Author:
Ruan Peilin,Feng Xin,Cheng Anchun,Wang Mingshu,Zhang Wei,Wu Ying,Yang Qiao,Tian Bin,Ou Xuming,Sun Di,Zhang Shaqiu,Mao Sai,Zhu Dekang,Jia Renyong,Chen Shun,Liu Mafeng,Zhao Xin-Xin,Huang Juan,Gao Qun,Yu Yanling,Zhang Ling,Pan Leichang
Abstract
Duck plague caused by duck plague virus (DPV) is a highly contagious disease that can cause serious morbidity and death in waterfowl such as ducks and geese, and bring huge economic losses to the duck industry. In this study, on the basis of the duck plague virus gC gene deletion strain CHv-ΔgC, based on the duck plague virus bacterial artificial chromosome (BAC) platform in our laboratory, the gE gene was knocked out using the traceless deletion technology to obtain gC/gE double gene deletion candidate vaccine strain CHv-ΔgC/gE. The double gene deletion strain (CHv-ΔgC/gE) constructed in this study has greatly weakened virulence, no pathogenicity to ducks, and stable genetic characteristicsin vitroandin vivo. Ducks immunized with CHv-ΔgC/gE can produce neutralizing antibodies and ELISA antibody levels comparable to those of commercial duck plague attenuated vaccine immunization, and can resist 100 LD50CHv challenge of ducks, with good immune protection effect. It has the potential to be further developed into duck plague gC/gE double gene deletion, marked attenuated vaccine.
Funder
National Natural Science Foundation of China
Subject
Immunology,Immunology and Allergy
Cited by
3 articles.
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