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Series GSE286024 Query DataSets for GSE286024
Status Public on Jan 31, 2025
Title Novel insights into the genetic basis and proteotranscriptomic elucidation of virulence attenuation in Pseudomonas syringae pv. actinidiae variants
Organism Pseudomonas syringae pv. actinidiae
Experiment type Expression profiling by high throughput sequencing
Summary Pseudomonas syringae pv. actinidiae (Psa) is the causal agent of kiwifruit bacterial canker, but the factors affecting its pathogenicity in natural settings remain poorly explored. In this study, we isolated two Psa strains, G126 and G282 from infected kiwifruit orchards in Guizhou Province of China. Both isolates, categorized as Psa-biovar 3, were confirmed through Psa3-specific primers and phylogenomic analysis. Pathogenicity assays on kiwifruit cultivar ‘Hongyang’ leaves and branches showed significantly reduced numbers of necrotic spots and reduced lesions sizes upon infection with G282 compared to the G1 positive control strain, while G126 showed nonpathogenic phenotype. Additionally, both strains failed to induce a hypersensitive response in nonhost Nicotiana tabacum plants, and exhibited significantly reduced promoter activity of the hrpR/S, hrpL, and hrpA genes, which are crucial for the type III secretion system (T3SS). Genomic sequencing revealed that the T3SS of G126 was defective due to a single-nucleotide polymorphism in the hrpR gene, while G282 was entirely deficient in the type VI secretion system (T6SS), which potentially regulates the expression of T3SS genes. Transcriptomic analysis showed widespread alterations in key aspects of the secretion system, protein transport, and signal transduction, further supporting the phenotype characteristics exhibited by the strains. This study enhances our understanding of the genetic basis of nonpathogenic and partially pathogenic Psa isolates, highlighting the functional interdependencies between T3SS and T6SS.
 
Overall design RNA-seq profiling of wild-type strain G1, non-pathogenic strain G126 and Pathogenetic deficiency mutant G282 after 6-hour induction in HDM (hrp-derepressing medium) culture medium

Grant awarded to Zhao Zhibo: National Key Research and Development Program of China (Grant No. 2022YFD1400200)
Grant awarded to Zhao Zhibo: National Natural Science Foundation of China (Grant No. 31860486, 32001864)
Grant awarded to Zhao Zhibo: Fund for the China Agriculture Research System (Grant No. CARS-26-04A)
 
Contributor(s) Asif M, Hu R, Xie T, Zhao Z
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Submission date Jan 07, 2025
Last update date Jun 23, 2025
Contact name Muhammad Asif
E-mail(s) m.asifssa@hotmail.com
Phone 17800150073
Organization name Guizhou University
Department Plant Pathology
Street address college of agriculture, Guizhou university
City Guiyang
State/province Guizhou
ZIP/Postal code 550025
Country China
 
Platforms (1)
GPL35271 Illumina NovaSeq 6000 (Pseudomonas syringae pv. actinidiae)
Samples (9)
GSM8715101 G1_A_biol rep 1
GSM8715102 G1_A_biol rep 2
GSM8715103 G1_A_biol rep 3
Relations
BioProject PRJNA1207504

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE286024_RAW.tar 2.5 Mb (http)(custom) TAR (of CSV)
GSE286024_gene_count.txt.gz 324.6 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA

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