Evidence map›Paper›PMID 35145031›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Scale-dependent tipping points of bacterial colonization resistance.

Yuya Karita, David T Limmer, Oskar Hallatschek

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Exploring the relationship betweenComputational and structural biotechnology journal · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Impact ofPathogens (Basel, Switzerland) · 2024
    Article
  10. Article
  11. Exploring the impact ofCurrent research in parasitology & vector-borne diseases · 2024
    Article
  12. Proliferating active matter.Nature reviews. Physics · 2023
    Review
  13. Article
  14. Impact of crowding on the diversity of expanding populations.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Self-consistent dispersal puts tight constraints on the spatiotemporal organization of species-rich metacommunities.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Article
  17. 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

3 authors at 2 institutions in 1 country.

Yuya KaritaDepartment of Physics, University of California, Berkeley, CA 94720.ORCID 0000-0001-8581-3630
David T LimmerDepartment of Chemistry, University of California, Berkeley, CA 94720.ORCID 0000-0002-2766-0688
Oskar HallatschekDepartment of Physics, University of California, Berkeley, CA 94720; ohallats@berkeley.edu.ORCID 0000-0002-1312-5975
University of California, Berkeley · USLawrence Berkeley National Laboratory · US

Funding

Resolving the Mechano-Chemical Regulation of Microbial Populations in Microfluidic DevicesR01GM115851 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HALLATSCHEK, OSKAR · 2015 to 2023
$2.2M
High Performance Computing Cluster for Public Health Driven Molecular Science - Core FacilityS10OD023532 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI DURKIN, KATHLEEN A · 2017 to 2017
$434k
NIGMS NIH HHS R01 GM115851NIH HHS S10 OD023532
6 · The paper itself

Abstract

Bacteria are efficient colonizers of a wide range of secluded microhabitats, such as soil pores, skin follicles, or intestinal crypts. How the structural diversity of these habitats modulates microbial self-organization remains poorly understood, in part because of the difficulty to precisely manipulate the physical structure of microbial environments. Using a microfluidic device to grow bacteria in crypt-like incubation chambers of systematically varied lengths, we show that small variations in the physical structure of the microhabitat can drastically alter bacterial colonization success and resistance against invaders. Small crypts are uncolonizable; intermediately sized crypts can stably support dilute populations, while beyond a second critical length scale, populations phase separate into a dilute region and a jammed region. The jammed state is characterized by extreme colonization resistance, even if the resident strain is suppressed by an antibiotic. Combined with a flexible biophysical model, we demonstrate that colonization resistance and associated priority effects can be explained by a crowding-induced phase transition, which results from a competition between proliferation and density-dependent cell leakage. The emerging sensitivity to scale underscores the need to control for scale in microbial ecology experiments. Systematic flow-adjustable length-scale variations may serve as a promising strategy to elucidate further scale-sensitive tipping points and to rationally modulate the stability and resilience of microbial colonizers.

Indexed as

Lab-On-A-Chip DevicesAcetobacterAnti-Bacterial AgentsBacteriological TechniquesDrug Resistance, BacterialTetracyclineAnti-Bacterial AgentsTetracyclineactive mattercolonization resistancemicrobiome stabilitymicrofluidicsphase separation

Identifiers

PMID35145031
PMCPMC8851462
OpenAlexW4220968785

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.