The PB2 co-adaptation of H10N8 avian influenza virus increases the pathogenicity to chickens and mice.

Bo Li1,2,3,4,5 Guanming Su1 Chencheng Xiao1 Jiahao Zhang1,2,3,4,5 Huanan Li1,2,3,4,5 Na Sun1 Guangjie Lao1 Yuandi Yu1 Xingxing Ren1 Wenbao Qi1,2,3,4,5 Xiuhui Wang1,6 Ming Liao1,2,3,4,5
Affiliations 6 institutions
  1. National Avian Influenza Para-Reference Laboratory, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
  2. Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou, China.
  3. Key Laboratory of Zoonoses, Ministry of Agricultural and Rural Affairs of the People's Republic of China, Guangzhou, China.
  4. National and Regional Joint Engineering Laboratory for Medicament of Zoonoses Prevention and Control, National Development and Reform Commission of the People's Republic of China, Guangzhou, China.
  5. Key Laboratory of Zoonoses Prevention and Control of Guangdong Province, Guangzhou, China.
  6. Hebei Province Poultry Engineering Technology Research Center, Hebei University of Engineering, Handan, People's Republic of China.

Abstract

Avian influenza (AI) is an important zoonotic disease, which can be transmitted across species barriers to other hosts, especially humans, posing a serious threat to the poultry industry and public health. In recent years, human cases infected with the H10N8, H9N2, and H7N9 of avian influenza viruses (AIVs) have been identified frequently as have the internal genes of H7N9 and H10N8, which are derived from H9N2 viruses. The adaptive mutation of the PB2 gene is an important way for the H10N8, H9N2, and H7N9 AIVs to spread across species to adapt to new hosts. Several well-known adaptive mutations in the PB2 gene, such as E627K, D701N, and A588V, significantly enhanced the virulence of the AIVs in mammals. However, the co-adaptation of AIVs to avian and mammalian hosts is rarely studied. In this study, we found that the mutations of PB2-I292V, PB2-R389K, PB2-A588V, PB2-T598M/V, PB2-L648V, and PB2-T676M substitutions significantly increased after 2012. In addition, in our previous studies, we found that the human-origin and avian-origin of H10N8 AIVs with very high homology also have these six mutation differences in PB2 gene, and the avian-origin H10N8 strain known as JX102 with all the key amino acids on the PB2 protein in the pre-evolutionary stage, so JX102 was chosen as a model strain. Among them, PB2-A588V significantly enhanced the activity of polymerase in avian and mammalian cells. Notably, animal experiments showed that PB2-A588V substitution increased the pathogenicity and transmissibility in chickens and the virulence of mice. The combined mutations of PB2-F6 (including PB2-I292V, PB2-R389K, PB2-A588V, PB2-T598M, PB2-L648V, and PB2-T676M) obtained higher adaptability of AIVs in avians and mammals than that of the single mutation of PB2-A588V, which suggested that the PB2 588 site is a key co-adaptation site and that synergies with other mutation sites can further enhance this co-adaptability. The results of this study show that the emergence of co-adaptation not only increases the threat to avians and mammals but may also contribute to a pandemic among avians and cross the interspecies barrier to mammals.

Supporting text Virus Host Location
avian influenza virus 59 co-adaptation 1 PB2-A588V 1 Influenza A Virus, H10N8 Subtype 4 Influenza A Virus, H7N9 Subtype 87 Influenza A Virus, H9N2 Subtype 71 Influenza in Birds 341 Influenza, Human 286 Animals 1949 Chickens 146 Humans 1441 Mammals 92 Mice 253 Viral Proteins 152 Virulence 108

Evidence records

4 total
Experimental Infection
2 records · 1 evidence types
Evidence type
2 records
OVE4794
Key finding

PB2-A588V substitution in H10N8 avian influenza virus increased pathogenicity and transmissibility in chickens under controlled infection.

Virus
Host
Location
Not specified
Supporting text

Animal experiments showed that PB2-A588V substitution increased the pathogenicity and transmissibility in chickens.

Method
animal infection experiment | clinical and transmission assessment
Experimental system
animal infection experiment in chickens
OVE4795
Key finding

PB2-A588V substitution in H10N8 avian influenza virus increased virulence in mice under controlled infection.

Virus
Host
Location
Not specified
Supporting text

Animal experiments showed that PB2-A588V substitution increased the virulence of mice.

Method
animal infection experiment | clinical and survival or morbidity assessment
Experimental system
animal infection experiment in mice
Functional Mechanism
2 records · 1 evidence types
Evidence type
2 records
OVE4796
Key finding

The PB2-A588V mutation in H10N8 avian influenza virus significantly enhanced polymerase activity in avian and mammalian cells, indicating host-adaptive molecular change.

Virus
Host
Not specified
Location
Not specified
Supporting text

Among them, PB2-A588V significantly enhanced the activity of polymerase in avian and mammalian cells.

Genes or proteins
PB2 | polymerase
Mutations
PB2-A588V
Mechanism types
replication adaptation | host-range expansion
OVE4797
Key finding

Combined PB2 mutations including I292V, R389K, A588V, T598M, L648V, and T676M in H10N8 avian influenza virus increased adaptability in avian and mammalian hosts, demonstrating PB2 co-adaptation across hosts.

Virus
Host
Not specified
Location
Not specified
Supporting text

The combined mutations of PB2-F6 (including PB2-I292V, PB2-R389K, PB2-A588V, PB2-T598M, PB2-L648V, and PB2-T676M) obtained higher adaptability of AIVs in avians and mammals than that of the single mutation of PB2-A588V, which suggested that the PB2 588 site is a key co-adaptation site and that synergies with other mutation sites can further enhance this co-adaptability.

Genes or proteins
PB2
Mutations
PB2-I292V | PB2-R389K | PB2-A588V | PB2-T598M | PB2-L648V | PB2-T676M
Mechanism types
replication adaptation | host-range expansion | virulence adaptation