Evidence map›Paper›PMID 38704366›Full record

ArticleNature communications2024

An oxylipin signal confers protection against antifungal echinocandins in pathogenic aspergilli.

Dante G Calise, Sung Chul Park, Jin Woo Bok, Gustavo H Goldman, Nancy P Keller

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. ZfpA-regulated chitin synthesis inAntimicrobial agents and chemotherapy · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. The Influence ofJournal of fungi (Basel, Switzerland) · 2024
    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

5 authors.

Dante G CaliseDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0009-0009-0953-4029
Sung Chul ParkDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0009-0008-9081-7992
Jin Woo BokDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA.
Gustavo H GoldmanFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil.ORCID http://orcid.org/0000-0002-2986-350X
Nancy P KellerDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI, USA. npkeller@wisc.edu.ORCID http://orcid.org/0000-0002-4386-9473

Funding

Deciphering the phenotypic and genomic traits that underlie the evolution of pathogenicity differences among Aspergillus fumigatus and its close relativesR01AI153356 · NIAID · VANDERBILT UNIVERSITY · PI Antonis Rokas · 2022 to 2026
$3.5M
Comprehensive analysis of NRPS-derived metabolomes of three Aspergillus speciesR01GM112739 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI KELLER, NANCY P · 2015 to 2023
$2.8M
Bidirectional paracrine signaling in the establishment of invasive aspergillosisR01AI150669 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KELLER, NANCY P · 2021 to 2025
$2.4M
V. cholerae iron transport mechanisms and pathogenesisR01AI050669 · NIAID · UNIVERSITY OF TEXAS AUSTIN · PI PAYNE, SHELLEY M. · 2002 to 2006
$1.5M
NIAID NIH HHS R01 AI050669NIAID NIH HHS R01 AI150669NIAID NIH HHS R01 AI153356NIGMS NIH HHS R01 GM112739U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01 AI50669-03U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01 GM112739-08
6 · The paper itself

Abstract

Aspergillus fumigatus is the leading causative agent of life-threatening invasive aspergillosis in immunocompromised individuals. One antifungal class used to treat Aspergillus infections is the fungistatic echinocandins, semisynthetic drugs derived from naturally occurring fungal lipopeptides. By inhibiting beta-1,3-glucan synthesis, echinocandins cause both fungistatic stunting of hyphal growth and repeated fungicidal lysis of apical tip compartments. Here, we uncover an endogenous mechanism of echinocandin tolerance in A. fumigatus whereby the inducible oxylipin signal 5,8-diHODE confers protection against tip lysis via the transcription factor ZfpA. Treatment of A. fumigatus with echinocandins induces 5,8-diHODE synthesis by the fungal oxygenase PpoA in a ZfpA dependent manner resulting in a positive feedback loop. This protective 5,8-diHODE/ZfpA signaling relay is conserved among diverse isolates of A. fumigatus and in two other Aspergillus pathogens. Our findings reveal an oxylipin-directed growth program-possibly arisen through natural encounters with native echinocandin producing fungi-that enables echinocandin tolerance in pathogenic aspergilli.

Indexed as

Antifungal AgentsAspergillosisAspergillus fumigatusEchinocandinsFungal ProteinsOxylipinsGene Expression Regulation, FungalHyphaeSignal TransductionTranscription FactorsAntifungal AgentsEchinocandinsFungal ProteinsOxylipinsTranscription Factors

Identifiers

PMID38704366
PMCPMC11069582

What Socratic 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 Socratic graph.