<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/GSE343nnn/GSE343114/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Bacteroides thetaiotaomicron</species><species> mouse gut metagenome</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=GSE343114</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Mining Microbial Transcriptomes to Engineer Cell-Based Bacterial Biosensors in Gut-Resident Bacteroidaceae [DSS RNAseq]</name><description>The gastrointestinal tract is rich in metabolic, immune, and microbiome-derived signals that can inform the design of live biotherapeutics and diagnosis of intestinal disorders. Engineered cell-based biosensors can tap into this molecular information and report on their environment, yet their development in gut-resident symbionts has been limited by a lack of validated sensor systems. Here, we present a generalizable pipeline that leverages bacterial transcriptional profiling to identify environment-responsive systems for biosensor engineering. Candidate Sensors Systems (CSSs) mined from healthy, disease, and in vitro transcriptomes were assembled into a barcoded library in Bacteroidaceae chassis and screened in high-throughput in vivo to identify responsive promoters. A unique Bacteroidales ECF-type sigma factor operon with ties to sphingolipid metabolism and flux was highly responsive in chemically-induced colitis models. The biosensor responded robustly to disease and returned to baseline upon recovery, establishing an in vivo-driven strategy for discovering functional biosensors in non-model gut-resident bacteria.</description><dates><publication>2026/08/24</publication></dates><accession>GSE343114</accession><cross_references><GSM>GSM9946280</GSM><GSM>GSM9946287</GSM><GSM>GSM9946288</GSM><GSM>GSM9946285</GSM><GSM>GSM9946286</GSM><GSM>GSM9946283</GSM><GSM>GSM9946284</GSM><GSM>GSM9946281</GSM><GSM>GSM9946282</GSM><GSM>GSM9946269</GSM><GSM>GSM9946267</GSM><GSM>GSM9946289</GSM><GSM>GSM9946268</GSM><GSM>GSM9946290</GSM><GSM>GSM9946291</GSM><GSM>GSM9946276</GSM><GSM>GSM9946277</GSM><GSM>GSM9946274</GSM><GSM>GSM9946275</GSM><GSM>GSM9946294</GSM><GSM>GSM9946272</GSM><GSM>GSM9946273</GSM><GSM>GSM9946295</GSM><GSM>GSM9946270</GSM><GSM>GSM9946292</GSM><GSM>GSM9946293</GSM><GSM>GSM9946271</GSM><GSM>GSM9946278</GSM><GSM>GSM9946279</GSM><GPL>37350</GPL><GPL>37336</GPL><GSE>343114</GSE><taxon>Bacteroides thetaiotaomicron</taxon><taxon> mouse gut metagenome</taxon></cross_references></HashMap>