Evidence map›Paper›PMID 25668237›Full record

ArticleThe Journal of investigative dermatology2015

Pentobra: A Potent Antibiotic with Multiple Layers of Selective Antimicrobial Mechanisms against Propionibacterium Acnes.

Nathan W Schmidt, George W Agak, Stephanie Deshayes, Yang Yu, Alyssa Blacker, Jackson Champer, Wujing Xian, Andrea M Kasko, Jenny Kim, Gerard C L Wong

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Targeting Inflammation in Acne: Current Treatments and Future Prospects.American journal of clinical dermatology · 2023
    Article
  5. Biofilm and wound healing: from bench to bedside.European journal of medical research · 2023
    Review
  6. Article
  7. Article
  8. PEG-8 Laurate Fermentation ofInternational journal of molecular sciences · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Review
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.

Nathan W SchmidtDepartment of Bioengineering, University of California, Los Angeles, California, USA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.
George W AgakDivision of Dermatology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Stephanie DeshayesDepartment of Bioengineering, University of California, Los Angeles, California, USA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.
Yang YuDivision of Dermatology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Alyssa BlackerDepartment of Bioengineering, University of California, Los Angeles, California, USA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.
Jackson ChamperDivision of Dermatology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Wujing XianDepartment of Bioengineering, University of California, Los Angeles, California, USA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California, USA.
Andrea M KaskoDepartment of Bioengineering, University of California, Los Angeles, California, USA; California NanoSystems Institute, University of California, Los Angeles, California, USA.
Jenny KimDivision of Dermatology, David Geffen School of Medicine at UCLA, Los Angeles, California, USA; California NanoSystems Institute, University of California, Los Angeles, California, USA; Department of Dermatology, Greater Los Angeles Healthcare System Veterans Affairs, Los Angeles, California, USA.
Gerard C L WongDepartment of Bioengineering, University of California, Los Angeles, California, USA; Department of Chemistry and Biochemistry, University of California, Los Angeles, California, USA; California NanoSystems Institute, University of California, Los Angeles, California, USA. Electronic address: gclwong@seas.ucla.edu.
University of California, Los Angeles · USCalifornia NanoSystems Institute · USVA Greater Los Angeles Healthcare System · US

Funding

Antimicrobial Oligomers for BioDefense and Emerging Food Borne Infectious DiseaseU01AI082192 · NIAID · UNIVERSITY OF MASSACHUSETTS AMHERST · PI TEW, GREGORY N. · 2009 to 2013
$7.0M
PHOTOTUNABLE BIOMATERIALS TO ENGINEER COMPLEX 3D CELL MICROENVIRONMENTSDP2OD008533 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KASKO, ANDREA MARIE · 2011 to 2011
$2.3M
Innate Immunity in Acne VulgarisR01AR053542 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, JENNY J · 2009 to 2013
$1.3M
Dermatology Scientist Training ProgramT32AR058921 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MODLIN, ROBERT L · 2010 to 2014
$877k
NIAID NIH HHS 1UO1 AI082192-01NIAID NIH HHS U01 AI082192NIAMS NIH HHS AR58921NIAMS NIH HHS R01 AR053542NIAMS NIH HHS R01-AR-053542NIAMS NIH HHS T32 AR058921NIH HHS DP2 OD008533
6 · The paper itself

Abstract

Although antibiotics are a common treatment for acne, the difficulties inherent to effective antimicrobial penetration in sebum and selective antimicrobial action in the skin are compounded by increasing resistance of Propionibacterium acnes clinical isolates. To address these problems, we engineered Pentobra, a peptide-aminoglycoside molecule that has multiple mechanisms of antibacterial action and investigated whether it can be a potential candidate for the treatment of acne. Pentobra combines the potent ribosomal activity of aminoglycosides with the bacteria-selective membrane-permeabilizing abilities of antimicrobial peptides. Pentobra demonstrated potent and selective killing of P. acnes but not against human skin cells in vitro. In direct comparison, Pentobra demonstrated bactericidal activity and drastically outperformed free tobramycin (by 5-7 logs) against multiple P. acnes clinical strains. Moreover, electron microscopic studies showed that Pentobra had robust membrane activity, as treatment with Pentobra killed P. acnes cells and caused leakage of intracellular contents. Pentobra may also have potential anti-inflammatory effects as demonstrated by suppression of some P. acnes-induced chemokines. Importantly, the killing activity was maintained in sebaceous environments as Pentobra was bactericidal against clinical isolates in comedones extracts isolated from human donors. Our work demonstrates that equipping aminoglycosides with selective membrane activity is a viable approach for developing antibiotics against P. acnes that are effective in cutaneous environments.

Indexed as

Acne VulgarisAminoglycosidesAnti-Bacterial AgentsCell MembraneCytokinesDrug Resistance, BacterialEnzyme-Linked Immunosorbent AssayHumansMicrobial Sensitivity TestsMicroscopy, ElectronMonocytesPeptidesPropionibacterium acnesSkinSpecies SpecificityStem CellsAminoglycosidesAnti-Bacterial AgentsCytokinesPentobraPeptidesTobramycin

Identifiers

PMID25668237
PMCPMC4430421
OpenAlexW2037899894

What OpenQuestion holds

Textmetadata
LicenceTDM
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.