Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus

ABSTRACT The genus Malassezia includes 14 species that are found on the skin of humans and animals and are associated with a number of diseases. Recent genome sequencing projects have defined the gene content of all 14 species; however, to date, genetic manipulation has not been possible for any spe...

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Autores principales: Giuseppe Ianiri, Anna F. Averette, Joanne M. Kingsbury, Joseph Heitman, Alexander Idnurm
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Publicado: American Society for Microbiology 2016
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spelling oai:doaj.org-article:7f68717324fa463d9e5e1bf858e848802021-11-15T15:50:15ZGene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus10.1128/mBio.01853-162150-7511https://doaj.org/article/7f68717324fa463d9e5e1bf858e848802016-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01853-16https://doaj.org/toc/2150-7511ABSTRACT The genus Malassezia includes 14 species that are found on the skin of humans and animals and are associated with a number of diseases. Recent genome sequencing projects have defined the gene content of all 14 species; however, to date, genetic manipulation has not been possible for any species within this genus. Here, we develop and then optimize molecular tools for the transformation of Malassezia furfur and Malassezia sympodialis using Agrobacterium tumefaciens delivery of transfer DNA (T-DNA) molecules. These T-DNAs can insert randomly into the genome. In the case of M. furfur, targeted gene replacements were also achieved via homologous recombination, enabling deletion of the ADE2 gene for purine biosynthesis and of the LAC2 gene predicted to be involved in melanin biosynthesis. Hence, the introduction of exogenous DNA and direct gene manipulation are feasible in Malassezia species. IMPORTANCE Species in the genus Malassezia are a defining component of the microbiome of the surface of mammals. They are also associated with a wide range of skin disease symptoms. Many species are difficult to culture in vitro, and although genome sequences are available for the species in this genus, it has not been possible to assess gene function to date. In this study, we pursued a series of possible transformation methods and identified one that allows the introduction of DNA into two species of Malassezia, including the ability to make targeted integrations into the genome such that genes can be deleted. This research opens a new direction in terms of now being able to analyze gene functions in this little understood genus. These tools will contribute to define the mechanisms that lead to the commensalism and pathogenicity in this group of obligate fungi that are predominant on the skin of mammals.Giuseppe IaniriAnna F. AveretteJoanne M. KingsburyJoseph HeitmanAlexander IdnurmAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 7, Iss 6 (2016)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Giuseppe Ianiri
Anna F. Averette
Joanne M. Kingsbury
Joseph Heitman
Alexander Idnurm
Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
description ABSTRACT The genus Malassezia includes 14 species that are found on the skin of humans and animals and are associated with a number of diseases. Recent genome sequencing projects have defined the gene content of all 14 species; however, to date, genetic manipulation has not been possible for any species within this genus. Here, we develop and then optimize molecular tools for the transformation of Malassezia furfur and Malassezia sympodialis using Agrobacterium tumefaciens delivery of transfer DNA (T-DNA) molecules. These T-DNAs can insert randomly into the genome. In the case of M. furfur, targeted gene replacements were also achieved via homologous recombination, enabling deletion of the ADE2 gene for purine biosynthesis and of the LAC2 gene predicted to be involved in melanin biosynthesis. Hence, the introduction of exogenous DNA and direct gene manipulation are feasible in Malassezia species. IMPORTANCE Species in the genus Malassezia are a defining component of the microbiome of the surface of mammals. They are also associated with a wide range of skin disease symptoms. Many species are difficult to culture in vitro, and although genome sequences are available for the species in this genus, it has not been possible to assess gene function to date. In this study, we pursued a series of possible transformation methods and identified one that allows the introduction of DNA into two species of Malassezia, including the ability to make targeted integrations into the genome such that genes can be deleted. This research opens a new direction in terms of now being able to analyze gene functions in this little understood genus. These tools will contribute to define the mechanisms that lead to the commensalism and pathogenicity in this group of obligate fungi that are predominant on the skin of mammals.
format article
author Giuseppe Ianiri
Anna F. Averette
Joanne M. Kingsbury
Joseph Heitman
Alexander Idnurm
author_facet Giuseppe Ianiri
Anna F. Averette
Joanne M. Kingsbury
Joseph Heitman
Alexander Idnurm
author_sort Giuseppe Ianiri
title Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
title_short Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
title_full Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
title_fullStr Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
title_full_unstemmed Gene Function Analysis in the Ubiquitous Human Commensal and Pathogen <italic toggle="yes">Malassezia</italic> Genus
title_sort gene function analysis in the ubiquitous human commensal and pathogen <italic toggle="yes">malassezia</italic> genus
publisher American Society for Microbiology
publishDate 2016
url https://doaj.org/article/7f68717324fa463d9e5e1bf858e84880
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