Machine learning uncovers thePseudomonas syringaetranscriptome in microbial communities and during infection

Author:

Bajpe Heera,Rychel Kevin,Lamoureux Cameron R.,Sastry Anand V.ORCID,Palsson Bernhard O.ORCID

Abstract

AbstractThe transcriptional regulatory network (TRN) of the phytopathogenPseudomonas syringaepv.tomatoDC3000 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 ofP. syringaeis yet to be achieved. Here, we collected and decomposed a compendium of public RNA-seq data fromP. syringaeto obtain 45 independently modulated gene sets (iModulons) that quantitatively describe the TRN and its activity state across diverse conditions. Through iModulon analysis, we 1) untangle the complex interspecies interactions betweenP. syringaeand other terrestrial bacteria in cocultures, 2) expand the current understanding of theArabidopsis thaliana-P. syringaeinteraction, and 3) elucidate the AlgU-dependent regulation of flagellar gene expression. The modularized TRN yields a unique understanding of interaction-specific transcriptional regulation inP. syringae.ImportancePseudomonas syringaepv.tomatoDC3000 is a model plant pathogen that infects tomatoes andArabidopsis 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.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3