Evidence map›Paper›PMID 27647888›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Dynamics of Escherichia coli's passive response to a sudden decrease in external osmolarity.

Renata Buda, Yunxiao Liu, Jin Yang, Smitha Hegde, Keiran Stevenson, Fan Bai, Teuta Pilizota

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
  2. Morphogenesis of bacterial colonies in liquid crystalline environments.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  6. Review
  7. Stress-mediated growth determinesProceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Ethanolamine-induced assembly of microcompartments is required forbioRxiv : the preprint server for biology · 2024
    Article
  13. Article
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  15. Review
  16. Article
  17. Physicochemical homeostasis in bacteria.FEMS microbiology reviews · 2023
    Article
  18. Life science alliance · 2023
    Article
  19. Article
  20. 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

7 authors.

Renata BudaCentre for Synthetic and Systems Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, United Kingdom.
Yunxiao LiuBiodynamic Optical Imaging Centre (BIOPIC), School of Life Sciences, Peking University, Beijing 100871, China.
Jin YangBiodynamic Optical Imaging Centre (BIOPIC), School of Life Sciences, Peking University, Beijing 100871, China.
Smitha HegdeCentre for Synthetic and Systems Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, United Kingdom.
Keiran StevensonCentre for Synthetic and Systems Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, United Kingdom.
Fan BaiBiodynamic Optical Imaging Centre (BIOPIC), School of Life Sciences, Peking University, Beijing 100871, China teuta.pilizota@ed.ac.uk fbai@pku.edu.cn.
Teuta PilizotaCentre for Synthetic and Systems Biology, Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FF, United Kingdom; teuta.pilizota@ed.ac.uk fbai@pku.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For most cells, a sudden decrease in external osmolarity results in fast water influx that can burst the cell. To survive, cells rely on the passive response of mechanosensitive channels, which open under increased membrane tension and allow the release of cytoplasmic solutes and water. Although the gating and the molecular structure of mechanosensitive channels found in Escherichia coli have been extensively studied, the overall dynamics of the whole cellular response remain poorly understood. Here, we characterize E. coli's passive response to a sudden hypoosmotic shock (downshock) on a single-cell level. We show that initial fast volume expansion is followed by a slow volume recovery that can end below the initial value. Similar response patterns were observed at downshocks of a wide range of magnitudes. Although wild-type cells adapted to osmotic downshocks and resumed growing, cells of a double-mutant ([Formula: see text]) strain expanded, but failed to fully recover, often lysing or not resuming growth at high osmotic downshocks. We propose a theoretical model to explain our observations by simulating mechanosensitive channels opening, and subsequent solute efflux and water flux. The model illustrates how solute efflux, driven by mechanical pressure and solute chemical potential, competes with water influx to reduce cellular osmotic pressure and allow volume recovery. Our work highlights the vital role of mechanosensation in bacterial survival.

Indexed as

Osmolar ConcentrationCell Membrane PermeabilityEscherichia coliModels, BiologicalTime FactorsWaterWaterbacterial mechanosensingosmotic downshocksingle-cell imaging

Identifiers

PMID27647888
PMCPMC5056102

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.