Effect of probiotic supplementation on growth,nitrogen utilisation and serum cholesterol in broilers

1. The effect of dietary probiotic supplementation on the growth, nitrogen utilisation and serum cholesterol content of broiler chickens was studied in 2 trials.

2. In experiment 1, the birds receiving the 0, 75, 100, 125 mg probiotic/kg diets had weight gains of 1204.0, 1272.0, 1268.3 and 1210.5 g, respectively at the end of 8 weeks of feeding. The group of birds fed on the 75 mg probiotic supplemented diet retained significantly (P<0.01) more nitrogen than the control birds. Serum cholesterol content was lower in the probiotic‐supplemented birds (93.3 mg/100 ml) compared to the control birds (132.2 mg/100 ml).

3. In the second experiment the probiotic plus antibiotic‐supplemented group of birds had the maximum weight gain (1148.5 g) followed by antibiotic (1141.3 g), probiotic‐supplemented (1128.4 g) and control birds (1045.6 g) after 6 weeks. Nitrogen retention was greatest in the antibiotic—(48.5%) followed by the probiotic—(46.5%), probiotic plus antibiotic‐supplemented groups (46.3%) compared to 40.2% in control birds.

4. The apparent metabolisable energy was greatest in birds receiving the probiotic plus antibiotic‐supplemented diet (12.37 MJ/kg) followed by antibiotic—(12.00 MJ/kg), probiotic‐supplemented birds (11.92 MJ/kg) than in control birds (11.62 MJ/kg). Serum cholesterol was significantly (P<0.01) lower in probiotic‐supplemented birds (86.1 mg/dl) compared to 118.4 mg/dl in control birds.     

Influence of dietary magnesium content on laying performance and egg shell magnesium content in the domestic hen

1. The effects of feeding diets containing various amounts of magnesium on laying performance in the domestic hen were investigated.

2. A reduction in egg number, egg mass, egg shell thickness and egg shell magnesium content occurred in birds receiving diets containing either 207 or 132 mg Mg²⁺/kg even though the duration of egg formation was unaffected.

3. The progressive increase in magnesium content normally observed towards the outer surface of the hen's egg shell was not present in birds receiving a diet containing 207 mg Mg²⁺/kg.     

The response of cage‐reared broiler cockerels to dietary supplements of nitrovin,zinc bacitracin or penicillin used singly or in paired combinations

1. The effect of feeding diets supplemented with procaine penicillin (50 mg/kg), zinc bacitracin (25 mg/kg) or nitrovin (20 mg/kg) singly or in combinations on the performance of broiler cockerels from 1 to 56 d was assessed.

2. The growth of treated birds was significantly better than that of controls fed on a basal diet, but no combination of additives was significantly superior to the additives given singly.

3. Performance up to 56 d of birds fed continuously on a diet supplemented with zinc bacitracin (25 mg/kg) from 1 d old was better than that obtained when the supplement was either introduced or withdrawn at different ages.     

Feeding behaviour in chickens given diets containing medium chain triglyceride

1. The effect of dietary medium chain triglyceride (MCT) on short‐term food intake was compared with the effect of long chain triglyceride (LCT) in chickens. Maize oil was used as the LCT while glyceryl tricaprylate (C 8) and glyceryl tricaprate (C 10) were used as MCT. Cumulative food intake was determined during the 6 h after the start of feeding.

2. Chicks were given diets containing 200 g C 8/kg diet, 200 g C 10/kg diet or 200 g LCT/kg diet in experiment 1. As early as 30 min after feeding, cumulative food intake in both MCT‐supplemented diets decreased significantly compared with the diet containing LCT.

3. To determine if endogenous cholecystokinin (CCK) was responsible for the decrease in food intake caused by MCT, birds were injected with the CCK‐A receptor antagonist devazepide (DVZ, 1 mg/kg BW) before diet presentation. DVZ had no effect on food intake with either LCT‐ or MCT‐supplemented diets.

