Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd

Previously a strategy for monitoring of pigs intended for cell transplantation was developed and successfully applied to several representative herds in New Zealand. A designated pathogen-free (DPF) herd has been chosen as a good candidate for xenotransplantation. This herd has previously tested fre...

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Main Authors: O. Garkavenko, S. Wynyard, D. Nathu, D. Simond, M. Muzina, Z. Muzina, L. Scobie, R. D. Hector, M. C. Croxson, P. Tan, B. R. Elliott
Format: Article
Language:English
Published: SAGE Publishing 2008-12-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368908787648056
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spelling doaj-45d75c44c33a41a5bd900f4f50ae04502020-11-25T03:03:21ZengSAGE PublishingCell Transplantation0963-68971555-38922008-12-011710.3727/096368908787648056Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free HerdO. Garkavenko0S. Wynyard1D. Nathu2D. Simond3M. Muzina4Z. Muzina5L. Scobie6R. D. Hector7M. C. Croxson8P. Tan9B. R. Elliott10Living Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandCentre for Transplantation & Renal Research, Westmead Millennium Institute, Westmead Hospital, AustraliaLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandDepartment of Biological and Biomedical Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UKDepartment of Biological and Biomedical Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UKVirology Immunology Department, Auckland Hospital, Auckland, New ZealandLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandLiving Cell Technologies Ltd, Manukau 2025, Auckland, New ZealandPreviously a strategy for monitoring of pigs intended for cell transplantation was developed and successfully applied to several representative herds in New Zealand. A designated pathogen-free (DPF) herd has been chosen as a good candidate for xenotransplantation. This herd has previously tested free of infectious agents relevant to xenotransplantation and we present here an in depth study of porcine endogenous retrovirus (PERV) transmission. A panel of assays that describes the constraints for the transmission of PERV has been suggested. It includes a) infectivity test in coculture of DPF pig primary cells with both human and pig target cell lines; b) RT activity in supernatant of stimulated primary cells from DPF pigs; c) viral load in donor's blood plasma; d) PERV proviral copy number in DPF pig genome; e) PERV class C prevalence in the herd and its recombination potential. There was no evidence of PERV transmission from DPF pig tissue to either pig or human cells. Additionally, there was no evidence of PERV RNA present in pig blood plasma. PERV copy number differs in individual pigs from as low as 3 copies to 30 copies and the presence of PERV-C varied between animals and breeds. In all DPF pigs tested, a specific locus for PERV-C potentially associated with the recombination of PERV in miniature swine was absent. Presented data on the PERV transmission allows us to classify the DPF potential donors as “null” or noninfectious pigs.https://doi.org/10.3727/096368908787648056
collection DOAJ
language English
format Article
sources DOAJ
author O. Garkavenko
S. Wynyard
D. Nathu
D. Simond
M. Muzina
Z. Muzina
L. Scobie
R. D. Hector
M. C. Croxson
P. Tan
B. R. Elliott
spellingShingle O. Garkavenko
S. Wynyard
D. Nathu
D. Simond
M. Muzina
Z. Muzina
L. Scobie
R. D. Hector
M. C. Croxson
P. Tan
B. R. Elliott
Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
Cell Transplantation
author_facet O. Garkavenko
S. Wynyard
D. Nathu
D. Simond
M. Muzina
Z. Muzina
L. Scobie
R. D. Hector
M. C. Croxson
P. Tan
B. R. Elliott
author_sort O. Garkavenko
title Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
title_short Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
title_full Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
title_fullStr Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
title_full_unstemmed Porcine Endogenous Retrovirus (PERV) and its Transmission Characteristics: A Study of the New Zealand Designated Pathogen-Free Herd
title_sort porcine endogenous retrovirus (perv) and its transmission characteristics: a study of the new zealand designated pathogen-free herd
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2008-12-01
description Previously a strategy for monitoring of pigs intended for cell transplantation was developed and successfully applied to several representative herds in New Zealand. A designated pathogen-free (DPF) herd has been chosen as a good candidate for xenotransplantation. This herd has previously tested free of infectious agents relevant to xenotransplantation and we present here an in depth study of porcine endogenous retrovirus (PERV) transmission. A panel of assays that describes the constraints for the transmission of PERV has been suggested. It includes a) infectivity test in coculture of DPF pig primary cells with both human and pig target cell lines; b) RT activity in supernatant of stimulated primary cells from DPF pigs; c) viral load in donor's blood plasma; d) PERV proviral copy number in DPF pig genome; e) PERV class C prevalence in the herd and its recombination potential. There was no evidence of PERV transmission from DPF pig tissue to either pig or human cells. Additionally, there was no evidence of PERV RNA present in pig blood plasma. PERV copy number differs in individual pigs from as low as 3 copies to 30 copies and the presence of PERV-C varied between animals and breeds. In all DPF pigs tested, a specific locus for PERV-C potentially associated with the recombination of PERV in miniature swine was absent. Presented data on the PERV transmission allows us to classify the DPF potential donors as “null” or noninfectious pigs.
url https://doi.org/10.3727/096368908787648056
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