Evidence map›Paper›PMID 33462434›Full record

ArticleNature microbiology2021

Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis.

Sameh S M Soliman, Clara Baldin, Yiyou Gu, Shakti Singh, Teclegiorgis Gebremariam, Marc Swidergall, Abdullah Alqarihi, Eman G Youssef, Sondus Alkhazraji, Antonis Pikoulas and 11 more

Open access · greenAbstract read
In one paragraph

Article in Nature microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Innovation in antifungal therapy.EMBO molecular medicine · 2026
    Review
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  7. Article
  8. Review
  9. Article
  10. Article
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  12. Article
  13. Article
  14. Article
  15. Chronic cutaneous and mucosal mucormycosis:Emerging microbes & infections · 2025
    Article
  16. Synergistic interactions betweenProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Future Prospects and Challenges in Mucormycosis Research.Journal of fungi (Basel, Switzerland) · 2025
    Article

7 more citing papers are in PubMed but not listed here.

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

21 authors at 10 institutions in 6 countries.

Sameh S M Soliman *Division of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0002-7691-615X
Clara Baldin *Division of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.
Yiyou Gu *Division of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.
Shakti Singh *Division of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0001-6521-0998
Teclegiorgis GebremariamDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0002-2295-058X
Marc SwidergallDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0002-5261-6267
Abdullah AlqarihiDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0003-4408-6398
Eman G YoussefDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0002-3167-1347
Sondus AlkhazrajiDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.
Antonis PikoulasDepartment of Medicine, University of Crete and Foundation for Research and Technology, Heraklion, Greece.
Christina PerskeDepartment of Pathology, University Medicine Göttingen, Göttingen, Germany.
Vivek VenkataramaniDepartment of Pathology, University Medicine Göttingen, Göttingen, Germany.
Abigail RichDepartments of Immunology and Microbiology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-7301-1945
Vincent M BrunoDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA.
Julie Dunning HotoppDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-3862-986X
Nicolas J MantisNew York State Department of Health, Wadsworth Center, Albany, NY, USA.ORCID http://orcid.org/0000-0002-5083-8640
John E EdwardsDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.
Scott G FillerDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA.ORCID http://orcid.org/0000-0001-7278-3700
Georgios ChamilosDepartment of Medicine, University of Crete and Foundation for Research and Technology, Heraklion, Greece.
Ellen S VitettaDepartments of Immunology and Microbiology, UT Southwestern Medical Center, Dallas, TX, USA.
Ashraf S IbrahimDivision of Infectious Diseases, The Lundquist Institute for Biomedical Innovation, Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, CA, USA. ibrahim@lundquist.org.ORCID http://orcid.org/0000-0003-3787-8530
UCLA Medical Center · USUniversity of California, Los Angeles · USUniversitätsmedizin Göttingen · DEUniversity of Crete · GRUniversity of Maryland, Baltimore · USBeni-Suef University · EGInnsbruck Medical University · ATNew York State Department of Health · USSouthwestern Medical CenterVanderbilt University · US

Funding

Technology CoreU19AI110820 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI WHITE, OWEN R · 2014 to 2023
$36.5M
Novel Toxins and Receptors in Mucormycosis Pathogenesis and TreatmentR01AI063503 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI IBRAHIM, ASHRAF S. · 2006 to 2025
$7.3M
Endothelial invasion by yeast-phase CandidaR01AI124566 · NIAID · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI FILLER, SCOTT G, MITCHELL, AARON P · 2016 to 2020
$2.7M
Therapeutic targeting of growth factor receptors to treat MucormycosisR01AI141360 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BRUNO, VINCENT MICHAEL · 2019 to 2023
$2.5M
Novel Candida albicans host receptors during infection and immune responseR00DE026856 · NIDCR · LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER · PI SWIDERGALL, MARC · 2019 to 2021
$710k
Humanized monoclonal antibodies to treat mucormycosisR43AI138904 · NIAID · VITALEX BIOSCIENCES, LLC · PI IBRAHIM, ASHRAF S., LAZAR, GARY · 2018 to 2019
$600k
NIAID NIH HHS R01 AI063503NIAID NIH HHS R01 AI124566NIAID NIH HHS R01 AI141360NIAID NIH HHS R43 AI138904NIAID NIH HHS U19 AI110820NIDCR NIH HHS R00 DE026856
6 · The paper itself

Abstract

Fungi of the order Mucorales cause mucormycosis, a lethal infection with an incompletely understood pathogenesis. We demonstrate that Mucorales fungi produce a toxin, which plays a central role in virulence. Polyclonal antibodies against this toxin inhibit its ability to damage human cells in vitro and prevent hypovolemic shock, organ necrosis and death in mice with mucormycosis. Inhibition of the toxin in Rhizopus delemar through RNA interference compromises the ability of the fungus to damage host cells and attenuates virulence in mice. This 17 kDa toxin has structural and functional features of the plant toxin ricin, including the ability to inhibit protein synthesis through its N-glycosylase activity, the existence of a motif that mediates vascular leak and a lectin sequence. Antibodies against the toxin inhibit R. delemar- or toxin-mediated vascular permeability in vitro and cross react with ricin. A monoclonal anti-ricin B chain antibody binds to the toxin and also inhibits its ability to cause vascular permeability. Therefore, we propose the name 'mucoricin' for this toxin. Not only is mucoricin important in the pathogenesis of mucormycosis but our data suggest that a ricin-like toxin is produced by organisms beyond the plant and bacterial kingdoms. Importantly, mucoricin should be a promising therapeutic target.

Indexed as

AnimalsAntitoxinsApoptosisCapillary PermeabilityCells, CulturedCross ReactionsHumansHyphaeLectinsMiceMucoralesMucormycosisMycotoxinsNecrosisRhizopusRibosome Inactivating ProteinsAntitoxinsLectinsmucoricinMycotoxinsRibosome Inactivating ProteinsRicin

Identifiers

PMID33462434
PMCPMC7914224
OpenAlexW3124620674

What Socratic holds

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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 Socratic graph.