4. In experiment 3, chicks were given a choice between either diets containing LCT and C 8, LCT and C 10, or C 8 and C 10 to confirm whether or not the palatability of the diets was influenced by the dietary fat sources. There was no difference in food intake between C 8 and C 10‐supplemented diets. However, chicks preferred the LCT‐supplemented diet compared with either of the diets containing MCT.     

Effect of probiotic supplementation on serum/yolk cholesterol and on egg shell thickness in layers

1. The effect of probiotic supplementation on egg production, on serum and yolk cholesterol and on egg shell thickness in 24 White Leghorn layers was studied from 28–38 weeks of age.

2. In 3 treatments the diet was supplemented with 0, 100 and 150 mg probiotic/kg food.

3. In the 100 mg probiotic group, egg production improved by 5%, and shell thickness improved slightly, with fewer thin‐shelled eggs than in the control (8.6% compared to 18.6%).

4. The initial serum cholesterol concentration of 170.2 mg/dl in control birds remained similar throughout the 10‐week experimental period, whereas in the 150 mg group the initial value of 176.5 mg/dl decreased to 114.3 mg by week 10.

5. Yolk cholesterol concentration was 14.69 mg in the control group and 11.28 and 11.37 mg/g in the 100 and 150 mg probiotic groups respectively. Overall mean total egg cholesterol was thus reduced by probiotic supplementation.     

Sulphur amino acid requirement of laying hens and the effects of excess dietary methionine on laying performance

1. Individually‐caged laying hens were fed on maize‐soya bean meal diets containing 11.50 or 12.35 MJ ME/kg with sulphur amino acid (SAA) contents varying from 5.0 to 7.0 g/kg in period 1 (0 to 20 weeks); from 5.0 to 8.0 g/kg in period 2 (21 to 36 weeks) and from 5.0 to 10.0 g/kg in period 3 (37 to 52 weeks).

2. A SAA requirement of about 750 mg/hen d, of which about 425 mg was methionine, was found to be adequate for birds producing on average 51 g egg mass per hen d over 52 weeks. The SAA requirement was found to be higher for maximum efficiency of food utilisation than for maximum egg yield.

3. A diet containing 140 g protein/kg adequately supplemented with methionine and lysine, could sustain laying performance almost identical to that achieved on a diet containing 167 g protein/kg.

4. In diets with 140 g protein/kg the addition of 0.5 to 3.5 g dl‐methionine/kg diet in excess of the requirement did not affect egg production adversely, but food conversion efficiency was decreased.     

Laboratory model for the detection of poultry growth promotants

A laboratory model is described which allows the effective screening for compounds possessing antibacterial activity to increase growth and improve the conversion of food in poultry. The model utilises birds from 1 to 4 d of age with the supplements fed for 14 to 11 d, respectively, at 50 mg/kg in a high energy, commercial‐type broiler starter ration.

The antibiotics tested and found active in the screening test include penicillin, penicillin and streptomycin, zinc bacitracin, chlortetracycline, erythromycin, lincomycin, bambermycins (moenomycin), neomycin, novobiocin, fosfomycin and thiopeptin. The non‐antibiotic anti‐bacterial, nitrovin, was also effective. Diethyl‐stilbestrol, melengestrol acetate, zeranol and reserpine were inactive. Thus, the screening procedure is responsive to compounds possessing antibacterial activity but not to compounds with hormonal anabolic activity or tranquilising‐sedative activity.

The test also reflects the effects of “ clean ” and “ new ” quarters by increased growth and improved food conversion seen in both the unsupplemented and penicillin‐supplemented groups with the antibiotic effect temporarily lost or greatly reduced.

This laboratory test is quick and efficient, and the results obtained are consistant, reproducible and statistically significant.     

The feeding of penicillin to goslings

A total of 180 crossbred Chinese/Emden goslings were either housed indoors for 8 weeks or kept inside for 4 weeks and then allowed to graze. Within each experimental group the birds were fed on diets with or without added penicillin. The antibiotic was included at either 55 mg/kg or 110 mg/kg.

