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PMID: 11090754 Published · ppublish English Comparative Study Evaluation Study Journal Article

Analysis of human cytomegalovirus DNA in urines of newborns and infants by means of a new ultrarapid real-time PCR-system.

Schalasta G, Eggers M, Schmid M, Enders G

Abstract

Amplification techniques such as PCR are becoming increasingly popular in the field of diagnosis of human cytomegalovirus (HCMV) also, thus substituting conventional techniques like the time consuming HCMV antigen or cell culture assays. Current PCR protocols however, are labor intensive, and moreover, the need for extensive postamplification manipulations increases the risk of false positive results due to contamination with amplified products. to overcome these shortcomings, the new ultrarapid and semi-automated real-time LightCycler PCR-system (LC-PCR), which combines amplification and detection in a closed capillary system, was tested for its suitability in diagnosis of HCMV in urines. 73 urine samples from 64 newborns and infants suspected of having congenitally or postnatally acquired HCMV were tested with the LC-PCR and results were compared with those obtained in parallel with a conventional PCR-ELISA and the rapid shell vial assay for detection of HCMV early antigen (EA-assay). with these methods, 31 newborns/infants were found to be infected with HCMV. HCMV DNA was detected in 39 urines while the EA-assay was positive in 33 urines. All the EA positive samples were also positive for HCMV DNA. In the urines of the remaining 33 newborns (34 urine samples) neither HCMV DNA nor EA were detectable. The overall agreement of the two PCR tests was 100% while a 92% agreement was obtained between the PCR and the EA-assays. As the sensitivity of the three tests turned out to be quite similiar, the discrepancy observed in the positive rate between PCR and EA-assay is due to other factors which will be discussed in detail. However, while LC-PCR takes only about 2 h from sample preparation to result generation, the EA-assay, such as the conventional PCR-ELISA, needs 24-48 h. Furthermore, due to its capability to perform cycle-by-cycle monitoring, the LC instrument enables semi-quantitative analysis of HCMV viral-load. LC-PCR is a suitable new tool for routine analysis of HCMV in the urines of newborns and infants. Compared to the conventional PCR-ELISA a considerable increase in test rapidity and reliability is achieved without the need to sacrifice sensitivity.

MeSH Terms
Antigens, Viral/analysis Child, Preschool Cohort Studies Cytomegalovirus/genetics,immunology,isolation & purification Cytomegalovirus Infections/urine,virology DNA, Viral/urine Enzyme-Linked Immunosorbent Assay Fluorescence Humans Infant Infant, Newborn Polymerase Chain Reaction/methods Reagent Kits, Diagnostic Sensitivity and Specificity
Chemicals
Antigens, Viral DNA, Viral Reagent Kits, Diagnostic
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Schalasta G
Institute for Virology, Infectiology and Epidemiology and Medical Diagnostic Laboratory, Rosenbergstrasse 85, D-70193, Stuttgart, Germany. schalasta@labor-enders.de
Eggers M
Schmid M
Enders G
Article Info
Journal
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
Abbr.
J Clin Virol
ISSN
1386-6532
Published
2000-12-00
Pages
175-85
Language
English
Region
Netherlands
NLM ID
9815671
Subset
IM
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