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dc.contributor.authorFerreira Criado, Miria
dc.contributor.authorBertran, Kateri
dc.contributor.authorLee, Dong-Hun
dc.contributor.authorKillmaster, Lindsay
dc.contributor.authorStephens, Christopher B.
dc.contributor.authorSpackman, Erica
dc.contributor.authorSa e Silva, Mariana
dc.contributor.authorAtkins, Emily
dc.contributor.authorMebatsion, Teshome
dc.contributor.authorWidener, Justin
dc.contributor.authorPritchard, Nikki
dc.contributor.authorKing, Hallie
dc.contributor.authorSwayne, David E.
dc.contributor.otherProducció Animalca
dc.date.accessioned2019-11-14T15:38:29Z
dc.date.available2019-11-14T15:38:29Z
dc.date.issued2019-03-15
dc.identifier.citationCriado, Miria Ferreira, Kateri Bertran, Dong-Hun Lee, Lindsay Killmaster, Christopher B. Stephens, Erica Spackman, and Mariana Sa e Silva et al. 2019. "Efficacy Of Novel Recombinant Fowlpox Vaccine Against Recent Mexican H7N3 Highly Pathogenic Avian Influenza Virus". Vaccine 37 (16): 2232-2243. Elsevier BV. doi:10.1016/j.vaccine.2019.03.009.ca
dc.identifier.issn0264-410Xca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/553
dc.description.abstractSince 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 rFPV-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 rFPV-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.ca
dc.format.extent12ca
dc.language.isoengca
dc.publisherElsevierca
dc.relation.ispartofVaccineca
dc.rightsAttribution 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleEfficacy of novel recombinant fowlpox vaccine against recent Mexican H7N3 highly pathogenic avian influenza virusca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.1016/j.vaccine.2019.03.009ca
dc.contributor.groupSanitat Animalca


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Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/
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