Evidence map›Paper›PMID 26368015›Full record

ArticlePloS one2015

A Single Amino Acid in the M1 Protein Responsible for the Different Pathogenic Potentials of H5N1 Highly Pathogenic Avian Influenza Virus Strains.

Naganori Nao, Masahiro Kajihara, Rashid Manzoor, Junki Maruyama, Reiko Yoshida, Mieko Muramatsu, Hiroko Miyamoto, Manabu Igarashi, Nao Eguchi, Masahiro Sato and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

50 citing papers in PubMed, 64 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

15 authors at 1 institution in 2 countries.

Naganori NaoResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Masahiro KajiharaResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Rashid ManzoorResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Junki MaruyamaResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Reiko YoshidaResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Mieko MuramatsuResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Hiroko MiyamotoResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Manabu IgarashiResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Nao EguchiResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Masahiro SatoResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Tatsunari KondohResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Masatoshi OkamatsuGraduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Yoshihiro SakodaGraduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Hiroshi KidaResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan; Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan.
Ayato TakadaResearch Center for Zoonosis Control, Hokkaido University, Sapporo, Japan; Global Institution for Collaborative Research and Education, Hokkaido University, Sapporo, Japan; School of Veterinary Medicine, the University of Zambia, Lusaka, Zambia.
Hokkaido University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Two highly pathogenic avian influenza virus strains, A/duck/Hokkaido/WZ83/2010 (H5N1) (WZ83) and A/duck/Hokkaido/WZ101/2010 (H5N1) (WZ101), which were isolated from wild ducks in Japan, were found to be genetically similar, with only two amino acid differences in their M1 and PB1 proteins at positions 43 and 317, respectively. We found that both WZ83 and WZ101 caused lethal infection in chickens but WZ101 killed them more rapidly than WZ83. Interestingly, ducks experimentally infected with WZ83 showed no or only mild clinical symptoms, whereas WZ101 was highly lethal. We then generated reassortants between these viruses and found that exchange of the M gene segment completely switched the pathogenic phenotype in both chickens and ducks, indicating that the difference in the pathogenicity for these avian species between WZ83 and WZ101 was determined by only a single amino acid in the M1 protein. It was also found that WZ101 showed higher pathogenicity than WZ83 in mice and that WZ83, whose M gene was replaced with that of WZ101, showed higher pathogenicity than wild-type WZ83, although this reassortant virus was not fully pathogenic compared to wild-type WZ101. These results suggest that the amino acid at position 43 of the M1 protein is one of the factors contributing to the pathogenicity of H5N1 highly pathogenic avian influenza viruses in both avian and mammalian hosts.

Indexed as

Amino Acid SubstitutionMutation, MissenseAnimalsChick EmbryoDucksInfluenza A Virus, H5N1 SubtypeMiceOrthomyxoviridae InfectionsViral Matrix ProteinsM1 protein, Influenza A virusViral Matrix Proteins

Identifiers

PMID26368015
PMCPMC4569272
OpenAlexW1916745146

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.