Evidence map›Paper›PMID 36154276›Full record

ArticlemBio2022

PopB-PcrV Interactions Are Essential for Pore Formation in the Pseudomonas aeruginosa Type III Secretion System Translocon.

Emma Kundracik, Josephine Trichka, José Díaz Aponte, Alicia Roistacher, Arne Rietsch

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Mechanistic blockade ofAntimicrobial agents and chemotherapy · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Antibiotics (Basel, Switzerland) · 2023
    Article
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

5 authors at 2 institutions in 1 country.

Emma KundracikDepartment of Molecular Biology and Microbiology, Case Western Reserve Universitygrid.67105.35, Cleveland, Ohio, USA.ORCID 0000-0001-6648-1474
Josephine TrichkaExperimental Immunology Branch, National Cancer Institute, National Institutes of Healthgrid.94365.3d, Bethesda, Maryland, USA.ORCID 0000-0002-1997-3502
José Díaz AponteDepartment of Molecular Biology and Microbiology, Case Western Reserve Universitygrid.67105.35, Cleveland, Ohio, USA.
Alicia RoistacherDepartment of Molecular Biology and Microbiology, Case Western Reserve Universitygrid.67105.35, Cleveland, Ohio, USA.ORCID 0000-0001-9169-4279
Arne RietschDepartment of Molecular Biology and Microbiology, Case Western Reserve Universitygrid.67105.35, Cleveland, Ohio, USA.ORCID 0000-0002-1556-7064
Case Western Reserve University · USNational Institutes of Health · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
TISSUE CULTURE AND HYBRIDOMA MODULEP30EY011373 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Irina A Pikuleva · 1997 to 2026
$17.7M
P. aeruginosa type III secreted effectors in corneal diseaseR01EY022052 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI RIETSCH, ARNE · 2012 to 2019
$3.1M
Host cell factors controlling type III secretion effector translocationR21AI168028 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI RIETSCH, ARNE · 2022 to 2023
$443k
Type III Secretion Translocon Structure and FunctionR21AI107131 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI RIETSCH, ARNE · 2014 to 2015
$436k
NEI NIH HHS P30 EY011373NEI NIH HHS R01 EY022052NIAID NIH HHS R21 AI107131NIAID NIH HHS R21 AI168028NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

The type III secretion system (T3SS) is a syringe-like virulence factor that delivers bacterial proteins directly into the cytoplasm of host cells. An essential component of the system is the translocon, which creates a pore in the host cell membrane through which proteins are injected. In Pseudomonas aeruginosa, the translocation pore is formed by proteins PopB and PopD and attaches to the T3SS needle via the needle tip protein PcrV. The structure and stoichiometry of the multimeric pore are unknown. We took a genetic approach to map contact points within the system by taking advantage of the fact that the translocator proteins of P. aeruginosa and the related Aeromonas hydrophila T3SS are incompatible and cannot be freely exchanged. We created chimeric versions of P. aeruginosa PopB and A. hydrophila AopB to intentionally disrupt and restore protein-protein interactions. We identified a chimeric B-translocator that specifically disrupts an interaction with the needle tip protein. This disruption did not affect membrane insertion of the B-translocator but did prevent formation of the translocation pore, arguing that the needle tip protein drives the formation of the translocation pore.

Indexed as

Pseudomonas aeruginosaType III Secretion SystemsAntigens, BacterialBacterial ProteinsVirulence FactorsAntigens, BacterialBacterial ProteinsType III Secretion SystemsVirulence Factorspore formationT3SStranslocon

Identifiers

PMID36154276
PMCPMC9600203
OpenAlexW4297220006

What Socratic 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 Socratic graph.