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Bacteroides thetaiotaomicron VPI-5482

ABSTRACT: Infection leaves a genetic and functional mark on the gut population of a commensal bacterium

PROVIDER: PRJNA889354 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR21859303_1.fastq.gz	Fastqsanger.gz
	SRR21859303_2.fastq.gz	Fastqsanger.gz
	SRR21859304_1.fastq.gz	Fastqsanger.gz
	SRR21859304_2.fastq.gz	Fastqsanger.gz
	SRR21859305_1.fastq.gz	Fastqsanger.gz

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Expression data of Enterohemorrhagic E. coli O157:H7 (EHEC) strain 86-24 when cultured with Bacteroides thetaiotaomicron VPI-5482

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Expression data of Enterohemorrhagic E. coli O157:H7 (EHEC) strain 86-24 when cultured with Bacteroides thetaiotaomicron VPI-5482

Project description:Regulation of EHEC gene expression by the gut commensal bacterium B. thetaiotaomicron. EHEC is a human pathogen that colonizes in the colon where B. thetaiotaomicron is a predominant commensal. We used microarrays to evaluate global regulation of EHEC when cultured with B. thetaiotaomicron. EHEC and B. thetaiotaomicron were co-cultured in vitro under strict anaerobic conditions in low-glucose Dulbecco's modified Eagle's medium (DMEM). Total RNA from bacteria grown to mid-logarithmic phase was extracted and hybridized to an Affymetrix E. coli 2.0 gene chip according to manufacturer's specifications: http//www.affymetrix.com/support/technical/manual/expression_manual.affx

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Project description:Strain engineering identifies unstable genetic loci in Bacteroides thetaiotaomicron

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Project description:Dynamic genetic adaptation of Bacteroides thetaiotaomicron during murine gut colonization

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Genome-wide RNA-seq of Bacteroides thetaiotaomicron VPI-5482 with Bacteroides phage challenge

Project description:Purpose: Examining the transcriptome of Bacteroides thetaiotaomicron VPI-5482 challenged with Bacteroides phage to assess surface molecule expression changes Methods: Bacteroides thetaiotaomicron was grown in BPRM in vitro or Germ-Free mice were monocolonized with Bacteroides thetaiotaomicron and gavaged with ARB25 phage. Fold change was calculated as live phage versus heat-killed phage treated samples with n=3 biological replicates. Once cells reached an optical density corresponding to mid-log phase growth (absorbance between 0.4-0.5), RNA was isolated and rRNA depleted. Samples were multiplexed for sequencing on the Illumina HiSeq platform at the University of Michigan Sequencing Core. Data was analyzed using Arraystar software (DNASTAR, Inc.) using DEseq2 normalization with default parameters. Genes with significant up- or down-regulation were determined by the following criteria: genes with an average fold-change >5-fold and with at least 2/3 biological replicates with a normalized expression level >1% of the overall average, and a p-value < 0.05 (t test with Benjamini-Hochberg correction) Results: Specific capsule expression was increased in wild-type B. thetaiotaomicron during phage infection in vitro and in vivo. Many corresponding in vivo genes were upregulated as well as other surface layer proteins.

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Project description:Coordinate regulation of glycan degradation and polysaccharide capsule biosynthesis by a prominent human gut symbiont

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Project description:Bacteroides thetaiotaomicron VPI-5482 Raw sequence reads

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Bacteroides thetaiotaomicron VPI-5482

Project description:Bacteroides thetaiotaomicron VPI-5482 Transcriptome or Gene expression

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Project description:Tnseq of B. thetaiotaomicron