Evidence map›Paper›PMID 33219834›Full record

ReviewCurrent genetics2021

Heterogeneity in populations of enterohaemorrhagic Escherichia coli undergoing D-serine adaptation.

Nicky O'Boyle, Andrew J Roe

Open access · hybridAbstract readReview
In one paragraph

Review in Current genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

2 authors at 2 institutions in 1 country.

Nicky O'BoyleInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, G12 8TA, UK. nicky.oboyle@glasgow.ac.uk.ORCID http://orcid.org/0000-0002-8669-7237
Andrew J RoeInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, G12 8TA, UK. andrew.roe@glasgow.ac.uk.ORCID http://orcid.org/0000-0003-3698-6134
University of Glasgow · GBWellcome Centre for Molecular Parasitology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R006539/1
6 · The paper itself

Abstract

Phenotypic and genetic heterogeneities are conserved features of prokaryotic populations. During periods of stress, this programmed diversity increases the likelihood that variants within the population will survive the adverse conditions, allowing for proliferation. Phenotypic heterogeneity can have a mutational or indeed a non-mutational basis as observed in bet-hedging strategies adopted by antibiotic-tolerant persister cells. Genetic variants can arise by phase variation (slip-strand mispairing, promoter inversions etc.), nucleotide polymorphisms resulting from replication errors or larger rearrangements such as deletions and insertions. In the face of selective pressures, these alterations may be neutral, beneficial or deleterious.We recently described the genetic basis of tolerance to a normally toxic metabolite, D-serine (D-ser) in enterohaemorrhagic E. coli (EHEC). Here we summarize our work in the context of population dynamics, provide further discussion on the distinction between these tolerance mechanisms and the importance of heterogeneity for maximising adaptive potential.

Indexed as

Enterohemorrhagic Escherichia coliEscherichia coli InfectionsAdaptation, PhysiologicalAnti-Bacterial AgentsDrug Resistance, BacterialGenetic HeterogeneityHumansMutationSerineAnti-Bacterial AgentsSerineAdaptive evolutionEHECMetabolismMutationPathogenesis

Identifiers

PMID33219834
PMCPMC8032621
OpenAlexW3103870023

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.