Only when the goslings were fed throughout on a diet supplemented with penicillin at an inclusion rate of 110 mg/kg was there significant growth promotion.

No significant differences in the weights of the liver, gizzard, small intestine or caeca, or in the average weights of 1 cm lengths of the small intestines and caeca could be detected.     

Effects on egg production of including high residual lipid copra meal in laying hen diets

1. The effects on egg production of including copra meals of 220.9 (Copra‐1) and 205.0 (Copra‐2) g residual lipids/kg, in laying hen diets at up to 400 g/kg, were examined in two feeding trials. In a separate experiment, the dry matter retention and ME of a 400 g Copra‐2/kg diet were determined between 6 to 9, 9 to 12 and 12 to 15 d of feeding.

2. Food intakes, egg output and efficiencies of food utilisation (g eggs/g food) of hens fed on Copra‐1 at 100 and 200 g/kg diet were not significantly different from controls; while food intakes at 400 g Copra‐1/kg diet were similar to controls, egg output (6.0% lower), efficiency of food utilisation and body weights of hens were significantly reduced. Hens fed Copra‐2 at 400 g/kg diet had 5.0 and 6.9% lower food intakes and egg output, respectively, and lost body weight compared to controls; however, egg output increased to that of the control group by the 11th week of feeding.

3. Initially, dry matter retention of the 400 g Copra‐2/kg diet was similar to, and ME slightly higher than the control diet; however, both were reduced significantly in the second and third collection periods. The water content of excreta from hens fed on 400 g Copra‐2/kg diet was significantly higher than that from controls.

4. Complete replacement of dietary maize, mainly with copra (experiment 1) led to an increase in pale yolks, with the 400 g Copra‐1/kg diet producing cream‐coloured yolks. Inclusion of maize at 180.6 g/kg of the 400 g Copra‐2/kg diet (experiment 2) resulted in eggs with slightly golden‐yellow yolks.     

Effects of an induced pause in egg production and supplementation of the diet with iron on egg shell colour,quality and performance of brown egg layers

1. A pause in egg production was induced in brown‐egg laying hens, aged 68 weeks, by feeding them whole oats for 7 d. Subsequently, these hens, together with control groups, were given laying diets with either 400 or 600 mg/kg iron. The 200 mg/kg of supplemental iron was added in the form of either ferrous sulphate or iron proteinate (chelated iron).

2. The feeding of whole oats halted egg production in 5.7 ±0.22 d and the duration of the pause was 8.3 ±0.78 d.

3. The induction of a pause improved the subsequent rate of egg production, egg output, efficiency of food utilisation, albumen quality, egg specific gravity and shell colour. It also increased food intake and body weight gain but neither egg weight nor the rate of mortality were affected.

4. Neither supplementation of the diet with iron nor its source had any significant effect on laying performance, egg quality or shell colour.     

Comparative study of the effects of organic selenium on hen performance and productivity of broiler breeders

1. A 10-week experiment was conducted with Ross 308 broiler breeder chickens in cages to evaluate the influence of organic and inorganic sources of selenium (Se) supplementation. A total of 600 birds at 29 weeks of age were divided at random into 4 groups and fed on a maize–soya basal diet supplemented with different forms of Se.

2. The first (control) group was given the basal diet without Se supplementation, whereas the second, third and fourth groups were given, respectively, the basal diet with 0.3 mg/kg of inorganic Se in the form of sodium selenite or 0.3 and 0.5 mg/kg of organic Se in the form of Se enriched yeast (Se-yeast).

3. The experiment was carried out for 10 weeks to compare and evaluate the influence of Se supplementation on breeder performance, egg production, hatchability and the quality of eggs. Samples were collected for analysis at weeks 0, 5 and 10 of the experimental period.

