摘要
选用1日龄AA肉鸡240只,随机分为4个处理,每个处理6个重复,每个重复10只鸡。处理一为基础日粮组,处理二、三、四分别添加2.5%血浆蛋白粉(SDPP)替代基础日粮中部分蛋白饲喂7、14、21d后,换喂相同日粮直到49d试验结束。前期饲喂21d后,从每个处理中选择接近平均体质量健康鸡8只腹腔注射大肠杆菌O2攻毒。结果表明:(1)前期1-14d连续添加SDPP生产成绩最好,显著高于处理-(P〈0.05)。后期和全期以1-21d添加的生产性能略好,与1-14d差异不显著。(2)添加SDPP提高了肉鸡Ea、Et、脾脏指数、胸腺指数和法氏囊指数,极显著(P〈0.01)提高淋巴细胞转化率。(3)SDPP明显降低肉鸡死亡率。结果表明,在1-14d添加SDPP,可促进肉鸡生长,增强免疫功能,前期获得最佳ADG的时间是饲喂1-14d。该饲喂时间肉鸡抗菌能力最强。
The experiment was conducted to investigate the effect of SDPP supplied during different stages on growth performance and immune function of broilers. 240 1-day-old Arbor Acres broilers were randomly allotted into 4 treatments with 6 replicates of 10 broilers each (5 females and 5 males). Treatments consisted of the group fed basal diet and groups fed diets containing 2.5% SDPP from 1-7 d, the second weekend and the third weekend, respec-tively. Then all of the four treatments were replaced by the same basal diet. On the 22ed,eight chickens with proximal average body weight (M:F=1:1) selected from every treatment were enforced peritoneal injection with Escherichia, coli O2, respectively. The results showed that: (1)the group fed the diet with SDPP lasted 14 d had the best performance and was significantly better than the control(P〈0.05) ,the group fed the diet with SDPP from 1 to 21 d had a better performance during later stage and holo-stage, but had no significant difference compared with the group fed the diet with SDPP lasted 14d; (2) SDPP increased Ea,Et and immune organs index,and the lymphocyte proliferation response was significantly increased(P〈0.01);(3) SDPP obviously decreased mortality of the broilers. It is concluded that fed the diet with SDPP from 1 to 14 d has an auxoaction on performance and immune function of broiler. The optimal last time of feeding SDPP during the early stage is 14 d to get the best ADG and antibiotic ability.
出处
《中国兽医学报》
CAS
CSCD
北大核心
2009年第11期1485-1488,1494,共5页
Chinese Journal of Veterinary Science
基金
教育部长江学者和创新团队发展计划资助项目(IR-TO555)
关键词
血浆蛋白粉
肉鸡
生产性能
免疫功能
死亡率
broilers
spray-dried porcine plasma
performance
immune function
mortality