Evidence map›Paper›PMID 30427086›Full record

ArticleMolecular microbiology2019

The toxin from a ParDE toxin-antitoxin system found in Pseudomonas aeruginosa offers protection to cells challenged with anti-gyrase antibiotics.

Meenakumari Muthuramalingam, John C White, Tamiko Murphy, Jessica R Ames, Christina R Bourne

Open access · hybridAbstract read
In one paragraph

Article in Molecular microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

  1. Identification of a novel gene inAntimicrobial agents and chemotherapy · 2026
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  14. Comparative analysis of five type II TA systems identified inFrontiers in cellular and infection microbiology · 2023
    Article
  15. Plasmids Can Shift Bacterial Morphological Response against Antibiotic Stress.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  16. Cohabitation ofFrontiers in cellular and infection microbiology · 2023
    Article
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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

5 authors at 1 institution in 1 country.

Meenakumari MuthuramalingamThe University of Oklahoma, Department of Chemistry and Biochemistry, Norman, 73019, OK, USA.
John C WhiteThe University of Oklahoma, Department of Chemistry and Biochemistry, Norman, 73019, OK, USA.
Tamiko MurphyThe University of Oklahoma, Department of Chemistry and Biochemistry, Norman, 73019, OK, USA.
Jessica R AmesThe University of Oklahoma, Department of Chemistry and Biochemistry, Norman, 73019, OK, USA.
Christina R BourneThe University of Oklahoma, Department of Chemistry and Biochemistry, Norman, 73019, OK, USA.
University of Oklahoma · US

Funding

Structure-Function Studies of MsvR, a Methanogen-Specific Transcriptional RegulaP20GM103640 · NIGMS · UNIVERSITY OF OKLAHOMA · PI THOMAS, LEONARD M · 2012 to 2021
$20.4M
Biacore T200S10OD025014 · OD · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MCEVER, RODGER PAUL · 2018 to 2018
$322k
Institutional Development Award (IDeA)NIGMS NIH HHS P20 GM103640NIGMS NIH HHS P20GM103640NIH HHS S10 OD025014Oklahoma Center for the Advancement of Science and Technology HR17-099University of Oklahoma
6 · The paper itself

Abstract

Toxin-antitoxin systems are mediators of diverse activities in bacterial physiology. For the ParE-type toxins, their reported role of gyrase inhibition utilized during plasmid-segregation killing indicates they are toxic. However, their location throughout chromosomes leads to questions about function, including potential non-toxic outcomes. The current study has characterized a ParDE system from the opportunistic human pathogen Pseudomonas aeruginosa (Pa). We identified a protective function for this ParE toxin, PaParE, against effects of quinolone and other antibiotics. However, higher concentrations of PaParE are themselves toxic to cells, indicating the phenotypic outcome can vary based on its concentration. Our assays confirmed PaParE inhibition of gyrase-mediated supercoiling of DNA with an IC

Indexed as

Toxin-Antitoxin SystemsAnti-Bacterial AgentsBacterial ToxinsEscherichia coliInhibitory Concentration 50Pseudomonas aeruginosaQuinolonesTopoisomerase II InhibitorsAnti-Bacterial AgentsBacterial ToxinsQuinolonesTopoisomerase II Inhibitors

Identifiers

PMID30427086
PMCPMC6368863
OpenAlexW2901304806

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.