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SRX26122089: GSM8524055: WT_pH7.8modifiedKB_rep1; Pseudomonas syringae pv. tomato str. DC3000; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 15.9M spots, 2.4G bases, 950.6Mb downloads

External Id: GSM8524055_r1
Submitted by: Swingle Lab, USDA-ARS
Study: Environmental alkalization suppresses deployment of virulence strategies in Pseudomonas syringae pv. tomato DC3000
show Abstracthide Abstract
Plant pathogenic bacteria encounter a drastic increase in apoplastic pH during the early stages of plant immunity. The effects of alkalization on pathogen-host interactions have not been comprehensively characterized. Here we used a global transcriptomic approach to assess the impact of environmental alkalization on Pseudomonas syringae pv. tomato DC3000 in vitro. In addition to the Type 3 Secretion System (T3SS), we found expression of genes encoding other virulence factors such as iron uptake, and coronatine biosynthesis to be strongly affected by environmental alkalization. We also found activity of extracytoplasmic function sigma factor, AlgU, was induced at pH 5.5 and suppressed at pH 7.8, which are pH levels that this pathogen would likely experience before and during pattern triggered immunity, respectively. This pH-dependent control requires the presence of periplasmic proteases, AlgW and MucP, that function as part of the environmental sensing system that activates AlgU in specific conditions. This is the first example of pH-dependency of AlgU activity, suggesting a regulatory pathway model where pH affects the proteolysis-dependent activation of AlgU. These results contribute to deeper understanding of the role apoplastic pH has on host-pathogen interactions. Overall design: Comparative gene expression profiling analysis of RNA-seq data for Pst DC3000 WT and algU deletion strains across pH-modified KB media growth condition at pH 5.5, 6.5 and 7.8
Sample: WT_pH7.8modifiedKB_rep1
SAMN43821210 • SRS22684468 • All experiments • All runs
Library:
Name: GSM8524055
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was isolated with Trizol, with an extra chloroform extraction to remove residual phenol and addition of glyco-blue as a carrier to promote RNA precipitation. RNA concentration was determined with a Nanodrop and integrity assessed on a Fragment Analyzer. Directional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Directional Ultra II RNA Library Prep Kit for Illumina (New England Biolabs), with initial rRNA depletion.
Runs: 1 run, 15.9M spots, 2.4G bases, 950.6Mb
Run# of Spots# of BasesSizePublished
SRR3071890915,874,7972.4G950.6Mb2024-10-03

ID:
35261730

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