DNA Vaccine Co-Expressing Hemagglutinin and IFN-γ Provides Partial Protection to Ferrets against Lethal Challenge with Canine Distemper Virus

Author:

Zhao Jianjun1ORCID,Sun Yiyang1ORCID,Sui Ping1,Pan Hongjun2,Shi Yijun3,Chen Jie2,Zhang Hailing2,Wang Xiaolong4,Tao Rongshan5,Liu Mengjia6,Sun Dongbo1,Zheng Jiasan1

Affiliation:

1. Key Laboratory of Bovine Disease Control in Northeast China, Ministry of Agriculture and Rural Affairs, College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, Daqing 163319, China

2. Institute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences (CAAS), Changchun 130112, China

3. Yantai Animal Disease Control Center of Shandong Province, Yantai 264000, China

4. Agricultural Bureau of Shanyang Country, Shangluo 726400, China

5. The Key Laboratory of Environmental Pollution Monitoring and Disease Control, School of Public Health, Guizhou Medical University, Guiyang 550025, China

6. Jinan Customs in Shandong Province of the P.R. of China, Jinan 250000, China

Abstract

Canine distemper (CD), caused by canine distemper virus (CDV), is a highly contagious and lethal disease in domestic and wild carnivores. Although CDV live-attenuated vaccines have reduced the incidence of CD worldwide, low levels of protection are achieved in the presence of maternal antibodies in juvenile animals. Moreover, live-attenuated CDV vaccines may retain residual virulence in highly susceptible species and cause disease. Here, we generated several CDV DNA vaccine candidates based on the biscistronic vector (pIRES) co-expressing virus wild-type or codon-optimized hemagglutinin (H) and nucleocapsid (N) or ferret interferon (IFN)-γ, as a molecular adjuvant, respectively. Apparently, ferret (Mustela putorius furo)-specific codon optimization increased the expression of CDV H and N proteins. A ferret model of CDV was used to evaluate the protective immune response of the DNA vaccines. The results of the vaccinated ferrets showed that the DNA vaccine co-expressing the genes of codon-optimized H and ferret IFN-γ (poptiH-IRES-IFN) elicited the highest anti-CDV serum-neutralizing antibodies titer (1:14) and cytokine responses (upregulated TNF-α, IL-4, IL-2, and IFN-γ expression) after the third immunization. Following vaccination, the animals were challenged with a lethal CDV 5804Pe/H strain with a dose of 105.0 TCID50. Protective immune responses induced by the DNA vaccine alleviated clinical symptoms and pathological changes in CDV-infected ferrets. However, it cannot completely prevent virus replication and viremia in vivo as well as virus shedding due to the limited neutralizing antibody level, which eventually contributed to a survival rate of 75% (3/4) against CDV infection. Therefore, the improved strategies for the present DNA vaccines should be taken into consideration to develop more protective immunity, which includes increasing antigen expression or alternative delivery routes, such as gene gun injection.

Funder

National Natural Science Foundation of China

Key research and development projects in Heilongjiang Province

State Key Laboratory of Veterinary Biotechnology Open Project

Science and Technology Fund Project of Guizhou Provincial Health Commission

Heilongjiang Bayi Agricultural University Research Foundation for Advanced Talents

Heilongjiang Bayi Agricultural University Support Program for San Heng San Zong

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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