Evidence map›Paper›PMID 24245785›Full record

ArticleCellular microbiology2014

Strategies for maximizing ATP supply in the microsporidian Encephalitozoon cuniculi: direct binding of mitochondria to the parasitophorous vacuole and clustering of the mitochondrial porin VDAC.

Christian Hacker, Matthew Howell, David Bhella, John Lucocq

Open access · hybridAbstract read
In one paragraph

Article in Cellular microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.6field-weighted citation impact, top 21% 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

33 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The Pathogenic Mechanism ofMicroorganisms · 2024
    Article
  6. mBio · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. bioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Down-Regulation of Lipid Metabolism in the Hepatopancreas of ShrimpInternational journal of molecular sciences · 2022
    Article
  13. Heterologous Expressed NbSWP12 from MicrosporidiaJournal of fungi (Basel, Switzerland) · 2022
    Article
  14. Article
  15. Review
  16. Microsporidia, a Highly Adaptive Organism and Its Host Expansion to Humans.Frontiers in cellular and infection microbiology · 2022
    Review
  17. Article
  18. Human microsporidian pathogenJournal of cell science · 2021
    Article
  19. Proteomic Analysis ofMolecular & cellular proteomics : MCP · 2020
    Article
  20. Invasion of Host Cells by Microsporidia.Frontiers in microbiology · 2020
    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

4 authors at 2 institutions in 1 country.

Christian HackerSchool of Medicine, University of St Andrews, North Haugh, St Andrews, Fife, KF16 9TF, UK.
Matthew Howell
David Bhella
John Lucocq
University of St Andrews · GBMRC University of Glasgow Centre for Virus Research · GB

Funding

Medical Research Council MC_UP_A550_1029Medical Research Council MC_UU_12014/7Wellcome TrustWellcome Trust WT089803MA
6 · The paper itself

Abstract

Microsporidia are obligate intracellular parasites with extremely reduced genomes and a dependence on host-derived ATP. The microsporidium Encephalitozoon cuniculi proliferates within a membranous vacuole and we investigated how the ATP supply is optimized at the vacuole-host interface. Using spatial EM quantification (stereology), we found a single layer of mitochondria coating substantial proportions of the parasitophorous vacuole. Mitochondrial binding occurred preferentially over the vegetative 'meront' stages of the parasite, which bulged into the cytoplasm, thereby increasing the membrane surface available for mitochondrial interaction. In a broken cell system mitochondrial binding was maintained and was typified by electron dense structures (< 10 nm long) bridging between outer mitochondrial and vacuole membranes. In broken cells mitochondrial binding was sensitive to a range of protease treatments. The function of directly bound mitochondria, as measured by the membrane potential sensitive dye JC-1, was indistinguishable from other mitochondria in the cell although there was a generalized depression of the membrane potential in infected cells. Finally, quantitative immuno-EM revealed that the ATP-delivering mitochondrial porin, VDAC, was concentrated atthe mitochondria-vacuole interaction site. Thus E. cuniculi appears to maximize ATP supply by direct binding of mitochondria to the parasitophorous vacuole bringing this organelle within 0.020 microns of the growing vegetative form of the parasite. ATP-delivery is further enhanced by clustering of ATP transporting porins in those regions of the outer mitochondrial membrane lying closest to the parasite.

Indexed as

Energy MetabolismAdenosine TriphosphateAnimalsCell LineEncephalitozoon cuniculiImaging, Three-DimensionalMicroscopy, ElectronMitochondriaRabbitsVacuolesVoltage-Dependent Anion ChannelsAdenosine TriphosphateVoltage-Dependent Anion Channels

Identifiers

PMID24245785
PMCPMC4233961
OpenAlexW1576697330

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.