Evidence map›Paper›PMID 22252821›Full record

ArticleAntimicrobial agents and chemotherapy2012

Pharmacological inhibition of the ClpXP protease increases bacterial susceptibility to host cathelicidin antimicrobial peptides and cell envelope-active antibiotics.

Shauna M McGillivray, Dan N Tran, Nitya S Ramadoss, John N Alumasa, Cheryl Y Okumura, George Sakoulas, Micah M Vaughn, Dawn X Zhang, Kenneth C Keiler, Victor Nizet

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2012. 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
2.6field-weighted citation impact, top 10% 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, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Gausemycin A-ResistantMicroorganisms · 2023
    Article
  6. Antibiotics (Basel, Switzerland) · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Innate Immune Interactions betweenFrontiers in cellular and infection microbiology · 2018
    Article
  20. Tetrazole-BasedAntimicrobial agents and chemotherapy · 2017
    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

10 authors at 3 institutions in 1 country.

Shauna M McGillivrayDepartment of Biology, Texas Christian University, Fort Worth, Texas, USA. s.mcgillivray@tcu.edu
Dan N Tran
Nitya S Ramadoss
John N Alumasa
Cheryl Y Okumura
George Sakoulas
Micah M Vaughn
Dawn X Zhang
Kenneth C Keiler
Victor Nizet
University of California, San Diego · USPennsylvania State University · USTexas Christian University · US

Funding

Cathelicidins in Skin ImmunityR01AI052453 · NIAID · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI GALLO, RICHARD L, NIZET, VICTOR · 2002 to 2017
$5.3M
TRAINING & OUTREACH COREU54HD071600 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BEST, BROOKIE MANNING · 2011 to 2015
$3.6M
Proteolysis and Skin AntimicrobialsR01AR052728 · NIAMS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI GALLO, RICHARD L · 2006 to 2015
$3.3M
The Role of tmRNA in development of C. crescentusR01GM068720 · NIGMS · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI KEILER, KENNETH C · 2004 to 2014
$2.3M
NIAID NIH HHS AI052453NIAID NIH HHS R01 AI052453NIAMS NIH HHS AR052728NIAMS NIH HHS R01 AR052728NICHD NIH HHS HD071600NICHD NIH HHS U54 HD071600NIGMS NIH HHS GM06852NIGMS NIH HHS GM68720NIGMS NIH HHS R01 GM068720
6 · The paper itself

Abstract

The ClpXP protease is a critical bacterial intracellular protease that regulates protein turnover in many bacterial species. Here we identified a pharmacological inhibitor of the ClpXP protease, F2, and evaluated its action in Bacillus anthracis and Staphylococcus aureus. We found that F2 exhibited synergistic antimicrobial activity with cathelicidin antimicrobial peptides and antibiotics that target the cell well and/or cell membrane, such as penicillin and daptomycin, in B. anthracis and drug-resistant strains of S. aureus. ClpXP inhibition represents a novel therapeutic strategy to simultaneously sensitize pathogenic bacteria to host defenses and pharmaceutical antibiotics.

Indexed as

Amino Acid SequenceAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacillus anthracisBacteriaCathelicidinsCell MembraneDrug Resistance, BacterialDrug SynergismEndopeptidase ClpEscherichia coli ProteinsMethicillin-Resistant Staphylococcus aureusMolecular Sequence DataProtease InhibitorsStaphylococcus aureusTetrazolesAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCathelicidinsClpXP protease, E coliEndopeptidase ClpEscherichia coli ProteinsF2 protease inhibitorProtease InhibitorsTetrazoles

Identifiers

PMID22252821
PMCPMC3318395
OpenAlexW2130037065

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.