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Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line

Mouse hepatitis virus (MHV) strain JHM is a coronavirus that causes encephalitis and demyelination in susceptible rodents. The known receptors for MHV are all members of the carcinoembryonic antigen family. Although human forms of the MHV receptor can function as MHV receptors in some assays, no hum...

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Autores principales: Koetters, Peter J., Hassanieh, Loubna, Stohlman, Stephen A., Gallagher, Thomas, Lai, Michael M.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press. 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131271/
https://www.ncbi.nlm.nih.gov/pubmed/10562501
http://dx.doi.org/10.1006/viro.1999.9984
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author Koetters, Peter J.
Hassanieh, Loubna
Stohlman, Stephen A.
Gallagher, Thomas
Lai, Michael M.C.
author_facet Koetters, Peter J.
Hassanieh, Loubna
Stohlman, Stephen A.
Gallagher, Thomas
Lai, Michael M.C.
author_sort Koetters, Peter J.
collection PubMed
description Mouse hepatitis virus (MHV) strain JHM is a coronavirus that causes encephalitis and demyelination in susceptible rodents. The known receptors for MHV are all members of the carcinoembryonic antigen family. Although human forms of the MHV receptor can function as MHV receptors in some assays, no human cell line has been identified that can support wild-type MHV infection. Here we describe the infection of a human hepatocellular carcinoma cell line, HuH-7, with MHV. HuH-7 cells were susceptible to strains JHM-DL and JHM-DS, yielding virus titers nearly identical to those seen in mouse DBT cells. In contrast, HuH-7 cells were only marginally susceptible or completely resistant to infection by other MHV strains, including A59. JHM produced a strong cytopathic effect in HuH-7 cells with the formation of round plaques. Studies of various recombinant viruses between JHM and A59 strains suggested that the ability of JHM to infect HuH-7 cells was determined by multiple viral genetic elements. Blocking the viral spike (S) protein with a neutralizing antibody or a soluble form of the MHV receptor inhibited infection of HuH-7 cells, suggesting that infection is mediated through the S protein. Transfection with the prototype mouse receptor, biliary glycoprotein, rendered HuH-7 cells susceptible to infection by other MHV strains as well, suggesting that JHM uses a receptor distinct from the classical MHV receptor to infect HuH-7 cells. Possible implications for human disease are discussed.
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spelling pubmed-71312712020-04-08 Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line Koetters, Peter J. Hassanieh, Loubna Stohlman, Stephen A. Gallagher, Thomas Lai, Michael M.C. Virology Article Mouse hepatitis virus (MHV) strain JHM is a coronavirus that causes encephalitis and demyelination in susceptible rodents. The known receptors for MHV are all members of the carcinoembryonic antigen family. Although human forms of the MHV receptor can function as MHV receptors in some assays, no human cell line has been identified that can support wild-type MHV infection. Here we describe the infection of a human hepatocellular carcinoma cell line, HuH-7, with MHV. HuH-7 cells were susceptible to strains JHM-DL and JHM-DS, yielding virus titers nearly identical to those seen in mouse DBT cells. In contrast, HuH-7 cells were only marginally susceptible or completely resistant to infection by other MHV strains, including A59. JHM produced a strong cytopathic effect in HuH-7 cells with the formation of round plaques. Studies of various recombinant viruses between JHM and A59 strains suggested that the ability of JHM to infect HuH-7 cells was determined by multiple viral genetic elements. Blocking the viral spike (S) protein with a neutralizing antibody or a soluble form of the MHV receptor inhibited infection of HuH-7 cells, suggesting that infection is mediated through the S protein. Transfection with the prototype mouse receptor, biliary glycoprotein, rendered HuH-7 cells susceptible to infection by other MHV strains as well, suggesting that JHM uses a receptor distinct from the classical MHV receptor to infect HuH-7 cells. Possible implications for human disease are discussed. Academic Press. 1999-11-25 2002-05-25 /pmc/articles/PMC7131271/ /pubmed/10562501 http://dx.doi.org/10.1006/viro.1999.9984 Text en Copyright © 1999 Academic Press. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Koetters, Peter J.
Hassanieh, Loubna
Stohlman, Stephen A.
Gallagher, Thomas
Lai, Michael M.C.
Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title_full Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title_fullStr Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title_full_unstemmed Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title_short Mouse Hepatitis Virus Strain JHM Infects a Human Hepatocellular Carcinoma Cell Line
title_sort mouse hepatitis virus strain jhm infects a human hepatocellular carcinoma cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131271/
https://www.ncbi.nlm.nih.gov/pubmed/10562501
http://dx.doi.org/10.1006/viro.1999.9984
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