4. At the end of the experiment (39 weeks), there was a reduction in mortality in breeders given diets supplemented with 0.5 mg/kg of Se-yeast. Supplementation of feed with 0.5 mg/kg organic Se increased egg production, percentage of settable eggs and hatchability.

5. Selenium supplementation increased egg weight and specific gravity compared to the control diet. However, no significant variation was found in albumen or yolk protein content at the end of week 10.

6. Selenium accumulation and glutathione peroxidase (GSHPx) activity were lower in the egg albumen and yolk of control compared with Se-supplemented treatments. Se accumulation and GSHPx activity were higher in the group given 0.3 mg/kg organic compared to 0.3 mg/kg of inorganic Se.

7. The results favour the use of Se-yeast at the dose of 0.5 mg/kg in broiler breeder diets for better productivity of eggs, settable eggs, hatchability and higher Se accumulation and antioxidant status in eggs.     

Responses of laying hens to a low‐protein diet supplemented with essential amino acids,l‐glutamic acid and/or intact protein

1. Three sequential experiments, each lasting 8 weeks, were carried out on 576 singly‐caged light hybrids.

2. In experiment 1 egg production was 84% using a conventional control diet, 61% with a basal low‐protein diet, and 79% with the basal diet supplemented with 10 essential amino acids + L‐glutamic acid (GA).

3. In experiment 2 supplementation with lysine and methionine (L + M) alone increased egg production significantly from 54 to 72%, compared with 83% with the conventional diet.

4. In experiment 3 egg production was 55% with the basal diet, 71% with the basal diet + L + M, 75% with a diet containing 141 g protein/kg + L + M, and 73% with the conventional diet.

5. In all three experiments supplementation with GA alone either gave no significant response or a depression in production.

6. Daily intakes of 1.24 g nitrogen as non‐essential amino acids and 13 to 14 g total crude protein per bird resulted in good egg production. Supplementation of the basal diet with L + M resulted in a daily intake of 413 mg methionine/bird day which was considered adequate, and a daily intake of 710 mg lysine which was considered slightly inadequate.     

The effects of lactoferrin on the intestinal environment of broiler chickens

1. The influence of in-feed lactoferrin (Lf) on bird production, intestinal microbiota, mucosal immune system and gut microarchitecture was assessed in male Cobb 500 broiler chickens.

2. Birds were given one of four diets from day of hatch: Control (basal diet with no additives), ZnB (basal diet?+?50?mg/kg zinc bacitracin), Lf 250?mg/kg (basal diet?+?250?mg/kg Lf) and Lf 500?mg/kg (basal diet?+?500?mg/kg Lf); n?=?24 birds/treatment. An apparent metabolisable energy study was performed between d 25-32.

3. Lf did not affect growth rate or feed conversion in the period 0-21?d of age, nor performance or energy metabolism during the 7?d metabolism experiment which commenced at 25?d of age.

4. The profiles of caecal microbial communities were significantly different in birds given ZnB compared with birds given a diet with no additives, or supplemented with 250?mg/kg Lf. Birds given 250?mg/kg Lf also had a different microbial profile compared with birds given 500?mg/kg Lf.

5. In comparison to control birds, Lf treated birds showed some differences in the T cell proportions in caecal tonsil and spleen. No differences in ileal villus height, crypt depth or goblet cell proportions were observed amongst dietary treatments.

6. Whilst Lf had little effect on the measured parameters, the use of an integrated approach to study the influence of novel feed additives may facilitate a greater understanding of the relationships between nutrition, gut health and bird performance.     

Effects of restricting the amounts of medium or low‐energy diets fed to laying hens in different colony sizes

1. Light hybrid hens between 32 and 68 weeks of age kept 4, 5 or 8 birds to the cage received one of three energy intakes, from a medium‐ or low‐energy diet.

2. Ad libitum fed birds laid more and heavier eggs than any of those restricted. A decrease in daily egg output of about 5 g was associated with each 100 kJ decrease in daily intake of metabolisable energy.

