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Journal of Clinical Microbiology, July 2003, p. 3167-3174, Vol. 41, No. 7
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.7.3167-3174.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Comparison of LightCycler-Based PCR, COBAS Amplicor CMV Monitor, and pp65 Antigenemia Assays for Quantitative Measurement of Cytomegalovirus Viral Load in Peripheral Blood Specimens from Patients after Solid Organ Transplantation

Xiaoli L. Pang, Linda Chui, Jayne Fenton, Barbara LeBlanc, and Jutta K. Preiksaitis*

Provincial Laboratory for Public Health (Microbiology), University of Alberta Hospital, University of Alberta, Edmonton, Alberta T6G 2J2, Canada

Received 15 November 2002/ Returned for modification 19 March 2003/ Accepted 7 April 2003

In order to evaluate the LightCycler-based PCR (LC-PCR) as a diagnostic assay technique, a classical pp65 antigenemia assay and the commercially available COBAS Amplicor CMV Monitor (CACM) assay were compared to the LC-PCR assay for the detection and quantitation of cytomegalovirus (CMV) load in 404 parallel specimens of peripheral blood from 66 patients after solid organ transplantation. A good correlation existed among these three assays (r {cong} 0.6, P < 0.0001). The LC-PCR assay was the most sensitive (54% of specimens positive) compared to the CACM (48.6%) and the pp65 antigenemia (26%) assays. The LC-PCR assay detected all samples found positive by using both the CMV pp65 antigenemia assay and the CACM assay. The LC-PCR also had the widest dynamic range (from 250 to 107 DNA copies/ml of plasma). No cross-reactions were found among CMV and Epstein-Barr virus, varicella-zoster virus, or herpes simplex virus in the LC-PCR by using amplification with specifically designed primer pairs. Precision, expressed as the coefficient of variation, was <3% with standard DNA from cell cultures and between 6.55 and 14.1% with clinical specimens in repeat LC-PCR runs. One run of the LC-PCR took half of the time required for the semiautomated CACM procedure. Because of its sensitivity, specificity, cost-effectiveness, and simplicity, the LC-PCR assay could replace the pp65 antigenemia and the CACM assays as the preferred technique for the surveillance, diagnosis, and monitoring of response of CMV diseases in high-risk populations.

* Corresponding author. Mailing address: Provincial Laboratory for Public Health (Microbiology), University of Alberta Hospital, WMC 1B1.22, 8440-112 St., Edmonton, AB T6G 2J2, Canada. Phone: (780) 407-8903. Fax: (780) 407-8984. E-mail: J.Preiksaitis{at}provlab.ab.ca.

Journal of Clinical Microbiology, July 2003, p. 3167-3174, Vol. 41, No. 7
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.7.3167-3174.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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