Evidence map›Paper›PMID 33391219›Full record

ArticleFrontiers in microbiology2020

Variation and Molecular Basis for Enhancement of Receptor Binding of H9N2 Avian Influenza Viruses in China Isolates.

Yang Liu, Shuo Li, Huapeng Sun, Liangqi Pan, Xinxin Cui, Xuhui Zhu, Yaling Feng, Mingliang Li, Yanan Yu, Meihua Wu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Yang LiuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Shuo LiCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Huapeng SunCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Liangqi PanCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Xinxin CuiCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Xuhui ZhuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Yaling FengCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Mingliang LiCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Yanan YuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Meihua WuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Jiate LinCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Fengxiang XuCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Shaohua YuanCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Shujian HuangSchool of Life Science and Engineering, Foshan University, Foshan, China.
Hailiang SunCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Ming LiaoCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
South China Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, H9N2 avian influenza viruses (H9N2 AIVs) globally circulate in poultry and have acquired some adaptation to mammals. However, it is not clear what the molecular basis is for the variation in receptor-binding features of the H9N2 AIVs. The receptor-binding features of 92 H9N2 AIVs prevalent in China during 1994-2017 were characterized through solid-phase ELISA assay and reverse genetics. H9N2 AIVs that circulated in this period mostly belonged to clade h9.4.2. Two increasing incidents occurred in the ability of H9N2 AIVs to bind to avian-like receptors in 2002-2005 and 2011-2014. Two increasing incidents occurred in the strength of H9N2 AIVs to bind to human-like receptors in 2002-2005 and 2011-2017. We found that Q227M, D145G/N, S119R, and R246K mutations can significantly increase H9N2 AIVs to bind to both avian- and human-like receptors. A160D/N, Q156R, T205A, Q226L, V245I, V216L, D208E, T212I, R172Q, and S175N mutations can significantly enhance the strength of H9N2 AIVs to bind to human-like receptors. Our study also identified mutations T205A, D208E, V216L, Q226L, and V245I as the key sites leading to enhanced receptor binding of H9N2 AIVs during 2002-2005 and mutations S119R, D145G, Q156R, A160D, T212I, Q227M, and R246K as the key sites leading to enhanced receptor binding of H9N2 AIVs during 2011-2017. These findings further illustrate the receptor-binding characteristics of avian influenza viruses, which can be a potential threat to public health.

Indexed as

H9N2 AIVHAinfluenzareceptors binding sitevariation

Identifiers

PMID33391219
PMCPMC7773702
OpenAlexW3110742558

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.