Project description:Here we present genome-wide high-coverage genotyping data on a panel of 75 human samples from Western Balkan region, Europe, that are used in addition to public data in studing the genetic variation of Southern Europe that was sequenced to the avwerage depth of 1X.
Project description:Purpose: to determine the differentially expressed genes in the phase-variable rough and smooth colony isolates of C. difficile Methods: C. difficile R20291 was grown on BHIS agar to obtain distinct colonies. Individual rough and smooth colonies were chosen for propagation on BHIS-agar for 24 hours as described in Garrett, et al., PLoS Biology, 2019. Growth was collected from n = 2 biological replicates. RNA was purified using TriSure and chloroform, beadbeating, and isopropanol/ethanol precipitation. Quality was verified with Bioanalyzer Assay. Samples were submitted to Genewiz for depletion of rRNA using the TruSeq RiboZero Gold Kit, library preparation, and single-end sequencing on the Illumina HiSeq 2500 platform. RNA sequencing analysis was done using CLC Genomic Workbench v20. Reads were mapped to C. difficile R20291 genome using the software's default menalties for mismatch, deletion, and insertion differences from the reference genome. Transcript reads were normalized as RPKM. Results: 88 genes were differentially expressed between bacteria from rough versus smooth colonies, with equal to or greater than a 2-fold change and p < 0.05 with FDR correction.
Project description:This SuperSeries is composed of the following subset Series: GSE35612: Microarray analysis of gene expression in rams experimentally infected with a rough virulent strain of Brucella ovis (acute phase) GSE35613: Microarray analysis of gene expression in rams experimentally infected with a rough virulent strain of Brucella ovis (chronic 1 phase) GSE35614: Microarray analysis of gene expression in rams experimentally infected with a rough virulent strain of Brucella ovis (chronic 2 phase) Refer to individual Series
Project description:Clostridioides difficile introduces phenotypic heterogeneity into populations via phase variation. C. difficile modulates phase variation through invertible DNA sequences containing regulatory information, termed switches. Inversion of a switch controls expression of the adjacent genes in an ON/OFF manner, resulting in phenotypic switching. The C. difficile cmr switch (for ‘colony morphology regulator’) coordinates several phenotypes. When cmr is ON, C. difficile displays a rough colony morphology, surface motility, and cell chaining and elongation. When cmr is OFF, colonies are smooth, and high levels of swimming motility and biofilm formation are observed. Prior work has also linked colony morphology and cmr switch orientation to virulence in the hanster model of infection (Garrett et al., PLoS Biology, 2019). The cmr-ON orientation results in the expression of cmrRST, an operon encoding a signal transduction system. CmrS is a predicted histidine kinase, and CmrR and CmrT are response regulators. We have shown that CmrR and CmrT are responsible for the observed cmr-associated phenotypes (Garrett et al., PLoS Biology, 2019). The goal of this study is to identify the genes that are regulated by CmrR and CmrT and determine how these genes contribute to colony morphology and the other cmr-associated phenotypes. To identify genes important for C. difficile colony morphology, we conducted a multi-pronged RNA-Seq study comparing the following transcriptomes: (1) Rough vs. smooth colony variants of wild-type, (2) cmr-ON vs. cmr-OFF phase-locked strains, (3) Rough, smooth, cmr-ON, and cmr-OFF vs. a ΔcmrRΔcmrT mutant, and (4) Wild-type overexpressing either cmrR or cmrT vs. a no-overexpression condition. Transcription analyses revealed that CmrRST accounts for some, but not all, transcriptional differences between rough and smooth colony morphotypes. Fewer than 20 genes were differentially expressed by CmrR and/or CmrT (≥4-fold change, p<0.05). Most of those genes appeared in the rough vs. smooth and cmr-ON vs. -OFF datasets as well, and further phenotypic analyses of CmrRST-regulated genes revealed multiple genes that mediated rough colony development.
Project description:The macrophage-Brucella interaction is critical for the establishment of a chronic Brucella infection. Smooth virulent B. suis strain 1330 (S1330) prevents macrophage cell death. However, rough attenuated B. suis strain VTRS1 induces strong macrophage cell death. To further investigate the mechanism of VTRS1-induced macrophage cell death, microarrays were used to analyze temporal transcriptional responses of murine macrophage-like J774. A1 cells infected with S1330 or VTRS1.
Project description:Long rough dab (Hippoglossoides platessoides) is an important flatfish fish species in the north Atlantic arctic and sub-arctic marine foodweb that could be vulnerable to contaminant exposure from offshore petroleum related activities. The study was conducted to map transcriptome responses in long rough dab precision cut liver slice (PCLS) culture exposed to benzo[a]pyrene (BaP). BaP is a polyaromatic hydrocarbon (PAH) which is among the most toxic compounds found in crude oil. PCLS culture was performed under 10 µM BaP exposure for 72 h and transcriptome analysis (RNA-seq) analysis was performed to characterize de novo transcriptome of the liver and identify genes responding to BaP exposure.