A mutation in the hepatitis E virus RNA polymerase promotes its replication and associates with ribavirin treatment failure in organ transplant recipients.
Abstract
We analyzed blood samples collected from 15 patients with chronic hepatitis E who were recipients of solid-organ transplants. All patients cleared the hepatitis E virus (HEV) except for 2 (nonresponders); 1 patient died. A G1634R mutation in viral polymerase was detected in the HEV RNA of the nonresponders; this mutation did not provide the virus with resistance to ribavirin in vitro. However, the mutant form of a subgenomic replicon of genotype 3 HEV replicated more efficiently in vitro than HEV without this mutation, and the same was true for infectious virus, including in competition assays. Similar results were obtained for genotype 1 HEV. The G1634R mutation therefore appears to increase the replicative capacity of HEV in the human liver and hence reduce the efficacy of ribavirin.
Rega Institute for Medical Research, Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium.Department of Gastroenterology, Hepatology and Endocrinology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany.Rega Institute for Medical Research, Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium.MVZ für Lebertransplantation, University Hospital Hamburg Eppendorf, Hamburg, Germany.Department of Gastroenterology, Hepatology and Endocrinology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany.Department of Gastroenterology, Hepatology and Endocrinology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany.Department of Gastroenterology, Hepatology and Endocrinology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany.Department of Gastroenterology, Hepatology and Endocrinology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany.Rega Institute for Medical Research, Department of Microbiology and Immunology, University of Leuven, Leuven, Belgium. Electronic address: johan.neyts@rega.kuleuven.be. MeSH
Antiviral AgentsDNA-Directed RNA PolymerasesDose-Response Relationship, DrugDrug Resistance, ViralFemaleGenotypeHep G2 CellsHepatitis EHepatitis E virusHepatitis, ChronicHumansMaleMutagenesis, Site-DirectedMutationOrgan TransplantationPhenotypeRibavirinTime FactorsTransfectionTreatment FailureVirus Replication
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