Evidence map›Paper›PMID 24389279›Full record

ArticleThe Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases

Arachidonic acid affects biofilm formation and PGE2 level in Candida albicans and non-albicans species in presence of subinhibitory concentration of fluconazole and terbinafine.

Nripendra Nath Mishra, Shakir Ali, Praveen K Shukla

Open access · goldAbstract read
In one paragraph

Article in The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  3. Journal of fungi (Basel, Switzerland) · 2024
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  10. Antifungal Drug Repurposing.Antibiotics (Basel, Switzerland) · 2020
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  11. Transcriptome Analyses ofG3 (Bethesda, Md.) · 2020
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  12. Journal of fungi (Basel, Switzerland) · 2019
    Review
  13. Fungal Symbionts Produce Prostaglandin EFrontiers in cellular and infection microbiology · 2019
    Article
  14. Review
  15. Inhibition ofFrontiers in pharmacology · 2018
    Article
  16. Article
  17. Article
  18. Antimicrobial agents and chemotherapy · 2017
    Article
  19. 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

3 authors at 1 institution in 1 country.

Nripendra Nath MishraMedical Mycology Lab, Division of Fermentation Technology, CSIR-Central Drug Research Institute, B.S. 10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226021, India; Department of Biochemistry, Jamia Hamdard, New Delhi, India.
Shakir AliDepartment of Biochemistry, Jamia Hamdard, New Delhi, India.
Praveen K ShuklaMedical Mycology Lab, Division of Fermentation Technology, CSIR-Central Drug Research Institute, B.S. 10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226021, India. Electronic address: pk_shukla@cdri.res.in.
Jamia Hamdard · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Candida albicans utilizes arachidonic acid (AA) released during the course of infection (Candidiasis) from phospholipids of infected host cell membranes and synthesizes extracellular prostaglandin(s) which play an important role in hyphae formation and host cell damage. C. albicans biofilms secrete significantly more prostaglandin(s) and evidence suggests that Candida biofilms have dramatically reduced susceptibility to majority of antifungal drugs. AA influences the saturation level of lipids and fluidity of yeast cell membranes. Therefore the aim of this study was to evaluate the effect of AA alone or in combination with antifungal agents on biofilm formation and production of prostaglandin (PGE2) in C. albicans, C. parapsilosis, C. glabrata, C. tropicalis, and C. albicans amphotericin B resistant strain (AmBR). Maximum biofilm formation was found to be in the case of C. albicans compared to C. non-albicans species. However, among the non-albicans species C. tropicalis exhibited highest biofilm formation. Treatment with AA in combination with subinhibitory concentrations of fluconazole and terbinafine separately exhibited significant (p<0.05) reduction in biofilm formation against C. glabrata, C. parapsilosis, C. tropicalis and AmBR as compared to their individual effect. Further, these two antifungal agents in combination with AA caused an increase in production of prostaglandin from fungal cell itself which was significant (p<0.05) in case of all the strains tested.

Indexed as

Antifungal AgentsArachidonic AcidBiofilmsCandidaCandida albicansDinoprostoneFluconazoleMicrobial Sensitivity TestsMicroscopy, FluorescenceNaphthalenesTerbinafineAntifungal AgentsArachidonic AcidDinoprostoneFluconazoleNaphthalenesTerbinafineAmBRArachidonic acidCandida albicansCandida tropicalisFDAProstaglandin E2

Identifiers

PMID24389279
PMCPMC9427476
OpenAlexW2019648275

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.