance index and mortality of different experimental groups

 

Items

Control

Low MOS

Medium MOS

High MOS

P

 0-21 d ay

 

 

 

 

 

Initial BW (day1)

9.68±0.22

9.76±0.29

9.51±0.25

9.71±0.32

0.92

Live BW (day 21)

101.92±0.52c

104.56±0.91b

107.76±0.55a

94.6±0.99d

000

FI (g/bird)

190.95±1.85

209.33±7.31

198.2±2.6

193.87±4.7

0.08

BW gain (g/bird)

92.24±0.59c

94.8±0.97 b

98.25±0.57a

84.9±0.98d

0.000

FC (g/g)

2.07±.02abc

2.2±0.01cd

2.01±0.03b

2.28±0.05d

0.02

Performance Index*

44.56±0.43 c

43.04±1.5c

48.72±0.65a

37.21±0.78b

0.000

22-44 day

 

 

 

 

 

FI (g/bird)

396.66±8.8d

426.00±3.1cd

410.0±2.9abc

430.0±5.8a

0.01

BW gain (g/bird)

88.56±1.2d

97.68±1.4b

110.16±1.7a

89.4±1.5 c

0.000

FC (g/g)

4.48±0.09b

4.36±0.03c

3.72±0.02d

4.8±0.06a

0.000

Performance Index

19.79±0.44 c

22.39±0.16b

29.6±0.21a

18.59±0.24 d

0.000

0-42 day

 

 

 

 

 

B W (final)

190.48±1.2c

202.74±1.5b

217.92±1.7a

184.00±1.4d

0.000

FI (g/bird)

587.62±7.54c

635.33±2.4 a

608.2±5.3ab

623.87±8.6b

0.01

BW gain (g/bird)

180.8±1.2c

192.5±1.6b

208.41±1.7a

174.29±1.5d

0.000

FC (g/g)

3.25±0.04c

3.3±0.05b

2.91±0.03d

3.57±0.05a

0.000

Performance Index

55.64±0.75c

58.35±.95b

71.42±0.62a

48.71±0.66d

0.000

Mortality, %

20

8

8

12

 

Figures in the same raw with different superscript differ significantly (p< 0.05).

Values are reported as means ± SE.

Low MOS (1 g MOS /kg feed); medium (MOS 3 g MOS /kg feed) and high MOS (5 g MOS /kg feed) treatments in the first 3 weeks and last 3 weeks, respectively

FI=Feed intake                FC= Feed conversion                   FC= feed intake (g)/weight gain (g)

*Performance Index= weight gain (g)/ FC ratio

 

Table 4: Energy and Protein efficiency of growing Japanese quails fed the experimental diets

 

Items

Control

Low MOS

Medium MOS

High MOS

P

ME intake kcal/bird

 

 

 

 

 

0-21day

560.87±5.44

614.84±21.47

582.17±7.65

569.44±11.97

0.08

22-42 day

1165.07±25.9bc

1251.23±8.97ac

1204.23±8.47ab

1262.98±16.95a

0.01

0-42 day

1726.2±22.16b

1866.35±29.97 a

1786.67±15.5 a b

1832.69±25.3a

0.02

CP intake (g/bird)

 

 

 

 

 

0-21day

45.91±0.44

50.32±1.75

47.65±0.62

46.61±0.98

0.08

22-42 day

95.36±2.1b

102.41±0.73a

98.56±0.69ab

103.37±1.38a

0.01

0-42 day

141.27±1.81b

152.73±2.45a

146.21±1.26ab

149.98±2.06a

0.01

BW gain (g/bird)

 

 

 

 

 

0-21day

92.24±0.59c

94.8±0.79 b

98.25±0.57a

84.9±0.98d

0.000

22-42 day

88.56±1.2d

97.68±1.4b

110.16±1.7 a

89.4±1.5 c

0.000

0-42 day

180.8±1.2c

192.5±1.6b

208.41±1.7a

174.29±1.5d

0.000

EER*

 

 

 

 

 

0-21day

6.08±0.05bcd

6.48±0.22ac

5.92±0.07d

6.71±0.14a

0.02

22-42 day

13.16±0.29b

12.81±0.09b

10.93±0.07c

14.13±0.18a

0.000

0-42 day

9.54±0.12b

9.69±0.15b

8.57±0.08c

10.51±0.15a

0.01

PER**

 

 

 

 

 

0-21day

0.5±0.006abc

0.53±0.01ab

0.48±0.005c

0.55±0.01a

0.000

22-42 day

1.07±0.02b

1.05±0.007b

0.89±0.0c

1.15±0.01a

0.000

0-42 day

0.78±0.01b

0.79±0.01b

0.7±0.01c

0.86±0.0a

0.000

 

Figures in the same raw with different superscript differ significantly (p< 0.05).

