Evidence map›Paper›PMID 29062062›Full record

ArticleScientific reports2017

Localised genetic heterogeneity provides a novel mode of evolution in dsDNA phages.

Damian J Magill, Phillip A Kucher, Victor N Krylov, Elena A Pleteneva, John P Quinn, Leonid A Kulakov

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Host Range Expansion ofPHAGE (New Rochelle, N.Y.) · 2020
    Article
  5. 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

6 authors.

Damian J MagillQueen's University Belfast, School of Biological Sciences, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland.
Phillip A KucherQueen's University Belfast, School of Biological Sciences, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland.
Victor N KrylovDepartment of Microbiology, Laboratory for Genetics of Bacteriophages, I.I. Mechnikov Research Institute for Vaccines and Sera, Moscow, Russia.
Elena A PletenevaDepartment of Microbiology, Laboratory for Genetics of Bacteriophages, I.I. Mechnikov Research Institute for Vaccines and Sera, Moscow, Russia.
John P QuinnQueen's University Belfast, School of Biological Sciences, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland.
Leonid A KulakovQueen's University Belfast, School of Biological Sciences, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland. l.kulakov@qub.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Red Queen hypothesis posits that antagonistic co-evolution between interacting species results in recurrent natural selection via constant cycles of adaptation and counter-adaptation. Interactions such as these are at their most profound in host-parasite systems, with bacteria and their viruses providing the most intense of battlefields. Studies of bacteriophage evolution thus provide unparalleled insight into the remarkable elasticity of living entities. Here, we report a novel phenomenon underpinning the evolutionary trajectory of a group of dsDNA bacteriophages known as the phiKMVviruses. Employing deep next generation sequencing (NGS) analysis of nucleotide polymorphisms we discovered that this group of viruses generates enhanced intraspecies heterogeneity in their genomes. Our results show the localisation of variants to genes implicated in adsorption processes, as well as variation of the frequency and distribution of SNPs within and between members of the phiKMVviruses. We link error-prone DNA polymerase activity to the generation of variants. Critically, we show trans-activity of this phenomenon (the ability of a phiKMVvirus to dramatically increase genetic variability of a co-infecting phage), highlighting the potential of phages exhibiting such capabilities to influence the evolutionary path of other viruses on a global scale.

Indexed as

Evolution, MolecularBacteriophagesDNA-Directed DNA PolymeraseDNA, ViralHigh-Throughput Nucleotide SequencingModels, MolecularPhenotypeProtein ConformationSequence Analysis, DNADNA-Directed DNA PolymeraseDNA, Viral

Identifiers

PMID29062062
PMCPMC5653853

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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.