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Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients
Human Polyomavirus (HPyV) infections are common, ranging from 60% to 100%. In kidney transplant (KTx) recipients, HPyVs have been associated with allograft nephropathy, progressive multifocal leukoencephalopathy, and skin cancer. Whether such complications are caused by viral reactivation or primary...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696855/ https://www.ncbi.nlm.nih.gov/pubmed/33182443 http://dx.doi.org/10.3390/v12111280 |
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author | Signorini, Lucia Dolci, Maria Favi, Evaldo Colico, Caterina Ferraresso, Mariano Ticozzi, Rosalia Basile, Giuseppe Ferrante, Pasquale Delbue, Serena |
author_facet | Signorini, Lucia Dolci, Maria Favi, Evaldo Colico, Caterina Ferraresso, Mariano Ticozzi, Rosalia Basile, Giuseppe Ferrante, Pasquale Delbue, Serena |
author_sort | Signorini, Lucia |
collection | PubMed |
description | Human Polyomavirus (HPyV) infections are common, ranging from 60% to 100%. In kidney transplant (KTx) recipients, HPyVs have been associated with allograft nephropathy, progressive multifocal leukoencephalopathy, and skin cancer. Whether such complications are caused by viral reactivation or primary infection transmitted by the donor remains debated. This study aimed to investigate the replication pattern and genomic characterization of BK Polyomavirus (BKPyV), JC Polyomavirus (JCPyV), and Merkel Cell Polyomavirus (MCPyV) infections in KTx. Urine samples from 57 KTx donor/recipient pairs were collected immediately before organ retrieval/transplant and periodically up to post-operative day 540. Specimens were tested for the presence of BKPyV, JCPyV, and MCPyV genome by virus-specific Real-Time PCR and molecularly characterized. HPyVs genome was detected in 49.1% of donors and 77.2% of recipients. Sequences analysis revealed the archetypal strain for JCPyV, TU and Dunlop strains for BKPyV, and IIa-2 strain for MCPyV. VP1 genotyping showed a high frequency for JCPyV genotype 1 and BKPyV genotype I. Our experience demonstrates that after KTx, HPyVs genome remains stable over time with no emergence of quasi-species. HPyVs strains isolated in donor/recipient pairs are mostly identical, suggesting that viruses detected in the recipient may be transmitted by the allograft. |
format | Online Article Text |
id | pubmed-7696855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76968552020-11-29 Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients Signorini, Lucia Dolci, Maria Favi, Evaldo Colico, Caterina Ferraresso, Mariano Ticozzi, Rosalia Basile, Giuseppe Ferrante, Pasquale Delbue, Serena Viruses Article Human Polyomavirus (HPyV) infections are common, ranging from 60% to 100%. In kidney transplant (KTx) recipients, HPyVs have been associated with allograft nephropathy, progressive multifocal leukoencephalopathy, and skin cancer. Whether such complications are caused by viral reactivation or primary infection transmitted by the donor remains debated. This study aimed to investigate the replication pattern and genomic characterization of BK Polyomavirus (BKPyV), JC Polyomavirus (JCPyV), and Merkel Cell Polyomavirus (MCPyV) infections in KTx. Urine samples from 57 KTx donor/recipient pairs were collected immediately before organ retrieval/transplant and periodically up to post-operative day 540. Specimens were tested for the presence of BKPyV, JCPyV, and MCPyV genome by virus-specific Real-Time PCR and molecularly characterized. HPyVs genome was detected in 49.1% of donors and 77.2% of recipients. Sequences analysis revealed the archetypal strain for JCPyV, TU and Dunlop strains for BKPyV, and IIa-2 strain for MCPyV. VP1 genotyping showed a high frequency for JCPyV genotype 1 and BKPyV genotype I. Our experience demonstrates that after KTx, HPyVs genome remains stable over time with no emergence of quasi-species. HPyVs strains isolated in donor/recipient pairs are mostly identical, suggesting that viruses detected in the recipient may be transmitted by the allograft. MDPI 2020-11-09 /pmc/articles/PMC7696855/ /pubmed/33182443 http://dx.doi.org/10.3390/v12111280 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Signorini, Lucia Dolci, Maria Favi, Evaldo Colico, Caterina Ferraresso, Mariano Ticozzi, Rosalia Basile, Giuseppe Ferrante, Pasquale Delbue, Serena Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title | Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title_full | Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title_fullStr | Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title_full_unstemmed | Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title_short | Viral Genomic Characterization and Replication Pattern of Human Polyomaviruses in Kidney Transplant Recipients |
title_sort | viral genomic characterization and replication pattern of human polyomaviruses in kidney transplant recipients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696855/ https://www.ncbi.nlm.nih.gov/pubmed/33182443 http://dx.doi.org/10.3390/v12111280 |
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