Evidence map›Paper›PMID 37633922›Full record

ArticleScientific reports2023

Mechanical stimuli activate gene expression via a cell envelope stress sensing pathway.

Christine E Harper, Wenyao Zhang, Junsung Lee, Jung-Ho Shin, Megan R Keller, Ellen van Wijngaarden, Emily Chou, Zhaohong Wang, Tobias Dörr, Peng Chen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. 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
2.6field-weighted citation impact, top 10% 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, 17 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Christine E Harper *Sibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Wenyao Zhang *Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, 14853, USA.
Junsung LeeSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Jung-Ho ShinWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, 14853, USA.
Megan R KellerWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, 14853, USA.
Ellen van WijngaardenSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Emily ChouSibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, 14853, USA.
Zhaohong WangDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, 14853, USA.
Tobias DörrWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, 14853, USA. tdoerr@cornell.edu.
Peng ChenDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, 14853, USA. pc252@cornell.edu.
Christopher J HernandezDepartment of Bioengineering and Therapeutic Sciences and Orthopaedic Surgery, University of California, San Francisco, CA, 94143, USA. christopher.hernandez@ucsf.edu.
Cornell University · USUniversity of California, San Francisco · US

Funding

Cell envelope stress responses and the mechanism of antibiotic tolerance in Gram-negative pathogensR01AI143704 · NIAID · CORNELL UNIVERSITY · PI DOERR, TOBIAS · 2019 to 2023
$2.0M
NIAID NIH HHS R01 AI143704
6 · The paper itself

Abstract

Mechanosensitive mechanisms are often used to sense damage to tissue structure, stimulating matrix synthesis and repair. While this kind of mechanoregulatory process is well recognized in eukaryotic systems, it is not known whether such a process occurs in bacteria. In Vibrio cholerae, antibiotic-induced damage to the load-bearing cell wall promotes increased signaling by the two-component system VxrAB, which stimulates cell wall synthesis. Here we show that changes in mechanical stress within the cell envelope are sufficient to stimulate VxrAB signaling in the absence of antibiotics. We applied mechanical forces to individual bacteria using three distinct loading modalities: extrusion loading within a microfluidic device, direct compression and hydrostatic pressure. In all cases, VxrAB signaling, as indicated by a fluorescent protein reporter, was increased in cells submitted to greater magnitudes of mechanical loading, hence diverse forms of mechanical stimuli activate VxrAB signaling. Reduction in cell envelope stiffness following removal of the endopeptidase ShyA led to large increases in cell envelope deformation and substantially increased VxrAB response, further supporting the responsiveness of VxrAB. Our findings demonstrate a mechanosensitive gene regulatory system in bacteria and suggest that mechanical signals may contribute to the regulation of cell wall homeostasis.

Indexed as

Anti-Bacterial AgentsCell WallCell MembraneGene ExpressionHomeostasisAnti-Bacterial Agents

Identifiers

PMID37633922
PMCPMC10460444
OpenAlexW4386190251

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.