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Disruption of the Aspergillus fumigatus RNA interference machinery alters the conidial transcriptome

View ORCID ProfileAbdulrahman A. Kelani, View ORCID ProfileAlexander Bruch, View ORCID ProfileFlora Rivieccio, View ORCID ProfileCorissa Visser, View ORCID ProfileThomas Krüger, View ORCID ProfileDanielle Weaver, Xiaoqing Pan, Sascha Schäuble, Gianni Panagiotou, View ORCID ProfileOlaf Kniemeyer, View ORCID ProfileMichael J. Bromley, View ORCID ProfilePaul Bowyer, View ORCID ProfileAmelia E. Barber, View ORCID ProfileAxel A. Brakhage, View ORCID ProfileMatthew G. Blango
doi: https://doi.org/10.1101/2022.07.28.501871
Abdulrahman A. Kelani
1Junior Research Group RNA Biology of Fungal Infections, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Alexander Bruch
1Junior Research Group RNA Biology of Fungal Infections, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Flora Rivieccio
2Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
3Department of Microbiology and Molecular Biology, Institute of Microbiology, Friedrich Schiller University, Jena, Germany
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Corissa Visser
2Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
3Department of Microbiology and Molecular Biology, Institute of Microbiology, Friedrich Schiller University, Jena, Germany
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Thomas Krüger
2Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Danielle Weaver
4Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
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Xiaoqing Pan
1Junior Research Group RNA Biology of Fungal Infections, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Sascha Schäuble
5Department of Microbiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Gianni Panagiotou
5Department of Microbiome Dynamics, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
6Department of Medicine and State Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong, Hong Kong, China
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Olaf Kniemeyer
2Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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Michael J. Bromley
4Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
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Paul Bowyer
4Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom
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Amelia E. Barber
7Junior Research Group Fungal Informatics, Friedrich Schiller University, Jena, Germany
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Axel A. Brakhage
2Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
3Department of Microbiology and Molecular Biology, Institute of Microbiology, Friedrich Schiller University, Jena, Germany
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Matthew G. Blango
1Junior Research Group RNA Biology of Fungal Infections, Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute (Leibniz-HKI), Jena, Germany
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  • For correspondence: matthew.blango@leibniz-hki.de
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ABSTRACT

The RNA interference (RNAi) pathway has evolved numerous functionalities in eukaryotes, with many on display in Kingdom Fungi. RNAi can regulate gene expression, facilitate drug resistance, or even be altogether lost to improve growth potential in some fungal pathogens. In the WHO fungal priority pathogen, Aspergillus fumigatus, the RNAi system is known to be intact and functional. To extend our limited understanding of A. fumigatus RNAi, we first investigated the genetic variation in RNAi-associated genes in a collection of 217 environmental and 83 clinical genomes, where we found that RNAi components are conserved even in clinical strains. Using endogenously expressed inverted-repeat transgenes complementary to a conditionally essential gene (pabA) or a nonessential gene (pksP), we determined that a subset of the RNAi componentry is active in inverted-repeat transgene silencing in conidia and mycelium. Analysis of mRNA-seq data from RNAi double-knockout strains linked the A. fumigatus dicer-like enzymes (DclA/B) and RNA-dependent RNA polymerases (RrpA/B) to regulation of conidial ribosome biogenesis genes; however, surprisingly few endogenous small RNAs were identified in conidia that could explain this broad change. Although RNAi was not clearly linked to growth or stress response defects in the RNAi knockouts, serial passaging of RNAi knockout strains for six generations resulted in lineages with diminished spore production over time, indicating that loss of RNAi can exert a fitness cost on the fungus. Cumulatively, A. fumigatus RNAi appears to play an active role in defense against double-stranded RNA species alongside a previously unappreciated housekeeping function in regulation of conidial ribosomal biogenesis genes.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • The manuscript was updated to focus solely on the role of RNA interference in Aspergillus fumigatus. Several additional datasets were added, including mRNA-seq, sRNA-seq, and proteomics on conidia.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted February 14, 2023.
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Disruption of the Aspergillus fumigatus RNA interference machinery alters the conidial transcriptome
Abdulrahman A. Kelani, Alexander Bruch, Flora Rivieccio, Corissa Visser, Thomas Krüger, Danielle Weaver, Xiaoqing Pan, Sascha Schäuble, Gianni Panagiotou, Olaf Kniemeyer, Michael J. Bromley, Paul Bowyer, Amelia E. Barber, Axel A. Brakhage, Matthew G. Blango
bioRxiv 2022.07.28.501871; doi: https://doi.org/10.1101/2022.07.28.501871
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Disruption of the Aspergillus fumigatus RNA interference machinery alters the conidial transcriptome
Abdulrahman A. Kelani, Alexander Bruch, Flora Rivieccio, Corissa Visser, Thomas Krüger, Danielle Weaver, Xiaoqing Pan, Sascha Schäuble, Gianni Panagiotou, Olaf Kniemeyer, Michael J. Bromley, Paul Bowyer, Amelia E. Barber, Axel A. Brakhage, Matthew G. Blango
bioRxiv 2022.07.28.501871; doi: https://doi.org/10.1101/2022.07.28.501871

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