Cargando…

Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae

Infections with filamentous fungi are common to all animals, but attention is rising especially due to the increasing incidence and high mortality rates observed in immunocompromised human individuals. Here, Aspergillus fumigatus and other members of its genus are the leading causative agents. Attri...

Descripción completa

Detalles Bibliográficos
Autores principales: Novohradská, Silvia, Ferling, Iuliia, Hillmann, Falk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723301/
https://www.ncbi.nlm.nih.gov/pubmed/29259922
http://dx.doi.org/10.3389/fcimb.2017.00497
_version_ 1783285182045880320
author Novohradská, Silvia
Ferling, Iuliia
Hillmann, Falk
author_facet Novohradská, Silvia
Ferling, Iuliia
Hillmann, Falk
author_sort Novohradská, Silvia
collection PubMed
description Infections with filamentous fungi are common to all animals, but attention is rising especially due to the increasing incidence and high mortality rates observed in immunocompromised human individuals. Here, Aspergillus fumigatus and other members of its genus are the leading causative agents. Attributes like their saprophytic life-style in various ecological niches coupled with nutritional flexibility and a broad host range have fostered the hypothesis that environmental predators could have been the actual target for some of their virulence determinants. In this mini review, we have merged the recent findings focused on the potential dual-use of fungal defense strategies against innate immune cells and soil amoebae as natural phagocytes. Well-established virulence attributes like the melanized surface of fungal conidia or their capacity to produce toxic secondary metabolites have also been found to be protective against the model amoeba Dictyostelium discoideum. Some of the recent advances during interaction studies with human cells have further promoted the adaptation of other amoeba infection models, including the wide-spread generalist Acanthamoeba castellanii, or less prominent representatives like Vermamoeba vermiformis. We further highlight prospects and limits of these natural phagocyte models with regard to the infection biology of filamentous fungi and in comparison to the phagocytes of the innate immune system.
format Online
Article
Text
id pubmed-5723301
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-57233012017-12-19 Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae Novohradská, Silvia Ferling, Iuliia Hillmann, Falk Front Cell Infect Microbiol Microbiology Infections with filamentous fungi are common to all animals, but attention is rising especially due to the increasing incidence and high mortality rates observed in immunocompromised human individuals. Here, Aspergillus fumigatus and other members of its genus are the leading causative agents. Attributes like their saprophytic life-style in various ecological niches coupled with nutritional flexibility and a broad host range have fostered the hypothesis that environmental predators could have been the actual target for some of their virulence determinants. In this mini review, we have merged the recent findings focused on the potential dual-use of fungal defense strategies against innate immune cells and soil amoebae as natural phagocytes. Well-established virulence attributes like the melanized surface of fungal conidia or their capacity to produce toxic secondary metabolites have also been found to be protective against the model amoeba Dictyostelium discoideum. Some of the recent advances during interaction studies with human cells have further promoted the adaptation of other amoeba infection models, including the wide-spread generalist Acanthamoeba castellanii, or less prominent representatives like Vermamoeba vermiformis. We further highlight prospects and limits of these natural phagocyte models with regard to the infection biology of filamentous fungi and in comparison to the phagocytes of the innate immune system. Frontiers Media S.A. 2017-12-05 /pmc/articles/PMC5723301/ /pubmed/29259922 http://dx.doi.org/10.3389/fcimb.2017.00497 Text en Copyright © 2017 Novohradská, Ferling and Hillmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Novohradská, Silvia
Ferling, Iuliia
Hillmann, Falk
Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title_full Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title_fullStr Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title_full_unstemmed Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title_short Exploring Virulence Determinants of Filamentous Fungal Pathogens through Interactions with Soil Amoebae
title_sort exploring virulence determinants of filamentous fungal pathogens through interactions with soil amoebae
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723301/
https://www.ncbi.nlm.nih.gov/pubmed/29259922
http://dx.doi.org/10.3389/fcimb.2017.00497
work_keys_str_mv AT novohradskasilvia exploringvirulencedeterminantsoffilamentousfungalpathogensthroughinteractionswithsoilamoebae
AT ferlingiuliia exploringvirulencedeterminantsoffilamentousfungalpathogensthroughinteractionswithsoilamoebae
AT hillmannfalk exploringvirulencedeterminantsoffilamentousfungalpathogensthroughinteractionswithsoilamoebae