Evidence map›Paper›PMID 27796932›Full record

ArticleJournal of microbiology (Seoul, Korea)2016

The in vitro and in vivo efficacy of fluconazole in combination with farnesol against Candida albicans isolates using a murine vulvovaginitis model.

Aliz Bozó, Marianna Domán, László Majoros, Gábor Kardos, István Varga, Renátó Kovács

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2016. 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
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. The effects of tyrosol on yeasts: an overview of current knowledge.Applied microbiology and biotechnology · 2025
    Review
  2. Cyclodextrins in action: ModulatingBiotechnology reports (Amsterdam, Netherlands) · 2025
    Article
  3. Antifungal Activity and Type of Interaction ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Inhibiting roles of farnesol and HOG in morphological switching ofAmerican journal of translational research · 2020
    Review
  10. Frontiers in microbiology · 2020
    Article
  11. Antimicrobial agents and chemotherapy · 2019
    Article
  12. Article
  13. Methodologies forMicrobial cell (Graz, Austria) · 2018
    Review
  14. Article
  15. 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

6 authors at 1 institution in 1 country.

Aliz BozóDepartment of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Marianna DománDepartment of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
László MajorosDepartment of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Gábor KardosDepartment of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
István VargaDepartment of Periodontology, Faculty of Dentistry, University of Debrecen, Debrecen, 4032, Hungary.
Renátó KovácsDepartment of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary. kovacs.renato@med.unideb.hu.
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Farnesol is a quorum-sensing molecule that inhibits biofilm formation in Candida albicans. Previous in vitro data suggest that, in combination with certain antifungals, farnesol may have an adjuvant anti-biofilm agent. However, the in vivo efficacy of farnesol is very questionable. Therefore, the in vitro and in vivo activity of fluconazole combined with farnesol was evaluated against C. albicans biofilms using fractional inhibitory concentration index (FICI) determination, time-kill experiments and a murine vulvovaginitis model. The median biofilm MICs of fluconazole-sensitive C. albicans isolates ranged between 4 -> 512 mg/L and 150-300 μM for fluconazole and farnesol, respectively. These values were 512 -> 512 mg/L and > 300 μM for fluconazole-resistant clinical isolates. Farnesol decreased the median MICs of fluconazole by 2-64-fold for biofilms. Based on FICI, synergistic interaction was observed only in the case of the sessile SC5314 reference strain (FICIs: 0.16-0.27). In time-kill studies, only the 512 mg/L fluconazole and 512 mg/L fluconazole + 75 μM farnesol reduced biofilm mass significantly at each time point in the case of all isolates. The combination reduced the metabolic activity of biofilms for all isolates in a concentration- and time-dependent manner. Our findings revealed that farnesol alone was not protective in a murine vulvovaginitis model. Farnesol was not beneficial in combination with fluconazole for fluconazole-susceptible isolates, but partially increased fluconazole activity against one fluconazole-resistant isolate, but not the other one.

Indexed as

AnimalsAntifungal AgentsBiofilmsCandida albicansCandidiasisDisease Models, AnimalDrug Resistance, FungalDrug SynergismFarnesolFemaleFluconazoleMiceMicrobial Sensitivity TestsQuorum SensingVaginaVirulenceAntifungal AgentsFarnesolFluconazoleFIC indexfluconazole-resistantmurine vulvovaginitissynergytime-kill experiment

Identifiers

PMID27796932
OpenAlexW2540081690

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.