Newcastle disease virus (NDV) recombinant expressing Marek's disease virus (MDV) glycoprotein B significantly protects chickens against MDV and NDV challenges

被引:2
作者
He, Lei [1 ,2 ]
Spatz, Stephen [1 ]
Dunn, John R. [1 ]
Yu, Qingzhong [1 ,3 ]
机构
[1] USDA, ARS, US Natl Poultry Res Ctr, 934 Coll Stn Rd, Athens, GA 30605 USA
[2] Henan Univ Sci & Technol, Coll Anim Sci & Technol, Luoyang 471003, Henan, Peoples R China
[3] USDA, ARS, US Natl Poultry Res Ctr, Southeast Poultry Res Lab, 934 Coll Stn Rd, Athens, GA 30605 USA
基金
美国农业部;
关键词
Marek 's disease; MDV gB; Newcastle disease; NDV LaSota; Recombinant dual vaccine; AVIAN INFLUENZA; FOWLPOX VIRUSES; FIELD TRIALS; VACCINE; STRAIN; OVO; EFFICACY; CONSTRUCTION; IMMUNIZATION; SYNERGISM;
D O I
10.1016/j.vaccine.2023.08.038
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Marek's disease (MD) is a highly contagious viral neoplastic disease of chickens caused by Marek's disease virus (MDV), resulting in significant economic losses to the poultry industry worldwide. The commonly used live and/ or vectored MDV vaccines are expensive to produce and difficult to handle due to the requirement of liquid nitrogen for manufacturing and delivering frozen infected cells that are viable. In this study, we aimed to develop a Newcastle disease virus (NDV) vectored MDV vaccine that can be lyophilized, stored, and transported at 4 degrees C. Four NDV LaSota (LS) vaccine strain-based recombinant viruses expressing MDV glycoproteins gB, gC, gE, or gI were generated using reverse genetics technology. The biological assessments showed that these recombinant viruses were slightly attenuated in vivo yet retained similar growth kinetics and virus titers in vitro compared to the parental LaSota virus. Vaccination of leghorn chickens (Lines 15I5x71 F1 cross) with these recombinant viruses via intranasal and intraocular routes conferred different levels of protection against virulent MDV challenge. The recombinant expressing the MDV gB protein, rLS/MDV-gB, protected vaccinated birds significantly against MDV-induced tumor formation when challenged at 14 days post-vaccination (DPV) but moderately at 5 DPV. Whereas the other three recombinants provided little protection against the MDV challenge. All four recombinants conferred complete protection against the velogenic NDV challenge. These results demonstrated that the rLS/MDV-gB virus is a safe and efficacious dual vaccine candidate that can be lyophilized and potentially mass-administered via aerosol or drinking water to large chicken populations at a meager cost.
引用
收藏
页码:5884 / 5891
页数:8
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