A novel European H5N8 influenza A virus has increased virulence in ducks but low zoonotic potential.

Christian Grund1 Donata Hoffmann2 Reiner Ulrich3 Mahmoud Naguib1 Jan Schinköthe3 Bernd Hoffmann1 Timm Harder1 Sandra Saenger4 Katja Zscheppang5 Mario Tönnies6 Stefan Hippenstiel5 Andreas Hocke5 Thorsten Wolff4 Martin Beer7
Affiliations 7 institutions
  1. Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
  2. Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany. [email protected].
  3. Department of Experimental Animal Facilities and Biorisk Management, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
  4. Unit 17 Influenza and other Respiratory Viruses, Robert Koch Institut, Berlin, Germany.
  5. Department of Internal Medicine/Infectious Diseases and Respiratory Medicine, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  6. HELIOS Clinic Emil von Behring, Department of Thoracic Surgery, Chest Hospital Heckeshorn, Berlin, Germany.
  7. Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany. [email protected].

Abstract

We investigated in a unique setup of animal models and a human lung explant culture biological properties, including zoonotic potential, of a representative 2016 highly pathogenic avian influenza virus (HPAIV) H5N8, clade 2.3.4.4 group B (H5N8B), that spread rapidly in a huge and ongoing outbreak series in Europe and caused high mortality in waterfowl and domestic birds. HPAIV H5N8B showed increased virulence with rapid onset of severe disease and mortality in Pekin ducks due to pronounced neuro- and hepatotropism. Cross-species infection was evaluated in mice, ferrets, and in a human lung explant culture model. While the H5N8B isolate was highly virulent for Balb/c mice, virulence and transmissibility were grossly reduced in ferrets, which was mirrored by marginal replication in human lung cultures infected ex vivo. Our data indicate that the 2016 HPAIV H5N8B is avian-adapted with augmented virulence for waterfowl, but has low zoonotic potential. The here tested combination of animal studies with the inoculation of human explants provides a promising future workflow to evaluate zoonotic potential, mammalian replication competence and avian virulence of HPAIV.

Supporting text Virus Host Location
Animals 1948 Disease Outbreaks 170 Ducks 81 Ferrets 79 Humans 1440 Influenza A Virus, H5N8 Subtype 12 Influenza in Birds 341 Influenza, Human 286 Lung 65 Mice, Inbred BALB C 73 Poultry Diseases 74 Virulence 108 Virus Replication 191 Zoonoses 397

Evidence records

3 total
Experimental Infection
3 records · 2 evidence types
Evidence type
2 records
OVE3060
Key finding

HPAIV H5N8B infection caused rapid onset of severe disease and mortality in Pekin ducks, associated with pronounced neuro- and hepatotropism.

Virus
Host
Location
Not specified
Supporting text

HPAIV H5N8B showed increased virulence with rapid onset of severe disease and mortality in Pekin ducks due to pronounced neuro- and hepatotropism.

Method
controlled infection experiment | clinical observation of disease signs | pathological assessment of neuro- and hepatotropism
Experimental system
Pekin duck infection model
OVE3061
Key finding

The H5N8B isolate was highly virulent for Balb/c mice in experimental infection.

Virus
Host
Location
Not specified
Supporting text

While the H5N8B isolate was highly virulent for Balb/c mice, virulence and transmissibility were grossly reduced in ferrets.

Method
controlled infection experiment | clinical assessment of virulence | mortality monitoring
Experimental system
Balb/c mouse infection model
Evidence type
1 records
OVE3062
Key finding

H5N8B showed grossly reduced virulence in ferrets and only marginal replication in human lung cultures infected ex vivo.

Virus
Host
Location
Not specified
Supporting text

While the H5N8B isolate was highly virulent for Balb/c mice, virulence and transmissibility were grossly reduced in ferrets, which was mirrored by marginal replication in human lung cultures infected ex vivo.

Method
animal inoculation | ex vivo infection | replication assessment
Sample type
lung cultures
Experimental system
in vivo ferret infection model and ex vivo human lung culture system