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Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi

BACKGROUND: Millions of humans and animals suffer from superficial infections caused by a group of highly specialized filamentous fungi, the dermatophytes, which exclusively infect keratinized host structures. To provide broad insights into the molecular basis of the pathogenicity-associated traits,...

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Autores principales: Burmester, Anke, Shelest, Ekaterina, Glöckner, Gernot, Heddergott, Christoph, Schindler, Susann, Staib, Peter, Heidel, Andrew, Felder, Marius, Petzold, Andreas, Szafranski, Karol, Feuermann, Marc, Pedruzzi, Ivo, Priebe, Steffen, Groth, Marco, Winkler, Robert, Li, Wenjun, Kniemeyer, Olaf, Schroeckh, Volker, Hertweck, Christian, Hube, Bernhard, White, Theodore C, Platzer, Matthias, Guthke, Reinhard, Heitman, Joseph, Wöstemeyer, Johannes, Zipfel, Peter F, Monod, Michel, Brakhage, Axel A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091305/
https://www.ncbi.nlm.nih.gov/pubmed/21247460
http://dx.doi.org/10.1186/gb-2011-12-1-r7
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author Burmester, Anke
Shelest, Ekaterina
Glöckner, Gernot
Heddergott, Christoph
Schindler, Susann
Staib, Peter
Heidel, Andrew
Felder, Marius
Petzold, Andreas
Szafranski, Karol
Feuermann, Marc
Pedruzzi, Ivo
Priebe, Steffen
Groth, Marco
Winkler, Robert
Li, Wenjun
Kniemeyer, Olaf
Schroeckh, Volker
Hertweck, Christian
Hube, Bernhard
White, Theodore C
Platzer, Matthias
Guthke, Reinhard
Heitman, Joseph
Wöstemeyer, Johannes
Zipfel, Peter F
Monod, Michel
Brakhage, Axel A
author_facet Burmester, Anke
Shelest, Ekaterina
Glöckner, Gernot
Heddergott, Christoph
Schindler, Susann
Staib, Peter
Heidel, Andrew
Felder, Marius
Petzold, Andreas
Szafranski, Karol
Feuermann, Marc
Pedruzzi, Ivo
Priebe, Steffen
Groth, Marco
Winkler, Robert
Li, Wenjun
Kniemeyer, Olaf
Schroeckh, Volker
Hertweck, Christian
Hube, Bernhard
White, Theodore C
Platzer, Matthias
Guthke, Reinhard
Heitman, Joseph
Wöstemeyer, Johannes
Zipfel, Peter F
Monod, Michel
Brakhage, Axel A
author_sort Burmester, Anke
collection PubMed
description BACKGROUND: Millions of humans and animals suffer from superficial infections caused by a group of highly specialized filamentous fungi, the dermatophytes, which exclusively infect keratinized host structures. To provide broad insights into the molecular basis of the pathogenicity-associated traits, we report the first genome sequences of two closely phylogenetically related dermatophytes, Arthroderma benhamiae and Trichophyton verrucosum, both of which induce highly inflammatory infections in humans. RESULTS: 97% of the 22.5 megabase genome sequences of A. benhamiae and T. verrucosum are unambiguously alignable and collinear. To unravel dermatophyte-specific virulence-associated traits, we compared sets of potentially pathogenicity-associated proteins, such as secreted proteases and enzymes involved in secondary metabolite production, with those of closely related onygenales (Coccidioides species) and the mould Aspergillus fumigatus. The comparisons revealed expansion of several gene families in dermatophytes and disclosed the peculiarities of the dermatophyte secondary metabolite gene sets. Secretion of proteases and other hydrolytic enzymes by A. benhamiae was proven experimentally by a global secretome analysis during keratin degradation. Molecular insights into the interaction of A. benhamiae with human keratinocytes were obtained for the first time by global transcriptome profiling. Given that A. benhamiae is able to undergo mating, a detailed comparison of the genomes further unraveled the genetic basis of sexual reproduction in this species. CONCLUSIONS: Our results enlighten the genetic basis of fundamental and putatively virulence-related traits of dermatophytes, advancing future research on these medically important pathogens.
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spelling pubmed-30913052011-05-11 Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi Burmester, Anke Shelest, Ekaterina Glöckner, Gernot Heddergott, Christoph Schindler, Susann Staib, Peter Heidel, Andrew Felder, Marius Petzold, Andreas Szafranski, Karol Feuermann, Marc Pedruzzi, Ivo Priebe, Steffen Groth, Marco Winkler, Robert Li, Wenjun Kniemeyer, Olaf Schroeckh, Volker Hertweck, Christian Hube, Bernhard White, Theodore C Platzer, Matthias Guthke, Reinhard Heitman, Joseph Wöstemeyer, Johannes Zipfel, Peter F Monod, Michel Brakhage, Axel A Genome Biol Research BACKGROUND: Millions of humans and animals suffer from superficial infections caused by a group of highly specialized filamentous fungi, the dermatophytes, which exclusively infect keratinized host structures. To provide broad insights into the molecular basis of the pathogenicity-associated traits, we report the first genome sequences of two closely phylogenetically related dermatophytes, Arthroderma benhamiae and Trichophyton verrucosum, both of which induce highly inflammatory infections in humans. RESULTS: 97% of the 22.5 megabase genome sequences of A. benhamiae and T. verrucosum are unambiguously alignable and collinear. To unravel dermatophyte-specific virulence-associated traits, we compared sets of potentially pathogenicity-associated proteins, such as secreted proteases and enzymes involved in secondary metabolite production, with those of closely related onygenales (Coccidioides species) and the mould Aspergillus fumigatus. The comparisons revealed expansion of several gene families in dermatophytes and disclosed the peculiarities of the dermatophyte secondary metabolite gene sets. Secretion of proteases and other hydrolytic enzymes by A. benhamiae was proven experimentally by a global secretome analysis during keratin degradation. Molecular insights into the interaction of A. benhamiae with human keratinocytes were obtained for the first time by global transcriptome profiling. Given that A. benhamiae is able to undergo mating, a detailed comparison of the genomes further unraveled the genetic basis of sexual reproduction in this species. CONCLUSIONS: Our results enlighten the genetic basis of fundamental and putatively virulence-related traits of dermatophytes, advancing future research on these medically important pathogens. BioMed Central 2011 2011-01-19 /pmc/articles/PMC3091305/ /pubmed/21247460 http://dx.doi.org/10.1186/gb-2011-12-1-r7 Text en Copyright ©2011 Burmester et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Burmester, Anke
Shelest, Ekaterina
Glöckner, Gernot
Heddergott, Christoph
Schindler, Susann
Staib, Peter
Heidel, Andrew
Felder, Marius
Petzold, Andreas
Szafranski, Karol
Feuermann, Marc
Pedruzzi, Ivo
Priebe, Steffen
Groth, Marco
Winkler, Robert
Li, Wenjun
Kniemeyer, Olaf
Schroeckh, Volker
Hertweck, Christian
Hube, Bernhard
White, Theodore C
Platzer, Matthias
Guthke, Reinhard
Heitman, Joseph
Wöstemeyer, Johannes
Zipfel, Peter F
Monod, Michel
Brakhage, Axel A
Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title_full Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title_fullStr Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title_full_unstemmed Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title_short Comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
title_sort comparative and functional genomics provide insights into the pathogenicity of dermatophytic fungi
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091305/
https://www.ncbi.nlm.nih.gov/pubmed/21247460
http://dx.doi.org/10.1186/gb-2011-12-1-r7
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