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Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors
Merkel cell polyomavirus (MCPyV) has been detected in 80% of Merkel cell carcinomas (MCC). In the host, the MCPyV reservoir remains elusive. MCPyV DNA sequences were revealed in blood donor buffy coats. In this study, MCPyV DNA sequences were investigated in the sera (n = 190) of healthy blood donor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712532/ https://www.ncbi.nlm.nih.gov/pubmed/29238698 http://dx.doi.org/10.3389/fonc.2017.00294 |
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author | Mazzoni, Elisa Rotondo, John C. Marracino, Luisa Selvatici, Rita Bononi, Ilaria Torreggiani, Elena Touzé, Antoine Martini, Fernanda Tognon, Mauro G. |
author_facet | Mazzoni, Elisa Rotondo, John C. Marracino, Luisa Selvatici, Rita Bononi, Ilaria Torreggiani, Elena Touzé, Antoine Martini, Fernanda Tognon, Mauro G. |
author_sort | Mazzoni, Elisa |
collection | PubMed |
description | Merkel cell polyomavirus (MCPyV) has been detected in 80% of Merkel cell carcinomas (MCC). In the host, the MCPyV reservoir remains elusive. MCPyV DNA sequences were revealed in blood donor buffy coats. In this study, MCPyV DNA sequences were investigated in the sera (n = 190) of healthy blood donors. Two MCPyV DNA sequences, coding for the viral oncoprotein large T antigen (LT), were investigated using polymerase chain reaction (PCR) methods and DNA sequencing. Circulating MCPyV sequences were detected in sera with a prevalence of 2.6% (5/190), at low-DNA viral load, which is in the range of 1–4 and 1–5 copies/μl by real-time PCR and droplet digital PCR, respectively. DNA sequencing carried out in the five MCPyV-positive samples indicated that the two MCPyV LT sequences which were analyzed belong to the MKL-1 strain. Circulating MCPyV LT sequences are present in blood donor sera. MCPyV-positive samples from blood donors could represent a potential vehicle for MCPyV infection in receivers, whereas an increase in viral load may occur with multiple blood transfusions. In certain patient conditions, such as immune-depression/suppression, additional disease or old age, transfusion of MCPyV-positive samples could be an additional risk factor for MCC onset. |
format | Online Article Text |
id | pubmed-5712532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57125322017-12-13 Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors Mazzoni, Elisa Rotondo, John C. Marracino, Luisa Selvatici, Rita Bononi, Ilaria Torreggiani, Elena Touzé, Antoine Martini, Fernanda Tognon, Mauro G. Front Oncol Oncology Merkel cell polyomavirus (MCPyV) has been detected in 80% of Merkel cell carcinomas (MCC). In the host, the MCPyV reservoir remains elusive. MCPyV DNA sequences were revealed in blood donor buffy coats. In this study, MCPyV DNA sequences were investigated in the sera (n = 190) of healthy blood donors. Two MCPyV DNA sequences, coding for the viral oncoprotein large T antigen (LT), were investigated using polymerase chain reaction (PCR) methods and DNA sequencing. Circulating MCPyV sequences were detected in sera with a prevalence of 2.6% (5/190), at low-DNA viral load, which is in the range of 1–4 and 1–5 copies/μl by real-time PCR and droplet digital PCR, respectively. DNA sequencing carried out in the five MCPyV-positive samples indicated that the two MCPyV LT sequences which were analyzed belong to the MKL-1 strain. Circulating MCPyV LT sequences are present in blood donor sera. MCPyV-positive samples from blood donors could represent a potential vehicle for MCPyV infection in receivers, whereas an increase in viral load may occur with multiple blood transfusions. In certain patient conditions, such as immune-depression/suppression, additional disease or old age, transfusion of MCPyV-positive samples could be an additional risk factor for MCC onset. Frontiers Media S.A. 2017-11-29 /pmc/articles/PMC5712532/ /pubmed/29238698 http://dx.doi.org/10.3389/fonc.2017.00294 Text en Copyright © 2017 Mazzoni, Rotondo, Marracino, Selvatici, Bononi, Torreggiani, Touzé, Martini and Tognon. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Mazzoni, Elisa Rotondo, John C. Marracino, Luisa Selvatici, Rita Bononi, Ilaria Torreggiani, Elena Touzé, Antoine Martini, Fernanda Tognon, Mauro G. Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title | Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title_full | Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title_fullStr | Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title_full_unstemmed | Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title_short | Detection of Merkel Cell Polyomavirus DNA in Serum Samples of Healthy Blood Donors |
title_sort | detection of merkel cell polyomavirus dna in serum samples of healthy blood donors |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712532/ https://www.ncbi.nlm.nih.gov/pubmed/29238698 http://dx.doi.org/10.3389/fonc.2017.00294 |
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