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Measurement of Epstein-Barr virus DNA load using a novel quantification standard containing two EBV DNA targets and SYBR Green I dye

dc.contributor.authorLay, Meav-Lang J
dc.contributor.authorLucas, Robyn
dc.contributor.authorRatnamohan, Mala
dc.contributor.authorTaylor, Janette
dc.contributor.authorPonsonby, Anne-Louise
dc.contributor.authorDwyer, Dominic E
dc.contributor.authorAusimmune Investigator Group (AIG)
dc.date.accessioned2016-01-12T02:39:09Z
dc.date.available2016-01-12T02:39:09Z
dc.date.issued2010-09-22
dc.date.updated2016-02-24T11:16:26Z
dc.description.abstractBACKGROUND Reactivation of Epstein-Barr virus (EBV) infection may cause serious, life-threatening complications in immunocompromised individuals. EBV DNA is often detected in EBV-associated disease states, with viral load believed to be a reflection of virus activity. Two separate real-time quantitative polymerase chain reaction (QPCR) assays using SYBR Green I dye and a single quantification standard containing two EBV genes, Epstein-Barr nuclear antigen-1 (EBNA-1) and BamHI fragment H rightward open reading frame-1 (BHRF-1), were developed to detect and measure absolute EBV DNA load in patients with various EBV-associated diseases. EBV DNA loads and viral capsid antigen (VCA) IgG antibody titres were also quantified on a population sample. RESULTS EBV DNA was measurable in ethylenediaminetetraacetic acid (EDTA) whole blood, peripheral blood mononuclear cells (PBMCs), plasma and cerebrospinal fluid (CSF) samples. EBV DNA loads were detectable from 8.0 × 10² to 1.3 × 10⁸ copies/ml in post-transplant lymphoproliferative disease (n = 5), 1.5 × 10³ to 2.0 × 10⁵ copies/ml in infectious mononucleosis (n = 7), 7.5 × 10⁴ to 1.1 × 10⁵ copies/ml in EBV-associated haemophagocytic syndrome (n = 1), 2.0 × 10² to 5.6 × 10³ copies/ml in HIV-infected patients (n = 12), and 2.0 × 10² to 9.1 × 10⁴ copies/ml in the population sample (n = 218). EBNA-1 and BHRF-1 DNA were detected in 11.0% and 21.6% of the population sample respectively. There was a modest correlation between VCA IgG antibody titre and BHRF-1 DNA load (rho = 0.13, p = 0.05) but not EBNA-1 DNA load (rho = 0.11, p = 0.11). CONCLUSION Two sensitive and specific real-time PCR assays using SYBR Green I dye and a single quantification standard containing two EBV DNA targets, were developed for the detection and measurement of EBV DNA load in a variety of clinical samples. These assays have application in the investigation of EBV-related illnesses in immunocompromised individuals.
dc.description.sponsorshipThe Ausimmune Study is funded by the National Multiple Sclerosis Society of the USA, the National Health & Medical Research Council (Project Grant 316901) and Multiple Sclerosis Research Australia.en_AU
dc.identifier.issn1743-422Xen_AU
dc.identifier.urihttp://hdl.handle.net/1885/95324
dc.publisherBioMed Central
dc.rights© Lay et al. 2010 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/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceVirology Journal
dc.subjectadolescent
dc.subjectadult
dc.subjectantibodies, viral
dc.subjectblood
dc.subjectcerebrospinal fluid
dc.subjectepstein-barr virus infections
dc.subjectfemale
dc.subjectherpesvirus 4, human
dc.subjecthumans
dc.subjectimmunoglobulin g
dc.subjectleukocytes, mononuclear
dc.subjectmale
dc.subjectmiddle aged
dc.subjectorganic chemicals
dc.subjectplasma
dc.subjectreference standards
dc.subjectsensitivity and specificity
dc.subjectstaining and labeling
dc.subjectviral load
dc.subjectyoung adult
dc.titleMeasurement of Epstein-Barr virus DNA load using a novel quantification standard containing two EBV DNA targets and SYBR Green I dye
dc.typeJournal article
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage252en_AU
local.contributor.affiliationLay, Meav-Lang, Westmead Hospital, Australiaen_AU
local.contributor.affiliationLucas, Robyn, College of Medicine, Biology and Environment, CMBE Research School of Population Health, Natl Centre for Epidemiology & Population Health, The Australian National Universityen_AU
local.contributor.affiliationRatnamohan, Mala, Institute of Clinical Pathology & Medical Research, Australiaen_AU
local.contributor.affiliationTaylor, Janet L, University of Sydney, Australiaen_AU
local.contributor.affiliationPonsonby, Anne-Louise, Murdoch Children's Research Institute, Australiaen_AU
local.contributor.affiliationDwyer, Dominic, University of Sydney, Australiaen_AU
local.contributor.authoruidu4002313en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor111706en_AU
local.identifier.ariespublicationu4637548xPUB164en_AU
local.identifier.citationvolume7en_AU
local.identifier.doi10.1186/1743-422X-7-252en_AU
local.identifier.essn1743-422Xen_AU
local.identifier.scopusID2-s2.0-77956858734
local.identifier.thomsonID000283422700001
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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