Values are reported as means ± SE

* EER= Energy efficiency ratio = Energy intake (kcal)/weight gain (g),

** PER = Protein efficiency ratio= protein intake (g)/weight gain (g)

 

 Table 5: The effects of dietary treatments on carcass characteristics and absolute organ weight (g) of growing Japanese quails

 

Items

Control

Low MOS

Medium MOS

High MOS

P

Live weight

193.00±2.41c

204.2±4.43 b

214.00±2.6 a

188.8±5.97d

0.000

Carcass weight

131.6±2.62d

145.2±4.86 b

159.6±3.03 a

132.2±2.22c

0.000

Dressing %

68.18±0.84c

71.1±1.88ab

74.56±0.59 a

70.57±1.04b

0.02

Offals weight

61.4±1.7

59.00±4.2

54.4±0.87

55.6±2.37

0.25

Offals, %

31.82±0.9a

28.88±1.89ab

25.99±0.59b

29.93±1.04a

0.01

Edible giblet wt

14.18±0.6

13.6±0.82

14.6±0.23

13.00±0.75

0.36

Edible giblet %

7.34±0.26

6.68±0.24

6.83±0.18

6.88±0.34

0.45

Liver

5.7±0.27 b

5.28±0.42b

6.78±0.13a

5.68±0.42b

0.04

Gizzard

3.46±0.18 a

3.32±0.31ab

3.98±0.26 a

2.6±0.2b

0.01

Heart

2.33±0.09

2.36±0.16

2.34±0.1

2.28±0.08

0.96

Spleen

0.13±0.02

0.13±0.01

0.15±0.03

0.09±0.01

0.44

Head

12.48±0.5

12.5±1.59

12.22±0.6

11.00±0.07

0.65

Abdominal fat

3.4±0.6a

2.7±0.33ab

1.5±0.16 b

2.5±0.35ab

0.03

Legs

5.62±0.96a

4.38±0.28 b

5.56±0.06 b

3.9±0.32b

0.01

 

 

Figures in the same raw with different superscript differ significantly (p< 0.05).

Values are reported as means ± SE.                                    n=5             n=number of birds

Offals weight= weight of (blood +feather +head+legs)

Edible Giblet weight = weight of (liver+ skinned gizzard+heart+abdominal fat)

Dressing %, offals %, giblet % are calculated in relation to live weight

 

Table 6:  Effect of MOS on carcass meat composition of Japanese quail

 

Items

Control 

Low MOS

Medium MOS

High MOS

P

Moisture

72.0±0.57

71.67±1.4

74.00±0.58

72.35±1.2

0.37

Crude protein

20.83±0.44

21.63±0.6

21.96±0.08

21.66±0.33

0.11

Fat

3.67±0.35a

2.60±0.31b

1.97±0.09 b

2.17±0.27 b

0.01

Ash

1.40±0.05b

1.67±0.09a

1.3±0.06 b

1.5±0.05a

0.01

 

Figures in the same raw with different superscript differ significantly (p< 0.05).

Values are reported as means ± SE.

 n=3                 n=number of birds

Table 7: Effects of dietary treatments on some serum parameters of growing Japanese quails

 

Items

Control 

Low MOS

Medium MOS

High MOS

P

Total protein, g/dl

3.18±0.06 b

4.30±0.22a

4.16±0.12b

4.08±0.1b

0.000

Albumen, g/dl

1.54±0.09

1.96±0.10

1.70±0.14

1.64±0.14

0.11

Glucose mg/dl

319.8±3.39b

366±5.78a

348.00±1.92a

340.2±6.93b

0.000

T. Choles., mg/dl

191.4±3.4a

172.0±4.06 b

164.8±5.00 b

177.6±4.7 b

0.004

T. lipids, mg/dl

655.0±10.2a

554.0±10.4 b

587.00±5.38 b

580.27±7.74 c

0.000

Triglyceride, mg /dl

110.4±1.6a

85.2±2.85c

81.00±3.7 c

94.8±3.38b

0.000

 

Figures in the same raw with different superscript differ significantly (p< 0.05).

