Evidence map›Paper›PMID 26748339›Full record

ArticleGenome biology and evolution2016

Mycobacterial Pan-Genome Analysis Suggests Important Role of Plasmids in the Radiation of Type VII Secretion Systems.

Emilie Dumas, Eva Christina Boritsch, Mathias Vandenbogaert, Ricardo C Rodríguez de la Vega, Jean-Michel Thiberge, Valerie Caro, Jean-Louis Gaillard, Beate Heym, Fabienne Girard-Misguich, Roland Brosch and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 105 citations in OpenAlex.

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  4. Giant linear plasmids in Mycobacterium avium harbour a tRNA array unit.DNA research : an international journal for rapid publication of reports on genes and genomes · 2026
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  8. Loss of the ESX-5 secretion locus inProceedings of the National Academy of Sciences of the United States of America · 2025
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  12. Genomic and phenotypic characterization ofMicrobiology spectrum · 2024
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  13. Review
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  17. Virulence Factors ofPathogens (Basel, Switzerland) · 2023
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  20. Pathogens (Basel, Switzerland) · 2022
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6 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

11 authors at 4 institutions in 1 country.

Emilie DumasINSERM U1173, UFR Simone Weil, Versailles-Saint-en-Quentin University, Saint-Quentin-en-Yvelines 78180, France.
Eva Christina BoritschInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, 75724, Paris Cedex 15, France.
Mathias VandenbogaertInstitut Pasteur, Genotyping of Pathogens and Public Health, 75724, Paris Cedex 15, France.
Ricardo C Rodríguez de la VegaUMR8079, Ecologie Systématique Evolution, Univ. Paris-Sud, CNRS, Université Paris-Saclay, Orsay 91400, France.
Jean-Michel ThibergeInstitut Pasteur, Genotyping of Pathogens and Public Health, 75724, Paris Cedex 15, France.
Valerie CaroInstitut Pasteur, Genotyping of Pathogens and Public Health, 75724, Paris Cedex 15, France.
Jean-Louis GaillardINSERM U1173, UFR Simone Weil, Versailles-Saint-en-Quentin University, Saint-Quentin-en-Yvelines 78180, France AP-HP, Hôpital Ambroise Paré, Service De Microbiologie Et Hygiène, Boulogne-Billancourt, France.
Beate HeymINSERM U1173, UFR Simone Weil, Versailles-Saint-en-Quentin University, Saint-Quentin-en-Yvelines 78180, France AP-HP, Hôpital Ambroise Paré, Service De Microbiologie Et Hygiène, Boulogne-Billancourt, France.
Fabienne Girard-MisguichINSERM U1173, UFR Simone Weil, Versailles-Saint-en-Quentin University, Saint-Quentin-en-Yvelines 78180, France.
Roland BroschInstitut Pasteur, Unit for Integrated Mycobacterial Pathogenomics, 75724, Paris Cedex 15, France roland.brosch@pasteur.fr guillaume.sapriel@uvsq.fr.
Guillaume SaprielINSERM U1173, UFR Simone Weil, Versailles-Saint-en-Quentin University, Saint-Quentin-en-Yvelines 78180, France UMR 8212, LSCE, Versailles-Saint-Quentin University, Saint-Quentin-en-Yvelines 78180, France Atelier De Bio-Informatique. Institut De Systématique, Evolution, Biodiversité, ISYEB, UMR 7205, CNRS, MNHN, UPMC, EPHE. Muséum National D'histoire Naturelle, Cedex 05, Paris 75231, France roland.brosch@pasteur.fr guillaume.sapriel@uvsq.fr.
Institut Pasteur · FRInserm · FRCentre National de la Recherche Scientifique · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In mycobacteria, various type VII secretion systems corresponding to different ESX (ESAT-6 secretory) types, are contributing to pathogenicity, iron acquisition, and/or conjugation. In addition to the known chromosomal ESX loci, the existence of plasmid-encoded ESX systems was recently reported. To investigate the potential role of ESX-encoding plasmids on mycobacterial evolution, we analyzed a large representative collection of mycobacterial genomes, including both chromosomal and plasmid-borne sequences. Data obtained for chromosomal ESX loci confirmed the previous five classical ESX types and identified a novel mycobacterial ESX-4-like type, termed ESX-4-bis. Moreover, analysis of the plasmid-encoded ESX loci showed extensive diversification, with at least seven new ESX profiles, identified. Three of them (ESX-P clusters 1-3) were found in multiple plasmids, while four corresponded to singletons. Our phylogenetic and gene-order-analyses revealed two main groups of ESX types: 1) ancestral types, including ESX-4 and ESX-4-like systems from mycobacterial and non-mycobacterial actinobacteria and 2) mycobacteria-specific ESX systems, including ESX-1-2-3-5 systems and the plasmid-encoded ESX types. Synteny analysis revealed that ESX-P systems are part of phylogenetic groups that derived from a common ancestor, which diversified and resulted in the different ESX types through extensive gene rearrangements. A converging body of evidence, derived from composition bias-, phylogenetic-, and synteny analyses points to a scenario in which ESX-encoding plasmids have been a major driving force for acquisition and diversification of type VII systems in mycobacteria, which likely played (and possibly still play) important roles in the adaptation to new environments and hosts during evolution of mycobacterial pathogenesis.

Indexed as

Evolution, MolecularGenome, BacterialGene RearrangementGene Transfer, HorizontalMycobacteriumPhylogenyPlasmidsSyntenyType IV Secretion SystemsType IV Secretion SystemsESX/type VII secretion systemshorizontal gene transfermycobacteriamycobacterial evolutionphylogenytuberculosisvirulence

Identifiers

PMID26748339
PMCPMC4779608
OpenAlexW2223993952

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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.