Literature detail

Environmental connections of novel avian-origin H7N9 influenza virus infection and virus adaptation to the human.

Jun Li1 Xinfen Yu Xiaoying Pu Li Xie Yongxiang Sun Haixia Xiao Fenjuan Wang Hua Din Ying Wu Di Liu Guoqiu Zhao Jun Liu Jingcao Pan
Affiliations 1 institutions
  1. Hangzhou Center for Disease Control and Prevention, Hangzhou 310021, China.
PMID 23657795 2013 Sci China Life Sci eng ppublish
PubMed DOI Browse context

Article

Publication summary

A novel H7N9 influenza A virus has been discovered as the causative identity of the emerging acute respiratory infection cases in Shanghai, China. This virus has also been identified in cases of infection in the neighboring area Hangzhou City in Zhejiang Province. In this study, epidemiologic, clinical, and virological data from three patients in Hangzhou who were confirmed to be infected by the novel H7N9 influenza A virus were collected and analyzed. Human respiratory specimens and chicken feces from a contacted free market were tested for influenza virus by real-time reverse transcription PCR (RT-PCR) and sequencing. The clinical features of the three cases were similar featured with high fever and severe respiratory symptoms; however, only one of the patients died. A certain degree of diversity was observed among the three Hangzhou viruses sequenced from human samples compared with other reported H7N9 influenza A viruses. The sequences of the novel avian-origin H7N9 influenza viruses from Hangzhou City contained important amino acid substitutions related to human adaptation. One of the Hangzhou viruses had gained a novel amino acid substitution (Q226I) in the receptor binding region of hemagglutinin. More importantly, the virus sequenced from the chicken feces had a 627E substitution in the PB2 protein instead of the mammalian-adapted 627K substitution that was found in the PB2 proteins from the Hangzhou viruses from the three patients. Therefore, the newly-emerging H7N9 virus might be under adaptation pressure that will help it "jump" from avian to human hosts. The significance of these substitutions needs further exploration, with both laboratory experiments and extensive field surveillance.

Adaptation, Physiological Adult Aged Animals Base Sequence Birds China Environmental Exposure Geography Host-Pathogen Interactions Humans Influenza A Virus, H7N9 Subtype Influenza, Human Male Molecular Sequence Data Mutation Phylogeny Sequence Analysis, DNA

Structured evidence records

Evidence records

5 total
2 records
Extraction confidence 0.95
Key finding

The H7N9 virus from Hangzhou acquired a Q226I amino acid substitution in the hemagglutinin receptor binding region, indicating adaptation to human receptor usage.

Virus
Host
Not specified
Location
Not specified
Supporting text

One of the Hangzhou viruses had gained a novel amino acid substitution (Q226I) in the receptor binding region of hemagglutinin.

Genes or proteins
hemagglutinin
Mutations
Q226I
Mechanism types
receptor_binding; host_adaptation
Extraction confidence 0.95
Key finding

PB2 protein sequences from human-derived H7N9 viruses contained the mammalian-adaptive 627K substitution, differing from avian viruses with 627E, consistent with adaptation to human hosts.

Virus
Host
Not specified
Location
Not specified
Supporting text

The virus sequenced from the chicken feces had a 627E substitution in the PB2 protein instead of the mammalian-adapted 627K substitution that was found in the PB2 proteins from the Hangzhou viruses from the three patients.

Genes or proteins
PB2
Mutations
E627K
Mechanism types
polymerase_activity; host_adaptation
1 records
Extraction confidence 0.80
Key finding

Sequenced H7N9 influenza A viruses from humans and a chicken in Hangzhou showed Q226I substitution in hemagglutinin and PB2 627K/627E polymorphism, indicating genomic evolution associated with adaptation from avian to human hosts.

Virus
Location
Not specified
Supporting text

Human respiratory specimens and chicken feces from a contacted free market were tested for influenza virus by RT-PCR and sequencing. The sequences of the novel avian-origin H7N9 influenza viruses from Hangzhou City contained important amino acid substitutions related to human adaptation. One of the Hangzhou viruses had gained a novel amino acid substitution (Q226I) in the receptor binding region of hemagglutinin. More importantly, the virus sequenced from the chicken feces had a 627E substitution in the PB2 protein instead of the mammalian-adapted 627K substitution that was found in the PB2 proteins from the Hangzhou viruses from the three patients.

Genes or proteins
hemagglutinin; PB2
Analysis methods
sequencing
1 records
Extraction confidence 0.95
Key finding

Avian-origin H7N9 influenza A virus was detected in both chickens and humans, supporting an avian-to-human spillover in Hangzhou, China.

Virus
Location
Supporting text

Human respiratory specimens and chicken feces from a contacted free market were tested for influenza virus by real-time RT-PCR and sequencing. The newly-emerging H7N9 virus might be under adaptation pressure that will help it 'jump' from avian to human hosts.

Method
real-time RT-PCR; sequencing
Study design
field surveillance
Transmission direction
animal-to-human
Geographic raw
Hangzhou City, Zhejiang Province, China
Country inferred
China
1 records
Extraction confidence 0.70
Key finding

H7N9 influenza A virus was detected in chicken feces collected at a live poultry market and in human respiratory specimens from infected patients in Hangzhou, China, indicating active zoonotic surveillance at the animal-human interface.

Virus
Location
Supporting text

Human respiratory specimens and chicken feces from a contacted free market were tested for influenza virus by real-time reverse transcription PCR (RT-PCR) and sequencing.

Method
real-time reverse transcription PCR; sequencing
Sample type
feces
Geographic raw
Hangzhou, China
Country inferred
China