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LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly
Potent antimicrobial metabolites are produced by filamentous fungi in pure culture, but their ecological functions in nature are often unknown. Using an antibacterial Penicillium isolate and a cheese rind microbial community, we demonstrate that a fungal specialized metabolite can regulate the diver...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294623/ https://www.ncbi.nlm.nih.gov/pubmed/37162223 http://dx.doi.org/10.1128/mbio.00769-23 |
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author | Tannous, Joanna Cosetta, Casey M. Drott, Milton T. Rush, Tomás A. Abraham, Paul E. Giannone, Richard J. Keller, Nancy P. Wolfe, Benjamin E. |
author_facet | Tannous, Joanna Cosetta, Casey M. Drott, Milton T. Rush, Tomás A. Abraham, Paul E. Giannone, Richard J. Keller, Nancy P. Wolfe, Benjamin E. |
author_sort | Tannous, Joanna |
collection | PubMed |
description | Potent antimicrobial metabolites are produced by filamentous fungi in pure culture, but their ecological functions in nature are often unknown. Using an antibacterial Penicillium isolate and a cheese rind microbial community, we demonstrate that a fungal specialized metabolite can regulate the diversity of bacterial communities. Inactivation of the global regulator, LaeA, resulted in the loss of antibacterial activity in the Penicillium isolate. Cheese rind bacterial communities assembled with the laeA deletion strain had significantly higher bacterial abundances than the wild-type strain. RNA-sequencing and metabolite profiling demonstrated a striking reduction in the expression and production of the natural product pseurotin in the laeA deletion strain. Inactivation of a core gene in the pseurotin biosynthetic cluster restored bacterial community composition, confirming the role of pseurotins in mediating bacterial community assembly. Our discovery demonstrates how global regulators of fungal transcription can control the assembly of bacterial communities and highlights an ecological role for a widespread class of fungal specialized metabolites. |
format | Online Article Text |
id | pubmed-10294623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-102946232023-06-28 LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly Tannous, Joanna Cosetta, Casey M. Drott, Milton T. Rush, Tomás A. Abraham, Paul E. Giannone, Richard J. Keller, Nancy P. Wolfe, Benjamin E. mBio Research Article Potent antimicrobial metabolites are produced by filamentous fungi in pure culture, but their ecological functions in nature are often unknown. Using an antibacterial Penicillium isolate and a cheese rind microbial community, we demonstrate that a fungal specialized metabolite can regulate the diversity of bacterial communities. Inactivation of the global regulator, LaeA, resulted in the loss of antibacterial activity in the Penicillium isolate. Cheese rind bacterial communities assembled with the laeA deletion strain had significantly higher bacterial abundances than the wild-type strain. RNA-sequencing and metabolite profiling demonstrated a striking reduction in the expression and production of the natural product pseurotin in the laeA deletion strain. Inactivation of a core gene in the pseurotin biosynthetic cluster restored bacterial community composition, confirming the role of pseurotins in mediating bacterial community assembly. Our discovery demonstrates how global regulators of fungal transcription can control the assembly of bacterial communities and highlights an ecological role for a widespread class of fungal specialized metabolites. American Society for Microbiology 2023-05-09 /pmc/articles/PMC10294623/ /pubmed/37162223 http://dx.doi.org/10.1128/mbio.00769-23 Text en https://doi.org/10.1128/AuthorWarrantyLicense.v1This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. |
spellingShingle | Research Article Tannous, Joanna Cosetta, Casey M. Drott, Milton T. Rush, Tomás A. Abraham, Paul E. Giannone, Richard J. Keller, Nancy P. Wolfe, Benjamin E. LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title | LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title_full | LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title_fullStr | LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title_full_unstemmed | LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title_short | LaeA-Regulated Fungal Traits Mediate Bacterial Community Assembly |
title_sort | laea-regulated fungal traits mediate bacterial community assembly |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294623/ https://www.ncbi.nlm.nih.gov/pubmed/37162223 http://dx.doi.org/10.1128/mbio.00769-23 |
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