Evidence map›Paper›PMID 27259462›Full record

ArticleEMBO reports2016

Mitochondria mediate septin cage assembly to promote autophagy of Shigella.

Andrea Sirianni, Sina Krokowski, Damián Lobato-Márquez, Stephen Buranyi, Julia Pfanzelter, Dieter Galea, Alexandra Willis, Siân Culley, Ricardo Henriques, Gerald Larrouy-Maumus and 4 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
6.1field-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

60 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
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  11. The mitochondrial carboxylase PCCA interacts withApplied and environmental microbiology · 2024
    Article
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  14. Mitochondrial Dysfunction in Bacterial Infections.Pathogens (Basel, Switzerland) · 2023
    Review
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Andrea SirianniSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Sina KrokowskiSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Damián Lobato-MárquezSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Stephen BuranyiSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Julia PfanzelterCellular Signalling and Cytoskeletal Function Laboratory, The Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, UK.
Dieter GaleaSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Alexandra WillisSection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Siân CulleyQuantitative Imaging and NanoBiophysics Group, MRC Laboratory for Molecular Cell Biology, Department of Cell and Developmental Biology, University College London, London, UK.
Ricardo HenriquesQuantitative Imaging and NanoBiophysics Group, MRC Laboratory for Molecular Cell Biology, Department of Cell and Developmental Biology, University College London, London, UK.
Gerald Larrouy-MaumusFaculty of Natural Sciences, Department of Life Sciences, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Michael HollinsheadDepartment of Pathology, University of Cambridge, Cambridge, UK.
Vanessa Sancho-ShimizuSection of Virology, St. Mary's Medical School, Imperial College London, London, UK Section of Paediatrics, St. Mary's Medical School, Imperial College London, London, UK.
Michael WayCellular Signalling and Cytoskeletal Function Laboratory, The Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, UK Section of Virology, St. Mary's Medical School, Imperial College London, London, UK.
Serge MostowySection of Microbiology, MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK s.mostowy@imperial.ac.uk.ORCID 0000-0002-7286-6503
Imperial College London · GBMRC Laboratory for Molecular Cell Biology · GBThe Honourable Society of Lincoln's Inn · GBSt Mary's Hospital · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M022374/1Medical Research Council MR/J006874/1Medical Research Council MR/K015826/1MRF_ C0483Wellcome TrustWellcome Trust WT097411MA
6 · The paper itself

Abstract

Septins, cytoskeletal proteins with well-characterised roles in cytokinesis, form cage-like structures around cytosolic Shigella flexneri and promote their targeting to autophagosomes. However, the processes underlying septin cage assembly, and whether they influence S. flexneri proliferation, remain to be established. Using single-cell analysis, we show that the septin cages inhibit S. flexneri proliferation. To study mechanisms of septin cage assembly, we used proteomics and found mitochondrial proteins associate with septins in S. flexneri-infected cells. Strikingly, mitochondria associated with S. flexneri promote septin assembly into cages that entrap bacteria for autophagy. We demonstrate that the cytosolic GTPase dynamin-related protein 1 (Drp1) interacts with septins to enhance mitochondrial fission. To avoid autophagy, actin-polymerising Shigella fragment mitochondria to escape from septin caging. Our results demonstrate a role for mitochondria in anti-Shigella autophagy and uncover a fundamental link between septin assembly and mitochondria.

Indexed as

AutophagyCell Cycle ProteinsCell LineCytoskeletal ProteinsHumansMitochondriaMitochondrial DynamicsMitochondrial ProteinsModels, BiologicalProtein BindingSeptinsShigellaCell Cycle ProteinsCytoskeletal ProteinsMitochondrial ProteinsSeptinsautophagycytoskeletonmitochondriaseptinShigella

Identifiers

PMID27259462
PMCPMC4931556
OpenAlexW2415172195

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.