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Status |
Public on Jul 06, 2023 |
Title |
Vero76 cells, R. rickettsii st. Morgan, 24hpi, Rep3 |
Sample type |
SRA |
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Source name |
Vero76 (ATCC CCL-81)
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Organism |
Chlorocebus aethiops |
Characteristics |
cell line: Vero76 (ATCC CCL-81) agent: R. rickettsii st. Morgan time: 24 hour post infection
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Treatment protocol |
Vero76 cells in 6-well plates (2/replicate) were infected with R. rickettsii Morgan or Iowa at a multiplicity of infection (MOI) of 30 for a 4 hr time point and MOI of 1 for 24 and 48 hr time points. Cultures were centrifuged at 2000 RPM for 5 min at room temperature to synchronize infections, and were incubated at 34ºC for 4, 24, or 48 hr prior to harvesting by scraping into Trizol. Purified rickettsiae of each strain were also extracted into Trizol. All conditions were performed in triplicate.
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Growth protocol |
Vero76 cells (ATCC® CCL-81™) were grown in RPMI medium plus 5 % heat-inactivated fetal bovine serum (FBS) at 37˚C in a 5% CO2 atmosphere.
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Extracted molecule |
total RNA |
Extraction protocol |
RNA containing aqueous phase was extracted using Qiagen AllPrep DNA/RNA 96-well system (Valencia, CA). The RNA yield was determined by spectrophotometry at 260 nm and 280nm and the integrity was assessed using the Agilent 2100 Bioanalyzer using RNA 6000 Pico kit (Agilent Technologies, Santa Clara, Ca). The average RNA Integrity Number (RIN) was 9.2. Ribo-Zero Epidemiology kits (Illumina, Inc, San Deigo, CA) were used to deplete the samples of ribosomal RNAs prior to library preparation with the TruSeq Total RNA-Seq Library Prep Kit (Illumina), starting at the Elute-Frag-Prime step without further modification. Final libraries were assessed on a BioAnalyzer DNA1000 chip (Agilent Technologies, Santa Clara, CA) and quantified using the Kapa Quantification Kit for Illumina MiSeq (v3 chemistry )Sequencing (Roche, Basel, Switzerland).
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina MiSeq |
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Description |
12706
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Data processing |
RNA-Seek (https://github.com/OpenOmics/RNA-seek) A custom hybrid reference genome database was built with Chlorocebus sabaeus (Green Monkey) reference genome (GCA_000409795.2) – background of Vero cells, and R. rickettsii str. Iowa genome (GCA_000017445.3) using ‘build’ function in RNA-Seek pipeline. Initial data preprocessing included read quality check with FASTQC v0.11.5, screening for sources of contamination (FQScreen v0.9.3, Kraken v2.0.8), removal of adapters and short sequences, and quality trimming with Cutadapt v1.18. Preprocessed reads were then mapped to the hybrid genome reference using STAR v2.7.6a aligner, and reads mapping to C. sabaeus and R. rickettsia genes were quantified using RSEM v1.3.0. The gene quantification data was split between C. sabaeus and R. rickettsia genes. The R. rickettsia gene expression data was further differential gene expression analyses. Assembly: Hybrid genome (Chlorocebus sabaeus + R. rickettsii str. Iowa) Supplementary files format and content: tab-delimited text files include RPKM counts (non-normalized) for R. rickettesia strain Iowa genes
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Submission date |
Mar 07, 2023 |
Last update date |
Jul 06, 2023 |
Contact name |
Neelam Redekar |
Organization name |
NIH
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Department |
NIAID
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Street address |
9000 rockville pike
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platform ID |
GPL33219 |
Series (1) |
GSE226832 |
Identification of an outer membrane protease of Rickettsia rickettsii responsible for maturation of surface exposed autotransporters |
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Relations |
BioSample |
SAMN33614065 |
SRA |
SRX19581786 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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