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Viral miRNAs in plasma and urine divulge JC polyomavirus infection
BACKGROUND: JC polyomavirus (JCPyV) is a widespread human polyomavirus that usually resides latently in its host, but can be reactivated under immune-compromised conditions potentially causing Progressive Multifocal Leukoencephalopathy (PML). JCPyV encodes its own microRNA, jcv-miR-J1. METHODS: We h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168162/ https://www.ncbi.nlm.nih.gov/pubmed/25178457 http://dx.doi.org/10.1186/1743-422X-11-158 |
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author | Lagatie, Ole Van Loy, Tom Tritsmans, Luc Stuyver, Lieven J |
author_facet | Lagatie, Ole Van Loy, Tom Tritsmans, Luc Stuyver, Lieven J |
author_sort | Lagatie, Ole |
collection | PubMed |
description | BACKGROUND: JC polyomavirus (JCPyV) is a widespread human polyomavirus that usually resides latently in its host, but can be reactivated under immune-compromised conditions potentially causing Progressive Multifocal Leukoencephalopathy (PML). JCPyV encodes its own microRNA, jcv-miR-J1. METHODS: We have investigated in 50 healthy subjects whether jcv-miR-J1-5p (and its variant jcv-miR-J1a-5p) can be detected in plasma or urine. RESULTS: We found that the overall detection rate of JCPyV miRNA was 74% (37/50) in plasma and 62% (31/50) in urine. Subjects were further categorized based on JCPyV VP1 serology status and viral shedding. In seronegative subjects, JCPyV miRNA was found in 86% (12/14) and 57% (8/14) of plasma and urine samples, respectively. In seropositive subjects, the detection rate was 69% (25/36) and 64% (23/36) for plasma and urine, respectively. Furthermore, in seropositive subjects shedding virus in urine, higher levels of urinary viral miRNAs were observed, compared to non-shedding seropositive subjects (P < 0.001). No correlation was observed between urinary and plasma miRNAs. CONCLUSION: These data indicate that analysis of circulating viral miRNAs divulge the presence of latent JCPyV infection allowing further stratification of seropositive individuals. Also, our data indicate higher infection rates than would be expected from serology alone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-422X-11-158) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4168162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41681622014-09-20 Viral miRNAs in plasma and urine divulge JC polyomavirus infection Lagatie, Ole Van Loy, Tom Tritsmans, Luc Stuyver, Lieven J Virol J Research BACKGROUND: JC polyomavirus (JCPyV) is a widespread human polyomavirus that usually resides latently in its host, but can be reactivated under immune-compromised conditions potentially causing Progressive Multifocal Leukoencephalopathy (PML). JCPyV encodes its own microRNA, jcv-miR-J1. METHODS: We have investigated in 50 healthy subjects whether jcv-miR-J1-5p (and its variant jcv-miR-J1a-5p) can be detected in plasma or urine. RESULTS: We found that the overall detection rate of JCPyV miRNA was 74% (37/50) in plasma and 62% (31/50) in urine. Subjects were further categorized based on JCPyV VP1 serology status and viral shedding. In seronegative subjects, JCPyV miRNA was found in 86% (12/14) and 57% (8/14) of plasma and urine samples, respectively. In seropositive subjects, the detection rate was 69% (25/36) and 64% (23/36) for plasma and urine, respectively. Furthermore, in seropositive subjects shedding virus in urine, higher levels of urinary viral miRNAs were observed, compared to non-shedding seropositive subjects (P < 0.001). No correlation was observed between urinary and plasma miRNAs. CONCLUSION: These data indicate that analysis of circulating viral miRNAs divulge the presence of latent JCPyV infection allowing further stratification of seropositive individuals. Also, our data indicate higher infection rates than would be expected from serology alone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1743-422X-11-158) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-02 /pmc/articles/PMC4168162/ /pubmed/25178457 http://dx.doi.org/10.1186/1743-422X-11-158 Text en © Lagatie et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lagatie, Ole Van Loy, Tom Tritsmans, Luc Stuyver, Lieven J Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title | Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title_full | Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title_fullStr | Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title_full_unstemmed | Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title_short | Viral miRNAs in plasma and urine divulge JC polyomavirus infection |
title_sort | viral mirnas in plasma and urine divulge jc polyomavirus infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168162/ https://www.ncbi.nlm.nih.gov/pubmed/25178457 http://dx.doi.org/10.1186/1743-422X-11-158 |
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