Efficacy of novel recombinant fowlpox vaccine against recent Mexican H7N3 highly pathogenic avian influenza virus

被引:20
作者
Criado, Miria Ferreira [1 ]
Bertran, Kateri [1 ,4 ]
Lee, Dong-Hun [1 ,5 ]
Killmaster, Lindsay [1 ]
Stephens, Christopher B. [1 ]
Spackman, Erica [1 ]
Sa e Silva, Mariana [2 ]
Atkins, Emily [2 ]
Mebatsion, Teshome [2 ]
Widener, Justin [2 ]
Pritchard, Nikki [3 ]
King, Hallie [2 ]
Swayne, David E. [1 ]
机构
[1] ARS, Exot & Emerging Avian Viral Dis Res Unit, Southeast Poultry Res Lab, US Natl Poultry Res Ctr,USDA, Athens, GA 30604 USA
[2] Boehringer Ingelheim Anim Hlth, Athens, GA 30601 USA
[3] Boehringer Ingelheim Anim Hlth, Gainesville, GA 30503 USA
[4] Inst Agrifood Res & Technol, Ctr Recerca Sanitat Anim, Campus Univ Autonoma Barcelona, Bellaterra 08193, Spain
[5] Univ Connecticut, Dept Pathobiol & Vet Sci, Storrs, CT 06269 USA
关键词
Chickens; High pathogenicity avian influenza; H7N3; Immunity; Recombinant fowlpox virus vaccine; Vaccine; T-CELL RECOGNITION; GLYCOSYLATION SITES; N-GLYCOSYLATION; HEMAGGLUTININ; H5; PROTECTION; EVOLUTION; MODULATE; POULTRY; PCR;
D O I
10.1016/j.vaccine.2019.03.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since 2012, H7N3 highly pathogenic avian influenza (HPAI) has produced negative economic and animal welfare impacts on poultry in central Mexico. In the present study, chickens were vaccinated with two different recombinant fowlpox virus vaccines (rFPV-H7/3002 with 2015 H7 hemagglutinin [HA] gene insert, and rFPV-H7/2155 with 2002 H7 HA gene insert), and were then challenged three weeks later with H7N3 HPAI virus (A/chicken/Jalisco/CPA-37905/2015). The rEPV-H7/3002 vaccine conferred 100% protection against mortality and morbidity, and significantly reduced virus shed titers from the respiratory and gastrointestinal tracts. In contrast, 100% of sham and rEPV-H7/2155 vaccinated birds shed virus at higher titers and died within 4 days. Pre- (15/20) and post- (20/20) challenge serum of birds vaccinated with rFPV-H7/3002 had antibodies detectable by hemagglutination inhibition (HI) assay using challenge virus antigen. However, only a few birds (3/20) in the rFPV-H7/2155 vaccinated group had antibodies that reacted against the challenge strain but all birds had antibodies that reacted against the homologous vaccine antigen (A/turkey/Virginia/SEP-66/2002) (20/20). One possible explanation for differences in vaccines efficacy is the antigenic drift between circulating viruses and vaccines. Molecular analysis demonstrated that the Mexican H7N3 strains have continued to rapidly evolve since 2012. In addition, we identified in silico three potential new N-glycosylation sites on the globular head of the H7 HA of A/chicken/Jalisco/CPA-37905/2015 challenge virus, which were absent in 2012 H7N3 outbreak virus. Our results suggested that mutations in the HA antigenic sites including increased glycosylation sites, accumulated in the new circulating Mexican H7 HPAIV strains, altered the recognition of neutralizing antibodies from the older vaccine strain rFPV-H7/2155. Therefore, the protective efficacy of novel rFPV-H7/3002 against recent outbreak Mexican H7N3 HPAIV confirms the importance of frequent updating of vaccines seed strains for long-term effective control of H7 HPAI virus. Published by Elsevier Ltd.
引用
收藏
页码:2232 / 2243
页数:12
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