An integrated genomic and transcriptomic survey of mucormycosis-causing fungi
Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contr...
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| Vydáno v: | Nature communications Ročník 7; číslo 1; s. 12218 - 11 |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
London
Nature Publishing Group UK
22.07.2016
Nature Publishing Group Nature Portfolio |
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| ISSN: | 2041-1723, 2041-1723 |
| On-line přístup: | Získat plný text |
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| Abstract | Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative
Rhizopus
and
Mucor
strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets.
Fungi of the order Mucorales can cause life-threatening infections. Here, Chibucos
et al
. present genomic and transcriptomic analyses of a diverse set of Mucorales fungi, shedding light on their evolution and identifying potential therapeutic targets in the pathogens and the host. |
|---|---|
| AbstractList | Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets. Fungi of the order Mucorales can cause life-threatening infections. Here, Chibucos et al. present genomic and transcriptomic analyses of a diverse set of Mucorales fungi, shedding light on their evolution and identifying potential therapeutic targets in the pathogens and the host. Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets. Fungi of the order Mucorales can cause life-threatening infections. Here, Chibucos et al . present genomic and transcriptomic analyses of a diverse set of Mucorales fungi, shedding light on their evolution and identifying potential therapeutic targets in the pathogens and the host. Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets.Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets. Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets. Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three representative Rhizopus and Mucor strains and with human airway epithelial cells during fungal invasion, to reveal key host and fungal determinants contributing to pathogenesis. Analysis of the host transcriptional response to Mucorales reveals platelet-derived growth factor receptor B (PDGFRB) signaling as part of a core response to divergent pathogenic fungi; inhibition of PDGFRB reduces Mucorales-induced damage to host cells. The unique presence of CotH invasins in all invasive Mucorales, and the correlation between CotH gene copy number and clinical prevalence, are consistent with an important role for these proteins in mucormycosis pathogenesis. Our work provides insight into the evolution of this medically and economically important group of fungi, and identifies several molecular pathways that might be exploited as potential therapeutic targets. Fungi of the order Mucorales can cause life-threatening infections. Here, Chibucos et al. present genomic and transcriptomic analyses of a diverse set of Mucorales fungi, shedding light on their evolution and identifying potential therapeutic targets in the pathogens and the host. |
| ArticleNumber | 12218 |
| Author | Crabtree, Jonathan Skory, Christopher D. Etienne, Kizee A. Fraser, Claire M. Lee, Hongkyu Chibucos, Marcus C. Filler, Scott G. Ibrahim, Ashraf S. Orvis, Joshua Gebremariam, Teclegiorgis O’Connor, Timothy D. Shetty, Amol C. Soliman, Sameh Kumari, Priti Rasko, David A. Hazen, Tracy H. Daugherty, Sean Lockhart, Shawn R. Bruno, Vincent M. |
| Author_xml | – sequence: 1 givenname: Marcus C. orcidid: 0000-0001-9586-0780 surname: Chibucos fullname: Chibucos, Marcus C. organization: Department of Microbiology and Immunology, University of Maryland School of Medicine, Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 2 givenname: Sameh surname: Soliman fullname: Soliman, Sameh organization: Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, Present address: Department of Medicinal Chemistry, College of Pharmacy, University of Sharjah, P.O. Box 27272, Sharjah, UAE – sequence: 3 givenname: Teclegiorgis surname: Gebremariam fullname: Gebremariam, Teclegiorgis organization: Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center – sequence: 4 givenname: Hongkyu surname: Lee fullname: Lee, Hongkyu organization: Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center – sequence: 5 givenname: Sean surname: Daugherty fullname: Daugherty, Sean organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 6 givenname: Joshua surname: Orvis fullname: Orvis, Joshua organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 7 givenname: Amol C. surname: Shetty fullname: Shetty, Amol C. organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 8 givenname: Jonathan surname: Crabtree fullname: Crabtree, Jonathan organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 9 givenname: Tracy H. surname: Hazen fullname: Hazen, Tracy H. organization: Department of Microbiology and Immunology, University of Maryland School of Medicine, Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 10 givenname: Kizee A. surname: Etienne fullname: Etienne, Kizee A. organization: Fungal Reference Laboratory, Mycotic Diseases Branch, Centers for Disease Control and Prevention – sequence: 11 givenname: Priti surname: Kumari fullname: Kumari, Priti organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 12 givenname: Timothy D. surname: O’Connor fullname: O’Connor, Timothy D. organization: Institute for Genome Sciences, University of Maryland School of Medicine, Department of Medicine, University of Maryland School of Medicine – sequence: 13 givenname: David A. surname: Rasko fullname: Rasko, David A. organization: Department of Microbiology and Immunology, University of Maryland School of Medicine, Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 14 givenname: Scott G. surname: Filler fullname: Filler, Scott G. organization: Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, David Geffen School of Medicine at UCLA – sequence: 15 givenname: Claire M. surname: Fraser fullname: Fraser, Claire M. organization: Institute for Genome Sciences, University of Maryland School of Medicine – sequence: 16 givenname: Shawn R. surname: Lockhart fullname: Lockhart, Shawn R. organization: Fungal Reference Laboratory, Mycotic Diseases Branch, Centers for Disease Control and Prevention – sequence: 17 givenname: Christopher D. surname: Skory fullname: Skory, Christopher D. organization: National Center for Agriculture Utilization Research, USDA, Agricultural Research Service – sequence: 18 givenname: Ashraf S. surname: Ibrahim fullname: Ibrahim, Ashraf S. email: ibrahim@labiomed.org organization: Division of Infectious Diseases, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, David Geffen School of Medicine at UCLA – sequence: 19 givenname: Vincent M. surname: Bruno fullname: Bruno, Vincent M. email: vbruno@som.umaryland.edu organization: Department of Microbiology and Immunology, University of Maryland School of Medicine, Institute for Genome Sciences, University of Maryland School of Medicine |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27447865$$D View this record in MEDLINE/PubMed |
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| Copyright | The Author(s) 2016 Copyright Nature Publishing Group Jul 2016 Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2016 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Present address: Department of Medicinal Chemistry, College of Pharmacy, University of Sharjah, P.O. Box 27272, Sharjah, UAE. |
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| Snippet | Mucormycosis is a life-threatening infection caused by Mucorales fungi. Here we sequence 30 fungal genomes, and perform transcriptomics with three... Fungi of the order Mucorales can cause life-threatening infections. Here, Chibucos et al. present genomic and transcriptomic analyses of a diverse set of... |
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| Title | An integrated genomic and transcriptomic survey of mucormycosis-causing fungi |
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