Tarpey I, Orbell S J, Britton P, Casais R, Hodgson T, Lin F, Hogan E, Cavanagh D
Intervet UK, Walton Manor, Walton, Milton Keynes, Bucks, UK.
Vaccine. 2006 Nov 17;24(47-48):6830-8. doi: 10.1016/j.vaccine.2006.06.040. Epub 2006 Jul 5.
Commercial vaccines for in ovo vaccination have not yet been developed for infectious bronchitis virus (IBV), the major coronavirus in the poultry industry. Recombinant IBVs based on the Beaudette strain expressing the Beaudette spike protein (Beau-R) or that from the virulent M41 strain (BeauR-M41(S)) were assessed for their potential as prototype vaccines for application to 18-day-old embryos. Pathogenicity was assessed by observing the effect on hatchability, and/or the production of nasal discharge and/or the effects on ciliary activity in the trachea at various time points post hatch. In contrast to commercial IBV vaccines given in ovo, the Beau-R and BeauR-M41(S) strains did not reduce hatchability or cause nasal discharge, and caused minimal damage to the ciliated epithelium of the trachea. The presence of the spike protein from a virulent virus did not increase the pathogenicity of the virus according to the criteria used. Assessment of the BeauR-M41(S) strain for efficacy showed that it protected up to 90% of chicks against challenge with virulent IB virus (M41) in a dose dependent manner. Further egg passage of the BeauR-M41(S) strain (BeauR-M41(S) EP10) did not increase its pathogenicity though it did improve its efficacy, based on serology and protection against a virulent challenge. BeauR-M41(S) EP10 was more efficacious than BeauR-M41(S) protecting more birds against virulent challenge and providing a better serological antibody response. BeauR-M41(S) EP10 induced a serological response similar to that of a commercial vaccine given at day-old though the commercial vaccine provided slightly higher efficacy. These results are promising for the development of embryo safe efficacious IBV vaccines for in ovo application.
针对家禽业主要冠状病毒传染性支气管炎病毒(IBV),尚未开发出用于卵内接种的商业疫苗。对基于表达Beaudette刺突蛋白的Beaudette毒株(Beau-R)或强毒株M41(BeauR-M41(S))构建的重组IBV进行了评估,以确定其作为适用于18日龄胚胎的原型疫苗的潜力。通过观察对孵化率的影响、鼻液分泌情况和/或孵化后不同时间点对气管纤毛活动的影响来评估致病性。与卵内接种的商业IBV疫苗不同,Beau-R和BeauR-M41(S)毒株不会降低孵化率或引起鼻液分泌,对气管纤毛上皮的损伤也最小。根据所使用的标准,来自强毒株的刺突蛋白的存在并未增加病毒的致病性。对BeauR-M41(S)毒株的效力评估表明,它能以剂量依赖的方式保护高达90%的雏鸡免受强毒IB病毒(M41)的攻击。基于血清学和对强毒攻击的保护作用,BeauR-M41(S)毒株的进一步传代(BeauR-M41(S) EP10)虽然没有增加其致病性,但确实提高了其效力。BeauR-M41(S) EP10比BeauR-M41(S)更有效,能保护更多的鸡免受强毒攻击,并产生更好的血清学抗体反应。BeauR-M41(S) EP10诱导的血清学反应与一日龄接种的商业疫苗相似,不过商业疫苗的效力略高。这些结果为开发用于卵内接种的胚胎安全有效IBV疫苗带来了希望。