Literature detail

Equine and Canine Influenza H3N8 Viruses Show Minimal Biological Differences Despite Phylogenetic Divergence.

Kurtis H Feng1 Gaelle Gonzalez2 Lingquan Deng3 Hai Yu4 Victor L Tse5 Lu Huang1 Kai Huang1 Brian R Wasik1 Bin Zhou6 David E Wentworth6 Edward C Holmes7 Xi Chen4 Ajit Varki3 Pablo R Murcia2 Colin R Parrish8
Affiliations 8 institutions
  1. Department of Microbiology and Immunology, Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
  2. Medical Research Council-University of Glasgow Centre for Virus Research, Glasgow, Scotland, United Kingdom.
  3. Cellular and Molecular Medicine, Glycobiology Research and Training Center, University of California, San Diego, La Jolla, California, USA.
  4. Department of Chemistry, University of California, Davis, Davis, California, USA.
  5. Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
  6. Infectious Disease Group, J. Craig Venter Institute, Rockville, Maryland, USA.
  7. Marie Bashir Institute for Infectious Diseases and Biosecurity, Charles Perkins Centre, School of Biological Sciences and Sydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
  8. Department of Microbiology and Immunology, Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA [email protected].
PMID 25903329 2015 J Virol eng ppublish
PubMed DOI Browse context

Article

Publication summary

The A/H3N8 canine influenza virus (CIV) emerged from A/H3N8 equine influenza virus (EIV) around the year 2000 through the transfer of a single virus from horses to dogs. We defined and compared the biological properties of EIV and CIV by examining their genetic variation, infection, and growth in different cell cultures, receptor specificity, hemagglutinin (HA) cleavage, and infection and growth in horse and dog tracheal explant cultures. Comparison of sequences of viruses from horses and dogs revealed mutations that may be linked to host adaptation and tropism. We prepared infectious clones of representative EIV and CIV strains that were similar to the consensus sequences of viruses from each host. The rescued viruses, including HA and neuraminidase (NA) double reassortants, exhibited similar degrees of long-term growth in MDCK cells. Different host cells showed various levels of susceptibility to infection, but no differences in infectivity were seen when comparing viruses. All viruses preferred α2-3- over α2-6-linked sialic acids for infections, and glycan microarray analysis showed that EIV and CIV HA-Fc fusion proteins bound only to α2-3-linked sialic acids. Cleavage assays showed that EIV and CIV HA proteins required trypsin for efficient cleavage, and no differences in cleavage efficiency were seen. Inoculation of the viruses into tracheal explants revealed similar levels of infection and replication by each virus in dog trachea, although EIV was more infectious in horse trachea than CIV. Influenza A viruses can cross species barriers and cause severe disease in their new hosts. Infections with highly pathogenic avian H5N1 virus and, more recently, avian H7N9 virus have resulted in high rates of lethality in humans. Unfortunately, our current understanding of how influenza viruses jump species barriers is limited. Our aim was to provide an overview and biological characterization of H3N8 equine and canine influenza viruses using various experimental approaches, since the canine virus emerged from horses approximately 15 years ago. We showed that although there were numerous genetic differences between the equine and canine viruses, this variation did not result in dramatic biological differences between the viruses from the two hosts, and the viruses appeared phenotypically equivalent in most assays we conducted. These findings suggest that the cross-species transmission and adaptation of influenza viruses may be mediated by subtle changes in virus biology.

Genetic Variation Adaptation, Biological Animals Cell Line Dogs Hemagglutinin Glycoproteins, Influenza Virus Horses Influenza A Virus, H3N8 Subtype Mutation Phylogeny Protein Binding Receptors, Virus Sialic Acids Trachea Viral Tropism Virus Attachment

Structured evidence records

Evidence records

10 total
2 records
Extraction confidence 0.80
Key finding

Sequence comparison and phylogenetic analysis identified genetic divergence and host-associated mutations between equine and canine H3N8 influenza viruses.

Virus
Location
Not specified
Supporting text

Comparison of sequences of viruses from horses and dogs revealed mutations that may be linked to host adaptation and tropism. The title indicates phylogenetic divergence between equine and canine H3N8 influenza viruses.

Analysis methods
sequence comparison; phylogenetic analysis
Extraction confidence 0.80
Key finding

Canine and equine H3N8 influenza viruses exhibited host-associated genetic differences following cross-species transmission from horses to dogs.

