Evidence map›Paper›PMID 36857394›Full record

ArticlePLoS pathogens2023

Influenza A virus reassortment is strain dependent.

Kishana Y Taylor, Ilechukwu Agu, Ivy José, Sari Mäntynen, A J Campbell, Courtney Mattson, Tsui-Wen Chou, Bin Zhou, David Gresham, Elodie Ghedin and 1 more

Open access · goldFull text read
In one paragraph

Article in PLoS pathogens, 2023. 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
6.0field-weighted citation impact, top 3% 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, 28 citations in OpenAlex.

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  10. Mechanistic insights into the small-molecule inhibition of influenza A virus entry.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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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

11 authors at 3 institutions in 1 country.

Kishana Y TaylorDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
Ilechukwu AguDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
Ivy JoséDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
Sari MäntynenDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
A J CampbellDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
Courtney MattsonDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.
Tsui-Wen ChouCenter for Genomics and Systems Biology + Department of Biology New York University New York, United States of America.
Bin ZhouCenter for Genomics and Systems Biology + Department of Biology New York University New York, United States of America.
David GreshamCenter for Genomics and Systems Biology + Department of Biology New York University New York, United States of America.
Elodie GhedinCenter for Genomics and Systems Biology + Department of Biology New York University New York, United States of America.
Samuel L Díaz MuñozDepartment of Microbiology and Molecular Genetics University of California, Davis Davis, California.ORCID 0000-0003-2967-9806
University of California, Davis · USNew York University · USNational Institute of Allergy and Infectious Diseases · US

Funding

Genomic profiling of influenza infections to identify biomarkers of disease severityZIAAI001323 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GHEDIN, ELODIE · 2020 to 2025
$8.0M
Dissecting the drivers of avian influenza virus reassortment in the wild bird reservoirR00AI119401 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DIAZ, SAMUEL L · 2017 to 2018
$493k
High-throughput studies of reassortment and coinfection of influenza virusesK99AI119401 · NIAID · NEW YORK UNIVERSITY · PI DIAZ, SAMUEL L · 2016 to 2016
$112k
NIAID NIH HHS K99 AI119401NIAID NIH HHS R00 AI119401
6 · The paper itself

Abstract

RNA viruses can exchange genetic material during coinfection, an interaction that creates novel strains with implications for viral evolution and public health. Influenza A viral genetic exchange can occur when genome segments from distinct strains reassort in coinfected cells. Predicting potential genomic reassortment between influenza strains has been a long-standing goal. Experimental coinfection studies have shed light on factors that limit or promote reassortment. However, determining the reassortment potential between diverse Influenza A strains has remained elusive. To address this challenge, we developed a high throughput genotyping approach to quantify reassortment among a diverse panel of human influenza virus strains encompassing two pandemics (swine and avian origin), three specific epidemics, and both circulating human subtypes A/H1N1 and A/H3N2. We found that reassortment frequency (the proportion of reassortants generated) is an emergent property of specific pairs of strains where strain identity is a predictor of reassortment frequency. We detect little evidence that antigenic subtype drives reassortment as intersubtype (H1N1xH3N2) and intrasubtype reassortment frequencies were, on average, similar. Instead, our data suggest that certain strains bias the reassortment frequency up or down, independently of the coinfecting partner. We observe that viral productivity is also an emergent property of coinfections, but uncorrelated to reassortment frequency; thus viral productivity is a separate factor affecting the total number of reassortants produced. Assortment of individual segments among progeny and pairwise segment combinations within progeny generally favored homologous combinations. These outcomes were not related to strain similarity or shared subtype but reassortment frequency was closely correlated to the proportion of both unique genotypes and of progeny with heterologous pairwise segment combinations. We provide experimental evidence that viral genetic exchange is potentially an individual social trait subject to natural selection, which implies the propensity for reassortment is not evenly shared among strains. This study highlights the need for research incorporating diverse strains to discover the traits that shift the reassortment potential to realize the goal of predicting influenza virus evolution resulting from segment exchange.

Indexed as

CoinfectionInfluenza A virusInfluenza A Virus, H1N1 SubtypeInfluenza, HumanOrthomyxoviridae InfectionsAnimalsHumansInfluenza A Virus, H3N2 SubtypeReassortant VirusesSwine

Identifiers

PMID36857394
PMCPMC10010518
OpenAlexW4322720367

What OpenQuestion holds

Textfull text, public
LicenceCC0
measurements read49
identifiers read12
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.