Awad Faez, Hutton Sally, Forrester Anne, Baylis Matthew, Ganapathy Kannan
a Institute of Infection and Global Health, Leahurst Campus, Neston, Cheshire , UK.
b Faculty of Veterinary Medicine , University of Omar Al-Mukhtar , Al-Bayda , Libya.
Avian Pathol. 2016;45(2):169-77. doi: 10.1080/03079457.2015.1137866.
Groups of one-day-old broiler chicks were vaccinated via the oculo-nasal route with different live infectious bronchitis virus (IBV) vaccines: Massachusetts (Mass), 793B, D274 or Arkansas (Ark). Clinical signs and gross lesions were evaluated. Five chicks from each group were humanely killed at intervals and their tracheas collected for ciliary activity assessment and for the detection of CD4+, CD8+ and IgA-bearing B cells by immunohistochemistry (IHC). Blood samples were collected at intervals for the detection of anti-IBV antibodies. At 21 days post-vaccination (dpv), protection conferred by different vaccination regimes against virulent M41, QX and 793B was assessed. All vaccination programmes were able to induce high levels of CD4+, CD8+ and IgA-bearing B cells in the trachea. Significantly higher levels of CD4+ and CD8+ expression were observed in the Mass2 + 793B2-vaccinated group compared to the other groups (subscripts indicate different manufacturers). Protection studies showed that the group of chicks vaccinated with Mass2 + 793B2 produced 92% ciliary protection against QX challenge; compared to 53%, 68% and 73% ciliary protection against the same challenge virus by Mass1 + D274, Mass1 + 793B1 and Mass3 + Ark, respectively. All vaccination programmes produced more than 85% ciliary protection against M41 and 793B challenges. It appears that the variable levels of protection provided by different heterologous live IBV vaccinations are dependent on the levels of local tracheal immunity induced by the respective vaccine combination. The Mass2 + 793B2 group showed the worst clinical signs, higher mortality and severe lesions following vaccination, but had the highest tracheal immune responses and demonstrated the best protection against all three challenge viruses.
将一日龄的肉鸡雏鸡分组,通过眼鼻途径用不同的传染性支气管炎病毒(IBV)活疫苗进行接种:马萨诸塞州(Mass)株、793B株、D274株或阿肯色州(Ark)株。评估临床症状和大体病变。每隔一段时间对每组的5只雏鸡实施安乐死,并收集它们的气管用于评估纤毛活性,以及通过免疫组织化学(IHC)检测CD4⁺、CD8⁺和含IgA的B细胞。每隔一段时间采集血样用于检测抗IBV抗体。在接种疫苗后21天(dpv),评估不同接种方案对强毒株M41、QX和793B的保护作用。所有接种方案均能在气管中诱导高水平的CD4⁺、CD8⁺和含IgA的B细胞。与其他组相比,接种Mass2 + 793B2疫苗的组中CD4⁺和CD8⁺表达水平显著更高(下标表示不同的生产商)。保护研究表明,接种Mass2 + 793B2疫苗的雏鸡组对QX攻击产生了92%的纤毛保护;相比之下,接种Mass1 + D274、Mass1 + 793B1和Mass3 + Ark疫苗的组对同一攻击病毒的纤毛保护率分别为53%、68%和73%。所有接种方案对M41和793B攻击均产生了超过85%的纤毛保护。不同的异源IBV活疫苗接种所提供的保护水平似乎取决于各自疫苗组合诱导的局部气管免疫水平。Mass2 + 793B2组在接种疫苗后表现出最严重的临床症状、更高的死亡率和严重病变,但具有最高的气管免疫反应,并对所有三种攻击病毒表现出最佳保护。