Values are reported as means ± SE.                   n=5            n= number of birds

 


DISCUSSION

 

Animals reared under commercial field conditions are subjected to stress, depending on the pathogen load in their environment. Stress is generally accompanied by suppression of body weight and feed intake, which could be the cause of the decline in production. Probiotics, prebiotics and organic acids have been used in the early period of the bird life to prevent the detrimental effects of stress. The addition of specific mannan oligosaccharide (MOS), derived from the outer cell wall of Saccharomyces cerevisiae, to a broiler chicken diet has been reported to improve their growth performance (Hooge, 2004; Rosen, 2007, Yang et al., 2008). Also these observations had been depicted in Japanese quails in previous studies (Stanely et al., 2000; Ghosh et al., 2007; Cakir et al., 2008; Sahin et al., 2008).This improvement in growth performance was achieved by saving energy and protein for body growth, which otherwise would be used to combat the growth of pathogenic bacteria (Samarasinghe et al., 2003). By binding pathogenic bacteria possessing type 1 fimbriae, MOS can prevent them from attaching to the gut lining, and this improving its integrity (Loddi et al., 2002). Gut microflora increase energy costs by modifying the rate of energy-consuming reactions such as protein turnover within the chicken GIT (Choct, 1999). The improvement in quails performance by MOS supplementation in this trail was supported by a lot of researches which explain the effect of prebiotics in enhancing resistance to enteric diseases, promoting growth. The authors of these researches  ascribed this effect to: (1) inhibits colonization of enteric pathogens by blocking bacterial adhesion to gut lining (Spring   et al., 2000; Valancony et al., 2001), (2) enhances immunity (Ferket, 2002; Humphrey et al.,2002), (3), brush border mucin barrier (Iji et al., 2001; Loddi     et al., 2002), (4) and integrity of the gut lining (Ferket, 2002) and (5) and reduces enterocyte turnover rate (Spring et al., 2000). These properties have the potential to enhance growth rate, feed conversion efficiency and livability in commercial broilers and turkeys and to increase egg production (Hooge, 2004).

 

The adverse effect of high MOS level on quail's performance was also observed by Biggs et al. (2007) who reported that high dosage of prebiotics can have negative effects on the gut system and retard the growth rate of birds. In an experiment with rat Ten Bruggencate et al. (2003) reported that rapid fermentation of prebiotics (fructo-oligosaccharides) leading to high concentrations of organic acids, impaired the barrier function, which reduced the ability of rats to resist salmonella infection in high dietary supplementation. The low MOS level induced slight improvement in growth performance, carcass characteristics, energy and protein efficiency in relation to the control group. 

 

The improvements of carcass weights, dressing percentages, offal's weights and the decrease in abdominal fat in medium MOS supplemented quails were in harmony with the results of previous studies on Japanese quails (Falaki et al., 2011) and broilers (Bozkurt et al., 2008; Zhou et al., 2009). It was hypothesized that a decrease in intestinal pathogen challenge provided by MOS would result in improvement in nutrient utilization and allocation leading to benefits in lean muscle gain (Ferket, 2004). The improvements of carcass characteristics confirm the results of body weight and body gain in medium MOS supplemented birds. Spring et al. (2000) ascribed this result could be due to decreased proliferation of pathogenic bacteria. The decrease in abdominal fat was consistent with results of Ammerman et al. (1989) who concluded that the addition of 0.3% oligofructose to the bird's ration decreased the percent of abdominal fat.

 

Recently, an increasing number of consumers have been demanding that food products be safe and healthy. Therefore, low-fat chickens are currently very popular products in international markets. Interestingly, in this study, the triglycerides, total cholesterol and total lipids concentration in blood decreased in concomitant with a significant decrease in carcass fat % as a response to MOS treatments. Triglycerides are secreted from the liver into the blood by triglyceride- rich lipoproteins; therefore, impaired hepatic lipogenesis results in decreased triglyceride concentrations in plasma. These results agreed with the results of earlier studies in which prebiotics found to lower the concentration of blood lipids in quails (Sharifi et al., 2011), broilers (Li et al., 2007; Ashayerizadeh et al., 2009; Rabie et al., 2010) and in piglets (Tang et al., 2005). 

        

The reduction in serum total cholesterol of quails fed probiotic and prebiotic supplemented diets could be attributed to the reduced absorption and or synthesis of cholesterol in the gastro-intestinal tract (Mohan     et al., 1996; Ghiyasi et al., 2008). The most important mechanism by which prebiotic eliminates cholesterol would likely be through reducing lipid absorption in intestine by binding bile acids, which results in increased cholesterol elimination and hepatic synthesis of new bile acids (Zhang et al., 2003; Taherpour et al., 2009).

 

The response of some physiological variables was non linear and tended to peak at medium and low concentrations of MOS. Based on the results of the current study, it can be concluded that, responses of Japanese quails to MOS supplementation are influenced by the level of supplementation. Therefore, this factor need to be carefully considered in order to obtain maximal growth-promoting effects of MOS in Japanese quails production.

 

Acknowledgements 

The authors are thankful to Dr Yaser Abdel Galil Ahmed, the head of the quail production unit, Faculty of Veterinary Medicine, SouthValleyUniversity for his help and support to perform this work.

