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How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation
Porcine cytomegalovirus (PCMV), that is actually a porcine roseolovirus (PRV), is a common herpesvirus in domestic pigs and wild boars. In xenotransplantation, PCMV/PRV has been shown to significantly reduce the survival time of pig kidneys and hearts in preclinical trials with different non-human p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747970/ https://www.ncbi.nlm.nih.gov/pubmed/36513687 http://dx.doi.org/10.1038/s41598-022-25624-1 |
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author | Halecker, S. Hansen, S. Krabben, L. Ebner, F. Kaufer, B. Denner, J. |
author_facet | Halecker, S. Hansen, S. Krabben, L. Ebner, F. Kaufer, B. Denner, J. |
author_sort | Halecker, S. |
collection | PubMed |
description | Porcine cytomegalovirus (PCMV), that is actually a porcine roseolovirus (PRV), is a common herpesvirus in domestic pigs and wild boars. In xenotransplantation, PCMV/PRV has been shown to significantly reduce the survival time of pig kidneys and hearts in preclinical trials with different non-human primates. Furthermore, PCMV/PRV has been transmitted in the first pig to human heart xenotransplantation and contributed to the death of the patient. Although transmitted to the recipient, there is no evidence that PCMV/PRV can infect primate cells including human cells. PCMV/PRV is closely related to the human herpesviruses 6 and 7, and only distantly related to the human CMV (HCMV). Antiviral drugs used for the treatment of HCMV are less effective against PCMV/PRV. However, there are well described strategies to eliminate the virus from pig facilities. In order to detect the virus and to eliminate it, highly sensitive detection methods and the knowledge of how, where and when to screen the donor pigs is required. Here, a comparative testing of organs from pigs of different ages using polymerase chain reaction (PCR)-based and immunological methods was performed. Testing young piglets, PCMV/PRV was detected effectively by PCR in blood, bronchoalveolar lavage fluid, tonsils and heart. In adult animals, detection by PCR was not successful in most cases, because the virus load was below the detection limit or the virus was in its latent stage. Therefore, detection of antibodies against selected recombinant proteins corresponding to epitopes detected by nearly all infected animals in a Western blot assay is advantageous. By contrast, immunological testing is not beneficial in young animals as piglets might have PCMV/PRV-specific antibodies obtained from their infected mother via the colostrum. Using a thoughtful combination of PCR-based and immunological methods, detection of PCMV/PRV in donor pigs for xenotransplantation is feasible and a controlled elimination of the virus by early weaning or other methods is possible. |
format | Online Article Text |
id | pubmed-9747970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97479702022-12-15 How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation Halecker, S. Hansen, S. Krabben, L. Ebner, F. Kaufer, B. Denner, J. Sci Rep Article Porcine cytomegalovirus (PCMV), that is actually a porcine roseolovirus (PRV), is a common herpesvirus in domestic pigs and wild boars. In xenotransplantation, PCMV/PRV has been shown to significantly reduce the survival time of pig kidneys and hearts in preclinical trials with different non-human primates. Furthermore, PCMV/PRV has been transmitted in the first pig to human heart xenotransplantation and contributed to the death of the patient. Although transmitted to the recipient, there is no evidence that PCMV/PRV can infect primate cells including human cells. PCMV/PRV is closely related to the human herpesviruses 6 and 7, and only distantly related to the human CMV (HCMV). Antiviral drugs used for the treatment of HCMV are less effective against PCMV/PRV. However, there are well described strategies to eliminate the virus from pig facilities. In order to detect the virus and to eliminate it, highly sensitive detection methods and the knowledge of how, where and when to screen the donor pigs is required. Here, a comparative testing of organs from pigs of different ages using polymerase chain reaction (PCR)-based and immunological methods was performed. Testing young piglets, PCMV/PRV was detected effectively by PCR in blood, bronchoalveolar lavage fluid, tonsils and heart. In adult animals, detection by PCR was not successful in most cases, because the virus load was below the detection limit or the virus was in its latent stage. Therefore, detection of antibodies against selected recombinant proteins corresponding to epitopes detected by nearly all infected animals in a Western blot assay is advantageous. By contrast, immunological testing is not beneficial in young animals as piglets might have PCMV/PRV-specific antibodies obtained from their infected mother via the colostrum. Using a thoughtful combination of PCR-based and immunological methods, detection of PCMV/PRV in donor pigs for xenotransplantation is feasible and a controlled elimination of the virus by early weaning or other methods is possible. Nature Publishing Group UK 2022-12-13 /pmc/articles/PMC9747970/ /pubmed/36513687 http://dx.doi.org/10.1038/s41598-022-25624-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Halecker, S. Hansen, S. Krabben, L. Ebner, F. Kaufer, B. Denner, J. How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title | How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title_full | How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title_fullStr | How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title_full_unstemmed | How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title_short | How, where and when to screen for porcine cytomegalovirus (PCMV) in donor pigs for xenotransplantation |
title_sort | how, where and when to screen for porcine cytomegalovirus (pcmv) in donor pigs for xenotransplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747970/ https://www.ncbi.nlm.nih.gov/pubmed/36513687 http://dx.doi.org/10.1038/s41598-022-25624-1 |
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