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Truncated chicken MDA5 enhances the immune response to inactivated NDV vaccine

Authors :
Qingsong Han
Xinglong Wang
Shuxia Zhang
Yanqing Jia
Zengqi Yang
Zhili Chu
Xiaolong Gao
Xinxin Qiu
Fathalrhman Eisa Addoma Adam
Xiangwei Wang
Source :
Veterinary Immunology and Immunopathology. 208:44-52
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Melanoma Differentiation-Associated protein 5 (MDA5) is a cytoplasmic sensor for viral invasion and plays an important role in regulation of the immune response against Newcastle disease virus (NDV) in chickens. MDA5 was used as an adjuvant to enhance the humoral immune response against influenza virus. In the current study, truncated chicken MDA5 [1–483 aa, chMDA5(483aa)] expressed by recombinant adenovirus was administered to specific-pathogen-free (SPF) chickens to improve the immune response induced by inactivated NDV vaccine. A total of 156 SPF chickens were divided into six groups, and after two rounds of immunization, the humoral immune response, cell-mediated immune (CMI) response and the protective efficacy of the vaccines against NDV challenge were evaluated. The results showed that co-administration of chMDA5(483aa) expressed by adenovirus increased the NDV-specific antibody response by 1.7 times and chickens received chMDA5(483aa) also gained a higher level of CMI response. Consistently, the protective efficacy of the inactivated NDV vaccine against virulent NDV (vNDV) challenge was improved by co-administrate with chMDA5(483aa), as indicated by the reduced morbidity and pathological lesions, lower levels of viral load in organs and reduced virus shedding. Our study demonstrated that chMDA5(433aa) expressed by adenovirus could enhance the immune efficacy of inactivated NDV vaccine in chickens and could be a potential adjuvant candidate in developing chicken NDV vaccines.

Details

ISSN :
01652427
Volume :
208
Database :
OpenAIRE
Journal :
Veterinary Immunology and Immunopathology
Accession number :
edsair.doi.dedup.....89396c820d3cba429d73fe82b0e93d21
Full Text :
https://doi.org/10.1016/j.vetimm.2018.11.019