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Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis
Talaromyces (Penicillium) marneffei is an important dimorphic mycosis endemic in Southeast Asia and Southern China, but the origin and maintenance of virulence traits in this organism remains obscure. Several pathogenic fungi, including Cryptococcus neoformans, Aspergillus fumigatus, Blastomyces der...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574045/ https://www.ncbi.nlm.nih.gov/pubmed/36262181 http://dx.doi.org/10.3389/fcimb.2022.1023067 |
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author | Pruksaphon, Kritsada Nosanchuk, Joshua D. Thammasit, Patcharin Pongpom, Monsicha Youngchim, Sirida |
author_facet | Pruksaphon, Kritsada Nosanchuk, Joshua D. Thammasit, Patcharin Pongpom, Monsicha Youngchim, Sirida |
author_sort | Pruksaphon, Kritsada |
collection | PubMed |
description | Talaromyces (Penicillium) marneffei is an important dimorphic mycosis endemic in Southeast Asia and Southern China, but the origin and maintenance of virulence traits in this organism remains obscure. Several pathogenic fungi, including Cryptococcus neoformans, Aspergillus fumigatus, Blastomyces dermatitidis, Sporothrix schenckii, Histoplasma capsulatum and Paracoccidioides spp. interact with free living soil amoebae and data suggests that fungal pathogenic strategies may emerge from environmental interactions of these fungi with ubiquitous phagocytic microorganisms. In this study, we examined the interactions of T. marneffei with the soil amoeba Acanthamoeba castellanii. T. marneffei was rapidly ingested by A. castellanii and phagocytosis of fungal cells resulted in amoeba death after 24 h of contact. Co-culture also resulted in a rapid transition for conidia to the fission-yeast form. In addition, well-established virulence factors such as melanin and a yeast specific mannoprotein of T. marneffei were expressed during interaction with A. castellanii at 37°C. Our findings support the assumption that soil amoebae environmental predators play a role in the selection and maintenance of particular features in T. marneffei that impart virulence to this clinically important dimorphic fungus in mammalian hosts. |
format | Online Article Text |
id | pubmed-9574045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95740452022-10-18 Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis Pruksaphon, Kritsada Nosanchuk, Joshua D. Thammasit, Patcharin Pongpom, Monsicha Youngchim, Sirida Front Cell Infect Microbiol Cellular and Infection Microbiology Talaromyces (Penicillium) marneffei is an important dimorphic mycosis endemic in Southeast Asia and Southern China, but the origin and maintenance of virulence traits in this organism remains obscure. Several pathogenic fungi, including Cryptococcus neoformans, Aspergillus fumigatus, Blastomyces dermatitidis, Sporothrix schenckii, Histoplasma capsulatum and Paracoccidioides spp. interact with free living soil amoebae and data suggests that fungal pathogenic strategies may emerge from environmental interactions of these fungi with ubiquitous phagocytic microorganisms. In this study, we examined the interactions of T. marneffei with the soil amoeba Acanthamoeba castellanii. T. marneffei was rapidly ingested by A. castellanii and phagocytosis of fungal cells resulted in amoeba death after 24 h of contact. Co-culture also resulted in a rapid transition for conidia to the fission-yeast form. In addition, well-established virulence factors such as melanin and a yeast specific mannoprotein of T. marneffei were expressed during interaction with A. castellanii at 37°C. Our findings support the assumption that soil amoebae environmental predators play a role in the selection and maintenance of particular features in T. marneffei that impart virulence to this clinically important dimorphic fungus in mammalian hosts. Frontiers Media S.A. 2022-10-03 /pmc/articles/PMC9574045/ /pubmed/36262181 http://dx.doi.org/10.3389/fcimb.2022.1023067 Text en Copyright © 2022 Pruksaphon, Nosanchuk, Thammasit, Pongpom and Youngchim https://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) and the copyright owner(s) 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 | Cellular and Infection Microbiology Pruksaphon, Kritsada Nosanchuk, Joshua D. Thammasit, Patcharin Pongpom, Monsicha Youngchim, Sirida Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title | Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title_full | Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title_fullStr | Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title_full_unstemmed | Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title_short | Interaction of Talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
title_sort | interaction of talaromyces marneffei with free living soil amoeba as a model of fungal pathogenesis |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574045/ https://www.ncbi.nlm.nih.gov/pubmed/36262181 http://dx.doi.org/10.3389/fcimb.2022.1023067 |
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