Viral miRNAs in plasma and urine divulge JC polyomavirus infection

被引:37
作者
Lagatie, Ole [1 ]
Van Loy, Tom [1 ]
Tritsmans, Luc [2 ]
Stuyver, Lieven J. [1 ]
机构
[1] Janssen Diagnost, B-2340 Beerse, Belgium
[2] Janssen Res & Dev, B-2340 Beerse, Belgium
关键词
JC Polyomavirus; Viral microRNA; Circulating microRNA; Progressive Multifocal Leukoencephalopathy; Biomarker; Viral activity; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; VIRUS-DNA; BK-VIRUS; MICRORNAS; BLOOD; ANTIBODY; PREVALENCE; RISK; PML; REPLICATION;
D O I
10.1186/1743-422X-11-158
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:9
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