Evidence map›Paper›PMID 40991669›Full record

ArticlePLoS pathogens2025

T6SS4 is heterogeneously expressed in Yersinia pseudotuberculosis and is a target for transcriptional and post-transcriptional regulation.

Anna Kerwien, Britta Körner, Ines Meyer, Yannick Teschke, Cassandra Sophie Köster, Ileana Paula Salto, Petra Dersch, Anne-Sophie Herbrüggen

Abstract read
In one paragraph

Article in PLoS pathogens, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Regulator-derived growth and fitness costs ofbioRxiv : the preprint server for biology · 2026
    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

8 authors.

Anna KerwienInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Britta KörnerInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Ines MeyerInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Yannick TeschkeInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Cassandra Sophie KösterInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Ileana Paula SaltoInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.
Petra DerschInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.ORCID 0000-0001-8177-3280
Anne-Sophie HerbrüggenInstitute for Infectiology, Center for Molecular Biology of Inflammation (ZMBE), University of Münster, Münster, Germany.ORCID 0000-0002-6341-5575

Funding

German Research Foundation (DFG)University of Münster
6 · The paper itself

Abstract

The type VI secretion system (T6SS) is a complex secretion system encoded by many Gram-negative bacteria to translocate effector proteins directly into target cells. Due to its high complexity and energy-intensive firing process, regulation of the T6SS is tightly controlled in many organisms. Y. pseudotuberculosis encodes four complete T6SS clusters but lacks genes implicated in T6SS gene regulation in other microorganisms, indicating a distinct control mechanism. Here, we could show that the T6SS4 of Y. pseudotuberculosis is heterogeneously expressed within a population, which is determined by the transcriptional T6SS4 activator RovC. Moreover, the T6SS4 and RovC are embedded in a complex and global regulatory network, including the global post-transcriptional regulator CsrA, the Yersinia modulator A (YmoA), the global protease Lon, and RNases (PNP and RNase III). Post-transcriptional processing of the T6SS4 polycistron and different transcript stability within the operon also achieve a higher regulatory complexity. In summary, our work provides new insights into the sophisticated and complex regulatory network of the T6SS4 of Y. pseudotuberculosis, which clearly differs from regulation in other organisms.

Indexed as

Bacterial ProteinsGene Expression Regulation, BacterialType VI Secretion SystemsYersinia pseudotuberculosisOperonRNA Processing, Post-TranscriptionalTranscription, GeneticYersinia pseudotuberculosis InfectionsBacterial ProteinsType VI Secretion Systems

Identifiers

PMID40991669
PMCPMC12503267

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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.