Evidence map›Paper›PMID 31407245›Full record

ArticleMolecular biology reports2019

The efflux pump inhibitor tetrandrine exhibits synergism with fluconazole or voriconazole against Candida parapsilosis.

Ya-Jing Zhao, Wei-Da Liu, Yong-Nian Shen, Dong-Mei Li, Kun-Ju Zhu, Hong Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. BioMed research international · 2023
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  7. Deciphering the Role ofIndian journal of microbiology · 2022
    Review
  8. Review
  9. Antifungal activity of Acylhydrazone derivatives againstAntimicrobial agents and chemotherapy · 2021
    Article
  10. Article
  11. A critical review: traditional uses, phytochemistry, pharmacology and toxicology ofPhytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2020
    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 4 institutions in 2 countries.

Ya-Jing ZhaoThe First Affiliated Hospital of Jinan University, 601 Huangpu Avenue West, Guangzhou, 510632, China.
Wei-Da LiuDepartment of Mycology, Institute of Dermatology, Chinese Academy of Medical Science and Peking Union Medical College, Nanjing, China.
Yong-Nian ShenDepartment of Mycology, Institute of Dermatology, Chinese Academy of Medical Science and Peking Union Medical College, Nanjing, China.
Dong-Mei LiDepartment of Microbiology and Immunology, Georgetown University Medical Center, Washington, DC, USA.
Kun-Ju ZhuThe First Affiliated Hospital of Jinan University, 601 Huangpu Avenue West, Guangzhou, 510632, China.
Hong ZhangThe First Affiliated Hospital of Jinan University, 601 Huangpu Avenue West, Guangzhou, 510632, China. tzhangh@jnu.edu.cn.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNJinan University · CNFirst Affiliated Hospital of Jinan University · CNGeorgetown University Medical Center · US

Funding

National Nature Science Foundation of China 81471995
6 · The paper itself

Abstract

In the last two decades, with the wide use of azoles, antifungal resistance among Candida parapsilosis has considered a matter of concern worldwide. The aim of this study is to evaluate the antifungal potentials of tetrandrine (TET) alone and in combination with fluconazole (FLC)/voriconazole (VRC) against C. parapsilosis. Susceptibility tests were performed by microdilution method, checkerboard assay, time-kill test, spot assay. Subsequently, rhodamine 6G efflux test and the expressions of transporter related genes, namely CDR1 and MDR1 for C. parapsilosis were analyzed by qRT-PCR. The susceptibility test showed that TET presented strong synergism with FLC and VRC with fractional inhibitory concentration index (FICI) in a range of 0.094-0.562. The susceptibility results were also confirmed by spot assay and time-kill studies. With TET treatment, a vast quantity of rhodamine 6G could not be pumped out from the cells as considerably intracellular red fluorescence was accumulated. Meanwhile, the expressions of efflux-associated genes presented varying degrees of inhibition. These results indicated that TET was a decent antifungal synergist to promote the antifungal efficacy of FLC/VRC, and the underlying antifungal mechanism might be associated with the inhibition of efflux pump and the elevation of intracellular drug content.

Indexed as

Antifungal AgentsBenzylisoquinolinesCandida parapsilosisDrug Resistance, FungalDrug SynergismFluconazoleFungal ProteinsMicrobial Sensitivity TestsVoriconazoleAntifungal AgentsBenzylisoquinolinesFluconazoleFungal ProteinstetrandrineVoriconazoleCandida parapsilosisFluconazole (FLC)SynergismTetrandrine (TET)Voriconazole (VRC)

Identifiers

PMID31407245
OpenAlexW2967136546

What Socratic 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 Socratic graph.