Evidence map›Paper›PMID 30156554›Full record

ArticleeLife2018

Long read sequencing reveals poxvirus evolution through rapid homogenization of gene arrays.

Thomas A Sasani, Kelsey R Cone, Aaron R Quinlan, Nels C Elde

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Poxvirus Recombination.Pathogens (Basel, Switzerland) · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Thomas A Sasani *Department of Human Genetics, University of Utah, Salt Lake, United States.ORCID 0000-0003-2317-1374
Kelsey R Cone *Department of Human Genetics, University of Utah, Salt Lake, United States.ORCID 0000-0002-4547-7174
Aaron R Quinlan *Department of Human Genetics, University of Utah, Salt Lake, United States.ORCID 0000-0003-1756-0859
Nels C Elde *Department of Human Genetics, University of Utah, Salt Lake, United States.ORCID 0000-0002-0426-1377
University of Utah · US

Funding

TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
Training Program in Microbial PathogenesisT32AI055434 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI MULVEY, MATTHEW A, PLANELLES, VICENTE · 2004 to 2025
$6.0M
New algorithms and tools for large-scale genomic analysesR01HG006693 · NHGRI · UNIVERSITY OF VIRGINIA · PI QUINLAN, AARON R · 2012 to 2018
$3.1M
Software for exploring all forms of genetic variation in any speciesR01GM124355 · NIGMS · UNIVERSITY OF UTAH · PI QUINLAN, AARON R · 2017 to 2020
$1.8M
Evolutionary innovations from host-microbe interactionsR35GM134936 · NIGMS · UNIVERSITY OF UTAH · PI ELDE, NELS C. · 2020 to 2024
$1.7M
Mechanisms of mimicry underlying the evolution of a model poxvirusR01GM114514 · NIGMS · UNIVERSITY OF UTAH · PI ELDE, NELS C. · 2015 to 2019
$1.6M
Burroughs Wellcome Fund 1015462NHGRI NIH HHS R01 HG006693NIAID NIH HHS T32 AI055434NIGMS NIH HHS R01 GM114514NIGMS NIH HHS R01 GM124355NIGMS NIH HHS R35 GM134936NIGMS NIH HHS T32 GM007464NIH HHS R01GM114514NIH HHS R01GM124355NIH HHS R01HG006693NIH HHS T32AI055434NIH HHS T32GM007464University of Utah Equipment Grant
6 · The paper itself

Abstract

Poxvirus adaptation can involve combinations of recombination-driven gene copy number variation and beneficial single nucleotide variants (SNVs) at the same loci. How these distinct mechanisms of genetic diversification might simultaneously facilitate adaptation to host immune defenses is unknown. We performed experimental evolution with vaccinia virus populations harboring a SNV in a gene actively undergoing copy number amplification. Using long sequencing reads from the Oxford Nanopore Technologies platform, we phased SNVs within large gene copy arrays for the first time. Our analysis uncovered a mechanism of adaptive SNV homogenization reminiscent of gene conversion, which is actively driven by selection. This study reveals a new mechanism for the fluid gain of beneficial mutations in genetic regions undergoing active recombination in viruses and illustrates the value of long read sequencing technologies for investigating complex genome dynamics in diverse biological systems.

Indexed as

Evolution, MolecularHigh-Throughput Nucleotide SequencingAdaptation, PhysiologicalDNA Copy Number VariationsGene ConversionPolymorphism, Single NucleotideRecombination, GeneticVaccinia viruscopy number variationevolutionary biologyexperimental evolutiongene conversionlong read sequencingpoxvirusvaccinia virusvirus

Identifiers

PMID30156554
PMCPMC6115191
OpenAlexW2950595312

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.