Evidence map›Paper›PMID 28639145›Full record

ArticleInfectious diseases and therapy2017

In vitro and In vivo Activity of Theaflavin-Epicatechin Combinations versus Multidrug-Resistant Acinetobacter baumannii.

Jonathan W Betts, Michael Hornsey, David W Wareham, Roberto M La Ragione

Abstract read
In one paragraph

Article in Infectious diseases and therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Theaflavin AmelioratesInternational journal of molecular sciences · 2023
    Article
  4. The VirtuousAntibiotics (Basel, Switzerland) · 2023
    Review
  5. Multidrug-ResistantAntibiotics (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Review
  8. Article
  9. Pathogens (Basel, Switzerland) · 2021
    Review
  10. Frontiers in cellular and infection microbiology · 2021
    Review
  11. Article
  12. Review
  13. New solvent options forVirulence · 2019
    Article
  14. Investigation of NovelAntimicrobial agents and chemotherapy · 2019
    Article
  15. The Mechanisms of Disease Caused byFrontiers in microbiology · 2019
    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

4 authors.

Jonathan W BettsDepartment of Pathology and Infectious Diseases, School of Veterinary Medicine, University of Surrey, Guildford, UK.
Michael HornseyDepartment of Pathology and Infectious Diseases, School of Veterinary Medicine, University of Surrey, Guildford, UK. mike.hornsey@surrey.ac.uk.ORCID http://orcid.org/0000-0001-8990-2059
David W WarehamAntimicrobial Research Group, Blizard Institute, Queen Mary University of London, London, UK.
Roberto M La RagioneDepartment of Pathology and Infectious Diseases, School of Veterinary Medicine, University of Surrey, Guildford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcinetobacter baumannii is an important human nosocomial pathogen; most clinical isolates are multidrug-resistant (MDR). Infections caused by A. baumannii often lead to high morbidity and mortality, with limited treatment options. Owing to the small number of anti-Gram-negative antibiotics in the development pipeline, researchers are looking to other natural compounds. The aim of this study was to determine the in vitro kill kinetics, in vivo efficacy and toxicity of theaflavin-epicatechin combinations against MDR A. baumannii.

methodsKill-kinetic assays were performed in Mueller-Hinton 2 broth over 24 h. Toxicity of the compound in the insect model, Galleria mellonella was investigated. The effect of theaflavin-epicatechin combinations on mortality and morbidity were assessed in Acinetobacter baumannii-infected G. mellonella. Larvae were scored for morbidity (melanisation: scale; 0-4) and mortality over 96 h.

resultsKill-kinetic assays revealed that monotherapy had bacteriostatic activity over 24 h, whereas theaflavin-epicatechin combinations were bactericidal (a >3 log reduction in bacterial numbers at 24 h compared with the starting inoculum). Both polyphenols were non-toxic to G. mellonella at concentrations of up to 1000 mg/kg. In vivo treatment assays showed that the combination significantly increased (t test; p ≤ 0.05) larval survival at 96 h to 86% [±17 standard deviation percentage points (pp)] compared to monotherapy with theaflavin (52% ± 14 pp), epicatechin (44% ± 25 pp) or PBS (31% ± 13 pp). Morbidity was also lower in larvae treated with the combination, compared with monotherapy.

conclusionPolyphenol combinations produce effective antibacterial action against A. baumannii and show great potential for the treatment of infections caused by MDR A. baumannii.

Indexed as

AcinetobacterGalleria mellonellaIn vivoMultidrug-resistantPolyphenols

Identifiers

PMID28639145
PMCPMC5595775

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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.