Long-Term Protection against Virulent Newcastle Disease Virus (NDV) in Chickens Immunized with a Single Dose of Recombinant Turkey Herpesvirus Expressing NDV F Protein

被引:1
作者
Shi, Bin [1 ]
Yang, Guifu [1 ]
Xiao, Yue [1 ]
Qian, Kun [1 ,2 ]
Shao, Hongxia [1 ,2 ]
Xu, Moru [1 ,2 ]
Qin, Aijian [1 ,2 ]
机构
[1] Yangzhou Univ, Key Lab Avian Prevent Med, Minist Educ, 12 East Wenhui Rd, Yangzhou 225009, Peoples R China
[2] Jiangsu Coinnovat Ctr Prevent & Control Important, 12 East Wenhui Rd, Yangzhou 225009, Peoples R China
关键词
Newcastle disease virus; recombinant turkey herpesvirus; insertion site; humoral immunity; long-term protection; INFECTIOUS BURSAL DISEASE; LARYNGOTRACHEITIS VIRUS; MAREKS DISEASES; FUSION PROTEIN; GENOTYPE VII; IN-OVO; VACCINE; EFFICACY; CHALLENGE; ONSET;
D O I
10.3390/vaccines12060604
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Newcastle disease (ND) is a significant infectious disease in poultry, causing substantial economic losses in developing countries. To control ND, chickens must be vaccinated multiple times a year. In order to develop an improved vaccine that provides long-term protection, the F gene from genotype VII NDV was inserted into the herpesvirus of turkey (HVT) vaccine virus using CRISPR/Cas9-mediated NHEJ repair and Cre/LoxP technology. The immunogenicity and protective efficacy of the resulting recombinant vaccines were evaluated through antibody assays and virus challenge experiments. Two recombinant vaccines, rHVT-005/006-F and rHVT-US2-F, were generated, both exhibiting growth rates comparable with those of HVT in vitro and consistently expressing the F protein. One-day-old specific pathogen-free (SPF) chickens immunized with 2000 PFU/bird of either rHVT-005/006-F or rHVT-US2-F developed robust humoral immunity and were completely protected against challenge with the NDV F48E8 strain at 4 weeks post-vaccination (wpv). Furthermore, a single dose of these vaccines provided sustained protection for at least 52 wpv. Our study identifies rHVT-005/006-F and rHVT-US2-F as promising ND vaccine candidates, offering long-term protection with a single administration. Moreover, HVT-005/006 demonstrates promise for accommodating additional foreign genes, facilitating the construction of multiplex vaccines.
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页数:14
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