Cargando…
Distribution and impact of yeast thermal tolerance permissive for mammalian infection
BACKGROUND: From the viewpoint of fungal virulence in mammals, thermal tolerance can be defined as the ability to grow in the 35°C to 40°C range, which is essential for inhabiting these hosts. RESULTS: We used archival information in a fungal collection to analyze the relationship between thermal to...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381509/ https://www.ncbi.nlm.nih.gov/pubmed/25762372 http://dx.doi.org/10.1186/s12915-015-0127-3 |
_version_ | 1782364465514151936 |
---|---|
author | Robert, Vincent Cardinali, Gianluigi Casadevall, Arturo |
author_facet | Robert, Vincent Cardinali, Gianluigi Casadevall, Arturo |
author_sort | Robert, Vincent |
collection | PubMed |
description | BACKGROUND: From the viewpoint of fungal virulence in mammals, thermal tolerance can be defined as the ability to grow in the 35°C to 40°C range, which is essential for inhabiting these hosts. RESULTS: We used archival information in a fungal collection to analyze the relationship between thermal tolerance and genetic background for over 4,289 yeast strains belonging to 1,054 species. Fungal genetic relationships were inferred from hierarchical trees based on pairwise alignments using the rRNA internal transcribed spacer and large subunit rDNA (LSU) sequences. In addition, we searched for correlations between thermal tolerance and other archival information including antifungal susceptibility, carbon sources, and fermentative capacity. Thermal tolerance for growth at mammalian temperatures was not monophyletic, with thermally tolerant species being interspersed among families that include closely related species that are not thermal tolerant. Thermal tolerance and resistance to antifungal drugs were not correlated, suggesting that these two properties evolved independently. Nevertheless, the ability to grow at higher temperatures did correlate with origin from lower geographic latitudes, capacity for fermentation and assimilation of certain carbon sources. CONCLUSIONS: Thermal tolerance was significantly more common among ascomycetous than basidiomycetous yeasts, suggesting an explanation for the preponderance of ascomycetous yeasts among human pathogenic fungi. Analysis of strain maximum tolerable temperature as a function of collection time suggested that basidiomycetous yeasts are rapidly adapting to global warming. The analysis identified genera with a high prevalence of the thermal-tolerant species that could serve as sources of emerging pathogenic fungi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-015-0127-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4381509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43815092015-04-02 Distribution and impact of yeast thermal tolerance permissive for mammalian infection Robert, Vincent Cardinali, Gianluigi Casadevall, Arturo BMC Biol Research Article BACKGROUND: From the viewpoint of fungal virulence in mammals, thermal tolerance can be defined as the ability to grow in the 35°C to 40°C range, which is essential for inhabiting these hosts. RESULTS: We used archival information in a fungal collection to analyze the relationship between thermal tolerance and genetic background for over 4,289 yeast strains belonging to 1,054 species. Fungal genetic relationships were inferred from hierarchical trees based on pairwise alignments using the rRNA internal transcribed spacer and large subunit rDNA (LSU) sequences. In addition, we searched for correlations between thermal tolerance and other archival information including antifungal susceptibility, carbon sources, and fermentative capacity. Thermal tolerance for growth at mammalian temperatures was not monophyletic, with thermally tolerant species being interspersed among families that include closely related species that are not thermal tolerant. Thermal tolerance and resistance to antifungal drugs were not correlated, suggesting that these two properties evolved independently. Nevertheless, the ability to grow at higher temperatures did correlate with origin from lower geographic latitudes, capacity for fermentation and assimilation of certain carbon sources. CONCLUSIONS: Thermal tolerance was significantly more common among ascomycetous than basidiomycetous yeasts, suggesting an explanation for the preponderance of ascomycetous yeasts among human pathogenic fungi. Analysis of strain maximum tolerable temperature as a function of collection time suggested that basidiomycetous yeasts are rapidly adapting to global warming. The analysis identified genera with a high prevalence of the thermal-tolerant species that could serve as sources of emerging pathogenic fungi. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-015-0127-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-26 /pmc/articles/PMC4381509/ /pubmed/25762372 http://dx.doi.org/10.1186/s12915-015-0127-3 Text en © Robert et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Robert, Vincent Cardinali, Gianluigi Casadevall, Arturo Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title | Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title_full | Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title_fullStr | Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title_full_unstemmed | Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title_short | Distribution and impact of yeast thermal tolerance permissive for mammalian infection |
title_sort | distribution and impact of yeast thermal tolerance permissive for mammalian infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381509/ https://www.ncbi.nlm.nih.gov/pubmed/25762372 http://dx.doi.org/10.1186/s12915-015-0127-3 |
work_keys_str_mv | AT robertvincent distributionandimpactofyeastthermaltolerancepermissiveformammalianinfection AT cardinaligianluigi distributionandimpactofyeastthermaltolerancepermissiveformammalianinfection AT casadevallarturo distributionandimpactofyeastthermaltolerancepermissiveformammalianinfection |