Cargando…

Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo

Humanized pigs have been developed to reduce the incidence of immune rejection in xenotransplantation, but significant concerns remain, such as transmission of viral zoonosis. Porcine endogenous retroviruses (PERV), which exist in the genome of pigs, are produced as infectious virions from all porci...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Nayoung, Choi, Jiwon, Kim, Sehyun, Gwon, Yong-Dae, Cho, Yeondong, Yang, Jae Myung, Oh, Yu-Kyoung, Kim, Young bong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104465/
https://www.ncbi.nlm.nih.gov/pubmed/27832080
http://dx.doi.org/10.1371/journal.pone.0165156
_version_ 1782466754176352256
author Kim, Nayoung
Choi, Jiwon
Kim, Sehyun
Gwon, Yong-Dae
Cho, Yeondong
Yang, Jae Myung
Oh, Yu-Kyoung
Kim, Young bong
author_facet Kim, Nayoung
Choi, Jiwon
Kim, Sehyun
Gwon, Yong-Dae
Cho, Yeondong
Yang, Jae Myung
Oh, Yu-Kyoung
Kim, Young bong
author_sort Kim, Nayoung
collection PubMed
description Humanized pigs have been developed to reduce the incidence of immune rejection in xenotransplantation, but significant concerns remain, such as transmission of viral zoonosis. Porcine endogenous retroviruses (PERV), which exist in the genome of pigs, are produced as infectious virions from all porcine cells and cause zoonosis. Here, we examined the possibility of zoonosis of hosts under conditions of immune suppression or xenotransplantation of cells producing host-adapted viruses. Upon transplantation of PERV-producing porcine cells into mice, no transmission of PERV was detected, whereas, transmission of PERV from mice transplanted with mouse-adapted PERV-producing cells was detected. In addition, the frequency of PERV transmission was increased in CsA treated mice transplanted with PERV-producing murine cells, compared with PERV-producing porcine cells. Transmission of PERV to host animals did not affect weight but immune responses, in particular, the number of T cells from PERV-transmitted mice, were notably reduced. The observed risk of PERV zoonosis highlights the requirement for thorough evaluation of viral zoonosis under particular host conditions, such as immunosuppressive treatment and transplantation with host-adapted virus-producing cells.
format Online
Article
Text
id pubmed-5104465
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-51044652016-12-08 Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo Kim, Nayoung Choi, Jiwon Kim, Sehyun Gwon, Yong-Dae Cho, Yeondong Yang, Jae Myung Oh, Yu-Kyoung Kim, Young bong PLoS One Research Article Humanized pigs have been developed to reduce the incidence of immune rejection in xenotransplantation, but significant concerns remain, such as transmission of viral zoonosis. Porcine endogenous retroviruses (PERV), which exist in the genome of pigs, are produced as infectious virions from all porcine cells and cause zoonosis. Here, we examined the possibility of zoonosis of hosts under conditions of immune suppression or xenotransplantation of cells producing host-adapted viruses. Upon transplantation of PERV-producing porcine cells into mice, no transmission of PERV was detected, whereas, transmission of PERV from mice transplanted with mouse-adapted PERV-producing cells was detected. In addition, the frequency of PERV transmission was increased in CsA treated mice transplanted with PERV-producing murine cells, compared with PERV-producing porcine cells. Transmission of PERV to host animals did not affect weight but immune responses, in particular, the number of T cells from PERV-transmitted mice, were notably reduced. The observed risk of PERV zoonosis highlights the requirement for thorough evaluation of viral zoonosis under particular host conditions, such as immunosuppressive treatment and transplantation with host-adapted virus-producing cells. Public Library of Science 2016-11-10 /pmc/articles/PMC5104465/ /pubmed/27832080 http://dx.doi.org/10.1371/journal.pone.0165156 Text en © 2016 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kim, Nayoung
Choi, Jiwon
Kim, Sehyun
Gwon, Yong-Dae
Cho, Yeondong
Yang, Jae Myung
Oh, Yu-Kyoung
Kim, Young bong
Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title_full Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title_fullStr Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title_full_unstemmed Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title_short Transmission of Porcine Endogenous Retrovirus Produced from Different Recipient Cells In Vivo
title_sort transmission of porcine endogenous retrovirus produced from different recipient cells in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104465/
https://www.ncbi.nlm.nih.gov/pubmed/27832080
http://dx.doi.org/10.1371/journal.pone.0165156
work_keys_str_mv AT kimnayoung transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT choijiwon transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT kimsehyun transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT gwonyongdae transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT choyeondong transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT yangjaemyung transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT ohyukyoung transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo
AT kimyoungbong transmissionofporcineendogenousretrovirusproducedfromdifferentrecipientcellsinvivo