Evidence map›Paper›PMID 27815348›Full record

ArticleG3 (Bethesda, Md.)2017

The CgHaa1-Regulon Mediates Response and Tolerance to Acetic Acid Stress in the Human Pathogen Candida glabrata.

Ruben T Bernardo, Diana V Cunha, Can Wang, Leonel Pereira, Sónia Silva, Sara B Salazar, Markus S Schröder, Michiyo Okamoto, Azusa Takahashi-Nakaguchi, Hiroji Chibana and 5 more

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-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

21 citing papers in PubMed, 31 citations in OpenAlex.

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  14. Differential Regulation of Echinocandin Targets Fks1 and Fks2 inJournal of fungi (Basel, Switzerland) · 2020
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  17. A Transcriptomics Approach To Unveiling the Mechanisms ofAntimicrobial agents and chemotherapy · 2019
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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

15 authors at 6 institutions in 3 countries.

Ruben T BernardoDepartment of Bioengineering, Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001, Portugal.
Diana V CunhaDepartment of Bioengineering, Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001, Portugal.
Can WangSchool of Biomolecular and Biomedical Sciences, Conway Institute, University College of Dublin, Belfield, Dublin 4, Ireland.
Leonel PereiraCentre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal.
Sónia SilvaCentre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal.
Sara B SalazarDepartment of Bioengineering, Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001, Portugal.
Markus S SchröderSchool of Biomolecular and Biomedical Sciences, Conway Institute, University College of Dublin, Belfield, Dublin 4, Ireland.
Michiyo OkamotoMedical Mycology Research Center, Chiba University, Chuo-ku, 260-8673, Japan.
Azusa Takahashi-NakaguchiMedical Mycology Research Center, Chiba University, Chuo-ku, 260-8673, Japan.
Hiroji ChibanaMedical Mycology Research Center, Chiba University, Chuo-ku, 260-8673, Japan.
Toshihiro AoyamaDepartment of Electronic and Information Engineering, Suzuka National College of Technology, Unver, Mie 510-0294, Japan.
Isabel Sá-CorreiaDepartment of Bioengineering, Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001, Portugal.
Joana AzeredoCentre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal.
Geraldine ButlerSchool of Biomolecular and Biomedical Sciences, Conway Institute, University College of Dublin, Belfield, Dublin 4, Ireland.
Nuno Pereira MiraDepartment of Bioengineering, Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, 1049-001, Portugal nuno.mira@tecnico.ulisboa.pt.
Chiba University Hospital · JPInstitute for Biotechnology and Bioengineering · PTUniversity College Dublin · IEUniversity of Minho · PTUniversity of Lisbon · PTNational Institute of Technology, Suzuka College · JP

Funding

Wellcome Trust
6 · The paper itself

Abstract

To thrive in the acidic vaginal tract, Candida glabrata has to cope with high concentrations of acetic acid. The mechanisms underlying C. glabrata tolerance to acetic acid at low pH remain largely uncharacterized. In this work, the essential role of the CgHaa1 transcription factor (encoded by ORF CAGL0L09339g) in the response and tolerance of C. glabrata to acetic acid is demonstrated. Transcriptomic analysis showed that CgHaa1 regulates, directly or indirectly, the expression of about 75% of the genes activated under acetic acid stress. CgHaa1-activated targets are involved in multiple physiological functions including membrane transport, metabolism of carbohydrates and amino acids, regulation of the activity of the plasma membrane H

Indexed as

Acetic AcidCandida glabrataCandidiasisEpithelial CellsEvolution, MolecularFemaleFungal ProteinsGene Expression Regulation, FungalGene Regulatory NetworksHSP30 Heat-Shock ProteinsHumansHydrogen-Ion ConcentrationMembrane Transport ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsStress, PhysiologicalAcetic AcidFungal ProteinsHaa1 protein, S cerevisiaeHSP30 Heat-Shock ProteinsMembrane Transport ProteinsSaccharomyces cerevisiae ProteinsTranscription Factorsacetic acidCandida glabrataCgHaa1vaginal candidiasisvaginal dysbiosis

Identifiers

PMID27815348
PMCPMC5217100
OpenAlexW2555979423

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.