Mouse lung-adapted mutation of E190G in hemagglutinin from H5N1 influenza virus contributes to attenuation in mice.

Pengfei Han1 Yi Hu1 Wei Sun1 Sen Zhang1 Yuchang Li1 Xiaoyan Wu1 Yinhui Yang1 Qingyu Zhu1 Tao Jiang1 Jing Li1 Chengfeng Qin1
Affiliations 1 institutions
  1. Department of Virology, State Key Laboratory of Pathogens and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, PR China.

Abstract

The highly pathogenic H5N1 avian influenza virus is one of the greatest influenza pandemic threats since 2003. The association of the receptor binding domain (RBD) with the virulence of influenza virus is rarely addressed, particularly of H5N1 influenza viruses. In this study, BALB/c mice were intranasally infected with A/Vietnam/1194/2004 (VN1194, H5N1). The mouse lung-adapted variants were isolated and the mutation of E190G (H3 numbering) in the RBD was recognized. The recombinant virus, rVN-E190G carrying E190G in hemagglutinin (HA) was designed and rescued using reverse genetics techniques. The receptor binding activity, growth curve and pathogenicity in mice of the rVN-E190G were investigated. Results demonstrated that rVN-E190G virus increased the binding avidity to α2,6 SA (sialic acid) and reduced the affinity to α2,3 SA, meanwhile weakened the viral replication in vitro. Moreover, the virulence assessment demonstrated that rVN-E190G was attenuated in mice. These results indicated that the mutation E190G in HA decreases H5N1 viral replication in vitro and significantly attenuates virulence in vivo. These findings identify one of the determinants in RBD which can be associated with H5N1 virulence in mice.

Supporting text Virus Host Location
attenuation 2 H5N1 82 hemagglutinin 31 mouse model 5 receptor binding domain 7 Adaptation, Biological 25 Mutation, Missense 26 Animals 1948 Body Weight 2 Female 289 Hemagglutinin Glycoproteins, Influenza Virus 180 Influenza A Virus, H5N1 Subtype 300 Lung 65 Mice, Inbred BALB C 73 Orthomyxoviridae Infections 228 Survival Analysis 7 Viral Load 36 Viral Plaque Assay 5 Virulence 108 Virulence Factors 9 Virus Attachment 55 Virus Replication 191 hemagglutinin, avian influenza A virus 26

Evidence records

4 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE2101
Key finding

Mouse lung‑adapted variants of H5N1 influenza virus (A/Vietnam/1194/2004) were isolated from infected mice.

Virus
Host
Location
Not specified
Supporting text

BALB/c mice were intranasally infected with A/Vietnam/1194/2004 (VN1194, H5N1). The mouse lung‑adapted variants were isolated and the mutation of E190G (H3 numbering) in the RBD was recognized.

Sample type
lung tissue
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE2100
Key finding

The recombinant H5N1 influenza virus rVN-E190G carrying the E190G mutation in hemagglutinin was attenuated in BALB/c mice compared to the parental H5N1 virus.

Virus
Host
Location
Not specified
Supporting text

Moreover, the virulence assessment demonstrated that rVN-E190G was attenuated in mice.

Method
intranasal infection | virulence assessment
Experimental system
in vivo infection model using BALB/c mice
Functional Mechanism
2 records · 2 evidence types
Evidence type
1 records
OVE2099
Key finding

The recombinant H5N1 virus rVN-E190G carrying the E190G mutation in hemagglutinin binds more strongly to α2,6-linked sialic acid and less to α2,3-linked sialic acid, indicating altered receptor specificity.

Virus
Host
Not specified
Location
Not specified
Supporting text

Results demonstrated that rVN-E190G virus increased the binding avidity to α2,6 SA (sialic acid) and reduced the affinity to α2,3 SA.

Method
receptor binding assay
Receptors
α2,6 SA | α2,3 SA
Evidence type
1 records
OVE2098
Key finding

Mutation E190G in hemagglutinin of H5N1 influenza virus decreases replication and virulence in mice, indicating receptor-binding adaptation affecting α2,6 versus α2,3 sialic acid affinity.

Virus
Host
Not specified
Location
Not specified
Supporting text

Results demonstrated that rVN-E190G virus increased the binding avidity to α2,6 SA and reduced the affinity to α2,3 SA, meanwhile weakened the viral replication in vitro. Moreover, the virulence assessment demonstrated that rVN-E190G was attenuated in mice.

Genes or proteins
hemagglutinin (HA)
Receptors
α2,6 sialic acid (SA) | α2,3 sialic acid (SA)
Mutations
E190G
Mechanism types
receptor binding | virulence adaptation | replication adaptation