3. For the same energy intake, egg output of birds fed on the low‐energy diet was markedly greater than that associated with the medium‐energy diet.

4. The mortality of birds receiving restricted quantities of the medium‐energy diet was two to three times greater than that associated with similar rationing of the low‐energy diet.     

Performance of laying hens fed on low sulphur amino acids diets supplemented with choline and methionine

1. Two experiments were carried out to examine the possibility of replacing a part of the methionine content with choline in a layers’ diet.

2. In the first a low methionine diet with 2.6 g methionine/kg was supplemented with 0.3, 0.6, 0.9 and 1.2 g DL‐methionine/kg. Choline at 1.12 g/kg was added to the diets, which contained 5.4, 6.0 and 6.6 g TSAA.

3. In the second diets with 3.02, 3.80, 4.53, 5.30, 6.04 and 6.51 g TSAA/kg were used and 0.94 g choline/kg was added to these diets.

4. Supplemental methionine increased egg production but not egg weight in the first experiment. When the low TSAA diet was supplemented with choline, egg output increased slightly but not significantly.

5. When supplemental methionine was added to the low protein and TSAA diets in experiment 2 it increased egg production and egg weight. Added choline did not increase egg production or egg weight, even with the diet very low in protein and TSAA. Body weight gain, food intake and feed conversion efficiency of food utilisation were improved by supplemental methionine but not choline.     

Response of broiler chicks to threonine‐supplemented diets to 4 weeks of age

1. Two experiments were carried out to determine the response of broiler chicks to threonine‐supplemented diets between 10 and 28 d and 7 and 21 d of age, respectively.

2. In the first experiment female broiler chicks were fed on 11 experimental diets. Two iso‐energetic basal diets (diets 1 and 2) were prepared with 200 and 160 g CP/kg and 7·6 and 6·0 g threonine/kg respectively. Both diets contained 11·5 g lysine and 8·7 g sulphur‐containing amino acids/kg. Diet 3 was composed of diet 2, supplemented with all essential and non‐essential amino acids (EAA and NEAA, respectively) except threonine, to the concentrations of the amino acids in diet 1. The NEAA were added as a combination of glutamic acid and glycine. Diets 4 to 11 had the same compositions as diet 3, but contained increasing amounts of threonine.

3. For birds fed on diet 2, gain was significantly lower and food/gain ratio was significantly higher than for birds fed on diet 1. Supplementation with EAA, NEAA and threonine to the same concentrations in diet 1 resulted in a performance similar to that found on diet 1.

4. In experiment 2, male and female broiler chicks both received 10 experimental diets. Diet 1 contained 220 g CP/kg and 8.5 g threonine/kg, diet 2 contained 160 g CP/kg from natural raw materials and 6 g threonine/kg. Both diets contained 12·4 g lysine and 9·3 g sulphur‐containing amino acids/kg. Basal diet 2 was supplemented with all EAA and NEAA to the concentrations of basal diet 1, except for threonine. Diets 3 to 10 had the same compositions as the supplemented diet 2, but contained increasing amounts of threonine.

5. For male and female chicks on diet 2, gain was significantly lower and food/gain ratio significantly higher than those on diet 1. Diet 10 (160 g CP/kg plus all EAA, including threonine, and NEAA supplemented to the concentrations of diet 1) resulted in the same performance as diet 1.

6. The results indicate that, when low protein maize‐soyabean meal diets supplemented with EAA and NEAA with 13·31 MJ ME/kg were fed to male and female broiler chicks until 21 d of age, improvements in gain and food/gain ratio were obtained when the dietary threonine content was increased to 7·25 g/kg. When female chicks were fed threonine‐supplemented diets to 28 d of age, improvement in gain and food/gain ratio was obtained when the threonine concentrations were increased to 6·32 g/kg diet.

7. Curves have been fitted to the data, from which a cost‐benefit analyses can be made and an optimum threonine dose calculated, using local prices.     

