Evidence map›Paper›PMID 32808698›Full record

ArticleMolecular microbiology2020

Expanded role of the Cu-sensing transcription factor Mac1p in Candida albicans.

Edward M Culbertson, Vincent M Bruno, Brendan P Cormack, Valeria C Culotta

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Journal of fungi (Basel, Switzerland) · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Metals at the Host-Fungal Pathogen Battleground.Annual review of microbiology · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Journal of fungi (Basel, Switzerland) · 2023
    Article
  13. Article
  14. Sub-lethal concentrations of chlorhexidine inhibitJournal of oral microbiology · 2023
    Article
  15. Article
  16. Article
  17. Ceruloplasmin as a source of Cu for a fungal pathogen.Journal of inorganic biochemistry · 2021
    Article
  18. 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

4 authors at 2 institutions in 1 country.

Edward M CulbertsonThe Department of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Vincent M BrunoDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA.
Brendan P CormackDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-2554-9345
Valeria C CulottaThe Department of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.ORCID 0000-0002-3213-1326
Johns Hopkins University · USUniversity of Maryland, Baltimore · US

Funding

Technology CoreU19AI110820 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI RASKO, DAVID A · 2014 to 2023
$36.5M
Copper as a nutrient for Candida albicans at the host-pathogen interfaceR01AI119949 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CULOTTA, VALERIA C · 2015 to 2019
$2.3M
Cuproproteins for Redox BiologyR35GM136644 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CULOTTA, VALERIA C · 2020 to 2024
$2.2M
Kidney Cu Homeostasis and Ceruloplasmin during Infection and InflammationF31DK111114 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI CULBERTSON, EDWARD MCLOUTH · 2016 to 2019
$177k
NIAID NIH HHS R01 AI119949NIAID NIH HHS U19 AI110820NIDDK NIH HHS F31 DK111114NIGMS NIH HHS R35 GM136644
6 · The paper itself

Abstract

As part of the innate immune response, the host withholds metal micronutrients such as Cu from invading pathogens, and microbes respond through metal starvation stress responses. With the opportunistic fungal pathogen Candida albicans, the Cu-sensing transcription factor Mac1p governs the cellular response to Cu starvation by controlling Cu import. Mac1p additionally controls reactive oxygen species (ROS) homeostasis by repressing a Cu-containing superoxide dismutase (SOD1) and inducing Mn-containing SOD3 as a non-Cu alternative. We show here that C. albicans Mac1p is essential for virulence in a mouse model for disseminated candidiasis and that the cellular functions of Mac1p extend beyond Cu uptake and ROS homeostasis. Specifically, mac1∆/∆ mutants are profoundly deficient in mitochondrial respiration and Fe accumulation, both Cu-dependent processes. Surprisingly, these deficiencies are not simply the product of impaired Cu uptake; rather mac1∆/∆ mutants appear defective in Cu allocation. The respiratory defect of mac1∆/∆ mutants was greatly improved by a sod1∆/∆ mutation, demonstrating a role for SOD1 repression by Mac1p in preserving respiration. Mac1p downregulates the major Cu consumer SOD1 to spare Cu for respiration that is essential for virulence of this fungal pathogen. The implications for such Cu homeostasis control in other pathogenic fungi are discussed.

Indexed as

AnimalsCandida albicansCandidiasisCopperFungal ProteinsGene Expression Regulation, FungalHost Microbial InteractionsIronMiceMitochondriaMutationReactive Oxygen SpeciesStress, PhysiologicalSuperoxide DismutaseTranscription FactorsVirulenceCopperFungal ProteinsIronReactive Oxygen SpeciesSuperoxide DismutaseTranscription FactorsCandida albicanscell respirationcopperironsuperoxide dismutase

Identifiers

PMID32808698
PMCPMC7856572
OpenAlexW3080393910

What OpenQuestion holds

Textmetadata
LicenceTDM
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.