首页> 美国卫生研究院文献>EFSA Journal >Safety and efficacy of B‐Act® (Bacillus licheniformis DSM 28710) as a feed additive for turkeys for fattening turkeys reared for breeding and minor poultry species for fattening or raised for laying
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Safety and efficacy of B‐Act® (Bacillus licheniformis DSM 28710) as a feed additive for turkeys for fattening turkeys reared for breeding and minor poultry species for fattening or raised for laying

机译:B‐Act®(地衣芽孢杆菌)的安全性和有效性DSM 28710)用作火鸡育肥的饲料添加剂火鸡饲养用于育种次要家禽品种用于育肥或饲养用于产蛋

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摘要

Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed was asked to deliver a scientific opinion on the safety and efficacy of B‐Act when used in feed for turkeys for fattening, reared for breeding and minor poultry species for fattening or raised for laying. B‐Act is a preparation containing viable spores of a strain. This species is considered by to be suitable for the qualified presumption of safety ( ) approach to safety assessment, which requires the identity of the strain to be established and evidence that it is not toxigenic and does not show acquired resistance to relevant antibiotics. In a previous opinion, the strain was found to meet the criteria for the approach. Since no concerns are expected from other components of the additive, B‐Act is presumed safe for the target species, consumers and the environment. In the same opinion, no conclusions could be drawn on the skin/eye irritation or skin sensitisation potential of the additive, but B‐Act was considered a potential respiratory sensitiser. Since the use of B‐Act with the target species is considered unlikely to introduce hazards for users of the product not already considered, the conclusions previously reached apply to the current application. B‐Act at the recommended dose of 1.6 × 10  colony forming units ( )/kg feed has the potential to be efficacious in turkeys for fattening. Since the same dose is proposed for the minor poultry species for fattening or raised for laying, the conclusions can be extended/extrapolated to these species. The conclusions on the compatibility of B‐Act with coccidiostats previously drawn apply to the current application provided that the maximum authorised concentrations of the coccidiostats for the target species are equal/lower than those for chickens.
机译:应欧洲委员会的要求,动物饲料中使用的添加剂和产品或物质小组被要求对B-Act在火鸡,育肥和小规模饲养的饲料中使用时的安全性和有效性发表科学意见。家禽品种,用于育肥或饲养。 B-Act是一种含有菌株活孢子的制剂。该物种被认为适合用于安全性评估的合格安全性推定()方法,该方法要求确定菌株的身份并证明其不是产毒的,并且不显示对相关抗生素的耐药性。在以前的意见中,发现该菌株符合该方法的标准。由于不会担心添加剂的其他成分,因此可以认为B-Act对目标物种,消费者和环境都是安全的。在同一意见中,无法就该添加剂的皮肤/眼睛刺激或皮肤致敏潜力得出任何结论,但B-Act被认为是潜在的呼吸致敏剂。由于认为将B-Act与目标物种一起使用不会给尚未考虑产品的用户带来危害,因此先前得出的结论适用于当前应用。 B-Act的建议剂量为1.6×10菌落形成单位()/ kg饲料,可能对火鸡育肥有效。由于建议对次要家禽品种进行相同剂量的育肥或饲养,因此结论可以扩展/外推到这些品种。先前得出的B-Act与抗球虫药的相容性结论适用于当前应用,只要目标物种的抗球虫药的最大授权浓度等于/低于鸡的水平即可。

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