Evidence map›Paper›PMID 33757767›Full record

ArticleThe Journal of biological chemistry

The PorX/PorY system is a virulence factor of Porphyromonas gingivalis and mediates the activation of the type IX secretion system.

Dezhi Yang, Chizhou Jiang, Bo Ning, Wei Kong, Yixin Shi

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. The survival status ofJournal of oral microbiology · 2026
    Review
  3. Article
  4. Article
  5. Advances in the type IX secretion system: an exploration focusing onCurrent research in microbial sciences · 2025
    Review
  6. Article
  7. Structure-function analysis of PorXScientific reports · 2024
    Article
  8. Article
  9. Article
  10. A PorX/PorY and σmSphere · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Dezhi YangThe School of Life Sciences, Arizona State University, Tempe, Arizona, USA; Biodesign Center for Immunotherapy, Vaccines and Virotherapy, Arizona State University, Tempe, Arizona, USA.
Chizhou JiangThe School of Life Sciences, Arizona State University, Tempe, Arizona, USA; Biodesign Center for Immunotherapy, Vaccines and Virotherapy, Arizona State University, Tempe, Arizona, USA.
Bo NingThe Center for Cellular and Molecular Diagnostics, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Wei KongBiodesign Center for Immunotherapy, Vaccines and Virotherapy, Arizona State University, Tempe, Arizona, USA. Electronic address: wei.kong@asu.edu.
Yixin ShiThe School of Life Sciences, Arizona State University, Tempe, Arizona, USA; Biodesign Center for Immunotherapy, Vaccines and Virotherapy, Arizona State University, Tempe, Arizona, USA. Electronic address: yixin.shi@asu.edu.
Arizona State University · USTulane University · US

Funding

Study of the PorX-PorY two-component system in Porphyromonas gingivalisR01DE024607 · NIDCR · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI SHI, YIXIN · 2015 to 2018
$1.5M
NIDCR NIH HHS R01 DE024607
6 · The paper itself

Abstract

PorX/PorY is a two-component system (TCS) of Porphyromonas gingivalis that governs transcription of numerous genes including those encoding a type IX secretion system (T9SS) for gingipain secretion and heme accumulation. Here, an in vitro analysis showed that the response regulator PorX specifically bound to two regions in the promoter of porT, a known PorX-regulated T9SS gene, thus demonstrating that PorX/PorY can directly regulate specific target genes. A truncated PorX protein containing the N-terminal receiver and effector domains retained a wild-type ability in both transcription regulation and heme accumulation, ruling out the role of the C-terminal ALP domain in gene regulation. The PorX/PorY system was the only TCS essential for heme accumulation and concomitantly responded to hemin to stimulate transcription of several known PorX-dependent genes in a concentration-dependent manner. We found that PorX/PorY activated the sigH gene, which encodes a sigma factor known for P. gingivalis adaptation to hydrogen peroxide (H

Indexed as

AnimalsBacterial ProteinsBacterial Secretion SystemsGene Expression Regulation, BacterialMiceMutationPorphyromonas gingivalisProtein Processing, Post-TranslationalVirulence FactorsBacterial ProteinsBacterial Secretion SystemsVirulence FactorsPorphyromonas gingivalisthe PorX/PorY systemthe two-component systemthe type IX secretion systemtranscription regulationvirulence

Identifiers

PMID33757767
PMCPMC8050853
OpenAlexW3136078105

What OpenQuestion 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 OpenQuestion graph.