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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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 |
format | Article |
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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><identifier>ISSN: 2058-5276</identifier><identifier>EISSN: 2058-5276</identifier><identifier>DOI: 10.1038/s41564-020-00837-0</identifier><identifier>PMID: 33462434</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>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</subject><ispartof>Nature microbiology, 2021-03, Vol.6 (3), p.313-326</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-97a82038fc486bb35ebdf0e86ab76bc2ba7a8459fd1f420d567cf64a80e862753</citedby><cites>FETCH-LOGICAL-c523t-97a82038fc486bb35ebdf0e86ab76bc2ba7a8459fd1f420d567cf64a80e862753</cites><orcidid>0000-0001-6521-0998 ; 0000-0002-5083-8640 ; 0000-0003-3787-8530 ; 0000-0002-2295-058X ; 0000-0002-5261-6267 ; 0000-0002-7301-1945 ; 0000-0003-3862-986X ; 0000-0001-7278-3700 ; 0000-0002-7691-615X ; 0000-0002-3167-1347 ; 0000-0003-4408-6398</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41564-020-00837-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41564-020-00837-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33462434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soliman, Sameh S. 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 & 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. M.</creator><creator>Baldin, Clara</creator><creator>Gu, Yiyou</creator><creator>Singh, Shakti</creator><creator>Gebremariam, Teclegiorgis</creator><creator>Swidergall, Marc</creator><creator>Alqarihi, Abdullah</creator><creator>Youssef, Eman G.</creator><creator>Alkhazraji, Sondus</creator><creator>Pikoulas, Antonis</creator><creator>Perske, Christina</creator><creator>Venkataramani, Vivek</creator><creator>Rich, Abigail</creator><creator>Bruno, Vincent M.</creator><creator>Hotopp, Julie Dunning</creator><creator>Mantis, Nicolas J.</creator><creator>Edwards, John E.</creator><creator>Filler, Scott G.</creator><creator>Chamilos, Georgios</creator><creator>Vitetta, Ellen S.</creator><creator>Ibrahim, Ashraf S.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><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></search><sort><creationdate>20210301</creationdate><title>Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis</title><author>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.</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 & 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. 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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soliman, Sameh S. M.</au><au>Baldin, Clara</au><au>Gu, Yiyou</au><au>Singh, Shakti</au><au>Gebremariam, Teclegiorgis</au><au>Swidergall, Marc</au><au>Alqarihi, Abdullah</au><au>Youssef, Eman G.</au><au>Alkhazraji, Sondus</au><au>Pikoulas, Antonis</au><au>Perske, Christina</au><au>Venkataramani, Vivek</au><au>Rich, Abigail</au><au>Bruno, Vincent M.</au><au>Hotopp, Julie Dunning</au><au>Mantis, Nicolas J.</au><au>Edwards, John E.</au><au>Filler, Scott G.</au><au>Chamilos, Georgios</au><au>Vitetta, Ellen S.</au><au>Ibrahim, Ashraf S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis</atitle><jtitle>Nature microbiology</jtitle><stitle>Nat Microbiol</stitle><addtitle>Nat Microbiol</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>6</volume><issue>3</issue><spage>313</spage><epage>326</epage><pages>313-326</pages><issn>2058-5276</issn><eissn>2058-5276</eissn><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.
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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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7914224 |
source | MEDLINE; SpringerLink Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T15%3A02%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mucoricin%20is%20a%20ricin-like%20toxin%20that%20is%20critical%20for%20the%20pathogenesis%20of%20mucormycosis&rft.jtitle=Nature%20microbiology&rft.au=Soliman,%20Sameh%20S.%20M.&rft.date=2021-03-01&rft.volume=6&rft.issue=3&rft.spage=313&rft.epage=326&rft.pages=313-326&rft.issn=2058-5276&rft.eissn=2058-5276&rft_id=info:doi/10.1038/s41564-020-00837-0&rft_dat=%3Cproquest_pubme%3E2493255135%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2493255135&rft_id=info:pmid/33462434&rfr_iscdi=true |