Evidence map›Paper›PMID 38536895›Full record

ArticlePLoS pathogens2024

The read-through transcription-mediated autoactivation circuit for virulence regulator expression drives robust type III secretion system 2 expression in Vibrio parahaemolyticus.

Dhira Saraswati Anggramukti, Eiji Ishii, Andre Pratama, Mohamad Al Kadi, Tetsuya Iida, Toshio Kodama, Shigeaki Matsuda

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
4.9field-weighted citation impact, top 6% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Dhira Saraswati AnggramuktiDepartment of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Eiji IshiiDepartment of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.ORCID 0000-0001-7899-252X
Andre PratamaDepartment of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.ORCID 0000-0001-5384-4475
Mohamad Al KadiHuman Immunology (Single Cell Genomics), WPI Immunology Frontier Research Center, Osaka University, Osaka, Japan.
Tetsuya IidaDepartment of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Toshio KodamaDepartment of Bacteriology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Shigeaki MatsudaDepartment of Bacterial Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.ORCID 0000-0001-8430-9723
Osaka International Cancer Institute · JPThe University of Osaka · JPNagasaki University · JP

Funding

Chemo-Sero-Therapeutic Research InstituteInstitute for FermentationScientific Research from the Japan Society for the Promotion of Science
6 · The paper itself

Abstract

Vibrio parahaemolyticus is the leading cause of seafood-borne gastroenteritis in humans worldwide. The major virulence factor responsible for the enteropathogenicity of this pathogen is type III secretion system 2 (T3SS2), which is encoded on the 80-kb V. parahaemolyticus pathogenicity island (Vp-PAI), the gene expression of which is governed by the OmpR-family transcriptional regulator VtrB. Here, we found a positive autoregulatory feature of vtrB transcription, which is often observed with transcriptional regulators of bacteria, but the regulation was not canonically dependent on its own promoter. Instead, this autoactivation was induced by heterogeneous transcripts derived from the VtrB-regulated operon upstream of vtrB. VtrB-activated transcription overcame the intrinsic terminator downstream of the operon, resulting in transcription read-through with read-in transcription of the vtrB gene and thus completing the autoregulatory loop for vtrB gene expression. The dampening of read-through transcription with an exogenous strong terminator reduced vtrB gene expression. Furthermore, a V. parahaemolyticus mutant with defects in the vtrB autoregulatory loop also showed compromises in T3SS2 expression and T3SS2-dependent cytotoxicity in vitro and enterotoxicity in vivo, indicating that this autoregulatory loop is essential for sustained vtrB activation and the consequent robust expression of T3SS2 genes for pathogenicity. Taken together, these findings demonstrate that the regulatory loop for vtrB gene expression based on read-through transcription from the upstream operon is a crucial pathway in T3SS2 gene regulatory network to ensure T3SS2-mediated virulence of V. parahaemolyticus.

Indexed as

Vibrio InfectionsVibrio parahaemolyticusBacterial ProteinsGene Expression Regulation, BacterialHumansPromoter Regions, GeneticType III Secretion SystemsVirulenceVirulence FactorsBacterial ProteinsType III Secretion SystemsVirulence Factors

Identifiers

PMID38536895
PMCPMC10971746
OpenAlexW4393218665

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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.