Evidence map›Paper›PMID 37333331›Full record

ArticlebioRxiv : the preprint server for biology2023

Direct measurement of dynamic attractant gradients reveals breakdown of the Patlak-Keller-Segel chemotaxis model.

Trung V Phan, Henry H Mattingly, Lam Vo, Jonathan S Marvin, Loren L Looger, Thierry Emonet

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Trung V PhanDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT.
Henry H MattinglyCenter for Computational Biology, Flatiron Institute, New York, NY.
Lam VoDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT.
Jonathan S MarvinJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA.
Loren L LoogerJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA.
Thierry EmonetDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT.

Funding

Resolving the Conflicts between Phenotypic Diversity and Collective Migration in Bacterial PopulationsF32GM131583 · NIGMS · YALE UNIVERSITY · PI MATTINGLY, HENRY H · 2019 to 2020
$127k
NIGMS NIH HHS F32 GM131583
6 · The paper itself

Abstract

Chemotactic bacteria not only navigate chemical gradients, but also shape their environments by consuming and secreting attractants. Investigating how these processes influence the dynamics of bacterial populations has been challenging because of a lack of experimental methods for measuring spatial profiles of chemoattractants in real time. Here, we use a fluorescent sensor for aspartate to directly measure bacterially generated chemoattractant gradients during collective migration. Our measurements show that the standard Patlak-Keller-Segel model for collective chemotactic bacterial migration breaks down at high cell densities. To address this, we propose modifications to the model that consider the impact of cell density on bacterial chemotaxis and attractant consumption. With these changes, the model explains our experimental data across all cell densities, offering new insight into chemotactic dynamics. Our findings highlight the significance of considering cell density effects on bacterial behavior, and the potential for fluorescent metabolite sensors to shed light on the complex emergent dynamics of bacterial communities.

Identifiers

PMID37333331
PMCPMC10274659

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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.