Evidence map›Paper›PMID 41316864›Full record

ArticleMolecular biology and evolution2025

Unraveling the Prevalence and Multifaceted Roles of Accessory Peptide Deformylases in Bacterial Adaptation and Resistance.

Morgan Lambérioux, Magaly Ducos-Galand, Pierre-Alexandre Kaminski, Eloi Littner, Jean-Michel Betton, Ariel Mechaly, Ahmed Haouz, Didier Mazel

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Bacterial peptide deformylase inhibitors induce prophages in competitors.bioRxiv : the preprint server for biology · 2025
    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

8 authors.

Morgan LambériouxUnité Plasticité du Génome Bactérien, CNRS UMR3525, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0009-0005-7510-2225
Magaly Ducos-GalandUnité Plasticité du Génome Bactérien, CNRS UMR3525, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0009-0001-3300-3537
Pierre-Alexandre KaminskiUnité Plasticité du Génome Bactérien, CNRS UMR3525, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0001-9841-6837
Eloi LittnerCollège Doctoral, Sorbonne Université, Paris, France.ORCID 0000-0002-8793-9584
Jean-Michel BettonStress Adaptation and Metabolism in Enterobacteria, UMR UMR6047, Institut Pasteur, Université de Paris-Cité, Paris, France.ORCID 0000-0002-6523-6343
Ariel MechalyCrystallography Platform-C2RT, CNRS UMR3528, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-5305-7495
Ahmed HaouzCrystallography Platform-C2RT, CNRS UMR3528, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0003-1196-1635
Didier MazelUnité Plasticité du Génome Bactérien, CNRS UMR3525, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0001-6482-6002

Funding

Centre National de la Recherche ScientifiqueFondation pour la Recherche Médicale Equipe FRM EQU202103012569Fondation pour la Recherche Médicale Equipe FRM FDM202106013531Institut PasteurPfizer Innovation France
6 · The paper itself

Abstract

Peptide deformylases (PDFs) are enzymes that are essential for bacterial viability and attractive targets for antibiotic development. Yet, despite their conserved function, many bacteria encode multiple PDFs, a genomic feature whose prevalence and implications remain largely unexplored. Here, we reveal that nearly half of all bacterial genomes carry more than one PDF gene, frequently embedded within mobile genetic elements such as plasmids and integrons. In Vibrio cholerae, the accessory PDF (Def2VCH) confers reduced susceptibility to actinonin (ACT), the most studied PDF inhibitor, while still supporting bacterial growth in the absence of the canonical PDF copies (Def1VCH). Crystallographic analysis shows that this reduced susceptibility stems from an arginine-to-tyrosine substitution that probably reduces ACT binding. Strikingly, this resistance signature is shared by integron-encoded PDFs, and transfer of an integron-encoded PDF cassette from Pseudoxanthomonas into a susceptible V. cholerae is sufficient to abolish ACT susceptibility. These findings reveal a hidden reservoir of resistance within the bacterial mobilome and shed light on potential mechanisms of bacterial resilience to environmental PDF inhibitors.

Indexed as

AmidohydrolasesDrug Resistance, BacterialVibrio choleraeBacterial ProteinsIntegronsAmidohydrolasesBacterial Proteinspeptide deformylaseantibiotic resistancebacterial genome evolutiongene duplicationmobile genetic elementspeptide deformylase

Identifiers

PMID41316864
PMCPMC12690207

What Socratic 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 Socratic graph.