 

REFERENCES

 

Ammerman, E.; Quarles, C. and Twining, P.V. (1989): Evaluation of fructo-ligosaccharides on performance and carcass yield of male broilers. Poult. Sci. 68: 167.

AOAC, (2005): Official Methods of Analysis. 18th Edn., Horwitz, W. (Ed.). Association of Analytical Chemists, AOAC International, ArlingtonVirginia, USA.

Ashayerizadeh, A.; Dabiri, N.; Ashayerizadeh, O.;  Mirzadeh, K.H.;  Roshanfekr, H.; Mamooee, M. (2009): Effect of dietary antibiotic, probiotic and prebiotic as growth promoters, on growth performance, carcass characteristics and hematological indices of broiler chickens. Pak. J. Biol. Sci. 12: 52-57.

Biggs, P.; Parsons, C.M. and Fahey, G.C. (2007): Effects of Several Oligosaccharides on Growth Performance, Nutrient Digestibilities, and Caecal Microbial Populations in Young Chicks. Poult. Sci. 86: 2327-2336.

Bozkurt, M.; Kucukyilmaz, K.; Katil, A.U.; Cinar, M. (2008): Growth performance and slaughter characteristics of broiler chickens fed with antibiotics, mannan oligosaccharide ad dextran oligosaccharide supplemented diet. Int. J. Poult. Sci., 7 (10): 969-977.

Çakir, S.; Midilli, M.; Erol, H.; Şimsek, N.;  Çinar, M.;  Altintas, A.; Alp, H.; Altintas, L.; Cengiz, Ö. and Antalyali, A. (2008): Use of combined probiotic-prebiotic, organic acid and avilamycin in diets of Japanese quails. Revue Méd. Vet., 159 (11): 565-569.

Choct, M. (1999): Soluble non-starch polysaccharides affect net utilization of energy by chickens. Recent Advances in Animal Nutrition in Australia, 12: 31–35.

Chung, C.H. and Day, D.F. (2004): Efficacy of Leuconostoc mesenteroides (ATCC 13146) isomaltoologosacharidesas a poultry prebiotic. Poult. Sci.,83: 1302-1306.

Duncan, D.B. (1955): Multiple range test and multiple F-tests. Biometrics. 11: 1-42.

Falaki, M.; Shams Shargh, M.; Dastar, B. and Zerehdaran, S. (2011): Effect of different levels of probiotic and prebiotic on performance and carcass characteristics of broiler chickens. Journal of Animal and Veterinary Advances, 10 (3): 378-384.

Ferket, P.R. (2002): Use of oligosaccharides and gut modifiers as replacements for dietary antibiotics. Proc. 63rd Minnesota Nutrition Conference, September 17-18, pp: 169–82. Eagan, MN.

Ferket, P.R. (2004): Alternatives to antibiotics in poultry production: responses, practical experience and recommendations. Nutritional biotechnology in the feed and food industries: Proceedings of Alltech's 20th Annual Symposium, Kentucky, USA, pp: 56-67.

Ghosh, H.K.; Halder, G.; Samanta, G.; Paul, S.K. and Pyne, S.K. (2007): Effect of dietary supplementation of organic acid and mannan oligosaccharide on the performance and gut health of Japanese quails (Coutrnix coutrnix  Japonica). Asian Journal of Poultry Science 1, (1):1-7

Gibson, G.R. and Roberfroid, M. (1995): Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. Journal of Nutrition 125: 1401-1412.

Ghiyasi, M.; Rezaei, M. and Sayyahzadeh, H. (2008): Effect of prebiotic (fermacto) in low protein diet on performance and carcass characteristics of broiler chicks. Int. J. Poult. Sci. 6: 661-665.

Hooge, D.M. (2004): Meta-analysis of broiler chicken pen trials evaluating dietary mannan oligosaccharide, 1993-2003. Int. J. Poultry Sci. 3: 163–74.

Huang, R.L.; Ding, Z.Y.; Yang, C.B.; Yen, Y.L.; Xie, M.Y.; Wu, G.Y.; Li, T.G.; Li, L.L.; Tang, Z.R.; Kang, P.; Hou, Z.P.; Ding, D.; Xiang, H., Kong, X.F. and Guo, Y.M. (2007): Dietary oligochitosan supplementation enhances immune status of broilers. Journal of the Science of Food and Agriculture 87: 153-159

Humphrey, B.D.; Koutsos, E.A. and Klasing, K.C. (2002): Requirements and priorities of the immune system for nutrients. In: Jacques, K.A. and T.P. Lyons (eds.), Biotechnology in the Feed and Food Industry, Proceedings of Alltech’s 18th Annual Symposium, pp: 69–77.NottinghamUniversityPress, UK.

Iji, P.A.; Saki, A.A. and Tivey, D.R. (2001): Intestinal structure and function of broiler chickens on diets supplemented with a mannan oligosaccharide. J. Sci. Food Agric.81: 1186–92.

