<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE327nnn/GSE327564/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Pseudomonas syringae pv. tomato str. DC3000</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE327564</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>In planta transcriptome analysis of Pseudomonas syringae pv. tomato DC3000 two component regulator mutant cvsR during early infection and early exposure to pattern-triggered immunity in Arabidopsis thaliana</name><description>We extracted P. syringae transcriptome from infected A. thaliana tissue under naive or PTI preactivated tissue by flg22 treatment, through physical separation by low speed centrifugation at 5 hours post inoculation. We compared the transcriptome of wildtype strain and mutant strain of cvsR, a previous identified two component regulator. This study aim to understand bacterial response to PTI and the role of cvsR regulon in plant.</description><dates><publication>2026/04/14</publication></dates><accession>GSE327564</accession><cross_references><GSM>GSM9661615</GSM><GSM>GSM9661614</GSM><GSM>GSM9661617</GSM><GSM>GSM9661606</GSM><GSM>GSM9661616</GSM><GSM>GSM9661605</GSM><GSM>GSM9661619</GSM><GSM>GSM9661608</GSM><GSM>GSM9661607</GSM><GSM>GSM9661618</GSM><GSM>GSM9661609</GSM><GSM>GSM9661620</GSM><GSM>GSM9661622</GSM><GSM>GSM9661611</GSM><GSM>GSM9661610</GSM><GSM>GSM9661621</GSM><GSM>GSM9661613</GSM><GSM>GSM9661612</GSM><GPL>34917</GPL><GSE>327564</GSE><taxon>Pseudomonas syringae pv. tomato str. DC3000</taxon></cross_references></HashMap>