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Hepatitis C Virus Infects and Perturbs Liver Stem Cells

View ORCID ProfileNathan L Meyers, View ORCID ProfileTal Ashuach, View ORCID ProfileDanielle E Lyons, Camille R Simoneau, Ann L Erickson, Mehdi Bouhaddou, Thong T. Nguyen, Mir M Khalid, Taha Y Taha, Vaishaali Natarajan, Jody L Baron, Norma Neff, Fabio Zanini, Tokameh Mahmoud, Stephen R Quake, Nevan J Krogan, Stewart Cooper, View ORCID ProfileTodd C McDevitt, Nir Yosef, Melanie Ott
doi: https://doi.org/10.1101/2021.10.26.465357
Nathan L Meyers
1Gladstone Institute of Virology, San Francisco, CA, USA
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Tal Ashuach
2Department of Electrical Engineering and Computer Science and Center for Computational Biology, University of California Berkeley, Berkeley, CA, USA
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  • ORCID record for Tal Ashuach
Danielle E Lyons
1Gladstone Institute of Virology, San Francisco, CA, USA
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Camille R Simoneau
1Gladstone Institute of Virology, San Francisco, CA, USA
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Ann L Erickson
3California Pacific Medical Center Research Institute, San Francisco, CA, USA
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Mehdi Bouhaddou
4Cellular and Molecular Pharmacology, University of California, San Francisco, CA, USA
5Gladstone Institute of Data Science and Biotechnology, San Francisco, CA, USA
6Quantitative Biosciences Institute, University of California, San Francisco, CA, USA
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Thong T. Nguyen
1Gladstone Institute of Virology, San Francisco, CA, USA
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Mir M Khalid
1Gladstone Institute of Virology, San Francisco, CA, USA
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Taha Y Taha
1Gladstone Institute of Virology, San Francisco, CA, USA
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Vaishaali Natarajan
7Gladstone Institute of Cardiovascular Disease, San Francisco, CA, USA
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Jody L Baron
8Department of Medicine, University of California San Francisco, San Francisco, CA, USA
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Norma Neff
9Chan Zuckerburg Biohub, San Francisco, CA, USA
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Fabio Zanini
10Department of Bioengineering, Stanford University, Stanford, CA, USA
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Tokameh Mahmoud
11Department of Biochemistry, Erasmus University Medical Center, Rotterdam, the Netherlands
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Stephen R Quake
9Chan Zuckerburg Biohub, San Francisco, CA, USA
10Department of Bioengineering, Stanford University, Stanford, CA, USA
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Nevan J Krogan
4Cellular and Molecular Pharmacology, University of California, San Francisco, CA, USA
5Gladstone Institute of Data Science and Biotechnology, San Francisco, CA, USA
6Quantitative Biosciences Institute, University of California, San Francisco, CA, USA
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Stewart Cooper
3California Pacific Medical Center Research Institute, San Francisco, CA, USA
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Todd C McDevitt
7Gladstone Institute of Cardiovascular Disease, San Francisco, CA, USA
12Bioengineering & Therapeutic Sciences, University of California San Francisco, San Francisco, CA, USA
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  • ORCID record for Todd C McDevitt
Nir Yosef
2Department of Electrical Engineering and Computer Science and Center for Computational Biology, University of California Berkeley, Berkeley, CA, USA
13Ragon Institute of Massachusetts General Hospital, MIT and Harvard, Cambridge, MA, USA
14Chan Zuckerberg Biohub Investigator, San Francisco, CA, USA
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Melanie Ott
1Gladstone Institute of Virology, San Francisco, CA, USA
8Department of Medicine, University of California San Francisco, San Francisco, CA, USA
15Liver Center, University of California San Francisco, San Francisco, CA, USA
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  • For correspondence: melanie.ott@gladstone.ucsf.edu
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Summary

Hepatitis C virus (HCV) is the leading cause of death from liver disease. How HCV infection causes lasting liver damage and increases cancer risk beyond viral clearance remains unclear. We identify bipotent liver stem cells as novel targets for HCV infection, and their erroneous differentiation as the potential cause of impaired liver regeneration and cancer development. We show 3D organoids generated from liver stem cells from actively HCV-infected individuals carry replicating virus and maintain low-grade infection over months. Organoids can be infected with a primary HCV isolate. Virus-inclusive single-cell RNA-sequencing uncovered extensive transcriptional reprogramming in HCV+ cells supporting hepatocytic differentiation, cancer stem cell development and viral replication while stem cell proliferation and interferon signaling are disrupted. Our data adds a pathogenesis factor – infection of liver stem cells – to the biology of HCV infection that explains persistent liver damage and enhanced cancer risk through an altered stem cell state.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted October 26, 2021.
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Hepatitis C Virus Infects and Perturbs Liver Stem Cells
Nathan L Meyers, Tal Ashuach, Danielle E Lyons, Camille R Simoneau, Ann L Erickson, Mehdi Bouhaddou, Thong T. Nguyen, Mir M Khalid, Taha Y Taha, Vaishaali Natarajan, Jody L Baron, Norma Neff, Fabio Zanini, Tokameh Mahmoud, Stephen R Quake, Nevan J Krogan, Stewart Cooper, Todd C McDevitt, Nir Yosef, Melanie Ott
bioRxiv 2021.10.26.465357; doi: https://doi.org/10.1101/2021.10.26.465357
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Hepatitis C Virus Infects and Perturbs Liver Stem Cells
Nathan L Meyers, Tal Ashuach, Danielle E Lyons, Camille R Simoneau, Ann L Erickson, Mehdi Bouhaddou, Thong T. Nguyen, Mir M Khalid, Taha Y Taha, Vaishaali Natarajan, Jody L Baron, Norma Neff, Fabio Zanini, Tokameh Mahmoud, Stephen R Quake, Nevan J Krogan, Stewart Cooper, Todd C McDevitt, Nir Yosef, Melanie Ott
bioRxiv 2021.10.26.465357; doi: https://doi.org/10.1101/2021.10.26.465357

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