Accurate laboratory tests for the diagnosis of active human herpesvirus 8 (HHV-8) infection are becoming essential to study the pathogenesis of HHV-8-associated tumors and for the clinical management of HHV-8-infected individuals. We have developed a highly sensitive, calibrated quantitative real-time PCR assay for the measurement of cell-free HHV-8 DNA in body fluids, based on the addition of a synthetic DNA calibrator prior to DNA extraction. The calibrator controls each sample for the presence of PCR inhibitors, determines a cutoff value of sensitivity for negative samples, and normalizes positive samples for the efficiency of DNA recovery. The assay shows a wide dynamic range of detection (between 1 and 106 viral genome equivalents/reaction) and a high degree of accuracy even in the presence of high amounts (up to 1 μg) of human genomic DNA. Moreover, the assay has a very high sensitivity (lower detection limit, 10 genome equivalents/ml) and a high degree of reproducibility and repeatability with a coefficient of variation (CV) of <15 and 23%, respectively. Furthermore, the use of the calibrator improves the accuracy of quantitation and decreases the intersample variability (CV, 9 and 6%, respectively). The sensitivity and specificity of the assay were tested with a series of clinical specimens obtained from patients affected by various HHV-8-related diseases, as well as from a wide number of controls. In conclusion, our calibrated real-time PCR assay provides a reliable high-throughput method for quantitation of HHV-8 DNA in clinical and laboratory specimens.

Broccolo, F., Locatelli, G., Sarmati, L., Piergiovanni, S., Veglia, F., Andreoni, M., et al. (2002). Calibrated real-time PCR assay for quantitation of human herpesvirus 8 DNA in biological fluids. JOURNAL OF CLINICAL MICROBIOLOGY, 40(12), 4652-4658 [10.1128/JCM.40.12.4652-4658.2002].

Calibrated real-time PCR assay for quantitation of human herpesvirus 8 DNA in biological fluids

SARMATI, LOREDANA;ANDREONI, MASSIMO;
2002-01-01

Abstract

Accurate laboratory tests for the diagnosis of active human herpesvirus 8 (HHV-8) infection are becoming essential to study the pathogenesis of HHV-8-associated tumors and for the clinical management of HHV-8-infected individuals. We have developed a highly sensitive, calibrated quantitative real-time PCR assay for the measurement of cell-free HHV-8 DNA in body fluids, based on the addition of a synthetic DNA calibrator prior to DNA extraction. The calibrator controls each sample for the presence of PCR inhibitors, determines a cutoff value of sensitivity for negative samples, and normalizes positive samples for the efficiency of DNA recovery. The assay shows a wide dynamic range of detection (between 1 and 106 viral genome equivalents/reaction) and a high degree of accuracy even in the presence of high amounts (up to 1 μg) of human genomic DNA. Moreover, the assay has a very high sensitivity (lower detection limit, 10 genome equivalents/ml) and a high degree of reproducibility and repeatability with a coefficient of variation (CV) of <15 and 23%, respectively. Furthermore, the use of the calibrator improves the accuracy of quantitation and decreases the intersample variability (CV, 9 and 6%, respectively). The sensitivity and specificity of the assay were tested with a series of clinical specimens obtained from patients affected by various HHV-8-related diseases, as well as from a wide number of controls. In conclusion, our calibrated real-time PCR assay provides a reliable high-throughput method for quantitation of HHV-8 DNA in clinical and laboratory specimens.
2002
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/17 - MALATTIE INFETTIVE
English
Con Impact Factor ISI
genomic DNA; virus DNA; article; body fluid; calibration; cell free system; controlled study; device; diagnostic accuracy; diagnostic value; DNA determination; DNA extraction; genome; Herpes virus infection; human; Human herpesvirus 8; major clinical study; nucleotide sequence; polymerase chain reaction; priority journal; quantitative analysis; reliability; reproducibility; sensitivity and specificity; time; virus detection; AIDS-Related Opportunistic Infections; Body Fluids; DNA Primers; DNA, Viral; Herpesviridae Infections; Herpesvirus 8, Human; Humans; Polymerase Chain Reaction; Reproducibility of Results; Sarcoma, Kaposi; Sensitivity and Specificity; Taq Polymerase; Viral Load; DNA viruses; Herpes; Herpesviridae; herpesvirus 8; Human herpesvirus 8
Broccolo, F., Locatelli, G., Sarmati, L., Piergiovanni, S., Veglia, F., Andreoni, M., et al. (2002). Calibrated real-time PCR assay for quantitation of human herpesvirus 8 DNA in biological fluids. JOURNAL OF CLINICAL MICROBIOLOGY, 40(12), 4652-4658 [10.1128/JCM.40.12.4652-4658.2002].
Broccolo, F; Locatelli, G; Sarmati, L; Piergiovanni, S; Veglia, F; Andreoni, M; Butto, S; Ensoli, B; Lusso, P; Malnati, Ms
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/49478
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