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Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection
The transcriptional regulatory network (TRN) of the phytopathogen Pseudomonas syringae pv. tomato DC3000 regulates its response to environmental stimuli, including interactions with hosts and neighboring bacteria. Despite the importance of transcriptional regulation during these agriculturally signi...
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/PMC10654099/ https://www.ncbi.nlm.nih.gov/pubmed/37638727 http://dx.doi.org/10.1128/msystems.00437-23 |
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author | Bajpe, Heera Rychel, Kevin Lamoureux, Cameron R. Sastry, Anand V. Palsson, Bernhard O. |
author_facet | Bajpe, Heera Rychel, Kevin Lamoureux, Cameron R. Sastry, Anand V. Palsson, Bernhard O. |
author_sort | Bajpe, Heera |
collection | PubMed |
description | The transcriptional regulatory network (TRN) of the phytopathogen Pseudomonas syringae pv. tomato DC3000 regulates its response to environmental stimuli, including interactions with hosts and neighboring bacteria. Despite the importance of transcriptional regulation during these agriculturally significant interactions, a comprehensive understanding of the TRN of P. syringae is yet to be achieved. Here, we collected and decomposed a compendium of public RNA-seq data from P. syringae to obtain 45 independently modulated gene sets (iModulons) that quantitatively describe the TRN and its activity state across diverse conditions. Through iModulon analysis, we (i) untangle the complex interspecies interactions between P. syringae and other terrestrial bacteria in cocultures, (ii) expand the current understanding of the Arabidopsis thaliana-P. syringae interaction, and (iii) elucidate the AlgU-dependent regulation of flagellar gene expression. The modularized TRN yields a unique understanding of interaction-specific transcriptional regulation in P. syringae. IMPORTANCE: Pseudomonas syringae pv. tomato DC3000 is a model plant pathogen that infects tomatoes and Arabidopsis thaliana. The current understanding of global transcriptional regulation in the pathogen is limited. Here, we applied iModulon analysis to a compendium of RNA-seq data to unravel its transcriptional regulatory network. We characterize each co-regulated gene set, revealing the activity of major regulators across diverse conditions. We provide new insights on the transcriptional dynamics in interactions with the plant immune system and with other bacterial species, such as AlgU-dependent regulation of flagellar genes during plant infection and downregulation of siderophore production in the presence of a siderophore cheater. This study demonstrates the novel application of iModulons in studying temporal dynamics during host-pathogen and microbe-microbe interactions, and reveals specific insights of interest. |
format | Online Article Text |
id | pubmed-10654099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-106540992023-08-28 Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection Bajpe, Heera Rychel, Kevin Lamoureux, Cameron R. Sastry, Anand V. Palsson, Bernhard O. mSystems Research Article The transcriptional regulatory network (TRN) of the phytopathogen Pseudomonas syringae pv. tomato DC3000 regulates its response to environmental stimuli, including interactions with hosts and neighboring bacteria. Despite the importance of transcriptional regulation during these agriculturally significant interactions, a comprehensive understanding of the TRN of P. syringae is yet to be achieved. Here, we collected and decomposed a compendium of public RNA-seq data from P. syringae to obtain 45 independently modulated gene sets (iModulons) that quantitatively describe the TRN and its activity state across diverse conditions. Through iModulon analysis, we (i) untangle the complex interspecies interactions between P. syringae and other terrestrial bacteria in cocultures, (ii) expand the current understanding of the Arabidopsis thaliana-P. syringae interaction, and (iii) elucidate the AlgU-dependent regulation of flagellar gene expression. The modularized TRN yields a unique understanding of interaction-specific transcriptional regulation in P. syringae. IMPORTANCE: Pseudomonas syringae pv. tomato DC3000 is a model plant pathogen that infects tomatoes and Arabidopsis thaliana. The current understanding of global transcriptional regulation in the pathogen is limited. Here, we applied iModulon analysis to a compendium of RNA-seq data to unravel its transcriptional regulatory network. We characterize each co-regulated gene set, revealing the activity of major regulators across diverse conditions. We provide new insights on the transcriptional dynamics in interactions with the plant immune system and with other bacterial species, such as AlgU-dependent regulation of flagellar genes during plant infection and downregulation of siderophore production in the presence of a siderophore cheater. This study demonstrates the novel application of iModulons in studying temporal dynamics during host-pathogen and microbe-microbe interactions, and reveals specific insights of interest. American Society for Microbiology 2023-08-28 /pmc/articles/PMC10654099/ /pubmed/37638727 http://dx.doi.org/10.1128/msystems.00437-23 Text en Copyright © 2023 Bajpe et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Bajpe, Heera Rychel, Kevin Lamoureux, Cameron R. Sastry, Anand V. Palsson, Bernhard O. Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title | Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title_full | Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title_fullStr | Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title_full_unstemmed | Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title_short | Machine learning uncovers the Pseudomonas syringae transcriptome in microbial communities and during infection |
title_sort | machine learning uncovers the pseudomonas syringae transcriptome in microbial communities and during infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654099/ https://www.ncbi.nlm.nih.gov/pubmed/37638727 http://dx.doi.org/10.1128/msystems.00437-23 |
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