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

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...

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Veröffentlicht in:Nature microbiology 2021-03, Vol.6 (3), p.313-326
Hauptverfasser: Soliman, Sameh S. M., Baldin, Clara, Gu, Yiyou, Singh, Shakti, Gebremariam, Teclegiorgis, Swidergall, Marc, Alqarihi, Abdullah, Youssef, Eman G., Alkhazraji, Sondus, Pikoulas, Antonis, Perske, Christina, Venkataramani, Vivek, Rich, Abigail, Bruno, Vincent M., Hotopp, Julie Dunning, Mantis, Nicolas J., Edwards, John E., Filler, Scott G., Chamilos, Georgios, Vitetta, Ellen S., Ibrahim, Ashraf S.
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container_issue 3
container_start_page 313
container_title Nature microbiology
container_volume 6
creator Soliman, Sameh S. M.
Baldin, Clara
Gu, Yiyou
Singh, Shakti
Gebremariam, Teclegiorgis
Swidergall, Marc
Alqarihi, Abdullah
Youssef, Eman G.
Alkhazraji, Sondus
Pikoulas, Antonis
Perske, Christina
Venkataramani, Vivek
Rich, Abigail
Bruno, Vincent M.
Hotopp, Julie Dunning
Mantis, Nicolas J.
Edwards, John E.
Filler, Scott G.
Chamilos, Georgios
Vitetta, Ellen S.
Ibrahim, Ashraf S.
description 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. Mucorales fungi produce a ricin-like toxin, mucoricin, which is required for fungal pathogenesis and represents a potential therapeutic target.
doi_str_mv 10.1038/s41564-020-00837-0
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M. ; Baldin, Clara ; Gu, Yiyou ; Singh, Shakti ; Gebremariam, Teclegiorgis ; Swidergall, Marc ; Alqarihi, Abdullah ; Youssef, Eman G. ; Alkhazraji, Sondus ; Pikoulas, Antonis ; Perske, Christina ; Venkataramani, Vivek ; Rich, Abigail ; Bruno, Vincent M. ; Hotopp, Julie Dunning ; Mantis, Nicolas J. ; Edwards, John E. ; Filler, Scott G. ; Chamilos, Georgios ; Vitetta, Ellen S. ; Ibrahim, Ashraf S.</creator><creatorcontrib>Soliman, Sameh S. M. ; Baldin, Clara ; Gu, Yiyou ; Singh, Shakti ; Gebremariam, Teclegiorgis ; Swidergall, Marc ; Alqarihi, Abdullah ; Youssef, Eman G. ; Alkhazraji, Sondus ; Pikoulas, Antonis ; Perske, Christina ; Venkataramani, Vivek ; Rich, Abigail ; Bruno, Vincent M. ; Hotopp, Julie Dunning ; Mantis, Nicolas J. ; Edwards, John E. ; Filler, Scott G. ; Chamilos, Georgios ; Vitetta, Ellen S. ; Ibrahim, Ashraf S.</creatorcontrib><description>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. 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M.</creatorcontrib><creatorcontrib>Baldin, Clara</creatorcontrib><creatorcontrib>Gu, Yiyou</creatorcontrib><creatorcontrib>Singh, Shakti</creatorcontrib><creatorcontrib>Gebremariam, Teclegiorgis</creatorcontrib><creatorcontrib>Swidergall, Marc</creatorcontrib><creatorcontrib>Alqarihi, Abdullah</creatorcontrib><creatorcontrib>Youssef, Eman G.</creatorcontrib><creatorcontrib>Alkhazraji, Sondus</creatorcontrib><creatorcontrib>Pikoulas, Antonis</creatorcontrib><creatorcontrib>Perske, Christina</creatorcontrib><creatorcontrib>Venkataramani, Vivek</creatorcontrib><creatorcontrib>Rich, Abigail</creatorcontrib><creatorcontrib>Bruno, Vincent M.</creatorcontrib><creatorcontrib>Hotopp, Julie Dunning</creatorcontrib><creatorcontrib>Mantis, Nicolas J.</creatorcontrib><creatorcontrib>Edwards, John E.</creatorcontrib><creatorcontrib>Filler, Scott G.</creatorcontrib><creatorcontrib>Chamilos, Georgios</creatorcontrib><creatorcontrib>Vitetta, Ellen S.</creatorcontrib><creatorcontrib>Ibrahim, Ashraf S.</creatorcontrib><title>Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis</title><title>Nature microbiology</title><addtitle>Nat Microbiol</addtitle><addtitle>Nat Microbiol</addtitle><description>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. Mucorales fungi produce a ricin-like toxin, mucoricin, which is required for fungal pathogenesis and represents a potential therapeutic target.