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Updates in the Language of Histoplasma Biodiversity

In a recent article, Sepúlveda et al. (mBio 8:e01339-17, 2017, https://doi.org/10.1128/mBio.01339-17) investigated the genetic structure and evolutionary history of the human pathogen Histoplasma. Using whole-genome resequencing data, Sepúlveda et al. found that the Histoplasma genus is composed of...

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Detalles Bibliográficos
Autor principal: Gladieux, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941069/
https://www.ncbi.nlm.nih.gov/pubmed/29739908
http://dx.doi.org/10.1128/mBio.00181-18
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author Gladieux, Pierre
author_facet Gladieux, Pierre
author_sort Gladieux, Pierre
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description In a recent article, Sepúlveda et al. (mBio 8:e01339-17, 2017, https://doi.org/10.1128/mBio.01339-17) investigated the genetic structure and evolutionary history of the human pathogen Histoplasma. Using whole-genome resequencing data, Sepúlveda et al. found that the Histoplasma genus is composed of at least four strongly differentiated lineages. Their tour de force is to use a smart combination of population genomic approaches to show that the advanced stage of intraspecific divergence observed within Histoplasma does not simply reflect population structure, but instead results from previously unidentified speciation events. The four independently evolving Histoplasma lineages are elevated to the species status and assigned names. The newly described species exhibit medically important differences in phenotype, and these findings, therefore, have important epidemiological implications. This work provides a blueprint for phylogenomic species recognition in fungi, opening the way for a new age of enlightenment in which fungal species are diagnosed using highly discriminatory tools within a hypothesis-testing framework.
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spelling pubmed-59410692018-05-15 Updates in the Language of Histoplasma Biodiversity Gladieux, Pierre mBio Commentary In a recent article, Sepúlveda et al. (mBio 8:e01339-17, 2017, https://doi.org/10.1128/mBio.01339-17) investigated the genetic structure and evolutionary history of the human pathogen Histoplasma. Using whole-genome resequencing data, Sepúlveda et al. found that the Histoplasma genus is composed of at least four strongly differentiated lineages. Their tour de force is to use a smart combination of population genomic approaches to show that the advanced stage of intraspecific divergence observed within Histoplasma does not simply reflect population structure, but instead results from previously unidentified speciation events. The four independently evolving Histoplasma lineages are elevated to the species status and assigned names. The newly described species exhibit medically important differences in phenotype, and these findings, therefore, have important epidemiological implications. This work provides a blueprint for phylogenomic species recognition in fungi, opening the way for a new age of enlightenment in which fungal species are diagnosed using highly discriminatory tools within a hypothesis-testing framework. American Society for Microbiology 2018-05-08 /pmc/articles/PMC5941069/ /pubmed/29739908 http://dx.doi.org/10.1128/mBio.00181-18 Text en Copyright © 2018 Gladieux. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Gladieux, Pierre
Updates in the Language of Histoplasma Biodiversity
title Updates in the Language of Histoplasma Biodiversity
title_full Updates in the Language of Histoplasma Biodiversity
title_fullStr Updates in the Language of Histoplasma Biodiversity
title_full_unstemmed Updates in the Language of Histoplasma Biodiversity
title_short Updates in the Language of Histoplasma Biodiversity
title_sort updates in the language of histoplasma biodiversity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941069/
https://www.ncbi.nlm.nih.gov/pubmed/29739908
http://dx.doi.org/10.1128/mBio.00181-18
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