Virus
Location
Not specified
Supporting text

Comparison of sequences of viruses from horses and dogs revealed mutations that may be linked to host adaptation and tropism.

Analysis methods
sequence comparison; phylogenetic analysis
2 records
Extraction confidence 0.90
Key finding

Equine influenza virus exhibited higher infectivity in horse tracheal explants than canine influenza virus, while both replicated similarly in dog trachea.

Virus
Location
Not specified
Supporting text

Inoculation of the viruses into tracheal explants revealed similar levels of infection and replication by each virus in dog trachea, although EIV was more infectious in horse trachea than CIV.

Method
inoculation; replication assay
Sample type
tracheal explant
Experimental system
ex vivo
Extraction confidence 0.90
Key finding

Equine and canine influenza H3N8 viruses showed similar infection and replication in dog tracheal explants.

Virus
Location
Not specified
Supporting text

Inoculation of the viruses into tracheal explants revealed similar levels of infection and replication by each virus in dog trachea, although EIV was more infectious in horse trachea than CIV.

Method
inoculation; replication assay
Sample type
tracheal explant
Experimental system
ex vivo
2 records
Extraction confidence 0.87
Key finding

Equine and canine influenza H3N8 viruses both preferentially bind to α2-3-linked sialic acid receptors, indicating conserved receptor specificity across hosts.

Virus
Location
Not specified
Supporting text

All viruses preferred α2-3- over α2-6-linked sialic acids for infections, and glycan microarray analysis showed that EIV and CIV HA-Fc fusion proteins bound only to α2-3-linked sialic acids.

Method
glycan microarray analysis
Receptors
α2-3-linked sialic acid
Extraction confidence 0.87
Key finding

Canine influenza H3N8 virus binds exclusively to α2-3-linked sialic acid receptors, similar to the equine progenitor virus.

Virus
Location
Not specified
Supporting text

All viruses preferred α2-3- over α2-6-linked sialic acids for infections, and glycan microarray analysis showed that EIV and CIV HA-Fc fusion proteins bound only to α2-3-linked sialic acids.

Method
glycan microarray analysis
Receptors
α2-3-linked sialic acid
1 records
Extraction confidence 0.90
Key finding

A/H3N8 canine influenza virus originated from equine influenza virus via a horse-to-dog transmission event.

Virus
Location
Not specified
Supporting text

The A/H3N8 canine influenza virus (CIV) emerged from A/H3N8 equine influenza virus (EIV) around the year 2000 through the transfer of a single virus from horses to dogs.

Method
sequencing; virus isolation; infection experiments
Study design
phylogenetic analysis
Transmission direction
animal-to-animal
1 records
Extraction confidence 0.88
Key finding

Equine and canine H3N8 influenza viruses carried sequence mutations associated with host adaptation and maintained α2-3-linked sialic acid receptor binding preference, indicating similar host-specific molecular adaptation patterns.

Virus
Host
Not specified
Location
Not specified
Supporting text

Comparison of sequences of viruses from horses and dogs revealed mutations that may be linked to host adaptation and tropism. All viruses preferred α2-3- over α2-6-linked sialic acids for infections, and glycan microarray analysis showed that EIV and CIV HA-Fc fusion proteins bound only to α2-3-linked sialic acids.

Genes or proteins
HA; NA
Receptors
α2-3-linked sialic acids
Mechanism types
receptor_binding; tropism; host_adaptation
1 records
Extraction confidence 0.75
Key finding

HA and NA double reassortant H3N8 influenza viruses derived from equine and canine lineages showed comparable replication phenotypes across tested host systems.

Host
Not specified
Location
Not specified
Supporting text

The rescued viruses, including HA and neuraminidase (NA) double reassortants, exhibited similar degrees of long-term growth in MDCK cells.

Event type
reassortment
Genes or segments
HA; NA
1 records
Extraction confidence 0.95
Key finding

Equine influenza A/H3N8 virus was transmitted from horses to dogs, establishing the A/H3N8 canine influenza virus lineage.

Virus
Location
Not specified
Supporting text

The A/H3N8 canine influenza virus (CIV) emerged from A/H3N8 equine influenza virus (EIV) around the year 2000 through the transfer of a single virus from horses to dogs.

Transmission direction
animal-to-human