The migratory waterfowl of the world are considered to be the natural reservoir of influenza A viruses. Of the 16 hemagglutinin subtypes of avian influenza viruses, the H6 subtype is commonly perpetuated in its natural hosts and is of concern due to its potential to be a precursor of highly pathogenic influenza viruses by reassortment. During routine influenza surveillance, we isolated an unconventional H6N5 subtype of avian influenza virus. Experimental infection of mice revealed that this isolate replicated efficiently in the lungs, subsequently spread systemically, and caused lethality. The isolate also productively infected ferrets, with direct evidence of contact transmission, but no disease or transmission was seen in pigs. Although the isolate possessed the conserved receptor-binding site sequences of avian influenza viruses, it exhibited relatively low replication efficiencies in ducks and chickens. Our genetic and molecular analyses of the isolate revealed that its PB1 sequence showed the highest evolutionary relationship to those of highly pathogenic H5N1 avian influenza viruses and that its PA protein had an isoleucine residue at position 97 (a representative virulence marker). Further studies will be required to examine why our isolate has the virologic characteristics of mammalian influenza viruses but the archetypal receptor binding profiles of avian influenza viruses, as well as to determine whether its potential virulence markers (PB1 analogous to those of H5N1 viruses or isoleucine residue at position 97 within PA) could render it highly pathogenic in mice.
AnimalsBirdsChick EmbryoChickensDucksFecesFerretsInfluenza A virusInfluenza in BirdsLungMiceMice, Inbred C57BLOrthomyxoviridae InfectionsRNA-Dependent RNA PolymeraseSwineViral ProteinsVirulenceinfluenza virus polymerase basic protein 1
Structured evidence records
Evidence records
11 total
Host Range Experiment5 records
Host Range ExperimentExtraction confidence 0.95
Key finding
Avian influenza H6N5 virus replicated systemically and was lethal in mice after experimental infection.
It exhibited relatively low replication efficiencies in ducks and chickens.
Method
replication assay
Experimental system
in vivo animal experiment
Cross Species Transmission2 records
Cross Species TransmissionExtraction confidence 0.90
Key finding
An avian influenza H6N5 virus originating from birds replicated lethally in mice and was transmissible among ferrets, demonstrating cross-species transmission from avian to mammalian hosts.
Experimental infection of mice revealed that this isolate replicated efficiently in the lungs, subsequently spread systemically, and caused lethality. The isolate also productively infected ferrets, with direct evidence of contact transmission.
Method
experimental infection
Study design
animal experiment
Transmission direction
animal-to-animal
Cross Species TransmissionExtraction confidence 0.90
Key finding
The avian influenza H6N5 virus productively infected ferrets and showed contact transmission, indicating avian-to-mammal cross-species infection capability.
The isolate also productively infected ferrets, with direct evidence of contact transmission.
Method
experimental infection
Study design
animal experiment
Transmission direction
animal-to-animal
Genomic Evolution1 records
Genomic EvolutionExtraction confidence 0.80
Key finding
Genetic analysis showed that the PB1 gene of the H6N5 isolate was most closely related to H5N1 viruses and that the PA protein contained an isoleucine at position 97, a known virulence marker.
Our genetic and molecular analyses of the isolate revealed that its PB1 sequence showed the highest evolutionary relationship to those of highly pathogenic H5N1 avian influenza viruses and that its PA protein had an isoleucine residue at position 97 (a representative virulence marker).
The H6N5 avian influenza virus retained conserved receptor-binding site sequences typical of avian influenza viruses, showing no receptor-level adaptation to mammalian-type receptors.
Although the isolate possessed the conserved receptor-binding site sequences of avian influenza viruses, it exhibited relatively low replication efficiencies in ducks and chickens.
Method
genetic analysis
Receptors
receptor-binding site sequences
Recombination Or Reassortment1 records
Recombination Or ReassortmentExtraction confidence 0.75
Key finding
The emergent H6N5 avian influenza virus appears to have acquired an H5N1-like PB1 segment through reassortment, linking segment exchange to mammalian infectivity.
Our genetic and molecular analyses of the isolate revealed that its PB1 sequence showed the highest evolutionary relationship to those of highly pathogenic H5N1 avian influenza viruses.
Event type
reassortment
Genes or segments
PB1
Zoonotic Surveillance1 records
Zoonotic SurveillanceExtraction confidence 0.95
Key finding
Routine influenza surveillance in migratory waterfowl led to the isolation of an H6N5 avian influenza virus.
2010. Emergence of H5N1 avian influenza viruses with reduced sensitivity to neuraminidase inhibitors and novel reassortants in Lao People's Democratic Republic
2002. Molecular evolution of H6 influenza viruses from poultry in Southeastern China: prevalence of H6N1 influenza viruses possessing seven A/Hong Kong/156/97 (H5N1)-like genes in poultry
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1997. Receptor specificity of influenza A viruses correlates with the agglutination of erythrocytes from different animal species. Virology 227:493–499
M., Sladen W. L., Webster R. G. 1988. Is the gene pool of influenza viruses in shorebirds and gulls different from that in wild ducks? Virology 163:247–250
2001. Antigenic and genetic characterization of swine influenza A (H1N1) viruses isolated from pneumonia patients in The Netherlands. Virology 282:301–306
M., Nicholson K. G., Zambon M. C. 2003. Sialic acid receptor specificity on erythrocytes affects detection of antibody to avian influenza haemagglutinin
J., Woolcock P. R., Krauss S. L., Webster R. G. 2002. Reassortment and interspecies transmission of North American H6N2 influenza viruses. Virology 295:44–53