Evidence map›Paper›PMID 35680894›Full record

ArticleNature communications2022

Evolutionary action of mutations reveals antimicrobial resistance genes in Escherichia coli.

David C Marciano, Chen Wang, Teng-Kuei Hsu, Thomas Bourquard, Benu Atri, Ralf B Nehring, Nicholas S Abel, Elizabeth A Bowling, Taylor J Chen, Pamela D Lurie and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Advances in adaptive laboratory evolution applications forSynthetic and systems biotechnology · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Genomic Pipeline for Analysis of Mutational Events in Bacteria.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Adaptive laboratory evolution ofFrontiers in microbiology · 2023
    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.

David C Marciano *Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. david.marciano@bcm.edu.ORCID 0000-0001-5237-5144
Chen Wang *Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0001-5769-2077
Teng-Kuei HsuThe Verna and Marrs McLean Department of Biochemistry & Molecular Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Thomas BourquardDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0002-9670-711X
Benu AtriStructural and Computational Biology & Molecular Biophysics Program, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0002-3514-013X
Ralf B NehringDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0001-5156-7734
Nicholas S AbelDepartment of Pharmacology, Baylor College of Medicine, Houston, TX, 77030, USA.
Elizabeth A BowlingThe Verna and Marrs McLean Department of Biochemistry & Molecular Biology, Baylor College of Medicine, Houston, TX, 77030, USA.
Taylor J ChenIntegrative Molecular & Biomedical Biosciences Program, Baylor College of Medicine, Houston, TX, 77030, USA.
Pamela D LurieDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0002-1383-0260
Panagiotis KatsonisDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0002-7172-1644
Susan M RosenbergDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0003-1444-473X
Christophe HermanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.ORCID 0000-0001-8954-7907
Olivier LichtargeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. lichtarge@bcm.edu.

Funding

Functional Determinnats in G Protein-coupled ReceptorsR01GM066099 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2003 to 2022
$7.5M
Decoding the impact of sex differences on Alzheimer's disease riskR01AG074009 · NIA · BAYLOR COLLEGE OF MEDICINE · PI AL-RAMAHI, ISMAEL, LICHTARGE, OLIVIER · 2021 to 2025
$6.0M
A Synthetic Platform for Non-Antibiotic Eradication of Bacterial InfectionsDP1AI152073 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI HERMAN, CHRISTOPHE · 2019 to 2023
$5.6M
Harnessing Proteins as Drugs: the Protectome of Cancer- and Aging-Prevention ProteinsDP1AG072751 · NIA · BAYLOR COLLEGE OF MEDICINE · PI ROSENBERG, SUSAN M · 2020 to 2024
$5.6M
A Knowledge Map to Find Alzheimer's Disease DrugsR01AG061105 · NIA · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2018 to 2022
$4.6M
Cognitive Computing of Alzheimer's Disease Genes and RiskU01AG068214 · NIA · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2021 to 2025
$4.4M
Mechanisms of Endogenous DNA Damage PromotionR01CA250905 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MILLER, KYLE M, ROSENBERG, SUSAN M · 2020 to 2024
$3.3M
MOLECULAR MECHANISMS OF STRESS-INDUCED MUTATIONR35GM122598 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI ROSENBERG, SUSAN M · 2017 to 2020
$2.4M
NCI NIH HHS R01 CA250905NIAID NIH HHS DP1 AI152073NIA NIH HHS DP1 AG072751NIA NIH HHS R01 AG061105NIA NIH HHS R01 AG074009NIA NIH HHS U01 AG068214NIGMS NIH HHS R01 GM066099NIGMS NIH HHS R35 GM122598
6 · The paper itself

Abstract

Since antibiotic development lags, we search for potential drug targets through directed evolution experiments. A challenge is that many resistance genes hide in a noisy mutational background as mutator clones emerge in the adaptive population. Here, to overcome this noise, we quantify the impact of mutations through evolutionary action (EA). After sequencing ciprofloxacin or colistin resistance strains grown under different mutational regimes, we find that an elevated sum of the evolutionary action of mutations in a gene identifies known resistance drivers. This EA integration approach also suggests new antibiotic resistance genes which are then shown to provide a fitness advantage in competition experiments. Moreover, EA integration analysis of clinical and environmental isolates of antibiotic resistant of E. coli identifies gene drivers of resistance where a standard approach fails. Together these results inform the genetic basis of de novo colistin resistance and support the robust discovery of phenotype-driving genes via the evolutionary action of genetic perturbations in fitness landscapes.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialEscherichia coliEscherichia coli ProteinsCiprofloxacinColistinMicrobial Sensitivity TestsMutationAnti-Bacterial AgentsCiprofloxacinColistinEscherichia coli Proteins

Identifiers

PMID35680894
PMCPMC9184624

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.