Evidence map›Paper›PMID 26832758›Full record

ArticleThe Journal of antimicrobial chemotherapy2016

Standard susceptibility testing overlooks potent azithromycin activity and cationic peptide synergy against MDR Stenotrophomonas maltophilia.

Monika Kumaraswamy, Leo Lin, Joshua Olson, Ching-Fang Sun, Poochit Nonejuie, Ross Corriden, Simon Döhrmann, Syed Raza Ali, Deirdre Amaro, Manfred Rohde and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Extended-Spectrum β-Lactamase-ProducingAntibiotics (Basel, Switzerland) · 2025
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  8. Measuring beta-lactam minimum inhibitory concentrations inJournal of clinical microbiology · 2024
    Review
  9. Article
  10. Article
  11. The NaHCOAntimicrobial agents and chemotherapy · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 2 institutions in 3 countries.

Monika KumaraswamyDivision of Infectious Diseases, University of California, San Diego, La Jolla, CA 92093, USA.
Leo LinDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Joshua OlsonDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Ching-Fang SunDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA School of Medicine, China Medical University, Taichung 40402, Taiwan.
Poochit NonejuieDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Ross CorridenDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Simon DöhrmannDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Syed Raza AliDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Deirdre AmaroDepartment of Pathology, University of California, San Diego, La Jolla, CA 92093, USA.
Manfred RohdeCentral Facility for Microscopy, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.
Joe PoglianoDivision of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
George SakoulasDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA.
Victor NizetDepartment of Pediatrics, University of California, San Diego, La Jolla, CA 92093, USA Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093, USA Rady Children's Hospital, San Diego, CA 92123, USA vnizet@ucsd.edu.
University of California, San Diego · USHelmholtz Centre for Infection Research · DE

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007198 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHI, NEIL C, INSEL, PAUL A · 1985 to 2024
$29.3M
RESEARCH IN INFECTIOUS DISEASEST32AI007036 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NIZET, VICTOR · 1985 to 2025
$9.2M
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
Identification of natural products targeting new pathways in bacteriaR01AI113295 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POGLIANO, JOSEPH A, POGLIANO, KIT J · 2014 to 2018
$3.3M
Proteolysis and Skin AntimicrobialsR01AR052728 · NIAMS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI GALLO, RICHARD L · 2006 to 2015
$3.3M
NIAID NIH HHS AI052453NIAID NIH HHS AI113295NIAID NIH HHS R01 AI113295NIAID NIH HHS R37 AI052453NIAID NIH HHS T32-AI007036NIAMS NIH HHS AR052728NICHD NIH HHS HD071600NIGMS NIH HHS T32 GM007198
6 · The paper itself

Abstract

objectivesThe Gram-negative bacillus Stenotrophomonas maltophilia (SM) is an emerging MDR opportunistic pathogen. Recent studies identify a potentially relevant activity of azithromycin against Gram-negative bacteria overlooked in standard bacteriological testing. We investigated azithromycin activity against SM in testing conditions incorporating mammalian tissue culture medium and host defence factors.

methodsMIC testing, chequerboard assays, time-kill assays and fluorescence microscopy were performed for azithromycin, the cationic peptide antibiotic colistin and the human defence peptide cathelicidin LL-37 alone or in combination in cation-adjusted Mueller-Hinton broth or mammalian tissue culture media. Azithromycin sensitization of SM to host immune clearance was tested in a human neutrophil killing assay and a murine pneumonia model.

resultsWe observed potent bactericidal activity of azithromycin against SM in mammalian tissue culture medium absent in bacteriological medium. Colistin and LL-37 strongly potentiated azithromycin killing of SM by increasing drug entry. Additionally, azithromycin sensitized SM to neutrophil killing and increased SM clearance in the murine pneumonia model.

conclusionsDespite lack of activity in standard MIC testing, azithromycin synergizes with cationic peptide antibiotics to kill SM in medium mimicking tissue fluid conditions. Azithromycin, alone or in combination with colistin, merits further exploration in therapy of drug-resistant SM infections.

Indexed as

Drug SynergismAnimalsAnti-Infective AgentsAntimicrobial Cationic PeptidesAzithromycinCathelicidinsColistinDisease Models, AnimalGram-Negative Bacterial InfectionsHumansMiceMicrobial Sensitivity TestsNeutrophilsPneumonia, BacterialStenotrophomonas maltophiliaTreatment OutcomeAnti-Infective AgentsAntimicrobial Cationic PeptidesAzithromycinCathelicidinsColistin

Identifiers

PMID26832758
PMCPMC4830416
OpenAlexW2254942567

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.