Evidence map›Paper›PMID 26077259›Full record

ArticleAntimicrobial agents and chemotherapy2015

Synergistic effect of membrane-active peptides polymyxin B and gramicidin S on multidrug-resistant strains and biofilms of Pseudomonas aeruginosa.

Marina Berditsch, Thomas Jäger, Nikola Strempel, Thomas Schwartz, Jörg Overhage, Anne S Ulrich

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed, 95 citations in OpenAlex.

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  14. Review
  15. A Novel Antimicrobial Peptide SpampcinInternational journal of molecular sciences · 2022
    Article
  16. Article
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  18. Article
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Marina BerditschInstitute of Organic Chemistry, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Thomas JägerInstitute of Organic Chemistry, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Nikola StrempelInstitute of Functional Interfaces, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Thomas SchwartzInstitute of Functional Interfaces, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Jörg OverhageInstitute of Functional Interfaces, Karlsruhe Institute of Technology, Karlsruhe, Germany.
Anne S UlrichInstitute of Organic Chemistry, Karlsruhe Institute of Technology, Karlsruhe, Germany Institute of Biological Interfaces, Karlsruhe Institute of Technology, Karlsruhe, Germany anne.ulrich@kit.edu.
Karlsruhe Institute of Technology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multidrug-resistant Pseudomonas aeruginosa is a major cause of severe hospital-acquired infections. Currently, polymyxin B (PMB) is a last-resort antibiotic for the treatment of infections caused by Gram-negative bacteria, despite its undesirable side effects. The delivery of drug combinations has been shown to reduce the required therapeutic doses of antibacterial agents and thereby their toxicity if a synergistic effect is present. In this study, we investigated the synergy between two cyclic antimicrobial peptides, PMB and gramicidin S (GS), against different P. aeruginosa isolates, using a quantitative checkerboard assay with resazurin as a growth indicator. Among the 28 strains that we studied, 20 strains showed a distinct synergistic effect, represented by a fractional inhibitory concentration index (FICI) of ≤0.5. Remarkably, several clinical P. aeruginosa isolates that grew as small-colony variants revealed a nonsynergistic effect, as indicated by FICIs between >0.5 and ≤0.70. In addition to inhibiting the growth of planktonic bacteria, the peptide combinations significantly decreased static biofilm growth compared with treatment with the individual peptides. There was also a faster and more prolonged effect when the combination of PMB and GS was used compared with single-peptide treatments on the metabolic activity of pregrown biofilms. The results of the present study define a synergistic interaction between two cyclic membrane-active peptides toward 17 multidrug-resistant P. aeruginosa and biofilms of P. aeruginosa strain PAO1. Thus, the application of PMB and GS in combination is a promising option for a topical medication and in the prevention of acute and chronic infections caused by multidrug-resistant or biofilm-forming P. aeruginosa.

Indexed as

Anti-Bacterial AgentsBiofilmsDrug Resistance, Multiple, BacterialGramicidinMicrobial Sensitivity TestsPolymyxin BPseudomonas aeruginosaAnti-Bacterial AgentsGramicidinPolymyxin B

Identifiers

PMID26077259
PMCPMC4538509
OpenAlexW1798723734

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.