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Status |
Public on Aug 10, 2019 |
Title |
Robust hepatitis E virus infection and transcriptional response in human hepatocytes |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
In this study, we established a protocol based on the HEV genotype 3 p6 (Kernow C-1) and the human hepatoma cell lines HepG2 and HepG2/C3A with different media conditions to produce HEV cell culture-derived particles (HEVcc) with viral titers between 10e5 to 10e6 FFU/mL. Viral titers could be further enhanced by an HEV variant harboring a mutation in the RNA-dependent RNA polymerase. These HEVcc particles were infectious in primary human hepatocytes. RNA sequencing studies of HEV infected primary human hepatocytes demonstrated a temporally structured transcriptional defense response. In conclusion, this robust cell culture model of HEV infection provides a powerful tool for studying viral-host interactions that should facilitate the discovery of antiviral drugs and vaccines for this important zoonotic pathogen.
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Overall design |
Primary human hepatocytes (PHH) were inoculated with cell culture-derived HEV particles and changes in transcriptional profiles were assessed using RNAseq.
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Contributor(s) |
Todt D, Friesland M, Steinmann E |
Citation(s) |
31896581 |
Submission date |
Aug 09, 2019 |
Last update date |
Jan 06, 2020 |
Contact name |
Daniel Todt |
E-mail(s) |
daniel.todt@rub.de
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Phone |
+492343222463
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Organization name |
Ruhr University Bochum
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Department |
Molecular & Medical Virology
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Street address |
Universitätsstr. 150
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City |
Bochum |
ZIP/Postal code |
44801 |
Country |
Germany |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (24)
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Relations |
BioProject |
PRJNA559467 |
SRA |
SRP217907 |