Evidence map›Paper›PMID 25713566›Full record

ArticleFrontiers in microbiology2015

PB2 segment promotes high-pathogenicity of H5N1 avian influenza viruses in mice.

Hailiang Sun, Pengfei Cui, Yafen Song, Yan Qi, Xiaokang Li, Wenbao Qi, Chenggang Xu, Peirong Jiao, Ming Liao

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Hailiang SunCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Pengfei CuiCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Yafen SongCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Yan QiCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Xiaokang LiCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Wenbao QiCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Chenggang XuCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Peirong JiaoCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.
Ming LiaoCollege of Veterinary Medicine, South China Agricultural University Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

H5N1 influenza viruses with high lethality are a continuing threat to humans and poultry. Recently, H5N1 high-pathogenicity avian influenza virus (HPAIV) has been shown to transmit through aerosols between ferrets in lab experiments by acquiring some mutation. This is another deeply aggravated threat of H5N1 HPAIV to humans. To further explore the molecular determinant of H5N1 HPAIV virulence in a mammalian model, we compared the virulence of A/Duck/Guangdong/212/2004 (DK212) and A/Quail/Guangdong/90/2004 (QL90). Though they were genetically similar, they had different pathogenicity in mice, as well as their 16 reassortants. The results indicated that a swap of the PB2 gene could dramatically decrease the virulence of rgDK212 in mice (1896-fold) but increase the virulence of rgQL90 in mice (60-fold). Furthermore, the polymerase activity assays showed that swapping PB2 genes between these two viruses significantly changed the activity of polymerase complexes in 293T cells. The mutation Ser715Asn in PB2 sharply attenuated the virulence of rgDK212 in mice (2710-fold). PB2 segment promotes high-pathogenicity of H5N1 avian influenza viruses in mice and 715 Ser in PB2 plays an important role in determining high virulence of DK212 in mice.

Indexed as

H5N1influenza virusmicemutantsreassortantvirulence

Identifiers

PMID25713566
PMCPMC4322641

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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.