Evidence map›Paper›PMID 24345876›Full record

ArticleInnate immunity2015

Microbicidal effects of α- and θ-defensins against antibiotic-resistant Staphylococcus aureus and Pseudomonas aeruginosa.

Kenneth P Tai, Karishma Kamdar, Jason Yamaki, Valerie V Le, Dat Tran, Patti Tran, Michael E Selsted, André J Ouellette, Annie Wong-Beringer

Open access · bronzeAbstract read
In one paragraph

Article in Innate immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 27% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  11. Frontiers in immunology · 2021
    Article
  12. Exposure ofThe Journal of biological chemistry · 2019
    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

9 authors at 2 institutions in 1 country.

Kenneth P TaiDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Karishma KamdarDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Jason YamakiTitus Family Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
Valerie V LeDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Dat TranDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Patti TranDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
Michael E SelstedDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.
André J OuelletteDepartment of Pathology and Laboratory Medicine, USC Norris Cancer Center, Keck School of Medicine, Los Angeles, CA, USA aouellet@usc.edu.
Annie Wong-BeringerTitus Family Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, School of Pharmacy, University of Southern California, Los Angeles, CA, USA.
USC Norris Comprehensive Cancer Center · USUniversity of Southern California · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
LOS ANGELES BASIN CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR031986 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2010 to 2011
$21.1M
MOLECULAR ASPECTS OF LEUKOCYTE ANTIMICROBIAL PEPTIDESR37AI022931 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SELSTED, MICHAEL E · 2000 to 2009
$3.7M
PEPTIDE EFFECTORS OF ENTERIC HOST DEFENSER01DK044632 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OUELLETTE, ANDRE J. · 1993 to 2010
$2.8M
Regulation of Mucosal Immunity by Pro- and Anti-inflammatory Salivary DefensinsR01DE021341 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SELSTED, MICHAEL E · 2010 to 2014
$1.9M
Physiologic Peptide Cyclization in Myeloid CellsR01AI058129 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI SELSTED, MICHAEL E · 2004 to 2008
$1.9M
STUDIES OF ALPHA-DEFENSINS IN PRIMATE INNATE IMMUNITYR01AI059346 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OUELLETTE, ANDRE J. · 2006 to 2010
$1.7M
MOLECULAR ASPECTS OF LEUKOCYTE ANTIMICROBIAL PEPTIDESR01AI022931 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SELSTED, MICHAEL E · 1986 to 2016
$1.7M
Impact of Fluoroquinolone resistance on Pseudomonas virulence and patient outcomeR21AI073467 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WONG-BERINGER, ANNIE · 2008 to 2009
$407k
PEPTIDE EFFECTORS OF ENTERIC HOST DEFENSER55DK044632 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI OUELLETTE, ANDRE J. · 1992 to 1992
–
NCI NIH HHS P30 CA014089NCI NIH HHS P30CA014089NCRR NIH HHS UL1 RR031986NCRR NIH HHS UL1RR031986NIAID NIH HHS AI022931NIAID NIH HHS AI058129NIAID NIH HHS AI059346NIAID NIH HHS AI073467NIAID NIH HHS R01 AI022931NIAID NIH HHS R01 AI058129NIAID NIH HHS R01 AI059346NIAID NIH HHS R21 AI073467NIAID NIH HHS R37 AI022931NIDCR NIH HHS DE021341NIDCR NIH HHS R01 DE021341NIDDK NIH HHS DK044632NIDDK NIH HHS R01 DK044632
6 · The paper itself

Abstract

Antibiotic-resistant bacterial pathogens threaten public health. Because many antibiotics target specific bacterial enzymes or reactions, corresponding genes may mutate under selection and lead to antibiotic resistance. Accordingly, antimicrobials that selectively target overall microbial cell integrity may offer alternative approaches to therapeutic design. Naturally occurring mammalian α- and θ-defensins are potent, non-toxic microbicides that may be useful for treating infections by antibiotic-resistant pathogens because certain defensin peptides disrupt bacterial, but not mammalian, cell membranes. To test this concept, clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA), including vancomycin heteroresistant strains, and ciprofloxacin-resistant Pseudomonas aeruginosa (Cip(R)-PA) were tested for sensitivity to α-defensins Crp-4, RMAD-4 and HNPs 1-3, and to RTD-1, macaque θ-defensin-1. In vitro, 3 μM Crp-4, RMAD-4 and RTD-1 reduced MRSA cell survival by 99%, regardless of vancomycin susceptibility. For PA clinical isolates that differ in fluoroquinolone resistance and virulence phenotype, peptide efficacy was independent of strain ciprofloxacin resistance, site of isolation or virulence factor expression. Thus, Crp-4, RMAD-4 and RTD-1 are effective in vitro antimicrobials against clinical isolates of MRSA and Cip(R)-PA, perhaps providing templates for development of α- and θ-defensin-based microbicides against antibiotic resistant or virulent infectious agents.

Indexed as

alpha-DefensinsAmino Acid SequenceBacteremiaBacterial InfectionsCiprofloxacinDefensinsDrug Resistance, BacterialMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular Sequence DataPseudomonas aeruginosaVancomycin Resistancealpha-DefensinsCiprofloxacinDefensinstheta-defensinAntimicrobial peptidesbacteremiaclinical isolatesExoSExoUpeptide therapeutics

Identifiers

PMID24345876
PMCPMC4062604
OpenAlexW2133801652

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.