Evidence map›Paper›PMID 25126112›Full record

ArticleJournal of biological engineering2014

Challenges in predicting the evolutionary maintenance of a phage transgene.

Matthew Schmerer, Ian J Molineux, Dilara Ally, Jabus Tyerman, Nicole Cecchini, James J Bull

Open access · goldAbstract read
In one paragraph

Article in Journal of biological engineering, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Pathogens (Basel, Switzerland) · 2024
    Review
  2. Review
  3. Article
  4. Basics for Improved Use of Phages for Therapy.Antibiotics (Basel, Switzerland) · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Recombinant vector vaccine evolution.PLoS computational biology · 2019
    Article
  9. Review
  10. Article
  11. Review
  12. 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 at 3 institutions in 1 country.

Matthew SchmererCenter for Computational Biology and Bioinformatics, The University of Texas at Austin, Austin, TX, USA.
Ian J MolineuxDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA ; Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, USA.
Dilara AllyBayer Crop Science - Biologics, 1540 Drew Ave, Unit 170, Davis, CA, USA.
Jabus TyermanTotal New Energies USA Inc., 5858 Horton Street, Suite 253, Emeryville, CA, USA.
Nicole CecchiniDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, USA.
James J BullCenter for Computational Biology and Bioinformatics, The University of Texas at Austin, Austin, TX, USA ; Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, USA ; Department of Integrative Biology, The University of Texas at Austin, Austin, TX, USA.
The University of Texas at Austin · USBayer (United States) · USTotal (United States) · US

Funding

Experimental viral evolution at high mutation rateR01GM057756 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI BULL, JAMES J · 1998 to 2013
$2.9M
NIGMS NIH HHS R01 GM057756
6 · The paper itself

Abstract

backgroundIn prior work, a phage engineered with a biofilm-degrading enzyme (dispersin B) cleared artificial, short-term biofilms more fully than the phage lacking the enzyme. An unresolved question is whether the transgene will be lost or maintained during phage growth - its loss would limit the utility of the engineering. Broadly supported evolutionary theory suggests that transgenes will be lost through a 'tragedy of the commons' mechanism unless the ecology of growth in biofilms meets specific requirements. We test that theory here.

resultsFunctional properties of the transgenic phage were identified. Consistent with the previous study, the dispersin phage was superior to unmodified phage at clearing short term biofilms grown in broth, shown here to be an effect attributable to free enzyme. However, the dispersin phage was only marginally better than control phages on short term biofilms in minimal media and was no better than control phages in clearing long term biofilms. There was little empirical support for the tragedy of the commons framework despite a strong theoretical foundation for its supposed relevance. The framework requires that the transgene imposes an intrinsic cost, yet the transgene was intrinsically neutral or beneficial when expressed from one part of the phage genome. Expressed from a different part of the genome, the transgene did behave as if intrinsically costly, but its maintenance did not benefit from spatially structured growth per se - violating the tragedy framework.

conclusionsOverall, the transgene was beneficial under many conditions, but no insight to its maintenance was attributable to the established evolutionary framework. The failure likely resides in system details that would be used to parameterize the models. Our study cautions against naive applications of evolutionary theory to synthetic biology, even qualitatively.

Indexed as

BiofilmEvolutionPhageSynthetic biologyTragedy of the commons

Identifiers

PMID25126112
PMCPMC4128545
OpenAlexW2138569895

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.