Inborr, J. (2000): Swedish poultry production without ın-feed antiobiotics - a testing ground or a model for the future? Australian Poultry Science Symposium, 2000: 12, 1-9.

Li, X.J.; Piao, X.S.; Kim, S.W.; Liu, P.; Wang, L.; Shen, Y.B.; Jung, S.C. and Lee, H.S. (2007): Effects of chito-oligosaccharide supplementation on performance, nutrient digestibility, and serum composition in broiler chickens. Poult. Sci. 86: 1107–1114.

Liong, M.T. and Shah, N.P. (2006): Effects of a Lactobacillus casei synbiotic on serum lipoprotein, intestinal microflora, and organic acids in rats. Journal of Dairy Science 89: 1390–1399.

Loddi, M.M.; Moraes, V.M.B.; Nakaghi, L.S.O.; Tucci, F.M.; Hannas, M.I.; Ariki, J. and Bruno, L.D.G. (2002): Mannan oligosaccharide and organic acids on intestinal morphology integrity of broilers evaluated by scanning electron microscopy. Proceedings of the 11th European Poultry Science Conference, Bremen, 121 pp.

Mohan, B.; Kadirvel, R.; Natarajan, A. and Bhaskaram, M. (1996): Effect of probiotic supplementation on growth, nitrogen utilization and serum cholesterol in broilers. Brit. Poultry Sci. 37: 395-401.

NRC, National Research Council, (1994): Nutrient Requirements of Poultry.  9th. Rev. (Edn.). NationalAcademy Press, Washington, DC., USA.

Rabie, M.H.; Ismail, F.S. and Sara, K.S. (2010): Effect of dietary energy level with probiotic and enzyme addition on performance, nutrient digestibility and carcass traits of broilers. Egypt. Poult. Sci. 30:179-201.

Rosen, G.D. (2007): Holo-analysis of the efficacy of Bio-Mos in broiler nutrition. British Poultry Science, 48: 21–26.

Sahin, T.; Kaya, I.; Unal, Y. and El Mali, D.A. (2008): Dietary supplementation of probiotic combination 9Combiotics) on performance, carcass quality, and blood parameters in growing quails. Journal of Animal and Veterinary Advances 7 (1): 1370-1373.

Samarasinghe, K.; Wenk, C.; Silva, K.F.S.T. and Gunasekera, J.M.D.M. (2003): Turmeric (Curcuma longa) root powder and mannanoligosaccharides as alternatives to antibiotics in broiler chicken diets. Asian-Australasian Journal of Animal Sciences 16: 1495-1500.

Sharifi, M.R.; Shams-Shargh, M.; Dastar, B. and Hassani, S. (2011): The effect of dietary protein levels and synbiotic on performance parameters, blood characteristics and carcass yields of Japanese quail (Coturnix coturnix Japonica). Italian Journal of Animal Science 10, 1

Spring, P.; Wenk, C.; Dawson, K.A. and Newman, K.E. (2000): The effects of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of Salmonella-challenged broiler chicks. Poult. Sci. 79: 205–211.

SPSS, (2001): Statistical package for the social sciences (SPSS® statistical software version 13. Inc., Chicago, IL for windows).

Stanley, V.G.; Brown, C. and Sefon, A.E. (2000): Comparative evaluation of a yeast culture, mannan oligosaccharide and antibiotic on performance of turkeys. Poult. Sci. 79: 205-2011.

Taherpour, K.; Moravej, H.; Shivazad, M.; Adibmoradi, M. and Yakhchali, B. (2009): Effects of dietary probiotic, prebiotic and butyric acid glycerides on performance and serum composition in broiler chickens. Afr. J. Biotechnol. 8: 2329-2334.

Tang,  Z.R.; Yin, Y.L.; Nyachoti, C.M.; Huang, R.L.; Li, T.J.; Yang, C.B.; Yang, X.J.; Gong, Peng, J.; Qi, D.S; Xing, J.J.; Sun, Z.H. and Fan, M.Z. (2005): Effect of dietary supplementation of chitosan and galacto-mannan-oligosaccharide on serum parameters and the insulin-like growth factor-I mRNA expression in early-weaned piglets. Domest. Anim. Endocrinol. 28: 430–441.

Ten Bruggencate, S.J.M.; Bovee-Oudenhoven, I.M.J.; Lettink-Wissink, M.L.G. and Van Der Meer, R. (2003): Dietary fructo-oligosaccharides dose-dependently increase translocation of salmonella in rats. Journal of Nutrition 133: 2313-2318.

