Evidence map›Paper›PMID 24331465›Full record

ArticleCell host & microbe2013

The globally disseminated M1T1 clone of group A Streptococcus evades autophagy for intracellular replication.

Timothy C Barnett, David Liebl, Lisa M Seymour, Christine M Gillen, Jin Yan Lim, Christopher N Larock, Mark R Davies, Benjamin L Schulz, Victor Nizet, Rohan D Teasdale and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 2 pooled it
10.4field-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

94 citing papers in PubMed, 2 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Pentamidine inhibition of streptopain attenuatesbioRxiv : the preprint server for biology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Group AInfection and immunity · 2024
    Article
  16. Interplay between group AMicrobiology and molecular biology reviews : MMBR · 2024
    Review
  17. Article
  18. Review
  19. Immunomodulating Enzymes fromMicroorganisms · 2024
    Review
  20. Breaking the cellular defense: the role of autophagy evasion inFrontiers in cellular and infection microbiology · 2024
    Article

34 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 3 countries.

Timothy C BarnettAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
David LieblInstitute for Molecular Bioscience, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Lisa M SeymourAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Christine M GillenAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Jin Yan LimAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Christopher N LarockDepartment of Pediatrics and Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Mark R DaviesAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Benjamin L SchulzAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Victor NizetDepartment of Pediatrics and Skaggs School of Pharmacy & Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Rohan D TeasdaleAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; Institute for Molecular Bioscience, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia.
Mark J WalkerAustralian Infectious Diseases Research Centre, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Queensland, St Lucia, QLD 4072, Australia. Electronic address: mark.walker@uq.edu.au.
University of Queensland · AUUniversity of California, San Diego · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2003 to 2013
$87.6M
GAS Switch from Colonizing Bacterium to Invasive PathogenR01AI077780 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NIZET, VICTOR · 2008 to 2019
$3.8M
Proteolysis and Skin AntimicrobialsR01AR052728 · NIAMS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI GALLO, RICHARD L · 2006 to 2015
$3.3M
NIAID NIH HHS AI057153NIAID NIH HHS AI077780NIAID NIH HHS R01 AI077780NIAMS NIH HHS AR052728NIAMS NIH HHS R01 AR052728
6 · The paper itself

Abstract

Autophagy is reported to be an important innate immune defense against the intracellular bacterial pathogen Group A Streptococcus (GAS). However, the GAS strains examined to date belong to serotypes infrequently associated with human disease. We find that the globally disseminated serotype M1T1 clone of GAS can evade autophagy and replicate efficiently in the cytosol of infected cells. Cytosolic M1T1 GAS (strain 5448), but not M6 GAS (strain JRS4), avoids ubiquitylation and recognition by the host autophagy marker LC3 and ubiquitin-LC3 adaptor proteins NDP52, p62, and NBR1. Expression of SpeB, a streptococcal cysteine protease, is critical for this process, as an isogenic M1T1 ΔspeB mutant is targeted to autophagy and attenuated for intracellular replication. SpeB degrades p62, NDP52, and NBR1 in vitro and within the host cell cytosol. These results uncover a proteolytic mechanism utilized by GAS to escape the host autophagy pathway that may underpin the success of the M1T1 clone.

Indexed as

AutophagyHost-Pathogen InteractionsImmune EvasionBacterial ProteinsCell LineCytosolExotoxinsHumansStreptococcus pyogenesVirulence FactorsBacterial Proteinserythrogenic toxinExotoxinsVirulence Factors

Identifiers

PMID24331465
PMCPMC3918495
OpenAlexW2135690913

What OpenQuestion holds

Textmetadata
LicenceTDM
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.