Journal of Clinical Virology
Volume 29, Issue 3 , Pages 171-178, March 2004

Automated detection of five human herpes virus DNAs by a set of LightCycler PCRs complemented with a single multiple internal control

Department of Laboratory Medicine (Zentral-Labor), Institute of Laboratory Medicine, General Hospital Linz, Allgemeines Krankenhaus, Krankenhausstrasse 9, A-4020 Linz, Austria

Received 25 February 2003; received in revised form 5 May 2003; accepted 6 May 2003.

Abstract 

Background: Herpes viruses represent important causes of morbidity and mortality especially in immuno-compromised patients. To assist in rapid diagnosis real-time PCR assays have been developed for the detection of herpes virus DNA in patient specimens. A recently described set of real-time PCR assays using LightCycler technology enabled parallel detection of DNA from cytomegalovirus (CMV), Epstein–Barr virus (EBV), herpes simplex virus type 1 and 2 (HSV-1/-2), and varicella-zoster virus (VZV) by using a single LightCycler program [J. Clin. Virol. 26 (2003) 85]. The set of assays lacked automation of DNA purification and of PCR mixture preparation, and was not furnished with measures to monitor for sample adequacy. Objectives: Development of a set of automated LightCycler-PCR assays for the detection CMV-, EBV-, HSV-1/-2- and VZV-DNA in plasma samples and complementation of the assays with internal amplification controls (ICs). Study design: The MagNA Pure LC instrument was used for automated DNA purification and automated preparation of PCR mixtures. A single multiple IC-DNA specific for all four herpes virus type-specific PCRs was generated and used in all four LightCycler assays. Detection limits were determined and clinical samples were evaluated. Results: With quantified herpes virus type-specific reference DNA spiked into EDTA plasma, the detection limits were found at 250 copies/ml of CMV-, EBV-, HSV-1/-2-DNA and at 500 copies/ml of VZV-DNA. The novel set of assays was evaluated by testing 112 EDTA plasma samples. The use of the IC led to the detection of PCR-inhibited samples. Conclusion: The set of automated LightCycler assays was found rapid, markedly labour saving and suitable for the routine diagnostic laboratory. The use of the one internal control molecule simplified the assay protocol and allowed monitoring for sample adequacy.

Keywords:  Cytomegalovirus (CMV), Epstein–Barr virus (EBV), Herpes simplex virus (HSV), Varicella-zoster virus (VZV), Real-time PCR, Internal control, MagnaPure LC, LightCycler

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PII: S1386-6532(03)00121-5

doi:10.1016/S1386-6532(03)00121-5

Journal of Clinical Virology
Volume 29, Issue 3 , Pages 171-178, March 2004