</description><subject>631/326/193/2542</subject><subject>692/420/254</subject><subject>Animals</subject><subject>Antitoxins - immunology</subject><subject>Antitoxins - pharmacology</subject><subject>Antitoxins - therapeutic use</subject><subject>Apoptosis</subject><subject>Biomedical and Life Sciences</subject><subject>Capillary Permeability</subject><subject>Cells, Cultured</subject><subject>Cross Reactions</subject><subject>Fungi</subject><subject>Humans</subject><subject>Hyphae - chemistry</subject><subject>Hyphae - pathogenicity</subject><subject>Infectious Diseases</subject><subject>Lectins - metabolism</subject><subject>Life Sciences</subject><subject>Medical Microbiology</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Mucorales</subject><subject>Mucorales - chemistry</subject><subject>Mucorales - classification</subject><subject>Mucorales - genetics</subject><subject>Mucorales - pathogenicity</subject><subject>Mucormycosis</subject><subject>Mucormycosis - microbiology</subject><subject>Mucormycosis - pathology</subject><subject>Mucormycosis - prevention &amp; control</subject><subject>Mycotoxins - chemistry</subject><subject>Mycotoxins - genetics</subject><subject>Mycotoxins - immunology</subject><subject>Mycotoxins - metabolism</subject><subject>N-Glycosylase</subject><subject>Necrosis</subject><subject>Parasitology</subject><subject>Pathogenesis</subject><subject>Permeability</subject><subject>Polyclonal antibodies</subject><subject>Protein biosynthesis</subject><subject>Rhizopus - chemistry</subject><subject>Rhizopus - genetics</subject><subject>Rhizopus - pathogenicity</subject><subject>Ribosome Inactivating Proteins - metabolism</subject><subject>Ricin</subject><subject>Ricin - chemistry</subject><subject>Ricin - immunology</subject><subject>Ricin - metabolism</subject><subject>RNA Interference</subject><subject>RNA-mediated interference</subject><subject>Structure-function relationships</subject><subject>Therapeutic applications</subject><subject>Therapeutic targets</subject><subject>Virology</subject><subject>Virulence</subject><subject>Virulence - drug effects</subject><subject>Virulence - genetics</subject><issn>2058-5276</issn><issn>2058-5276</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UctOwzAQtBCIotIf4IAicQ44fiW5IKGKl1TEhZ4tx7FblyQudoLo3-M0pZQLJ693ZmcfA8BFAq8TiLMbTxLKSAwRjCHMcBrDI3CGIM1iilJ2fBCPwMT7FYQwYYixjJ2CEcaEIYLJGZi_dNI6I00TGR-JaBvGlXlXUWu_QrZdiraHpDOtkaKKtHUhqaK1aJd2oRrlA2p1VPdC9Uba8D8HJ1pUXk127xjMH-7fpk_x7PXxeXo3iyVFuI3zVGQoLKMlyVhRYKqKUkOVMVGkrJCoEIFAaK7LRBMES8pSqRkRWc9BKcVjcDvorruiVqVUTetExdfO1MJtuBWG_0Uas-QL-8nTPCEoXGAMrnYCzn50yrd8ZTvXhJk5IjlGlCa4b4MGlnTWe6f0vkMCee8GH9zgwQ2-dYPDUHR5ONu-5Of2gYAHgg9Qs1Dut_c_st-dnJaL</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Soliman, Sameh S. 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M. ; Baldin, Clara ; Gu, Yiyou ; Singh, Shakti ; Gebremariam, Teclegiorgis ; Swidergall, Marc ; Alqarihi, Abdullah ; Youssef, Eman G. ; Alkhazraji, Sondus ; Pikoulas, Antonis ; Perske, Christina ; Venkataramani, Vivek ; Rich, Abigail ; Bruno, Vincent M. ; Hotopp, Julie Dunning ; Mantis, Nicolas J. ; Edwards, John E. ; Filler, Scott G. ; Chamilos, Georgios ; Vitetta, Ellen S. ; Ibrahim, Ashraf S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-97a82038fc486bb35ebdf0e86ab76bc2ba7a8459fd1f420d567cf64a80e862753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>631/326/193/2542</topic><topic>692/420/254</topic><topic>Animals</topic><topic>Antitoxins - immunology</topic><topic>Antitoxins - pharmacology</topic><topic>Antitoxins - therapeutic use</topic><topic>Apoptosis</topic><topic>Biomedical and Life Sciences</topic><topic>Capillary Permeability</topic><topic>Cells, Cultured</topic><topic>Cross Reactions</topic><topic>Fungi</topic><topic>Humans</topic><topic>Hyphae - chemistry</topic><topic>Hyphae - pathogenicity</topic><topic>Infectious Diseases</topic><topic>Lectins - metabolism</topic><topic>Life Sciences</topic><topic>Medical Microbiology</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Mucorales</topic><topic>Mucorales - chemistry</topic><topic>Mucorales - classification</topic><topic>Mucorales - genetics</topic><topic>Mucorales - pathogenicity</topic><topic>Mucormycosis</topic><topic>Mucormycosis - microbiology</topic><topic>Mucormycosis - pathology</topic><topic>Mucormycosis - prevention &amp; control</topic><topic>Mycotoxins - chemistry</topic><topic>Mycotoxins - genetics</topic><topic>Mycotoxins - immunology</topic><topic>Mycotoxins - metabolism</topic><topic>N-Glycosylase</topic><topic>Necrosis</topic><topic>Parasitology</topic><topic>Pathogenesis</topic><topic>Permeability</topic><topic>Polyclonal antibodies</topic><topic>Protein biosynthesis</topic><topic>Rhizopus - chemistry</topic><topic>Rhizopus - genetics</topic><topic>Rhizopus - pathogenicity</topic><topic>Ribosome Inactivating Proteins - metabolism</topic><topic>Ricin</topic><topic>Ricin - chemistry</topic><topic>Ricin - immunology</topic><topic>Ricin - metabolism</topic><topic>RNA Interference</topic><topic>RNA-mediated interference</topic><topic>Structure-function relationships</topic><topic>Therapeutic applications</topic><topic>Therapeutic targets</topic><topic>Virology</topic><topic>Virulence</topic><topic>Virulence - drug effects</topic><topic>Virulence - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soliman, Sameh S. 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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. Mucorales fungi produce a ricin-like toxin, mucoricin, which is required for fungal pathogenesis and represents a potential therapeutic target.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33462434</pmid><doi>10.1038/s41564-020-00837-0</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-6521-0998</orcidid><orcidid>https://orcid.org/0000-0002-5083-8640</orcidid><orcidid>https://orcid.org/0000-0003-3787-8530</orcidid><orcidid>https://orcid.org/0000-0002-2295-058X</orcidid><orcidid>https://orcid.org/0000-0002-5261-6267</orcidid><orcidid>https://orcid.org/0000-0002-7301-1945</orcidid><orcidid>https://orcid.org/0000-0003-3862-986X</orcidid><orcidid>https://orcid.org/0000-0001-7278-3700</orcidid><orcidid>https://orcid.org/0000-0002-7691-615X</orcidid><orcidid>https://orcid.org/0000-0002-3167-1347</orcidid><orcidid>https://orcid.org/0000-0003-4408-6398</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 2058-5276
ispartof Nature microbiology, 2021-03, Vol.6 (3), p.313-326
issn 2058-5276
2058-5276
language eng
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subjects 631/326/193/2542
692/420/254
Animals
Antitoxins - immunology
Antitoxins - pharmacology
Antitoxins - therapeutic use
Apoptosis
Biomedical and Life Sciences
Capillary Permeability
Cells, Cultured
Cross Reactions
Fungi
Humans
Hyphae - chemistry
Hyphae - pathogenicity
Infectious Diseases
Lectins - metabolism
Life Sciences
Medical Microbiology
Mice
Microbiology
Mucorales
Mucorales - chemistry
Mucorales - classification
Mucorales - genetics
Mucorales - pathogenicity
Mucormycosis
Mucormycosis - microbiology
Mucormycosis - pathology
Mucormycosis - prevention & control
Mycotoxins - chemistry
Mycotoxins - genetics
Mycotoxins - immunology
Mycotoxins - metabolism
N-Glycosylase
Necrosis
Parasitology
Pathogenesis
Permeability
Polyclonal antibodies
Protein biosynthesis
Rhizopus - chemistry
Rhizopus - genetics
Rhizopus - pathogenicity
Ribosome Inactivating Proteins - metabolism
Ricin
Ricin - chemistry
Ricin - immunology
Ricin - metabolism
RNA Interference
RNA-mediated interference
Structure-function relationships
Therapeutic applications
Therapeutic targets
Virology
Virulence
Virulence - drug effects
Virulence - genetics
title Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis
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