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Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis

A human betaretrovirus (HBRV) has been linked with the autoimmune liver disease, primary biliary cholangitis (PBC), and various cancers, including breast cancer and lymphoma. HBRV is closely related to the mouse mammary tumor virus, and represents the only exogenous betaretrovirus characterized in h...

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Autores principales: Goubran, Mariam, Wang, Weiwei, Indik, Stanislav, Faschinger, Alexander, Wasilenko, Shawn T., Bintner, Jasper, Carpenter, Eric J., Zhang, Guangzhi, Nuin, Paulo, Macintyre, Georgina, Wong, Gane K.-S., Mason, Andrew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146342/
https://www.ncbi.nlm.nih.gov/pubmed/35632628
http://dx.doi.org/10.3390/v14050886
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author Goubran, Mariam
Wang, Weiwei
Indik, Stanislav
Faschinger, Alexander
Wasilenko, Shawn T.
Bintner, Jasper
Carpenter, Eric J.
Zhang, Guangzhi
Nuin, Paulo
Macintyre, Georgina
Wong, Gane K.-S.
Mason, Andrew L.
author_facet Goubran, Mariam
Wang, Weiwei
Indik, Stanislav
Faschinger, Alexander
Wasilenko, Shawn T.
Bintner, Jasper
Carpenter, Eric J.
Zhang, Guangzhi
Nuin, Paulo
Macintyre, Georgina
Wong, Gane K.-S.
Mason, Andrew L.
author_sort Goubran, Mariam
collection PubMed
description A human betaretrovirus (HBRV) has been linked with the autoimmune liver disease, primary biliary cholangitis (PBC), and various cancers, including breast cancer and lymphoma. HBRV is closely related to the mouse mammary tumor virus, and represents the only exogenous betaretrovirus characterized in humans to date. Evidence of infection in patients with PBC has been demonstrated through the identification of proviral integration sites in lymphoid tissue, the major reservoir of infection, as well as biliary epithelium, which is the site of the disease process. Accordingly, we tested the hypothesis that patients with PBC harbor a transmissible betaretrovirus by co-cultivation of PBC patients’ lymph node homogenates with the HS578T breast cancer line. Because of the low level of HBRV replication, betaretrovirus producing cells were subcloned to optimize viral isolation and production. Evidence of infection was provided by electron microscopy, RT-PCR, in situ hybridization, cloning of the HBRV proviral genome and demonstration of more than 3400 integration sites. Further evidence of viral transmissibility was demonstrated by infection of biliary epithelial cells. While HBRV did not show a preference for integration proximal to specific genomic features, analyses of common insertion sites revealed evidence of integration proximal to cancer associated genes. These studies demonstrate the isolation of HBRV with features similar to mouse mammary tumor virus and confirm that patients with PBC display evidence of a transmissible viral infection.
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spelling pubmed-91463422022-05-29 Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis Goubran, Mariam Wang, Weiwei Indik, Stanislav Faschinger, Alexander Wasilenko, Shawn T. Bintner, Jasper Carpenter, Eric J. Zhang, Guangzhi Nuin, Paulo Macintyre, Georgina Wong, Gane K.-S. Mason, Andrew L. Viruses Article A human betaretrovirus (HBRV) has been linked with the autoimmune liver disease, primary biliary cholangitis (PBC), and various cancers, including breast cancer and lymphoma. HBRV is closely related to the mouse mammary tumor virus, and represents the only exogenous betaretrovirus characterized in humans to date. Evidence of infection in patients with PBC has been demonstrated through the identification of proviral integration sites in lymphoid tissue, the major reservoir of infection, as well as biliary epithelium, which is the site of the disease process. Accordingly, we tested the hypothesis that patients with PBC harbor a transmissible betaretrovirus by co-cultivation of PBC patients’ lymph node homogenates with the HS578T breast cancer line. Because of the low level of HBRV replication, betaretrovirus producing cells were subcloned to optimize viral isolation and production. Evidence of infection was provided by electron microscopy, RT-PCR, in situ hybridization, cloning of the HBRV proviral genome and demonstration of more than 3400 integration sites. Further evidence of viral transmissibility was demonstrated by infection of biliary epithelial cells. While HBRV did not show a preference for integration proximal to specific genomic features, analyses of common insertion sites revealed evidence of integration proximal to cancer associated genes. These studies demonstrate the isolation of HBRV with features similar to mouse mammary tumor virus and confirm that patients with PBC display evidence of a transmissible viral infection. MDPI 2022-04-24 /pmc/articles/PMC9146342/ /pubmed/35632628 http://dx.doi.org/10.3390/v14050886 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Goubran, Mariam
Wang, Weiwei
Indik, Stanislav
Faschinger, Alexander
Wasilenko, Shawn T.
Bintner, Jasper
Carpenter, Eric J.
Zhang, Guangzhi
Nuin, Paulo
Macintyre, Georgina
Wong, Gane K.-S.
Mason, Andrew L.
Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title_full Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title_fullStr Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title_full_unstemmed Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title_short Isolation of a Human Betaretrovirus from Patients with Primary Biliary Cholangitis
title_sort isolation of a human betaretrovirus from patients with primary biliary cholangitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146342/
https://www.ncbi.nlm.nih.gov/pubmed/35632628
http://dx.doi.org/10.3390/v14050886
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