Evidence map›Paper›PMID 29610312›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Robust, linear correlations between growth rates and β-lactam-mediated lysis rates.

Anna J Lee, Shangying Wang, Hannah R Meredith, Bihan Zhuang, Zhuojun Dai, Lingchong You

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
10.7field-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

96 citing papers in PubMed, 164 citations in OpenAlex.

  1. Contributions of intra- and extracellular antibiotic degradation to collective [Formula: see text]-lactam survival.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  19. Habitat fragmentation enhances microbial collective defence.Journal of the Royal Society, Interface · 2025
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36 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Anna J LeeDepartment of Biomedical Engineering, Duke University, Durham, NC 27708.
Shangying WangDepartment of Biomedical Engineering, Duke University, Durham, NC 27708.
Hannah R MeredithDepartment of Biomedical Engineering, Duke University, Durham, NC 27708.
Bihan ZhuangDepartment of Biomedical Engineering, Duke University, Durham, NC 27708.
Zhuojun DaiDepartment of Biomedical Engineering, Duke University, Durham, NC 27708.
Lingchong YouDepartment of Biomedical Engineering, Duke University, Durham, NC 27708; you@duke.edu.
Duke University · US

Funding

A comprehensive research resource to define mechanisms underlying microbial regulation of host metabolism in pediatric obesity and obesity-targeted therapeuticsR24DK110492 · NIDDK · DUKE UNIVERSITY · PI RAWLS, JOHN F, SEED, PATRICK C. · 2016 to 2020
$7.2M
Post-antibiotic effect and design of optimal antibiotic dosing protocolsR01GM098642 · NIGMS · DUKE UNIVERSITY · PI YOU, LINGCHONG · 2011 to 2025
$3.6M
A synthetic biology approach to analyze evolution of programmed bacterial deathR01GM110494 · NIGMS · DUKE UNIVERSITY · PI YOU, LINGCHONG · 2014 to 2017
$1.2M
NIDDK NIH HHS R24 DK110492NIGMS NIH HHS R01 GM098642NIGMS NIH HHS R01 GM110494
6 · The paper itself

Abstract

It is widely acknowledged that faster-growing bacteria are killed faster by β-lactam antibiotics. This notion serves as the foundation for the concept of bacterial persistence: dormant bacterial cells that do not grow are phenotypically tolerant against β-lactam treatment. Such correlation has often been invoked in the mathematical modeling of bacterial responses to antibiotics. Due to the lack of thorough quantification, however, it is unclear whether and to what extent the bacterial growth rate can predict the lysis rate upon β-lactam treatment under diverse conditions. Enabled by experimental automation, here we measured >1,000 growth/killing curves for eight combinations of antibiotics and bacterial species and strains, including clinical isolates of bacterial pathogens. We found that the lysis rate of a bacterial population linearly depends on the instantaneous growth rate of the population, regardless of how the latter is modulated. We further demonstrate that this predictive power at the population level can be explained by accounting for bacterial responses to the antibiotic treatment by single cells. This linear dependence of the lysis rate on the growth rate represents a dynamic signature associated with each bacterium-antibiotic pair and serves as the quantitative foundation for designing combination antibiotic therapy and predicting the population-structure change in a population with mixed phenotypes.

Indexed as

Anti-Bacterial AgentsBacterial LoadBacteriolysisBiomassCarbenicillinCulture MediaEscherichia coliHigh-Throughput Screening AssaysKineticsNephelometry and TurbidimetryRoboticsTemperatureAnti-Bacterial AgentsCarbenicillinCulture Mediaantibiotic resistancebeta-lactamsquantitative biologysystems biology

Identifiers

PMID29610312
PMCPMC5910845
OpenAlexW2795903858

What OpenQuestion holds

Textmetadata
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.