Valancony, H.; Humbert, F.; Rukelibuga, J.; Bougon, M.; Balaine, L. and Lalande, F. (2001): Comparison of some substitutes for antibiotic additives in diets for turkey poults. Effects on production and on resistance to salmonella colonization. Sci.Tech. Avicoles 35: 25–34.

Verdonk, J.M.A.J.; Shim, S.B.; Van Leeuwen, P. and Verstegen, M.W.A. (2005): Application of inulin-type fructans in animal feed and pet food. British Journal of Nutrition 93, S125-S138.

Xu, Z.R.; Hu, C.H.; Xia, M.S.; Zhan, X.A. and Wang, M.Q. (2003): Effects of dietary fructooligosaccharide on digestive enzyme activities, intestinal microflora and morphology of male broilers. Poult. Sci. 82: 1030– 1036.

Yang, Y.; Iji, P.A.; Kocher, A.; Thomson, E.; Mikkelsen, L.L. and Choct, M. (2007): Effects of mannan oligosaccharide in broiler chicken diets on growth performance, energy utilisation, nutrient digestibility and intestinal microflora British Poultry Science Volume 49, Number 2 (March 2008), pp. 186-194.

Yang, Y.; Iji, P.A.; Kocher, A.; Thomson, E.; Mikkelsen, L.L. and Choct, M. (2008): Effects of mannanoligosaccharide in broiler chicken diets on growth performance, net energy utilization, nutrient digestibility, and intestinal microflora. British Poultry Science 49:        186-194.

Zhang, W.F.; Li, D.F.; Lu, W.Q. and Yi, G.F. (2003): Effects of isomalto oligosaccharides on broiler performance and intestinal microflora. Poult. Sci.  82: 657–663.

Zhou, T.X.; Chen, Y.J.; Yoo, J.S.; Huang, Y.; Lee, J.H.; Jang, H.D.; Shin, S.O.; Kim, H.J.; Cho, J.H. and Kim, I.H. (2009): Effects of chito oligosaccharide supplementation on performance, blood characteristics, relative organ weight, and meat quality in broiler chickens. Poult. Sci. 88: 593–600

 

 


اثر إضافة  Mannan oligosaccharides (MOS)علي أداء ومواصفات الذبيحة في السمان الياباني النامي

 

شريف محمد عبد الرحيم ، زينهم شيخون

 

أجريت هذه التجربة لتقييم أثر إضافة ثلاث مستويات غذائية من MOS علي بعض الصفات الإنتاجية ومواصفات الذبيحة وبعض مکونات الدم في السمان الياباني النامي. لذلک تم استخدم عدد 100 طائر من السمان الياباني النامي عمر يوم تم تقسيمهما عشوائيا إلي عدد 4 مجموعات بکل منها عدد 25 طائر وقسمت کل مجموعة إلي 3 مکررات ( اثنان بهما 8 طيور وواحدة بها 9 طيور). غذيت المجموعة الأولي علي العليقة الضابطة بدون أي إضافات, في حين غذيت المجموعة الثانية والثالثة علي العليقه المقارنة بعد اضافة 1 جم MOS /کجم عليقه (مستوي منخفض), و 3 جم  MOS/کجم عليقه (مستوي متوسط) لکل منهما علي التوالي. اما المجموعة الرابعة فقد اٌضيف الي عليقتها 5جمMOS  /کجم عليقه (مستوي مرتفع). وذلک في تجربة استمرت ستة اسابيع. أظهرت النتائج أن إضافة المستوي المتوسط (3 جم MOS /کجم عليقة) أعطي أفضل أداء إنتاجي تمثل في تحسن معنوي في في کل من الزيادة في وزن الجسم ومعدل الکفاءة التحويلية للغذاء ومؤشر الأداء وکذلک نسبة التصافي والأجزاء المأکولة من الطائر مقارنة بالمستويات الأخرى وکذلک التي تمت تغذيتها علي العليقة الضابطة فقط. کما لوحظ أيضا أن إضافة المستوي المتوسط من MOS أدي إلي تحسن کفاءة تحويل الطاقة والبروتين. أوضحت النتائج أن المستوي المنخفض من MOS أدي إلي تحسن طفيف في الأداء الإنتاجي للطيور في حين کان اثر المستوي المرتفع سلبياً علي الأداء الإنتاجي للطيور. اوضحت النتائج ان إضافة  MOS أدت إلي انخفاض الکولسترول والدهون الکلية  والجليسريدات الثلاثية في دم السمان الياباني النامي عند جميع المستويات المضافة. وقد خلصت النتائج الي  أن المستوي المتوسط من MOS حقق أفضل النتائج مما يؤکد اهمية مراعاة مستوي إضافةMOS  إلي علائق السمان وذلک للحصول علي أعلي إنتاج دون الحاجة إلي استخدام المضادات الحيوية في هذا الصدد.

