Evidence map›Paper›PMID 24218478›Full record

ArticleInfection and immunity2014

Cyclic Di-GMP receptor PlzA controls virulence gene expression through RpoS in Borrelia burgdorferi.

Ming He, Jun-Jie Zhang, Meiping Ye, Yongliang Lou, X Frank Yang

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Virulence Regulation inMicroorganisms · 2025
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  5. Hitchhiker's Guide toJournal of bacteriology · 2024
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  8. bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
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  11. Article
  12. Interactions Between Ticks and Lyme Disease Spirochetes.Current issues in molecular biology · 2021
    Article
  13. TheFrontiers in microbiology · 2021
    Article
  14. Lyme Disease Pathogenesis.Current issues in molecular biology · 2021
    Review
  15. Gene Regulation and Transcriptomics.Current issues in molecular biology · 2021
    Article
  16. Role of HK2 in the Enzootic Cycle ofFrontiers in medicine · 2020
    Article
  17. Article
  18. The RpoS Gatekeeper inFrontiers in microbiology · 2019
    Article
  19. Article
  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

5 authors at 3 institutions in 2 countries.

Ming HeDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Jun-Jie Zhang
Meiping Ye
Yongliang Lou
X Frank Yang
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USWenzhou Medical University · CN

Funding

Regulatory Network of the Lyme Disease PathogenR01AI083640 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI X. Frank Yang · 2009 to 2026
$5.9M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015481 · NCRR · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIFE, ROSE S · 2001 to 2001
$1.6M
The mechanism of activation of the Rrp2-RpoN-RpoS pathway in Borrelia burgdorferiR21AI085242 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI YANG, X. FRANK · 2010 to 2011
$397k
NCRR NIH HHS C06 RR015481NCRR NIH HHS C06 RR015481-01NIAID NIH HHS AI083640NIAID NIH HHS AI085242NIAID NIH HHS R01 AI083640NIAID NIH HHS R21 AI085242
6 · The paper itself

Abstract

As an obligate pathogen, the Lyme disease spirochete Borrelia burgdorferi has a streamlined genome that encodes only two two-component signal transduction systems, Hk1-Rrp1 and Hk2-Rrp2 (in addition to CheA-CheY systems). The output of Hk1-Rrp1 is the production of the second messenger cyclic di-GMP (c-di-GMP), which is indispensable for B. burgdorferi to survive in the tick vector. The output of Hk2-Rrp2 is the transcriptional activation of the global regulator RpoS, which is essential for the pathogen to accomplish its tick-mouse transmission and to establish mammalian infection. Although evidence indicates that these two systems communicate with each other, how they are connected is not fully understood. In this study, we showed that the c-di-GMP-binding protein PlzA, a downstream effector of Rrp1, positively modulates the production of RpoS, a global regulator and downstream target of Rrp2. Thus, PlzA functions as a connector that links Hk1-Rrp1 with Hk2-Rrp2. We further showed that PlzA regulates rpoS expression through modulation of another regulator, BosR, at both the transcriptional and the posttranscriptional levels. In addition, PlzA was also capable of regulating rpoS expression independently of Rrp1, suggesting that besides being a c-di-GMP-binding protein, PlzA has other functions. Along with the previous finding of PlzA controlling motility, these studies demonstrate that PlzA is a multifunctional protein. These findings further reinforce the notion that B. burgdorferi utilizes its limited signaling systems and regulators to govern multiple cellular processes during its complex enzootic cycle between ticks and mammals.

Indexed as

Bacterial ProteinsBorrelia burgdorferiCarrier ProteinsCells, CulturedGene Expression Regulation, BacterialIntracellular Signaling Peptides and ProteinsLyme DiseaseSigma FactorSignal TransductionVirulenceBacterial ProteinsCarrier Proteinscyclic GMP-binding proteinIntracellular Signaling Peptides and ProteinsSigma Factorsigma factor KatF protein, Bacteria

Identifiers

PMID24218478
PMCPMC3911845
OpenAlexW2142899232

What OpenQuestion holds

Textmetadata
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.