Evidence map›Paper›PMID 27528665›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Key experimental evidence of chromosomal DNA transfer among selected tuberculosis-causing mycobacteria.

Eva C Boritsch, Varun Khanna, Alexandre Pawlik, Nadine Honoré, Victor H Navas, Laurence Ma, Christiane Bouchier, Torsten Seemann, Philip Supply, Timothy P Stinear and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
12.2field-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

68 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  13. Large-scale Pan Genomic Analysis ofEvolutionary bioinformatics online · 2024
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  15. Review
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  17. Article
  18. Mechanisms of Linezolid Resistance in Mycobacteria.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  19. Review
  20. Article

8 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 2 countries.

Eva C BoritschInstitut Pasteur (IP), Unit for Integrated Mycobacterial Pathogenomics, 75015 Paris, France;
Varun KhannaIP, Hub Bioinformatique et Biostatistique, C3BI, Unité de Services et de Recherche, USR 3756, IP CNRS, 75015 Paris, France;
Alexandre PawlikInstitut Pasteur (IP), Unit for Integrated Mycobacterial Pathogenomics, 75015 Paris, France;
Nadine HonoréInstitut Pasteur (IP), Unit for Integrated Mycobacterial Pathogenomics, 75015 Paris, France;
Victor H NavasIP, Lymphocyte Cell Biology Unit, 75015 Paris, France;
Laurence MaIP, PF1-Plate-Forme Génomique, 75015 Paris, France;
Christiane BouchierIP, PF1-Plate-Forme Génomique, 75015 Paris, France;
Torsten SeemannVictorian Life Sciences Computation Initiative, University of Melbourne, Carlton, VIC 3053, Australia;ORCID 0000-0001-6046-610X
Philip SupplyINSERM U1019, CNRS UMR 8204, Center for Infection and Immunity, Institut Pasteur de Lille, Université de Lille, 59000 Lille, France;
Timothy P StinearDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC 3000, Australia.ORCID 0000-0003-0150-123X
Roland BroschInstitut Pasteur (IP), Unit for Integrated Mycobacterial Pathogenomics, 75015 Paris, France; roland.brosch@pasteur.fr.ORCID 0000-0003-2587-3863
Institut Pasteur · FRCentre National de la Recherche Scientifique · FRInstitut de Génomique Fonctionnelle · FRThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Horizontal gene transfer (HGT) is a major driving force of bacterial diversification and evolution. For tuberculosis-causing mycobacteria, the impact of HGT in the emergence and distribution of dominant lineages remains a matter of debate. Here, by using fluorescence-assisted mating assays and whole genome sequencing, we present unique experimental evidence of chromosomal DNA transfer between tubercle bacilli of the early-branching Mycobacterium canettii clade. We found that the obtained recombinants had received multiple donor-derived DNA fragments in the size range of 100 bp to 118 kbp, fragments large enough to contain whole operons. Although the transfer frequency between M. canettii strains was low and no transfer could be observed among classical Mycobacterium tuberculosis complex (MTBC) strains, our study provides the proof of concept for genetic exchange in tubercle bacilli. This outstanding, now experimentally validated phenomenon presumably played a key role in the early evolution of the MTBC toward pathogenicity. Moreover, our findings also provide important information for the risk evaluation of potential transfer of drug resistance and fitness mutations among clinically relevant mycobacterial strains.

Indexed as

Gene Transfer, HorizontalDNA, BacterialEvolution, MolecularGenome, BacterialHumansMycobacteriumMycobacterium tuberculosisSpecies SpecificityTuberculosisWhole Genome SequencingDNA, BacterialDNA transferevolutionMycobacterium canettiirecombinationtuberculosis

Identifiers

PMID27528665
PMCPMC5024641
OpenAlexW2517845626

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.