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HuH-7-Lunet BLR Cells Propagate Rat Hepatitis E Virus (HEV) in a Cell Culture System Optimized for HEV
by
Schemmerer, Mathias
, Erl, Monika
, Wenzel, Jürgen J.
in
Animals
/ Antiviral agents
/ Antiviral drugs
/ Brief Report
/ Cell culture
/ Cell Culture Techniques
/ Cell Line
/ Experiments
/ Genomes
/ Genotypes
/ Hepatitis
/ Hepatitis C
/ Hepatitis E
/ hepatitis E virus
/ Hepatitis E virus - genetics
/ Hepatocytes
/ Infections
/ Liver
/ Liver cancer
/ Orthohepevirus C
/ rat HEV
/ Rats
/ Replication
/ Tumor cell lines
/ Viruses
/ zoonosis
2022
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HuH-7-Lunet BLR Cells Propagate Rat Hepatitis E Virus (HEV) in a Cell Culture System Optimized for HEV
by
Schemmerer, Mathias
, Erl, Monika
, Wenzel, Jürgen J.
in
Animals
/ Antiviral agents
/ Antiviral drugs
/ Brief Report
/ Cell culture
/ Cell Culture Techniques
/ Cell Line
/ Experiments
/ Genomes
/ Genotypes
/ Hepatitis
/ Hepatitis C
/ Hepatitis E
/ hepatitis E virus
/ Hepatitis E virus - genetics
/ Hepatocytes
/ Infections
/ Liver
/ Liver cancer
/ Orthohepevirus C
/ rat HEV
/ Rats
/ Replication
/ Tumor cell lines
/ Viruses
/ zoonosis
2022
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HuH-7-Lunet BLR Cells Propagate Rat Hepatitis E Virus (HEV) in a Cell Culture System Optimized for HEV
by
Schemmerer, Mathias
, Erl, Monika
, Wenzel, Jürgen J.
in
Animals
/ Antiviral agents
/ Antiviral drugs
/ Brief Report
/ Cell culture
/ Cell Culture Techniques
/ Cell Line
/ Experiments
/ Genomes
/ Genotypes
/ Hepatitis
/ Hepatitis C
/ Hepatitis E
/ hepatitis E virus
/ Hepatitis E virus - genetics
/ Hepatocytes
/ Infections
/ Liver
/ Liver cancer
/ Orthohepevirus C
/ rat HEV
/ Rats
/ Replication
/ Tumor cell lines
/ Viruses
/ zoonosis
2022
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HuH-7-Lunet BLR Cells Propagate Rat Hepatitis E Virus (HEV) in a Cell Culture System Optimized for HEV
Journal Article
HuH-7-Lunet BLR Cells Propagate Rat Hepatitis E Virus (HEV) in a Cell Culture System Optimized for HEV
2022
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Overview
The family Hepeviridae comprises the species Orthohepevirus A–D (HEV-A to -D). HEV-C genotype 1 (HEV-C1, rat HEV) is able to infect humans. This study investigated whether an optimized HEV-A cell culture system is able to propagate the cell culture-derived rat HEV, and if de novo isolation of the virus from rat liver is possible. We tested the liver carcinoma cell lines PLC/PRF/5, HuH-7, and HuH-7-Lunet BLR for their susceptibility to HEV-C1 strains. Cells were infected with the cell culture-derived HEV-C1 strain R63 and rat liver-derived strain R68. Cells were maintained in MEMM medium, which was refreshed every 3–4 days. The viral load of HEV-C1 was determined by RT-qPCR in the supernatant and expressed as genome copies per mL (c/mL). Rat HEV replication was most efficient in the newly introduced HuH-7-Lunet BLR cell line. Even if the rat HEV isolate had been pre-adapted to PLC/PRF/5 by multiple passages, replication in HuH-7-Lunet BLR was still at least equally effective. Only HuH-7-Lunet BLR cells were susceptible to the isolation of HEV-C1 from the liver homogenate. These results suggest HuH-7-Lunet BLR as the most permissive cell line for rat HEV. Our HEV-C1 cell culture system may be useful for basic research, the animal-free generation of large amounts of the virus as well as for the testing of antiviral compounds and drugs.
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