 

 

REFERENCES
 
Ammerman, E.; Quarles, C. and Twining, P.V. (1989): Evaluation of fructo-ligosaccharides on performance and carcass yield of male broilers. Poult. Sci. 68: 167.
AOAC, (2005): Official Methods of Analysis. 18th Edn., Horwitz, W. (Ed.). Association of Analytical Chemists, AOAC International, ArlingtonVirginia, USA.
Ashayerizadeh, A.; Dabiri, N.; Ashayerizadeh, O.;  Mirzadeh, K.H.;  Roshanfekr, H.; Mamooee, M. (2009): Effect of dietary antibiotic, probiotic and prebiotic as growth promoters, on growth performance, carcass characteristics and hematological indices of broiler chickens. Pak. J. Biol. Sci. 12: 52-57.
Biggs, P.; Parsons, C.M. and Fahey, G.C. (2007): Effects of Several Oligosaccharides on Growth Performance, Nutrient Digestibilities, and Caecal Microbial Populations in Young Chicks. Poult. Sci. 86: 2327-2336.
Bozkurt, M.; Kucukyilmaz, K.; Katil, A.U.; Cinar, M. (2008): Growth performance and slaughter characteristics of broiler chickens fed with antibiotics, mannan oligosaccharide ad dextran oligosaccharide supplemented diet. Int. J. Poult. Sci., 7 (10): 969-977.
Çakir, S.; Midilli, M.; Erol, H.; Şimsek, N.;  Çinar, M.;  Altintas, A.; Alp, H.; Altintas, L.; Cengiz, Ö. and Antalyali, A. (2008): Use of combined probiotic-prebiotic, organic acid and avilamycin in diets of Japanese quails. Revue Méd. Vet., 159 (11): 565-569.
Choct, M. (1999): Soluble non-starch polysaccharides affect net utilization of energy by chickens. Recent Advances in Animal Nutrition in Australia, 12: 31–35.
Chung, C.H. and Day, D.F. (2004): Efficacy of Leuconostoc mesenteroides (ATCC 13146) isomaltoologosacharidesas a poultry prebiotic. Poult. Sci.,83: 1302-1306.
Duncan, D.B. (1955): Multiple range test and multiple F-tests. Biometrics. 11: 1-42.
Falaki, M.; Shams Shargh, M.; Dastar, B. and Zerehdaran, S. (2011): Effect of different levels of probiotic and prebiotic on performance and carcass characteristics of broiler chickens. Journal of Animal and Veterinary Advances, 10 (3): 378-384.
Ferket, P.R. (2002): Use of oligosaccharides and gut modifiers as replacements for dietary antibiotics. Proc. 63rd Minnesota Nutrition Conference, September 17-18, pp: 169–82. Eagan, MN.
Ferket, P.R. (2004): Alternatives to antibiotics in poultry production: responses, practical experience and recommendations. Nutritional biotechnology in the feed and food industries: Proceedings of Alltech's 20th Annual Symposium, Kentucky, USA, pp: 56-67.
Ghosh, H.K.; Halder, G.; Samanta, G.; Paul, S.K. and Pyne, S.K. (2007): Effect of dietary supplementation of organic acid and mannan oligosaccharide on the performance and gut health of Japanese quails (Coutrnix coutrnix  Japonica). Asian Journal of Poultry Science 1, (1):1-7
Gibson, G.R. and Roberfroid, M. (1995): Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. Journal of Nutrition 125: 1401-1412.
Ghiyasi, M.; Rezaei, M. and Sayyahzadeh, H. (2008): Effect of prebiotic (fermacto) in low protein diet on performance and carcass characteristics of broiler chicks. Int. J. Poult. Sci. 6: 661-665.
Hooge, D.M. (2004): Meta-analysis of broiler chicken pen trials evaluating dietary mannan oligosaccharide, 1993-2003. Int. J. Poultry Sci. 3: 163–74.
Huang, R.L.; Ding, Z.Y.; Yang, C.B.; Yen, Y.L.; Xie, M.Y.; Wu, G.Y.; Li, T.G.; Li, L.L.; Tang, Z.R.; Kang, P.; Hou, Z.P.; Ding, D.; Xiang, H., Kong, X.F. and Guo, Y.M. (2007): Dietary oligochitosan supplementation enhances immune status of broilers. Journal of the Science of Food and Agriculture 87: 153-159
Humphrey, B.D.; Koutsos, E.A. and Klasing, K.C. (2002): Requirements and priorities of the immune system for nutrients. In: Jacques, K.A. and T.P. Lyons (eds.), Biotechnology in the Feed and Food Industry, Proceedings of Alltech’s 18th Annual Symposium, pp: 69–77.NottinghamUniversityPress, UK.
