Evidence map›Paper›PMID 26305782›Full record

ArticlePloS one2015

Beta-Lactamase Repressor BlaI Modulates Staphylococcus aureus Cathelicidin Antimicrobial Peptide Resistance and Virulence.

Morgan A Pence, Nina M Haste, Hiruy S Meharena, Joshua Olson, Richard L Gallo, Victor Nizet, Sascha A Kristian

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Isolation of a Methicillin-ResistantAntibiotics (Basel, Switzerland) · 2026
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  3. Microorganisms · 2025
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  5. Bibliometric analysis of hotspots inFrontiers in microbiology · 2025
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  6. Insights into Kinases of ESKAPE Pathogens for Therapeutic Interventions.Cardiovascular & hematological agents in medicinal chemistry · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Genotypic and Phenotypic Characterization of SomeInfection and drug resistance · 2023
    Article
  13. Vancomycin Resistance inMicroorganisms · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. A protease-mediated mechanism regulates the cytochromeProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. AnMicrobial genomics · 2019
    Article
  19. Article
  20. Evaluating the ototoxicity of an anti-MRSA peptide KR-12-a2.Brazilian journal of otorhinolaryngology
    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

7 authors at 2 institutions in 1 country.

Morgan A PenceBiomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, United States of America; Department of Pediatrics, School of Medicine, University of California San Diego, La Jolla, CA, United States of America.
Nina M HasteBiomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, United States of America; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA, United States of America.
Hiruy S MeharenaBiomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, United States of America.
Joshua OlsonDepartment of Pediatrics, School of Medicine, University of California San Diego, La Jolla, CA, United States of America.
Richard L GalloDepartment of Dermatology, School of Medicine, University of California San Diego, La Jolla, CA, United States of America; VA San Diego Healthcare System, San Diego, CA, United States of America.
Victor NizetDepartment of Pediatrics, School of Medicine, University of California San Diego, La Jolla, CA, United States of America; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA, United States of America.
Sascha A KristianDepartment of Pediatrics, School of Medicine, University of California San Diego, La Jolla, CA, United States of America.
University of California, San Diego · USVA San Diego Healthcare System · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SHUMAN, HOWARD A · 2003 to 2013
$87.6M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
Cathelicidins in Skin ImmunityR01AI052453 · NIAID · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI GALLO, RICHARD L, NIZET, VICTOR · 2002 to 2017
$5.3M
Cathelicidin in Skin ImmunityR37AI052453 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Richard L Gallo, Victor Nizet · 2019 to 2026
$4.6M
TRAINING & OUTREACH COREU54HD071600 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BEST, BROOKIE MANNING · 2011 to 2015
$3.6M
Skin barrier function and the microbiomeR01AI116576 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GALLO, RICHARD L, NAKATSUJI, TERUAKI · 2015 to 2019
$1.7M
New Antiobiotics Against Drug-Resistant Pathogens from Marine Natural ProductsF31GM090658 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HASTE, NINA MARIE · 2010 to 2011
$57k
NIAID NIH HHS AI052453NIAID NIH HHS AI057153NIAID NIH HHS HHSN272200700055CNIAID NIH HHS R01 AI052453NIAID NIH HHS R37 AI052453NIAID NIH HHS U54 AI057153NICHD NIH HHS HD071600NICHD NIH HHS U54 HD071600NIGMS NIH HHS 5 F31 GM090658-02NIGMS NIH HHS F31 GM090658NIGMS NIH HHS T32 GM008666
6 · The paper itself

Abstract

BlaI is a repressor of BlaZ, the beta-lactamase responsible for penicillin resistance in Staphylococcus aureus. Through screening a transposon library in S. aureus Newman for susceptibility to cathelicidin antimicrobial peptide, we discovered BlaI as a novel cathelicidin resistance factor. Additionally, through integrational mutagenesis in S. aureus Newman and MRSA Sanger 252 strains, we confirmed the role of BlaI in resistance to human and murine cathelidicin and showed that it contributes to virulence in human whole blood and murine infection models. We further demonstrated that BlaI could be a target for innate immune-based antimicrobial therapies; by removing BlaI through subinhibitory concentrations of 6-aminopenicillanic acid, we were able to sensitize S. aureus to LL-37 killing.

Indexed as

AnimalsAntimicrobial Cationic Peptidesbeta-LactamasesCathelicidinsDNA Transposable ElementsGene Expression Regulation, BacterialHumansMicePenicillanic AcidPenicillin ResistanceStaphylococcal InfectionsStaphylococcus aureusaminopenicillanic acidAntimicrobial Cationic Peptidesbeta-LactamasesCathelicidinsDNA Transposable ElementsPenicillanic Acid

Identifiers

PMID26305782
PMCPMC4549145
OpenAlexW1719468938

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.