Relationship between monensin and sulphur amino acid requirements IN broiler chickens

1. Diets containing 80, 100, 125, 150, 175 or 200 mg monensin/kg were fed to broiler chickens from 0 to 28 d in cages that prevented access to excreta.

2. Growth was depressed with 125 mg monensin or more/kg and food intake tended to decrease. Feathering was adversely affected with 175 mg or more/kg.

3. In a similar experiment, diets containing 8.8, 9.1, 9.4, 9.7 or 10.1 g total sulphur amino acids (SAA)/kg were supplemented with 125 or 80 mg monensin/kg and compared with a diet containing 8.8 g SAA and 33 mg robenidine/kg.

4. With 125 mg monensin/kg, body‐weight gain was significantly less than that of birds receiving robenidine if dietary SAA content was 9.4 g or less/kg. With 9.7 g SAA or more/kg, gain in birds receiving monensin was similar to that of birds receiving robenidine.

5. Monensin at 125 mg/kg therefore appears to increase the SAA requirement.     

Role of dietary γ‐linolenic acid in liver lipid metabolism in Japanese quail

1. The importance of linoleic acid (18:2n‐6) itself and of dietary y‐linolenic acid (18:3n‐6) as essential fatty acids (EFA) in Japanese quail were investigated with regard to liver lipid metabolism. Experimental diets were made by adding of 0, 2 or 4 g γ‐linolenic acid/kg, or 20 g linoleic acid/kg to an n‐6 EFA‐free diet. From 3 to 6 weeks of age, birds were fed equal amounts of experimental diets.

2. liver weight and lipid content in birds fed the 2 and 4 g γ‐linolenic acid/kg diet were significantly lower than those in birds fed the γ‐linolenic acid‐free diet. However, no significant difference was observed between the γ‐linolenic acid‐ and linoleic acid‐supplemented diets.

3. In birds fed the 4 g γ‐linolenic acid/kg diet, the proportion of arachidonic acid in the liver lipid was similar to that in quail fed the 20 g linoleic acid/kg diet, implying a conversion rate from linoleic acid to y‐linolenic acid of approximately 20% of whole body content.

4. It is concluded that linoleic acid itself is not essential for Japanese quail and that at least 2 g/kg of γ‐linolenic acid in the diet completely prevents liver enlargement accompanied by lipid accumulation.     

The nutrient intake of laying hens given a choice of diets,in relation to their production requirements

1. Sixty individually‐caged birds, each of two stocks, were offered either a complete diet (11.2 MJ ME, 173 g crude protein and 32 g Ca per kilogram) or a choice between the same diet and ground barley. All diets were offered ad libitum from 41 to 56 weeks of age.

2. Weight gain, rate of lay, mean egg weight, egg output, shell thickness and total food intake were unaffected by the treatments in either stock.

3. The mean intake of the complete diet was 825 and 845 g/kg of total intake with standard deviations between individuals of 73 and 61 g/kg respectively in the two stocks.

4. In birds given a choice of diet the one selected was related to output (P < 0.01).     

Incorporation of triticale in layer diets

1. Diets containing either maize or triticale were fed unsupplemented or supplemented with meat meal or groundnut oil to White Leghorn pullets for two periods of 11 weeks each.

2. The egg production of birds fed on the unsupplemented triticale diet was significantly higher than that of the birds fed on the unsupplemented maize diet, but was not significantly different from that of the birds fed on the maize plus meat meal diet.

3. Protein quality of the unsupplemented triticale diet as judged by efficiency of nitrogen retention was similar or inferior to that of the unsupplemented maize diet.

4. The higher protein content of triticale and the increased intake of these diets seemed to be responsible for the better performance observed.

5. Addition of groundnut oil to the triticale diet did not improve either egg weight or production.

6. It is concluded that the quantitative substitution for triticale of maize does not adversely affect egg production and egg weight.