Evidence map›Paper›PMID 34570829›Full record

ArticlePLoS pathogens2021

Influenza A virus segments five and six can harbor artificial introns allowing expanded coding capacity.

Heather M Froggatt, Kaitlyn N Burke, Ryan R Chaparian, Hector A Miranda, Xinyu Zhu, Benjamin S Chambers, Nicholas S Heaton

Abstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
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

7 authors.

Heather M FroggattDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.
Kaitlyn N BurkeDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.ORCID 0000-0002-4868-4494
Ryan R ChaparianDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.ORCID 0000-0003-3838-1868
Hector A MirandaDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.ORCID 0000-0003-4072-6634
Xinyu ZhuDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.
Benjamin S ChambersDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.ORCID 0000-0002-8095-5012
Nicholas S HeatonDepartment of Molecular Genetics and Microbiology Duke University School of Medicine Durham, North Carolina, United States of America.ORCID 0000-0002-5307-3428

Funding

Collaborative Influenza Vaccine Innovation Centers (CIVICs): Component A: Vaccine Center75N93019C00050 · NIAID · DUKE UNIVERSITY · PI MOODY, TONY · 2019 to 2025
$69.1M
The pathogenic effects of epithelial cells surviving direct influenza virus infectionR01AI137031 · NIAID · DUKE UNIVERSITY · PI Nicholas S Heaton · 2019 to 2026
$4.5M
Loss of cellular identity after influenza virus infection and effects on pulmonary functionR01HL142985 · NHLBI · DUKE UNIVERSITY · PI HEATON, NICHOLAS S · 2018 to 2022
$2.8M
NHLBI NIH HHS R01 HL142985NIAID NIH HHS 75N93019C00050NIAID NIH HHS R01 AI137031
6 · The paper itself

Abstract

Influenza A viruses encode their genomes across eight, negative sense RNA segments. The six largest segments produce mRNA transcripts that do not generally splice; however, the two smallest segments are actively spliced to produce the essential viral proteins NEP and M2. Thus, viral utilization of RNA splicing effectively expands the viral coding capacity without increasing the number of genomic segments. As a first step towards understanding why splicing is not more broadly utilized across genomic segments, we designed and inserted an artificial intron into the normally nonsplicing NA segment. This insertion was tolerated and, although viral mRNAs were incompletely spliced, we observed only minor effects on viral fitness. To take advantage of the unspliced viral RNAs, we encoded a reporter luciferase gene in frame with the viral ORF such that when the intron was not removed the reporter protein would be produced. This approach, which we also show can be applied to the NP encoding segment and in different viral genetic backgrounds, led to high levels of reporter protein expression with minimal effects on the kinetics of viral replication or the ability to cause disease in experimentally infected animals. These data together show that the influenza viral genome is more tolerant of splicing than previously appreciated and this knowledge can be leveraged to develop viral genetic platforms with utility for biotechnology applications.

Indexed as

AnimalsHumansInfluenza A virusIntronsRNA SplicingRNA, ViralRNA, Viral

Identifiers

PMID34570829
PMCPMC8496794

What OpenQuestion holds

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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.