Evidence map›Paper›PMID 32658892›Full record

ArticlePLoS genetics2020

A non-canonical RNAi pathway controls virulence and genome stability in Mucorales.

Carlos Pérez-Arques, María Isabel Navarro-Mendoza, Laura Murcia, Eusebio Navarro, Victoriano Garre, Francisco Esteban Nicolás

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  7. Article
  8. Challenges and Opportunities Arising from Host-International journal of molecular sciences · 2024
    Review
  9. Molecular mechanisms that govern infection and antifungal resistance in Mucorales.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  10. Article
  11. Journal of fungi (Basel, Switzerland) · 2023
    Review
  12. Heterochromatin and RNAi act independently to ensure genome stability in Mucorales human fungal pathogens.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Review
  14. Article
  15. Recent Advances and Future Directions in the Understanding of Mucormycosis.Frontiers in cellular and infection microbiology · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  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

6 authors at 1 institution in 1 country.

Carlos Pérez-ArquesDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.ORCID 0000-0003-1384-3608
María Isabel Navarro-MendozaDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.ORCID 0000-0002-3560-6155
Laura MurciaDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.
Eusebio NavarroDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.
Victoriano GarreDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.
Francisco Esteban NicolásDepartment of Genetics and Microbiology, Faculty of Biology, University of Murcia, Murcia, Spain.ORCID 0000-0003-3762-5971
Universidad de Murcia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epimutations in fungal pathogens are emerging as novel phenomena that could explain the fast-developing resistance to antifungal drugs and other stresses. These epimutations are generated by RNA interference (RNAi) mechanisms that transiently silence specific genes to overcome stressful stimuli. The early-diverging fungus Mucor circinelloides exercises a fine control over two interacting RNAi pathways to produce epimutants: the canonical RNAi pathway and a new RNAi degradative pathway. The latter is considered a non-canonical RNAi pathway (NCRIP) because it relies on RNA-dependent RNA polymerases (RdRPs) and a novel ribonuclease III-like named R3B2 to degrade target transcripts. Here in this work, we uncovered the role of NCRIP in regulating virulence processes and transposon movements through key components of the pathway, RdRP1 and R3B2. Mutants in these genes are unable to launch a proper virulence response to macrophage phagocytosis, resulting in a decreased virulence potential. The transcriptomic profile of rdrp1Δ and r3b2Δ mutants revealed a pre-exposure adaptation to the stressful phagosomal environment even when the strains are not confronted by macrophages. These results suggest that NCRIP represses key targets during regular growth and releases its control when a stressful environment challenges the fungus. NCRIP interacts with the RNAi canonical core to protect genome stability by controlling the expression of centromeric retrotransposable elements. In the absence of NCRIP, these retrotransposons are robustly repressed by the canonical RNAi machinery; thus, supporting the antagonistic role of NCRIP in containing the epimutational pathway. Both interacting RNAi pathways might be essential to govern host-pathogen interactions through transient adaptations, contributing to the unique traits of the emerging infection mucormycosis.

Indexed as

RNA InterferenceAntifungal AgentsDrug Resistance, FungalEpigenesis, GeneticFungal ProteinsGene Expression Regulation, FungalGenomic InstabilityHost-Pathogen InteractionsMucoralesMucormycosisMutationRibonuclease IIIRNA, MessengerSignal TransductionVirulenceAntifungal AgentsFungal ProteinsRibonuclease IIIRNA, Messenger

Identifiers

PMID32658892
PMCPMC7377519
OpenAlexW3040781519

What OpenQuestion holds

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LicenceCC BY
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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.