Diagnostic value of monitoring human cytomegalovirus late pp67 mRNA expression in renal-allograft recipients by nucleic acid sequence-based amplification.

M.J. Blok*, V.J. Goossens, S.J.V. Vanherle, B. Top, N. Tacken, M.J. Middeldorp, M.H. Christiaans, J.P. van Hooff, C.A.M.V.A. Bruggeman

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Department of Medical Microbiology, University Hospital Maastricht, The Netherlands. mbl@lmib.azm.nl

The diagnostic value of monitoring human cytomegalovirus (HCMV) late pp67 mRNA expression by nucleic acid sequence-based amplification (NASBA) after renal-allograft transplantation was evaluated. RNAs were isolated from 489 whole-blood specimens of 42 patients for the specific amplification of the late pp67 (UL65) mRNA. NASBA results were compared to results from the pp65 antigenemia assay, virus isolation by cell culture, and serology. The sensitivity value for NASBA proved to be higher than that for the antigenemia assay (50 versus 35%) for the detection of HCMV infection, while the sensitivity values of cell culture and NASBA were comparable (54 and 50%, respectively). NASBA detected the onset of HCMV infection simultaneously with cell culture and the antigenemia assay. Both the antigenemia assay and NASBA are very specific (100%) and highly predictive (100%) for the onset of HCMV infection. Antiviral therapy with ganciclovir resulted in negative results for cell culture, the antigenemia assay, and NASBA. In conclusion, monitoring HCMV pp67 mRNA expression by NASBA is a highly specific method for the detection of HCMV infection in renal-allograft recipients and is more sensitive than the antigenemia assay. Furthermore, NASBA can be used to monitor the progression of HCMV infections and the effect of antiviral therapy on viral activity.
Original languageEnglish
Pages (from-to)1341-1346
Number of pages6
JournalJournal of Clinical Microbiology
Volume36
Issue number5
DOIs
Publication statusPublished - 1 Jan 1998

Cite this