Evidence map›Paper›PMID 23205707›Full record

ArticleMolecular microbiology2013

YopK controls both rate and fidelity of Yop translocation.

Rebecca Dewoody, Peter M Merritt, Melanie M Marketon

Abstract read
In one paragraph

Article in Molecular microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Current Challenges inMicroorganisms · 2025
    Review
  2. Review
  3. Zoonoses (Shannon, Ireland) · 2023
    Article
  4. Review
  5. Heightened Virulence ofInfection and immunity · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Galectin-3 directs antimicrobial guanylate binding proteins to vacuoles furnished with bacterial secretion systems.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Review
  15. Article
  16. Article
  17. The Amino-Terminal Part of the Needle-Tip Translocator LcrV ofFrontiers in cellular and infection microbiology · 2016
    Article
  18. Review
  19. Review
  20. 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

3 authors.

Rebecca DewoodyDepartment of Biology, Indiana University, Bloomington, IN 47405, USA.
Peter M Merritt
Melanie M Marketon

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SHUMAN, HOWARD A · 2003 to 2013
$87.6M
TRAINING IN GENETICST32GM007757 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI KUMAR, JUSTIN P · 1985 to 2014
$8.1M
Bifunctional Control of Yop Translocation by YopKR01AI107055 · NIAID · TUFTS UNIVERSITY BOSTON · PI MARKETON, MELANIE · 2013 to 2017
$1.9M
Regulation of Yersinia Type III Secretion by YopKR21AI083660 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI MARKETON, MELANIE · 2009 to 2010
$402k
NIAID NIH HHS 2-U54-AI-057153NIAID NIH HHS R01 AI107055NIAID NIH HHS R21 AI083660NIAID NIH HHS R21AI083660NIAID NIH HHS U54 AI057153NIGMS NIH HHS T32 GM007757
6 · The paper itself

Abstract

Yersinia pestis, the causative agent of plague, utilizes a type III secretion system (T3SS) to intoxicate host cells. The injection of T3SS substrates must be carefully controlled, and dysregulation leads to altered infection kinetics and early clearance of Y. pestis. While the sequence of events leading up to cell contact and initiation of translocation has received much attention, the regulatory events that take place after effector translocation is less understood. Here we show that the regulator YopK is required to maintain fidelity of substrate specificity, in addition to controlling translocation rate. YopK was found to interact with YopD within targeted cells during Y. pestis infection, suggesting that YopK's regulatory mechanism involves a direct interaction with the translocation pore. In addition, we identified a single amino acid in YopK that is essential for translocation rate regulation but is dispensable for maintaining fidelity of translocation. Furthermore, we found that expression of YopK within host cells was sufficient to downregulate translocation rate, but it did not affect translocation fidelity. Together, our data support a model in which YopK is a bifunctional protein whose activities are genetically and spatially distinct such that fidelity control occurs within bacteria and rate control occurs within host cells.

Indexed as

Bacterial Secretion SystemsBacterial ProteinsDNA Mutational AnalysisModels, BiologicalProtein BindingProtein Interaction MappingProtein TransportYersinia pestisBacterial ProteinsBacterial Secretion Systems

Identifiers

PMID23205707
PMCPMC3545096

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Registered trials

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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.