Evidence map›Paper›PMID 33439894›Full record

ArticlePLoS pathogens2021

Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival.

Sariqa Wagley, Helen Morcrette, Andrea Kovacs-Simon, Zheng R Yang, Ann Power, Richard K Tennant, John Love, Neil Murray, Richard W Titball, Clive S Butler

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
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  10. Microbiology spectrum · 2025
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  12. Mini review: Persister cell control strategies.Frontiers in pharmacology · 2025
    Review
  13. Review
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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

10 authors at 1 institution in 1 country.

Sariqa WagleyBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.ORCID 0000-0002-7374-118X
Helen MorcretteBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
Andrea Kovacs-SimonBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
Zheng R YangBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
Ann PowerBioEconomy Centre, The Henry Wellcome Building for BioCatalysis, Biosciences, Exeter, United Kingdom.
Richard K TennantBioEconomy Centre, The Henry Wellcome Building for BioCatalysis, Biosciences, Exeter, United Kingdom.
John LoveBioEconomy Centre, The Henry Wellcome Building for BioCatalysis, Biosciences, Exeter, United Kingdom.
Neil MurrayLyons Seafoods, Fairfield House, Warminster, Wiltshire, United Kingdom.
Richard W TitballBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
Clive S ButlerBiosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, United Kingdom.
University of Exeter · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N016513/1
6 · The paper itself

Abstract

The viable but non culturable (VBNC) state is a condition in which bacterial cells are viable and metabolically active, but resistant to cultivation using a routine growth medium. We investigated the ability of V. parahaemolyticus to form VBNC cells, and to subsequently become resuscitated. The ability to control VBNC cell formation in the laboratory allowed us to selectively isolate VBNC cells using fluorescence activated cell sorting, and to differentiate subpopulations based on their metabolic activity, cell shape and the ability to cause disease in Galleria mellonella. Our results showed that two subpopulations (P1 and P2) of V. parahaemolyticus VBNC cells exist and can remain dormant in the VBNC state for long periods. VBNC subpopulation P2, had a better fitness for survival under stressful conditions and showed 100% revival under favourable conditions. Proteomic analysis of these subpopulations (at two different time points: 12 days (T12) and 50 days (T50) post VBNC) revealed that the proteome of P2 was more similar to that of the starting microcosm culture (T0) than the proteome of P1. Proteins that were significantly up or down-regulated between the different VBNC populations were identified and differentially regulated proteins were assigned into 23 functional groups, the majority being assigned to metabolism functional categories. A lactate dehydrogenase (lldD) protein, responsible for converting lactate to pyruvate, was significantly upregulated in all subpopulations of VBNC cells. Deletion of the lactate dehydrogenase (RIMD2210633:ΔlldD) gene caused cells to enter the VBNC state significantly more quickly compared to the wild-type, and adding lactate to VBNC cells aided their resuscitation and extended the resuscitation window. Addition of pyruvate to the RIMD2210633:ΔlldD strain restored the wild-type VBNC formation profile. This study suggests that lactate dehydrogenase may play a role in regulating the VBNC state.

Indexed as

Bacterial Physiological PhenomenaMicrobial ViabilityVirulenceBacterial ProteinsCells, CulturedCulture MediaGene Expression Regulation, BacterialProteomeVibrio InfectionsVibrio parahaemolyticusBacterial ProteinsCulture MediaProteome

Identifiers

PMID33439894
PMCPMC7837498
OpenAlexW3121085209

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.