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Infection courses, virological features and IFN-α responses of HBV genotypes in cell culture and animal models.
Zhang, Min; Zhang, Zhensheng; Imamura, Michio; Osawa, Mitsutaka; Teraoka, Yuji; Piotrowski, Jason; Ishida, Yuji; Sozzi, Vitina; Revill, Peter A; Saito, Takeshi; Chayama, Kazuaki; Liang, T Jake.
Afiliação
  • Zhang M; Liver Diseases Branch, NIDDK, NIH, Bethesda, MD, USA.
  • Zhang Z; Liver Diseases Branch, NIDDK, NIH, Bethesda, MD, USA.
  • Imamura M; Department of Gastroenterology and Metabolism, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima, Japan.
  • Osawa M; Department of Gastroenterology and Metabolism, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima, Japan.
  • Teraoka Y; Department of Gastroenterology and Metabolism, Graduate School of Biomedical & Health Science, Hiroshima University, Hiroshima, Japan.
  • Piotrowski J; Liver Diseases Branch, NIDDK, NIH, Bethesda, MD, USA.
  • Ishida Y; Division of Gastrointestinal and Liver Diseases, Department of Medicine, University of Southern California, Keck School of Medicine, Los Angeles, CA, USA; PhoenixBio Co., Ltd., Higashi-Hiroshima, Hiroshima, Japan.
  • Sozzi V; Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Revill PA; Victorian Infectious Diseases Reference Laboratory, Royal Melbourne Hospital at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
  • Saito T; Division of Gastrointestinal and Liver Diseases, Department of Medicine, University of Southern California, Keck School of Medicine, Los Angeles, CA, USA.
  • Chayama K; Collaborative Research Laboratory of Medical Innovation, Hiroshima University, Hiroshima, Japan.
  • Liang TJ; Liver Diseases Branch, NIDDK, NIH, Bethesda, MD, USA. Electronic address: jliang@nih.gov.
J Hepatol ; 75(6): 1335-1345, 2021 12.
Article em En | MEDLINE | ID: mdl-34363922
ABSTRACT
BACKGROUND &

AIMS:

HBV consists of 9 major genotypes (A to I), 1 minor strain (designated J) and multiple subtypes, which may be associated with different clinical characteristics. As only cell lines expressing genotype D3 have been established, herein, we aimed to establish stable cell lines producing high-titer cell culture-generated HBV (HBVcc) of different genotypes and to explore their infectivity, virological features and responses to treatment.

METHODS:

Stable cell lines producing high titers of HBV genotype A2, B2, C1, E, F1b and H were generated by transfecting plasmids containing a replication-competent 1.3x length HBV genome and an antibiotic marker into HepG2 cells that can support HBV replication. Clones with the highest levels of HBV DNA and/or HBeAg were selected and expanded for large-scale purification of HBVcc. HBVcc of different genotypes were tested in cells and a humanized chimeric mouse model.

RESULTS:

HBVcc genotypes were infectious in mouse-passaged primary human hepatocytes (PXB cells) and responded differently to human interferon (IFN)-α with variable kinetics of reduction in HBV DNA, HBeAg and HBsAg. HBVcc of all genotypes were infectious in humanized chimeric mice but with variable kinetics of viremia and viral antigen production. Treatment of infected mice with human IFN-α resulted in modest and variable reductions of viremia and viral antigenemia. HBVcc passaged in humanized chimeric mice (HBVmp) infected PXB cells much more efficiently than that of the original HBVcc viral stock.

CONCLUSIONS:

Herein, we generated stable cell lines producing HBV of various genotypes that are infectious in vitro and in vivo. We observe genotype-associated variations in viral antigen production, infection kinetics and responses to human IFN-α treatment in these models. LAY

SUMMARY:

Stable cell lines producing high-titer cell culture-generated hepatitis B virus (HBV) of various genotypes were established. HBV genotypes showed stable infectivity in both in vitro and in vivo models, which are valuable tools for antiviral development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genótipo / Hepatite B Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genótipo / Hepatite B Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos