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Series GSE234958 Query DataSets for GSE234958
Status Public on Jan 25, 2024
Title An expanded transcriptome atlas for Bacteroides thetaiotaomicron reveals a small RNA that modulates tetracycline sensitivity
Organism Bacteroides thetaiotaomicron
Experiment type Expression profiling by high throughput sequencing
Summary Gene expression plasticity allows bacteria to adapt to diverse environments, tie their metabolism to available nutrients, and cope with stress. This is particularly relevant in a niche as dynamic and hostile as the human intestinal tract, yet transcriptional networks remain largely unknown in gut Bacteroides spp. Here, we map transcriptional units and profile their expression levels in Bacteroides thetaiotaomicron over a suite of 15 defined experimental conditions that are relevant in vivo, such as variation of temperature, pH, and oxygen tension, exposure to antibiotic stress, and growth on simple carbohydrates or on host mucin-derived glycans. Thereby, we infer stress- and carbon source-specific transcriptional regulons, including conditional expression of capsular polysaccharides and polysaccharide utilization loci, and expand the annotation of small regulatory RNAs (sRNAs) in this organism. Integrating this comprehensive expression atlas with transposon mutant fitness data, we identify conditionally important sRNAs. One example is MasB, whose inactivation led to increased bacterial tolerance of tetracyclines. Using MS2 affinity purification coupled with RNA sequencing, we predict targets of this sRNA and discuss their potential role in the context of the MasB-associated phenotype. Together, this transcriptomic compendium in combination with functional sRNA genomics—publicly available through a new iteration of the ‘Theta-Base’ web browser (www.helmholtz-hiri.de/en/datasets/bacteroides-v2)—constitutes a valuable resource for the microbiome and sRNA research communities alike.
 
Overall design Samples 1-32: RNA-seq of Bacteroides thetaiotaomicron VPI-5482 (wild type) grown in TYG-medium and exposed to different stress conditions (Cold, Heat, Acid, Aerobe, H2O2, Deoxycholate, Bile salts and Gentamicin) or in minimal medium supplemented with different carbon sources (Glucose, Arabinose, Xylose, Maltose, GlcNAc, Mucin and Starvation). Two biological replicates per strain and condition. Samples 33, 34: Genome-wide mapping of transcription start sites via differential RNA-seq (dRNA-seq) of pooled RNA from the above mentioned samples 1-32. Two biological replicates. Samples 35-38: Identification of RNAs (RNA-seq) co-purified with MS2 aptamer tagged MasB sRNA in a masB deletion background and an untagged MasB control strain. Two biological replicates.
 
Contributor(s) Ryan D, Bornet E, Prezza G, Alampalli SV, de Carvalho TF, Felchle H, Ebbecke T, Hayward R, Deutschbauer AM, Barquist L, Westermann AJ
Citation(s) 38528147
Submission date Jun 14, 2023
Last update date Apr 17, 2024
Contact name Alexander J. Westermann
E-mail(s) alexander.westermann@helmholtz-hiri.de
Organization name Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI),
Street address Josef-Schneider-Straße 2/D15
City Würzburg
ZIP/Postal code 97080
Country Germany
 
Platforms (1)
GPL28094 Illumina NextSeq 500 (Bacteroides thetaiotaomicron)
Samples (40)
GSM7486729 MM-Glucose, R1
GSM7486730 MM-Xylose, R1
GSM7486731 MM-Arabinose, R1
Relations
BioProject PRJNA983800

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
GSE234958_MS2_counts.csv.csv.gz 97.1 Kb (ftp)(http) CSV
GSE234958_Pool_counts.csv.gz 244.8 Kb (ftp)(http) CSV
GSE234958_RNAseq_counts.xlsx 1.6 Mb (ftp)(http) XLSX
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Raw data are available in SRA
Processed data are available on Series record

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