Evidence map›Paper›PMID 40066990›Full record

ArticlemSphere2025

The Gcn5 lysine acetyltransferase mediates cell wall remodeling, antifungal drug resistance, and virulence of

Manju Chauhan, Raju Shivarathri, Ariel A Aptekmann, Anuradha Chowdhary, Karl Kuchler, Jigar V Desai, Neeraj Chauhan

Abstract read
In one paragraph

Article in mSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Microbiology and molecular biology reviews : MMBR · 2026
    Review
  6. Review
  7. Article
  8. 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

7 authors.

Manju Chauhan *Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.
Raju Shivarathri *Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.
Ariel A AptekmannCenter for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.
Anuradha ChowdharyMedical Mycology Unit, Department of Medical Mycology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, India.
Karl KuchlerMedical University of Vienna, Max Perutz Labs Vienna, Department of Medical Biochemistry, Campus Vienna Biocenter, Vienna, Austria.ORCID 0000-0003-2719-5955
Jigar V DesaiCenter for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.ORCID 0000-0002-8823-0796
Neeraj ChauhanCenter for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA.ORCID 0000-0002-9252-9897

Funding

Tissue specific immunity to fungal infectionsR01AI182977 · NIAID · HACKENSACK UNIVERSITY MEDICAL CENTER · PI NEERAJ CHAUHAN · 2025 to 2026
$1.7M
Identifying drug-resistant Candida species using SuperSelective primer PCRR21AI174118 · NIAID · HACKENSACK UNIVERSITY MEDICAL CENTER · PI CHAUHAN, NEERAJ · 2023 to 2024
$474k
HHS | NIH | All of Us Research Program (All of Us NIH) R01AI182977, R21AI174118New Jersey Health Foundation (NJHF) PC186-24NIAID NIH HHS R01 AI182977NIAID NIH HHS R21 AI174118
6 · The paper itself

Abstract

IMPORTANCE: Invasive fungal diseases affect approximately 6.5 million people every year, of which about 2.5 million people die worldwide. This number is expected to rise due to increasing numbers of immunosuppressed people, including the elderly, premature infants, organ transplant recipients, cancer, and HIV/AIDS patients. The Centers for Disease Control and Prevention (CDC) and the World Health Organization (WHO) have both recently emphasized a critical need for the development of new antifungal therapeutics to address expanding drug resistance among human fungal pathogens. The necessity of new antifungal drugs is also underscored by the fact that mortality due to invasive candidiasis has remained unchanged for several decades. However, the discovery of new drugs acting on antifungal drug targets is complicated because fungi are eukaryotes. This greatly limits the number of feasible fungal-specific drug targets. One class of molecules that fulfills the criterion of fungal specificity is chromatin modification enzymes such as lysine acetyltransferase (KATs). The fungal KATs are structurally less well conserved, and some modifications are only found in fungi, minimizing the risk of toxicity, thus making KATs new promising tools for antifungal therapy. We report here that Gcn5 lysine acetyltransferase mediates antifungal drug resistance and virulence of

Indexed as

Antifungal AgentsCandida aurisCell WallDrug Resistance, FungalFungal ProteinsLysine AcetyltransferasesAnimalsCandida albicansCandidiasisHumansMiceVirulenceAntifungal AgentsFungal ProteinsLysine AcetyltransferasesCandida auriscaspofunginCPTH2GCN5lysine acetyl transferasevirulence

Identifiers

PMID40066990
PMCPMC12039264

What OpenQuestion holds

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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.