Literature detail

Novel Highly Pathogenic Avian A(H5N2) and A(H5N8) Influenza Viruses of Clade 2.3.4.4 from North America Have Limited Capacity for Replication and Transmission in Mammals.

Bryan S Kaplan1 Marion Russier1 Trushar Jeevan1 Bindumadhav Marathe1 Elena A Govorkova1 Charles J Russell1 Mia Kim-Torchetti2 Young Ki Choi3 Ian Brown4 Takehiko Saito5 David E Stallknecht6 Scott Krauss1 Richard J Webby1
Affiliations 6 institutions
  1. Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  2. National Veterinary Services Laboratories, Science, Technology and Analysis Services, Veterinary Services, Animal and Plant Health Inspection Service, U.S. Department of Agriculture, Ames, Iowa, USA.
  3. College of Medicine and Medical Research Institute, Chungbuk National University, Cheongju, South Korea.
  4. Animal and Plant Health Agency, New Haw, Addlestone, Surrey, United Kingdom.
  5. Influenza and Prion Disease Research Center, National Institute of Animal Health, National Agriculture and Food Research Organization, Tsukuba, Ibaraki, Japan.
  6. Department of Population Health, College of Veterinary Medicine, The University of Georgia, Athens, Georgia, USA.
PMID 27303732 2016 mSphere eng epublish
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Article

Publication summary

Highly pathogenic influenza A(H5N8) viruses from clade 2.3.4.4 were introduced to North America by migratory birds in the fall of 2014. Reassortment of A(H5N8) viruses with avian viruses of North American lineage resulted in the generation of novel A(H5N2) viruses with novel genotypes. Through sequencing of recent avian influenza viruses, we identified PB1 and NP gene segments very similar to those in the viruses isolated from North American waterfowl prior to the introduction of A(H5N8) to North America, highlighting these bird species in the origin of reassortant A(H5N2) viruses. While they were highly virulent and transmissible in poultry, we found A(H5N2) viruses to be low pathogenic in mice and ferrets, and replication was limited in both hosts compared with those of recent highly pathogenic avian influenza (HPAI) H5N1 viruses. Molecular characterization of the hemagglutinin protein from A(H5N2) viruses showed that the receptor binding preference, cleavage, and pH of activation were highly adapted for replication in avian species and similar to those of other 2.3.4.4 viruses. In addition, North American and Eurasian clade 2.3.4.4 H5NX viruses replicated to significantly lower titers in differentiated normal human bronchial epithelial cells than did seasonal human A(H1N1) and highly pathogenic A(H5N1) viruses isolated from a human case. Thus, despite their having a high impact on poultry, our findings suggest that the recently emerging North American A(H5N2) viruses are not expected to pose a substantial threat to humans and other mammals without further reassortment and/or adaptation and that reassortment with North American viruses has not had a major impact on viral phenotype. IMPORTANCE Highly pathogenic H5 influenza viruses have been introduced into North America from Asia, causing extensive morbidity and mortality in domestic poultry. The introduced viruses have reassorted with North American avian influenza viruses, generating viral genotypes not seen on other continents. The experiments and analyses presented here were designed to assess the impact of this genetic diversification on viral phenotypes, particularly as regards mammalian hosts, by comparing the North American viruses with their Eurasian precursor viruses.

avian influenza virus H5N2 H5N8 mammals viral replication

Structured evidence records

Evidence records

7 total
3 records
Extraction confidence 1.00
Key finding

A(H5N2) influenza viruses showed low pathogenicity and limited replication in mice and ferrets relative to H5N1, indicating restricted host range in mammals.

Virus
Location
Not specified
Supporting text

We found A(H5N2) viruses to be low pathogenic in mice and ferrets, and replication was limited in both hosts compared with those of recent highly pathogenic avian influenza (HPAI) H5N1 viruses.

Method
experimental infection; replication assay
Experimental system
in vivo animal experiment
Extraction confidence 1.00
Key finding

A(H5N2) influenza viruses exhibited restricted replication in ferrets and were less pathogenic than H5N1, reflecting limited mammalian adaptation.

Virus
Location
Not specified
Supporting text

We found A(H5N2) viruses to be low pathogenic in mice and ferrets, and replication was limited in both hosts compared with those of recent highly pathogenic avian influenza (HPAI) H5N1 viruses.

Method
experimental infection; replication assay
Experimental system
in vivo animal experiment
Extraction confidence 1.00
Key finding

Clade 2.3.4.4 H5NX influenza viruses, including North American A(H5N2) and A(H5N8), replicated poorly in differentiated human bronchial epithelial cells compared with human-adapted influenza strains.

Virus
Location
Not specified
Supporting text

North American and Eurasian clade 2.3.4.4 H5NX viruses replicated to significantly lower titers in differentiated normal human bronchial epithelial cells than did seasonal human A(H1N1) and highly pathogenic A(H5N1) viruses isolated from a human case.

Method
replication assay
Sample type
bronchial epithelial cells
Experimental system
in vitro cell culture
1 records
Extraction confidence 0.70
Key finding

Eurasian H5N8 influenza viruses reassorted with North American avian influenza viruses, producing novel H5N2 genotypes, indicating viral exchange between distinct avian species populations.

Virus
Location
Supporting text

Reassortment of A(H5N8) viruses with avian viruses of North American lineage resulted in the generation of novel A(H5N2) viruses with novel genotypes.

Method
sequencing
Study design
phylogenetic analysis
Transmission direction
animal-to-animal
Geographic raw
North America
1 records
Extraction confidence 0.85
Key finding

Sequencing demonstrated that the novel North American A(H5N2) influenza viruses originated through reassortment of A(H5N8) with local avian viruses, acquiring PB1 and NP gene segments from North American waterfowl lineages.

Virus
Location
Not specified
Supporting text

Reassortment of A(H5N8) viruses with avian viruses of North American lineage resulted in the generation of novel A(H5N2) viruses with novel genotypes. Through sequencing of recent avian influenza viruses, we identified PB1 and NP gene segments very similar to those in the viruses isolated from North American waterfowl prior to the introduction of A(H5N8) to North America.

Genes or proteins
PB1; NP
Analysis methods
genome sequencing; reassortment analysis
1 records
Extraction confidence 0.90
Key finding

Hemagglutinin of A(H5N2) viruses exhibited avian-type receptor binding and pH activation properties, indicating molecular adaptation for replication in birds rather than mammals.

Virus
Host
Not specified
Location
Not specified
Supporting text

Molecular characterization of the hemagglutinin protein from A(H5N2) viruses showed that the receptor binding preference, cleavage, and pH of activation were highly adapted for replication in avian species and similar to those of other 2.3.4.4 viruses.

Genes or proteins
hemagglutinin
Mechanism types
receptor_binding; cell_entry
1 records
Extraction confidence 1.00
Key finding

A(H5N2) viruses emerged in North America through reassortment between introduced A(H5N8) viruses and North American avian influenza viruses, incorporating PB1 and NP gene segments from local waterfowl viruses.

Host
Not specified
Location
Not specified
Supporting text

Reassortment of A(H5N8) viruses with avian viruses of North American lineage resulted in the generation of novel A(H5N2) viruses with novel genotypes. Through sequencing, we identified PB1 and NP gene segments very similar to those in viruses isolated from North American waterfowl prior to the introduction of A(H5N8).

Event type
reassortment
Genes or segments
PB1; NP