Evidence map›Paper›PMID 23699254›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2013

Role of pore-forming toxins in bacterial infectious diseases.

Ferdinand C O Los, Tara M Randis, Raffi V Aroian, Adam J Ratner

Open access · bronzeAbstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 227 papers.

0numbers the graph read from it
0cells of the map it votes in
227citing papers in PubMed
26.1field-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

227 citing papers in PubMed, 389 citations in OpenAlex.

  1. Article
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  13. Enigmatic roles ofJournal of bacteriology · 2025
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  15. Review
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  19. Article
  20. Article

167 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

4 authors at 2 institutions in 1 country.

Ferdinand C O LosDepartment of Pediatrics, Columbia University, New York, New York, USA.
Tara M Randis
Raffi V Aroian
Adam J Ratner
Columbia University · USUniversity of California, San Diego · US

Funding

p38-mediated defense pathway against pore-forming toxinsR01GM071603 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI AROIAN, RAFFI V · 2006 to 2014
$2.5M
Gardnerella vaginalis: toxin production and pathogenesisR01AI092743 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RATNER, ADAM JONATHAN · 2011 to 2015
$2.0M
DNase For Prevention Of Reproductive Tract Infections In PregnancyR33AI098654 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RATNER, ADAM JONATHAN · 2014 to 2016
$1.6M
R21 Orphan nuclear receptorsR21AI111020 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RATNER, ADAM JONATHAN · 2014 to 2015
$451k
DNase For Prevention Of Reproductive Tract Infections In PregnancyR21AI098654 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI RATNER, ADAM JONATHAN · 2012 to 2013
$448k
NIAID NIH HHS R01 AI092743NIAID NIH HHS R21 AI098654NIAID NIH HHS R21 AI111020NIAID NIH HHS R33 AI098654NIGMS NIH HHS R01 GM071603
6 · The paper itself

Abstract

Pore-forming toxins (PFTs) are the most common bacterial cytotoxic proteins and are required for virulence in a large number of important pathogens, including Streptococcus pneumoniae, group A and B streptococci, Staphylococcus aureus, Escherichia coli, and Mycobacterium tuberculosis. PFTs generally disrupt host cell membranes, but they can have additional effects independent of pore formation. Substantial effort has been devoted to understanding the molecular mechanisms underlying the functions of certain model PFTs. Likewise, specific host pathways mediating survival and immune responses in the face of toxin-mediated cellular damage have been delineated. However, less is known about the overall functions of PFTs during infection in vivo. This review focuses on common themes in the area of PFT biology, with an emphasis on studies addressing the roles of PFTs in in vivo and ex vivo models of colonization or infection. Common functions of PFTs include disruption of epithelial barrier function and evasion of host immune responses, which contribute to bacterial growth and spreading. The widespread nature of PFTs make this group of toxins an attractive target for the development of new virulence-targeted therapies that may have broad activity against human pathogens.

Indexed as

AnimalsBacterial InfectionsBacterial ProteinsHost-Pathogen InteractionsHumansPore Forming Cytotoxic ProteinsBacterial ProteinsPore Forming Cytotoxic Proteins

Identifiers

PMID23699254
PMCPMC3668673
OpenAlexW2123109660

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.