Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lagatie, Ole, Van Loy, Tom, Tritsmans, Luc, Stuyver, Lieven J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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
_version_ 1782335500891193344
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
work_keys_str_mv AT lagatieole viralmirnasinplasmaandurinedivulgejcpolyomavirusinfection
AT vanloytom viralmirnasinplasmaandurinedivulgejcpolyomavirusinfection
AT tritsmansluc viralmirnasinplasmaandurinedivulgejcpolyomavirusinfection
AT stuyverlievenj viralmirnasinplasmaandurinedivulgejcpolyomavirusinfection