Evidence map›Paper›PMID 31976503›Full record

ArticleMetallomics : integrated biometal science2020

Changes in mammalian copper homeostasis during microbial infection.

Edward M Culbertson, Aslam A Khan, Abigael Muchenditsi, Svetlana Lutsenko, David J Sullivan, Michael J Petris, Brendan P Cormack, Valeria C Culotta

Abstract read
In one paragraph

Article in Metallomics : integrated biometal science, 2020. 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
–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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Metals at the Host-Fungal Pathogen Battleground.Annual review of microbiology · 2024
    Review
  8. Article
  9. Review
  10. Improved diagnostic markers for invasive pulmonary aspergillosis in COPD patients.Frontiers in cellular and infection microbiology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Demonstration ofMicrobiology spectrum · 2021
    Article
  17. Ceruloplasmin as a source of Cu for a fungal pathogen.Journal of inorganic biochemistry · 2021
    Article
  18. Article
  19. Article
  20. 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

8 authors.

Edward M CulbertsonThe Department of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA. vculott1@jhu.edu.
Aslam A KhanDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, USA.
Abigael MuchenditsiDepartment of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Svetlana LutsenkoDepartment of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
David J SullivanThe W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Michael J PetrisDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, USA.
Brendan P CormackDepartment of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Valeria C CulottaThe Department of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA. vculott1@jhu.edu.ORCID 0000-0002-3213-1326

Funding

Optimized Combination Antimalarial Drug TherapyR01AI111962 · NIAID · GEORGETOWN UNIVERSITY · PI ROEPE, PAUL D., SULLIVAN, DAVID JOSEPH · 2014 to 2018
$4.9M
AIDS Opportunistic Infectious: Virulence of C. glabrataR01AI046223 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 1999 to 2014
$4.9M
Copper Homeostasis and Liver FunctionR01DK117396 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI JAMES P HAMILTON, SVETLANA LUTSENKO · 2018 to 2026
$3.9M
GENETIC DETERMINANTS OF OXYGEN TOXICITYR01GM050016 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CULOTTA, VALERIA C · 1993 to 2018
$3.0M
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
Copper metabolism as a unique vulnerability in cancerR01CA190265 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI PETRIS, MICHAEL J. · 2015 to 2019
$1.7M
Copper and iron in nutritional immunityR01DK116859 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI PETRIS, MICHAEL J. · 2019 to 2022
$1.7M
Kidney Cu Homeostasis and Ceruloplasmin during Infection and InflammationF31DK111114 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI CULBERTSON, EDWARD MCLOUTH · 2016 to 2019
$177k
NCI NIH HHS R01 CA190265NIAID NIH HHS R01 AI046223NIAID NIH HHS R01 AI111962NIAID NIH HHS R01 AI119949NIDDK NIH HHS F31 DK111114NIDDK NIH HHS R01 DK116859NIDDK NIH HHS R01 DK117396NIGMS NIH HHS R01 GM050016
6 · The paper itself

Abstract

Animals carefully control homeostasis of Cu, a metal that is both potentially toxic and an essential nutrient. During infection, various shifts in Cu homeostasis can ensue. In mice infected with Candida albicans, serum Cu progressively rises and at late stages of infection, liver Cu rises, while kidney Cu declines. The basis for these changes in Cu homeostasis was poorly understood. We report here that the progressive rise in serum Cu is attributable to liver production of the multicopper oxidase ceruloplasmin (Cp). Through studies using Cp-/- mice, we find this elevated Cp helps recover serum Fe levels at late stages of infection, consistent with a role for Cp in loading transferrin with Fe. Cp also accounts for the elevation in liver Cu seen during infection, but not for the fluctuations in kidney Cu. The Cu exporting ATPase ATP7B is one candidate for kidney Cu control, but we find no change in the pattern of kidney Cu loss during infection of Atp7b-/- mice, implying alternative mechanisms. To test whether fungal infiltration of kidney tissue was required for kidney Cu loss, we explored other paradigms of infection. Infection with the intravascular malaria parasite Plasmodium berghei caused a rise in serum Cu and decrease in kidney Cu similar to that seen with C. albicans. Thus, dynamics in kidney Cu homeostasis appear to be a common feature among vastly different infection paradigms. The implications for such Cu homeostasis control in immunity are discussed.

Indexed as

AnimalsCandida albicansCandidiasisCeruloplasminCopperFemaleHomeostasisKidneyLiverMaleMiceMice, Inbred BALB CMice, Inbred C57BLCeruloplasminCopper

Identifiers

PMID31976503
PMCPMC7122220

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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.