4.7 Article

Pathobiology of highly pathogenic H5 avian influenza viruses in naturally infected Galliformes and Anseriformes in France during winter 2015-2016

Journal

VETERINARY RESEARCH
Volume 53, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13567-022-01028-x

Keywords

Highly pathogenic avian influenza; viral tropism; H5; pathology; sialic acids

Funding

  1. Direction Generale de l'Alimentation, Ministere de l'Agriculture et de l'Alimentation, France
  2. French Comite Interprofessionnel des Palmipedes a foie gras (CIFOG), France
  3. ERC Starting Grant from the European Commission [802780]
  4. Beijerinck Premium of the Royal Dutch Academy of Sciences
  5. Netherlands Organization for Scientific Research [NWO TOPPUNT 718.015.00]
  6. European Research Council (ERC) [802780] Funding Source: European Research Council (ERC)

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This study describes the pathobiological characteristics of the H5 highly pathogenic avian influenza outbreaks that occurred in Southwestern France in 2015-2016. The infection in chickens and guinea fowls was characterized by severe systemic vasculitis and parenchymal necrosis, while in ducks, the lesions were mild. Glycan-binding analyses revealed different affinities of the virus to the mucosae of different bird species, providing insights into its adaptability and transmission mechanisms.
In late 2015, an epizootic of Highly Pathogenic Avian Influenza (H5Nx) was registered in Southwestern France, including more than 70 outbreaks in commercial poultry flocks. Phylogenetic analyses suggested local emergence of H5 viruses which differed from A/goose/Guangdong/1/1996 clade 2.3.4.4b lineage and shared a unique polybasic cleavage site in their hemagglutinin protein. The present work provides an overview of the pathobiological picture associated with this epizootic in naturally infected chickens, guinea fowls and ducks. Upon necropsy examination, selected tissues were sampled for histopathology, immunohistochemistry and quantitative Real Time Polymerase Chain Reaction. In Galliformes, HPAIVs infection manifested as severe acute systemic vasculitis and parenchymal necrosis and was associated with endothelial expression of viral antigen. In ducks, lesions were mild and infrequent, with sparse antigenic detection in respiratory and digestive mucosae and leukocytes. Tissue quantifications of viral antigen and RNA were higher in chickens and guinea fowls compared to duck. Subsequently, recombinant HA (rHA) was generated from a H5 HPAIV isolated from an infected duck to investigate its glycan-binding affinity for avian mucosae. Glycan-binding analysis revealed strong affinity of rHA for 3'Sialyl-LacNAc and low affinity for Sialyl-Lewis(X), consistent with a duck-adapted virus similar to A/Duck/Mongolia/54/2001 (H5N2). K222R and S227R mutations on rHA sequence shifted affinity towards Sialyl-Lewis(X) and led to an increased affinity for chicken mucosa, confirming the involvement of these two mutations in the glycan-binding specificity of the HA. Interestingly, the rHA glycan binding pattern of guinea fowl appeared intermediate between duck and chicken. The present study presents a unique pathobiological description of the H5 HPAIVs outbreaks that occurred in 2015-2016 in Southwestern France.

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