Evidence map›Paper›PMID 38648521›Full record

ArticleMolecular biology and evolution2024

The Number and Pattern of Viral Genomic Reassortments are not Necessarily Identifiable from Segment Trees.

Qianying Lin, Emma E Goldberg, Thomas Leitner, Carmen Molina-París, Aaron A King, Ethan O Romero-Severson

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

3 citing papers in PubMed, 4 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

6 authors at 2 institutions in 1 country.

Qianying LinTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, USA.ORCID 0000-0001-8620-9910
Emma E GoldbergTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, USA.
Thomas LeitnerTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, USA.ORCID 0000-0001-8160-2588
Carmen Molina-ParísTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, USA.ORCID 0000-0001-9828-6737
Aaron A KingDepartment of Ecology & Evolutionary Biology, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-6159-3207
Ethan O Romero-SeversonTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM, USA.ORCID 0000-0002-8082-1225
Los Alamos National Laboratory · USSanta Fe Institute · US

Funding

Reconstructing HIV Epidemics from HIV PhylogeneticsR01AI087520 · NIAID · TRIAD NATIONAL SECURITY, LLC · PI Thomas K. Leitner · 2010 to 2026
$11.2M
Dynamical modeling of hospital transmission and antibiotic resistance evolution in a multidrug resistant nosocomial pathogenR01AI143852 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOODS, ROBERT J · 2019 to 2023
$2.9M
US-UK Collab: Modelling reassortment at the cellular, clinical, and phylogenetic level in emerging BunyavirusesR01AI167048 · NIAID · TRIAD NATIONAL SECURITY, LLC · PI MOLINA-PARIS, CARMEN · 2021 to 2025
$2.2M
National Science Foundation/National Institutes of Health Interface Program #1761603NIAID NIH HHS R01 AI087520NIAID NIH HHS R01 AI143852NIAID NIH HHS R01 AI167048NIH HHS #R01AI167048
6 · The paper itself

Abstract

Reassortment is an evolutionary process common in viruses with segmented genomes. These viruses can swap whole genomic segments during cellular co-infection, giving rise to novel progeny formed from the mixture of parental segments. Since large-scale genome rearrangements have the potential to generate new phenotypes, reassortment is important to both evolutionary biology and public health research. However, statistical inference of the pattern of reassortment events from phylogenetic data is exceptionally difficult, potentially involving inference of general graphs in which individual segment trees are embedded. In this paper, we argue that, in general, the number and pattern of reassortment events are not identifiable from segment trees alone, even with theoretically ideal data. We call this fact the fundamental problem of reassortment, which we illustrate using the concept of the "first-infection tree," a potentially counterfactual genealogy that would have been observed in the segment trees had no reassortment occurred. Further, we illustrate four additional problems that can arise logically in the inference of reassortment events and show, using simulated data, that these problems are not rare and can potentially distort our observation of reassortment even in small data sets. Finally, we discuss how existing methods can be augmented or adapted to account for not only the fundamental problem of reassortment, but also the four additional situations that can complicate the inference of reassortment.

Indexed as

Genome, ViralPhylogenyReassortant VirusesEvolution, MolecularModels, Geneticgenomic reassortmentmolecular epidemiologyphylodynamicspopulation genetics

Identifiers

PMID38648521
PMCPMC11152448
OpenAlexW4395012819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.