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Hcmv-miR-UL22A-5p: A Biomarker in Transplantation With Broad Impact on Host Gene Expression and Potential Immunological Implications
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4379028
Author(s) Lisboa, L. F.; Egli, A.; O'Shea, D.; Asberg, A.; Hartmann, A.; Rollag, H.; Pang, X. L.; Tyrrell, D. L.; Kumar, D.; Humar, A.
Author(s) at UniBasel Egli, Adrian
Year 2015
Title Hcmv-miR-UL22A-5p: A Biomarker in Transplantation With Broad Impact on Host Gene Expression and Potential Immunological Implications
Journal Am J Transplant
Volume 15
Number 7
Pages / Article-Number 1893-902
Keywords Biomarkers; Blotting, Western; Cohort Studies; Computational Biology; Cytomegalovirus/*genetics; Cytomegalovirus Infections/blood/*genetics/virology; Follow-Up Studies; *Gene Expression Profiling; *Gene Expression Regulation, Viral; Graft Rejection; Graft Survival; Host-Pathogen Interactions/*genetics/immunology; Humans; Immunoprecipitation; MicroRNAs/blood/*genetics; *Organ Transplantation; Prognosis; RNA, Viral/blood/genetics; Real-Time Polymerase Chain Reaction; Recurrence; Risk Factors; Virus Replication; infection and infectious agents; infectious disease; molecular biology: micro RNA; molecular biology: transcription factor; translational research / science; viral: Cytomegalovirus (CMV)
Mesh terms Biomarkers; Blotting, Western; Cohort Studies; Computational Biology; Cytomegalovirus, genetics; Cytomegalovirus Infections, virology; Follow-Up Studies; Gene Expression Profiling; Gene Expression Regulation, Viral; Graft Rejection; Graft Survival; Host-Pathogen Interactions, immunology; Humans; Immunoprecipitation; MicroRNAs, genetics; Organ Transplantation; Prognosis; RNA, Viral, genetics; Real-Time Polymerase Chain Reaction; Recurrence; Risk Factors; Virus Replication
Abstract Cytomegalovirus (CMV) encodes multiple microRNAs. While these have been partially characterized in vitro, their relevance to clinical CMV infection has not been evaluated. We analyzed samples from a cohort of solid organ transplant patients with CMV disease (n = 245) for viral microRNA expression. Several CMV microRNAs were readily detectable in patients with CMV disease in variable relative abundance. Expression level generally correlated with DNA viral load and the absence of viral microRNA was associated with faster viral clearance. Detection of hcmv-miR-UL22A-5p at baseline independently predicted the recurrence of CMV viremia upon discontinuation of antiviral therapy (OR 3.024, 95% CI: 1.35-6.8; p = 0.007). A combination of direct mRNA targeting by the microRNA and indirect modulation of gene expression involving isoforms of the transcriptional regulator C-MYC may be responsible for the broad effects seen in the association of gene transcripts with the RNA-induced silencing complex and in global protein expression upon hcmv-miR-UL22A-5p transfection. This novel study of in vivo viral microRNA expression profiles provides unique insight into the complexity of clinical CMV infection following transplantation. We provide evidence that viral microRNAs may have complex effects on gene expression and be associated with specific virologic and clinical outcomes, and thus could be further evaluated as biomarkers.
Publisher WILEY
ISSN/ISBN 1600-6143
edoc-URL https://edoc.unibas.ch/61730/
Full Text on edoc No
Digital Object Identifier DOI 10.1111/ajt.13222
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/25833298
ISI-Number WOS:000356494300025
Document type (ISI) Journal Article, Multicenter Study, Randomized Controlled Trial
 
   

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