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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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 |
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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 |
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