Evidence map›Paper›PMID 28494243›Full record

ArticleCell host & microbe2017

A Rab20-Dependent Membrane Trafficking Pathway Controls M. tuberculosis Replication by Regulating Phagosome Spaciousness and Integrity.

Laura Schnettger, Angela Rodgers, Urska Repnik, Rachel P Lai, Gang Pei, Martijn Verdoes, Robert J Wilkinson, Douglas B Young, Maximiliano G Gutierrez

Open access · hybridAbstract read
In one paragraph

Article in Cell host & microbe, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Delayed-Type Hypersensitivity toInternational journal of molecular sciences · 2026
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4 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

9 authors at 4 institutions in 4 countries.

Laura SchnettgerHost-Pathogen Interactions In Tuberculosis Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Angela RodgersMycobacterial Systems Biology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Urska RepnikDepartment of Biosciences, University of Oslo, Blindernveien 31, 0371 Oslo, Norway.
Rachel P LaiTuberculosis Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Gang PeiDepartment of Immunology, Max Planck Institute for Infection Biology, Charitéplatz 1, 10117 Berlin, Germany.
Martijn VerdoesRadboud Institute for Molecular Life Sciences (RIMLS), Geert Grooteplein 26/28, Nijmegen 6525 GA, the Netherlands.
Robert J WilkinsonTuberculosis Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Douglas B YoungMycobacterial Systems Biology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Maximiliano G GutierrezHost-Pathogen Interactions In Tuberculosis Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address: max.g@crick.ac.uk.
The Francis Crick Institute · GBCharité - Universitätsmedizin Berlin · DERadboud University Nijmegen · NLUniversity of Oslo · NO

Funding

Medical Research Council MC_U117588499Medical Research Council MC_UP_1202/11Wellcome Trust FC001092
6 · The paper itself

Abstract

The intracellular pathogen Mycobacterium tuberculosis (Mtb) lives within phagosomes and also disrupts these organelles to access the cytosol. The host pathways and mechanisms that contribute to maintaining Mtb phagosome integrity have not been investigated. Here, we examined the spatiotemporal dynamics of Mtb-containing phagosomes and identified an interferon-gamma-stimulated and Rab20-dependent membrane trafficking pathway in macrophages that maintains Mtb in spacious proteolytic phagolysosomes. This pathway functions to promote endosomal membrane influx in infected macrophages, and is required to preserve Mtb phagosome integrity and control Mtb replication. Rab20 is specifically and significantly upregulated in the sputum of human patients with active tuberculosis. Altogether, we uncover an immune-regulated cellular pathway of defense that promotes maintenance of Mtb within intact membrane-bound compartments for efficient elimination.

Indexed as

AnimalsAntigens, BacterialBacterial ProteinsCell Culture TechniquesDisease Models, AnimalEndosomesFemaleHost-Pathogen InteractionsHumansInterferon-gammaMacrophagesMembranesMiceMice, Inbred C57BLMycobacterium tuberculosisPhagosomesAntigens, BacterialBacterial ProteinsESAT-6 protein, Mycobacterium tuberculosisInterferon-gammaRab20 protein, humanrab GTP-Binding ProteinsmacrophagemycobacteriumphagosomeRab20Rab GTPasestuberculosis

Identifiers

PMID28494243
PMCPMC5432432
OpenAlexW2612426698

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.