The experiment was conducted at ICAR-Directorate of Poultry Research, Rajendranagar, Hyderabad, India from July to August 2017.
Rice-DDGS samples and experimental diets
Two lots of r-DDGS,
viz. high protein (57% CP) and medium protein (47% CP) were procured from the market (M/s M.I. Feed Industries, Thane, Maharashtra and M/s Prorich Agro Foods, Panchkula, Haryana, respectively) and analysed for proximate composition (
AOAC, 2016). The amino acid profile of r-DDGS was analysed employing wet chemistry (courtesy Evonik, Mumbai, India). A maize-soybean meal-based diet was compounded to serve as the control. Another 2 sets of diets were compounded containing high protein and medium protein r-DDGS, each at 5 and 10% level in the diet, thus making a total of 5 experimental diets (Table 1). All the diets were maintained
isocaloric and
isonitrogenous so as to eliminate the possible influence of nutrient variation on the performance and other variables of chickens
.
Chicks and management
A total of 300 numbers of Vanaraja straight run chicks were procured from the Experimental Hatchery of ICAR-Directorate of Poultry Research, Hyderabad at day-old and divided into 5 treatment groups with 10 replicates of 6 chicks each and housed in 3-tiered raised wire floor SS battery brooder pens (2' × 2.5'/replicate) in an open-sided poultry house. The chicks were brooded by providing supplementary heat till 4 weeks of age using incandescent bulbs. The chicks were vaccinated against Newcastle and Infectious bursal diseases as per the standard schedule. Each of these experimental groups was fed one of the five experimental diets
ad libitum from 0 to 6 weeks of age (Table 1). The nutrient concentration of various diets was maintained uniform during the experimental period to meet the requirements of Vanaraja chicks. The chicks were maintained under uniform managemental conditions throughout the trial.
Data collection
The effect of r-DDGS on body weight, feed intake and FCR (feed/body weight gain) was assessed at weekly intervals. The body weight was recorded prior to feeding the chicks. At 6 weeks of age, about two to three ml of blood was collected through the brachial vein from 10 chickens in each treatment group into non-heparinised tubes. Subsequently, serum was separated and analysed for the concentrations of total protein and cholesterol using reagent kits (Qualigens, Mumbai, India). At 6 weeks of age, one bird from each replicate (total 10 birds per treatment) were killed by decapitation and data on dressing yields and weights of visceral and lymphoid organs were recorded. Abdominal fat was collected as per
Fancher and Jensen (1989). The weights were expressed relative to kg live weight. A piece of breast muscle from each carcass was collected, dried in a hot air oven at 80°C for 12 hours and analysed for crude protein content
(AOAC, 2016). At the end of the experiment, a 3-day digestibility experiment was performed on a total of nine chicks, selected at random from each treatment and housed in three pens (2'×2.5') with three chicks each. The relative digestibility of dry matter was estimated by determining the proportion of the consumed amount that was retained. The experiment was conducted as per the guidelines of the Institute’s Animal Ethics Committee with their due approval.
Statistical analysis
The data were subjected to one-way analysis of variance under completely randomised design (
Snedecor and Cochran, 1968) using SPSS software (version 15) and the means were compared by multiple range test (
Duncan, 1955). The level of significance was considered at P≤0.05. Each replicate group was considered as the experimental unit for the data on body weight, feed intake, FCR and digestibility estimates, whereas for serum biochemical variables, the data of individual birds were considered for statistical analysis.