Zhang Jun-Feng, Park Jong-Yeol, Kim Sang-Won, Choi Yu-Ri, Cha Se-Yeoun, Jang Hyung-Kwan, Wei Bai, Kang Min
College of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang 471003, China.
Department of Avian Diseases, College of Veterinary Medicine and Center for Avian Disease, Jeonbuk National University, Iksan 54596, Republic of Korea.
Vaccines (Basel). 2024 Feb 23;12(3):226. doi: 10.3390/vaccines12030226.
Infectious bursal disease (IBD), caused by IBD virus (IBDV), is an extremely contagious immunosuppressive disease that causes major losses for the poultry industry worldwide. Recently, the novel variant IBDV (G2d) has been highly prevalent in Korea, but the current vaccines against this very virulent IBDV have limited efficacy against this novel variant. To develop a vaccine against this variant IBDV, a recombinant virus designated rHVT-VP2 was constructed by inserting the IBDV (G2d) VP2 gene into herpesvirus of turkeys (HVT) using CRISPR/Cas9 gene-editing technology. The PCR and sequencing results obtained showed that the recombinant virus rHVT-VP2 was successfully constructed. Vaccination with rHVT-VP2 generated IBDV-specific antibodies in specific pathogen-free chickens starting from 2 weeks post-immunization. Seven days after the challenge, the autopsy results showed that the bursa atrophy rates of the rHVT-VP2, HVT, vaccine A, and positive control groups were 0%, 100%, 60%, and 100%, respectively, and the BBIX values were 1.07 ± 0.22, 0.27 ± 0.05, 0.64 ± 0.33, and 0.32 ± 0.06, respectively. These results indicate that rHVT-VP2 can provide 100% protection against a challenge with the IBDV (G2d), whereas vaccine A only provides partial protection. In conclusion, vaccination with the recombinant virus rHVT-VP2 can provide chickens with effective protection against variant IBDV (G2d).
传染性法氏囊病(IBD)由传染性法氏囊病病毒(IBDV)引起,是一种极具传染性的免疫抑制性疾病,给全球家禽业造成重大损失。最近,新型变异IBDV(G2d)在韩国高度流行,但目前针对这种超强毒力IBDV的疫苗对这种新型变异株的效力有限。为开发针对这种变异IBDV的疫苗,利用CRISPR/Cas9基因编辑技术将IBDV(G2d)VP2基因插入火鸡疱疹病毒(HVT)中,构建了一种名为rHVT-VP2的重组病毒。获得的PCR和测序结果表明重组病毒rHVT-VP2构建成功。用rHVT-VP2免疫无特定病原体鸡后,从免疫后2周开始产生IBDV特异性抗体。攻毒7天后,尸检结果显示,rHVT-VP2、HVT、疫苗A和阳性对照组的法氏囊萎缩率分别为0%、100%、60%和100%,BBIX值分别为1.07±0.22、0.27±0.05、0.64±0.33和0.32±0.06。这些结果表明,rHVT-VP2可提供100%的保护以抵抗IBDV(G2d)攻毒,而疫苗A仅提供部分保护。总之,用重组病毒rHVT-VP2免疫可使鸡有效抵抗变异IBDV(G2d)。