A Novel Reassortant Avian H7N6 Influenza Virus Is Transmissible in Guinea Pigs via Respiratory Droplets.

Zongzheng Zhao1,2 Lina Liu1 Zhendong Guo2 Chunmao Zhang2 Zhongyi Wang2 Guoyuan Wen1 Wenting Zhang1 Yu Shang1 Tengfei Zhang1 Zuwu Jiao1 Ligong Chen3 Cheng Zhang3 Huan Cui3 Meilin Jin4 Chengyu Wang2 Qingping Luo1 Huabin Shao1
Affiliations 4 institutions
  1. Institute of Animal Husbandry and Veterinary Sciences, Hubei Academy of Agricultural Sciences, Wuhan, China.
  2. Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun, China.
  3. College of Veterinary Medicine, Hebei Agricultural University, Baoding, China.
  4. College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.

Abstract

Since 2013, H7N9 and H5N6 avian influenza viruses (AIVs) have caused sporadic human infections and deaths and continued to circulate in the poultry industry. Since 2014, H7N6 viruses which might be reassortants of H7N9 and H5N6 viruses, have been isolated in China. However, the biological properties of H7N6 viruses are unknown. Here, we characterize the receptor binding preference, pathogenicity and transmissibility of a H7N6 virus A/chicken/Hubei/00095/2017(H7N6) (abbreviated HB95), and a closely related H7N9 virus, A/chicken/Hubei/00093/2017(H7N9) (abbreviated HB93), which were isolated from poultry in Hubei Province, China, in 2017. Phylogenetic analyses demonstrated that the hemagglutinin (HA) gene of HB95 is closely related to those of HB93 and human-origin H7N9 viruses, and that the neuraminidase (NA) gene of HB95 shared the highest nucleotide similarity with those of H5N6 viruses. HB95 and HB93 had binding affinity for human-like α2, 6-linked sialic acid receptors and were virulent in mice without prior adaptation. In addition, in guinea pig model, HB93 was transmissible by direct contact, but HB95 was transmissible via respiratory droplets. These results revealed the potential threat to public health posed by H7N6 influenza viruses and emphasized the need for continued surveillance of the circulation of this subtype in poultry.

Supporting text Virus Host Location
avian H7N6 influenza A virus 1 pathogenicity 54 reassortment 36 receptor binding 30 transmissibility 13

Evidence records

8 total
Zoonotic Surveillance
2 records · 1 evidence types
Evidence type
2 records
OVE3227
Key finding

An H7N6 virus designated A/chicken/Hubei/00095/2017(H7N6) was isolated from poultry in Hubei Province, China, in 2017.

Virus
Host
Location
Not specified
Supporting text

A/chicken/Hubei/00095/2017(H7N6) (abbreviated HB95) ... which was isolated from poultry in Hubei Province, China, in 2017.

OVE3228
Key finding

An H7N9 virus designated A/chicken/Hubei/00093/2017(H7N9) was isolated from poultry in Hubei Province, China, in 2017.

Virus
Host
Location
Not specified
Supporting text

A closely related H7N9 virus, A/chicken/Hubei/00093/2017(H7N9) (abbreviated HB93) ... which was isolated from poultry in Hubei Province, China, in 2017.

Experimental Infection
4 records · 2 evidence types
Evidence type
2 records
OVE3231
Key finding

The avian influenza virus HB95 was virulent in mice without prior adaptation.

Virus
Host
Location
Not specified
Supporting text

HB95 and HB93 had binding affinity for human-like α2, 6-linked sialic acid receptors and were virulent in mice without prior adaptation.

Method
in vivo infection of mice | observation of disease signs and mortality
Experimental system
mouse infection model
OVE3232
Key finding

The avian influenza virus HB93 was virulent in mice without prior adaptation.

Virus
Host
Location
Not specified
Supporting text

HB95 and HB93 had binding affinity for human-like α2, 6-linked sialic acid receptors and were virulent in mice without prior adaptation.

Method
in vivo infection of mice | observation of disease signs and mortality
Experimental system
mouse infection model
Evidence type
2 records
OVE3234
Key finding

HB95 virus was experimentally transmissible between guinea pigs via respiratory droplets.

Virus
Host
Location
Not specified
Supporting text

In guinea pig model, HB95 was transmissible via respiratory droplets.

Method
animal transmission experiment | aerosol or respiratory droplet exposure assay
Experimental system
guinea pig respiratory droplet transmission model
OVE3233
Key finding

HB93 virus was experimentally transmissible between guinea pigs by direct contact.

Virus
Host
Location
Not specified
Supporting text

In guinea pig model, HB93 was transmissible by direct contact.

Method
animal transmission experiment | direct contact exposure assay
Experimental system
guinea pig contact transmission model
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE3229
Key finding

The H7N6 virus HB95 binds to human-like α2,6-linked sialic acid receptors, indicating human-type receptor affinity.

Virus
Host
Not specified
Location
Not specified
Supporting text

HB95 and HB93 had binding affinity for human-like α2,6-linked sialic acid receptors.

Method
receptor binding assay
Receptors
human-like α2,6-linked sialic acid receptor
Genomic Evolution
1 records · 1 evidence types
Evidence type
1 records
OVE3235
Key finding

H7N6 virus HB95 is a reassortant containing an HA gene related to H7N9 viruses and an NA gene derived from H5N6 viruses.

Virus
Host
Not specified
Location
Not specified
Supporting text

Phylogenetic analyses demonstrated that the hemagglutinin (HA) gene of HB95 is closely related to those of HB93 and human-origin H7N9 viruses, and that the neuraminidase (NA) gene of HB95 shared the highest nucleotide similarity with those of H5N6 viruses.

Event type
reassortment
Genes or segments
HA | NA