Evidence map›Paper›PMID 32001719›Full record

ArticleNPJ systems biology and applications2020

Mechanistic insights into bacterial metabolic reprogramming from omics-integrated genome-scale models.

Noushin Hadadi, Vikash Pandey, Anush Chiappino-Pepe, Marian Morales, Hector Gallart-Ayala, Florence Mehl, Julijana Ivanisevic, Vladimir Sentchilo, Jan R van der Meer

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in NPJ systems biology and applications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 54 citations in OpenAlex.

  1. The CpxR-GlvR regulatory axis ofFrontiers in cellular and infection microbiology · 2026
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  2. Reconstruction of a Genome-Scale Metabolic Model forInternational journal of molecular sciences · 2025
    Article
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  9. Multi-scale models of whole cells: progress and challenges.Frontiers in cell and developmental biology · 2023
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  17. Strategies for EnhancingFrontiers in bioengineering and biotechnology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Noushin HadadiDepartment of Fundamental Microbiology, University of Lausanne, 1015, Lausanne, Switzerland. Nouhin.hadadi@unige.ch.ORCID 0000-0001-6614-4910
Vikash PandeyLaboratory of Computational Systems Biotechnology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Anush Chiappino-PepeLaboratory of Computational Systems Biotechnology, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Marian MoralesDepartment of Fundamental Microbiology, University of Lausanne, 1015, Lausanne, Switzerland.
Hector Gallart-AyalaMetabolomics Platform, University of Lausanne, 1015, Lausanne, Switzerland.
Florence MehlMetabolomics Platform, University of Lausanne, 1015, Lausanne, Switzerland.
Julijana IvanisevicMetabolomics Platform, University of Lausanne, 1015, Lausanne, Switzerland.
Vladimir SentchiloDepartment of Fundamental Microbiology, University of Lausanne, 1015, Lausanne, Switzerland.
Jan R van der MeerDepartment of Fundamental Microbiology, University of Lausanne, 1015, Lausanne, Switzerland.
University of Lausanne · CHÉcole Polytechnique Fédérale de Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the adaptive responses of individual bacterial strains is crucial for microbiome engineering approaches that introduce new functionalities into complex microbiomes, such as xenobiotic compound metabolism for soil bioremediation. Adaptation requires metabolic reprogramming of the cell, which can be captured by multi-omics, but this data remains formidably challenging to interpret and predict. Here we present a new approach that combines genome-scale metabolic modeling with transcriptomics and exometabolomics, both of which are common tools for studying dynamic population behavior. As a realistic demonstration, we developed a genome-scale model of Pseudomonas veronii 1YdBTEX2, a candidate bioaugmentation agent for accelerated metabolism of mono-aromatic compounds in soil microbiomes, while simultaneously collecting experimental data of P. veronii metabolism during growth phase transitions. Predictions of the P. veronii growth rates and specific metabolic processes from the integrated model closely matched experimental observations. We conclude that integrative and network-based analysis can help build predictive models that accurately capture bacterial adaptation responses. Further development and testing of such models may considerably improve the successful establishment of bacterial inoculants in more complex systems.

Indexed as

Adaptation, BiologicalBacteriaBiochemical PhenomenaBiodegradation, EnvironmentalComputational BiologyGenomeMetabolic Networks and PathwaysModels, BiologicalPseudomonasSystems Analysis

Identifiers

PMID32001719
PMCPMC6946695
OpenAlexW3000694224

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.