Li Yanpeng, Kang Mengjiao, Su Shuai, Ding Jiabo, Cui Zhizhong, Zhu Hongfei
The Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Wei Sheng Wu Xue Bao. 2010 Jul;50(7):942-8.
To evaluate the immuno-protective effect of GX0101 deltameq-BAC containing an infectious meq-null Marek's disease virus genome.
One-day-old SPF birds were reared separately in isolators with positive filtered air. On day 1 of age, chickens immunized with 101 microg of GX0101A deltameq-BAC suspended in PBS, challenge infection with 500PFU very virulent rMD5 was performed at day 5 and 12 post-immunization separately. During 90 days after challenge, all bird were recorded and checked for necropsy. The samples of heart and liver were collected for histo-sections.
The protective index of the two vaccines used was 87 and 33 for CVI988/Rispens and GX0101 deltameq-BAC, respectively, after challenged with the very virulent virus rMd5 at day 5 post-immunization. When challenged with rMd5 at day 12 post-immunization, the protection index of GX0101 deltameq-BAC increased to 53%.
Except that GX0101 deltameq-BAC can confer protection against very virulent Marek's disease virus, a delay in the development of Marek's disease could be observed in some chickens vaccinated with GX0101 deltameq-BAC. On the other hand, compared with CVI988/Rispens, the reconstruction of GX0101 deltameq-BAC in the body is a prerequisite for access to protection. Therefore, there is a blank period after immunization, which provides a chance for infection with the wild Marek's disease virus.
评估含有传染性meq基因缺失的马立克氏病病毒基因组的GX0101三角体meq - BAC的免疫保护效果。
1日龄SPF鸡在装有正压过滤空气的隔离器中单独饲养。1日龄时,用101微克悬浮于PBS中的GX0101A三角体meq - BAC对鸡进行免疫,分别在免疫后第5天和第12天用500PFU超强毒rMD5进行攻毒感染。攻毒后90天内,记录所有鸡的情况并进行剖检检查。采集心脏和肝脏样本进行组织切片。
免疫后第5天用超强毒病毒rMd5攻毒后,所用两种疫苗CVI988/Rispens和GX0101三角体meq - BAC的保护指数分别为87和33。免疫后第12天用rMd5攻毒时,GX0101三角体meq - BAC的保护指数增至53%。
除GX0101三角体meq - BAC能对超强毒马立克氏病病毒提供保护外,在一些接种GX0101三角体meq - BAC的鸡中可观察到马立克氏病发病延迟。另一方面,与CVI988/Rispens相比,GX0101三角体meq - BAC在体内的重组是获得保护的前提条件。因此,免疫后存在一个空白期,这为野生马立克氏病病毒感染提供了机会。