Literature DB >> 32999029

Cross-Protection by Inactivated H5 Prepandemic Vaccine Seed Strains against Diverse Goose/Guangdong Lineage H5N1 Highly Pathogenic Avian Influenza Viruses.

Miria Ferreira Criado1, Mariana Sá E Silva1, Dong-Hun Lee1,2, Carolina Alves de Lima Salge3, Erica Spackman1, Ruben Donis4, Xiu-Feng Wan5,6,7,8,9, David E Swayne10.   

Abstract

The highly pathogenic avian influenza virus (HPAIV) H5N1 A/goose/Guangdong/1996 lineage (Gs/GD) is endemic in poultry across several countries in the world and has caused sporadic lethal infections in humans. Vaccines are important in HPAIV control both for poultry and in prepandemic preparedness for humans. This study assessed inactivated prepandemic vaccine strains in a One Health framework across human and agricultural and wildlife animal health, focusing on the genetic and antigenic diversity of field H5N1 Gs/GD viruses from the agricultural sector and assessing cross-protection in a chicken challenge model. Nearly half (47.92%) of the 48 combinations of vaccine and challenge viruses examined had bird protection of 80% or above. Most vaccinated groups had prolonged mean death times (MDT), and the virus-shedding titers were significantly lower than those of the sham-vaccinated group (P ≤ 0.05). The antibody titers in the prechallenge sera were not predictive of protection. Although vaccinated birds had higher titers of hemagglutination-inhibiting (HI) antibodies against the homologous vaccine antigen, most of them also had lower or no antibody titer against the challenge antigen. The comparison of all parameters and homologous or closely related vaccine and challenge viruses gave the best prediction of protection. Through additional analysis, we identified a pattern of epitope substitutions in the hemagglutinin (HA) of each challenge virus that impacted protection, regardless of the vaccine used. These changes were situated in the antigenic sites and/or reported epitopes associated with virus escape from antibody neutralization. As a result, this study highlights virus diversity, immune response complexity, and the importance of strain selection for vaccine development to control H5N1 HPAIV in the agricultural sector and for human prepandemic preparedness. We suggest that the engineering of specific antigenic sites can improve the immunogenicity of H5 vaccines.IMPORTANCE The sustained circulation of highly pathogenic avian influenza virus (HPAIV) H5N1 A/goose/Guangdong/1996 (Gs/GD) lineage in the agricultural sector and some wild birds has led to the evolution and selection of distinct viral lineages involved in escape from vaccine protection. Our results using inactivated vaccine candidates from the human pandemic preparedness program in a chicken challenge model identified critical antigenic conformational epitopes on H5 hemagglutinin (HA) from different clades that were associated with antibody recognition and escape. Even though other investigators have reported epitope mapping in the H5 HA, much of this information pertains to epitopes reactive to mouse antibodies. Our findings validate changes in antigenic epitopes of HA associated with virus escape from antibody neutralization in chickens, which has direct relevance to field protection and virus evolution. Therefore, knowledge of these immunodominant regions is essential to proactively develop diagnostic tests, improve surveillance platforms to monitor AIV outbreaks, and design more efficient and broad-spectrum agricultural and human prepandemic vaccines.

Entities:  

Keywords:  H5N1; chicken; goose/Guangdong lineage; highly pathogenic avian influenza; immunity; inactivated vaccine; influenza vaccines; vaccines

Year:  2020        PMID: 32999029     DOI: 10.1128/JVI.00720-20

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  4 in total

1.  Differential mitochondrial proteomic analysis of A549 cells infected with avian influenza virus subtypes H5 and H9.

Authors:  Yuting Yang; Yun Zhang; Changcheng Yang; Fang Fang; Ying Wang; Haiyan Chang; Ze Chen; Ping Chen
Journal:  Virol J       Date:  2021-02-18       Impact factor: 4.099

2.  Generation and Evaluation of Recombinant Thermostable Newcastle Disease Virus Expressing the HA of H9N2 Avian Influenza Virus.

Authors:  Xiaorong Zhang; Zongyi Bo; Chenchen Meng; Yin Chen; Chengcheng Zhang; Yongzhong Cao; Yantao Wu
Journal:  Viruses       Date:  2021-08-13       Impact factor: 5.048

3.  Selenium nanoparticles enhance the efficacy of homologous vaccine against the highly pathogenic avian influenza H5N1 virus in chickens.

Authors:  Nahed Yehia; Mohammed A AbdelSabour; Ahmed M Erfan; Zeinab Mohammed Ali; Reem A Soliman; Ahmed Samy; Mohamed Mohamed Soliman; Mohamed E Abd El-Hack; Mohamed T El-Saadony; Kawkab A Ahmed
Journal:  Saudi J Biol Sci       Date:  2021-11-25       Impact factor: 4.052

4.  Insight into the first multi-epitope-based peptide subunit vaccine against avian influenza A virus (H5N6): An immunoinformatics approach.

Authors:  Md Mukthar Mia; Mahamudul Hasan; Shakil Ahmed; Mohammad Nahian Rahman
Journal:  Infect Genet Evol       Date:  2022-08-22       Impact factor: 4.393

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.