Evidence map›Paper›PMID 28086090›Full record

ArticleCell2017

A Periplasmic Polymer Curves Vibrio cholerae and Promotes Pathogenesis.

Thomas M Bartlett, Benjamin P Bratton, Amit Duvshani, Amanda Miguel, Ying Sheng, Nicholas R Martin, Jeffrey P Nguyen, Alexandre Persat, Samantha M Desmarais, Michael S VanNieuwenhze and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
12.2field-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

56 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
  2. Cell-body curvature modulates stall frequency to enhancebioRxiv : the preprint server for biology · 2026
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  5. Dissecting the physics of bacterial biofilms with agent-based simulations.Current opinion in solid state & materials science · 2025
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  14. Review
  15. Small regulatory RNAs inmicroLife · 2023
    Review
  16. Article
  17. Article
  18. 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

14 authors at 5 institutions in 2 countries.

Thomas M BartlettDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Benjamin P BrattonDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Amit DuvshaniDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Amanda MiguelDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Ying ShengDepartment of Microbiology, Nanjing Agricultural University, Nanjing 210014, China.
Nicholas R MartinDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Jeffrey P NguyenLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Alexandre PersatDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Samantha M DesmaraisDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Michael S VanNieuwenhzeDepartment of Chemistry, Indiana University, Bloomington, Bloomington, IN 47405, USA.
Kerwyn Casey HuangDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jun ZhuDepartment of Microbiology, Nanjing Agricultural University, Nanjing 210014, China; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Joshua W ShaevitzLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Zemer GitaiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. Electronic address: zgitai@princeton.edu.
Princeton University · USStanford University · USIndiana University Bloomington · USNanjing Agricultural University · CNUniversity of Pennsylvania · US

Funding

Spatial Patterning During DevelopmentP50GM071508 · NIGMS · PRINCETON UNIVERSITY · PI POWELL, SUSAN M · 2004 to 2013
$30.6M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI COVERT, MARKUS W · 2013 to 2017
$10.9M
Mechano-microbiology: how physical forces control bacterial-host interactionsDP1AI124669 · NIAID · PRINCETON UNIVERSITY · PI GITAI, ZEMER · 2015 to 2019
$4.0M
Dynamics of bacterial peptidoglycan synthesisR01GM113172 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI BRUN, YVES V, VANNIEUWENHZE, MICHAEL S · 2015 to 2018
$3.5M
Engineering of cell shape and intracellular organizationDP2OD006466 · OD · STANFORD UNIVERSITY · PI HUANG, KERWYN C. · 2009 to 2009
$2.4M
ROS responses during Vibrio cholerae infectionR01AI120489 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ZHU, JUN · 2016 to 2020
$2.4M
Caulobacter cell shape and cytoskeletal regulationR01GM107384 · NIGMS · PRINCETON UNIVERSITY · PI GITAI, ZEMER · 2013 to 2016
$1.5M
NIAID NIH HHS DP1 AI124669NIAID NIH HHS R01 AI120489NIGMS NIH HHS P50 GM071508NIGMS NIH HHS P50 GM107615NIGMS NIH HHS R01 GM107384NIGMS NIH HHS R01 GM113172NIGMS NIH HHS T32 GM007388NIH HHS DP2 OD006466
6 · The paper itself

Abstract

Pathogenic Vibrio cholerae remains a major human health concern. V. cholerae has a characteristic curved rod morphology, with a longer outer face and a shorter inner face. The mechanism and function of this curvature were previously unknown. Here, we identify and characterize CrvA, the first curvature determinant in V. cholerae. CrvA self-assembles into filaments at the inner face of cell curvature. Unlike traditional cytoskeletons, CrvA localizes to the periplasm and thus can be considered a periskeletal element. To quantify how curvature forms, we developed QuASAR (quantitative analysis of sacculus architecture remodeling), which measures subcellular peptidoglycan dynamics. QuASAR reveals that CrvA asymmetrically patterns peptidoglycan insertion rather than removal, causing more material insertions into the outer face than the inner face. Furthermore, crvA is quorum regulated, and CrvA-dependent curvature increases at high cell density. Finally, we demonstrate that CrvA promotes motility in hydrogels and confers an advantage in host colonization and pathogenesis.

Indexed as

Amino Acid SequenceAnimalsBacterial ProteinsLocomotionMicePeptidoglycanPeriplasmSequence AlignmentVibrio choleraeVirulenceBacterial ProteinsCrvA protein, Vibrio choleraePeptidoglycanbacterial cytoskeletoncell shapefluorescent D-amino acidspathogenesispeptidoglycanperiskeletonquantitative cell biology

Identifiers

PMID28086090
PMCPMC5287421
OpenAlexW2578210508

What OpenQuestion holds

Textmetadata
LicenceTDM
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.