Iji, P.A.; Saki, A.A. and Tivey, D.R. (2001): Intestinal structure and function of broiler chickens on diets supplemented with a mannan oligosaccharide. J. Sci. Food Agric.81: 1186–92.
Inborr, J. (2000): Swedish poultry production without ın-feed antiobiotics - a testing ground or a model for the future? Australian Poultry Science Symposium, 2000: 12, 1-9.
Li, X.J.; Piao, X.S.; Kim, S.W.; Liu, P.; Wang, L.; Shen, Y.B.; Jung, S.C. and Lee, H.S. (2007): Effects of chito-oligosaccharide supplementation on performance, nutrient digestibility, and serum composition in broiler chickens. Poult. Sci. 86: 1107–1114.
Liong, M.T. and Shah, N.P. (2006): Effects of a Lactobacillus casei synbiotic on serum lipoprotein, intestinal microflora, and organic acids in rats. Journal of Dairy Science 89: 1390–1399.
Loddi, M.M.; Moraes, V.M.B.; Nakaghi, L.S.O.; Tucci, F.M.; Hannas, M.I.; Ariki, J. and Bruno, L.D.G. (2002): Mannan oligosaccharide and organic acids on intestinal morphology integrity of broilers evaluated by scanning electron microscopy. Proceedings of the 11th European Poultry Science Conference, Bremen, 121 pp.
Mohan, B.; Kadirvel, R.; Natarajan, A. and Bhaskaram, M. (1996): Effect of probiotic supplementation on growth, nitrogen utilization and serum cholesterol in broilers. Brit. Poultry Sci. 37: 395-401.
NRC, National Research Council, (1994): Nutrient Requirements of Poultry.  9th. Rev. (Edn.). NationalAcademy Press, Washington, DC., USA.
Rabie, M.H.; Ismail, F.S. and Sara, K.S. (2010): Effect of dietary energy level with probiotic and enzyme addition on performance, nutrient digestibility and carcass traits of broilers. Egypt. Poult. Sci. 30:179-201.
Rosen, G.D. (2007): Holo-analysis of the efficacy of Bio-Mos in broiler nutrition. British Poultry Science, 48: 21–26.
Sahin, T.; Kaya, I.; Unal, Y. and El Mali, D.A. (2008): Dietary supplementation of probiotic combination 9Combiotics) on performance, carcass quality, and blood parameters in growing quails. Journal of Animal and Veterinary Advances 7 (1): 1370-1373.
Samarasinghe, K.; Wenk, C.; Silva, K.F.S.T. and Gunasekera, J.M.D.M. (2003): Turmeric (Curcuma longa) root powder and mannanoligosaccharides as alternatives to antibiotics in broiler chicken diets. Asian-Australasian Journal of Animal Sciences 16: 1495-1500.
Sharifi, M.R.; Shams-Shargh, M.; Dastar, B. and Hassani, S. (2011): The effect of dietary protein levels and synbiotic on performance parameters, blood characteristics and carcass yields of Japanese quail (Coturnix coturnix Japonica). Italian Journal of Animal Science 10, 1
Spring, P.; Wenk, C.; Dawson, K.A. and Newman, K.E. (2000): The effects of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of Salmonella-challenged broiler chicks. Poult. Sci. 79: 205–211.
SPSS, (2001): Statistical package for the social sciences (SPSS® statistical software version 13. Inc., Chicago, IL for windows).
Stanley, V.G.; Brown, C. and Sefon, A.E. (2000): Comparative evaluation of a yeast culture, mannan oligosaccharide and antibiotic on performance of turkeys. Poult. Sci. 79: 205-2011.
Taherpour, K.; Moravej, H.; Shivazad, M.; Adibmoradi, M. and Yakhchali, B. (2009): Effects of dietary probiotic, prebiotic and butyric acid glycerides on performance and serum composition in broiler chickens. Afr. J. Biotechnol. 8: 2329-2334.
Tang,  Z.R.; Yin, Y.L.; Nyachoti, C.M.; Huang, R.L.; Li, T.J.; Yang, C.B.; Yang, X.J.; Gong, Peng, J.; Qi, D.S; Xing, J.J.; Sun, Z.H. and Fan, M.Z. (2005): Effect of dietary supplementation of chitosan and galacto-mannan-oligosaccharide on serum parameters and the insulin-like growth factor-I mRNA expression in early-weaned piglets. Domest. Anim. Endocrinol. 28: 430–441.
Ten Bruggencate, S.J.M.; Bovee-Oudenhoven, I.M.J.; Lettink-Wissink, M.L.G. and Van Der Meer, R. (2003): Dietary fructo-oligosaccharides dose-dependently increase translocation of salmonella in rats. Journal of Nutrition 133: 2313-2318.
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