Affiliation:
1. Divisionof Molecular Microbiology and Development of Genetic Diagnostics,Children's Cancer ResearchInstitute
2. Department ofVirology, University Medical Centre Rotterdam, Rotterdam, TheNetherlands
3. St. AnnaKinderspital, Vienna, Austria
Abstract
ABSTRACT
A
panel of 23 real-time PCR assays based on
Taq
Man
technology has been developed for the detection and monitoring of 16
different viruses and virus families including human polyomaviruses BK
virus and JC virus, human herpesviruses 6, 7, and 8, human
adenoviruses, herpes simplex viruses 1 and 2, varicella-zoster virus,
cytomegalovirus, Epstein-Barr virus, parvovirus B19, influenza A and B
viruses, parainfluenza viruses 1 to 3, enteroviruses, and respiratory
syncytial virus. The test systems presented have a broad dynamic range
and display high sensitivity, reproducibility, and specificity.
Moreover, the assays allow precise quantification of viral load in a
variety of clinical specimens. The ability to use uniform PCR
conditions for all assays permits simultaneous processing and detection
of many different viruses, thus economizing the diagnostic work. Our
observations based on more than 50,000 assays reveal the potential of
the real-time PCR tests to facilitate early diagnosis of infection and
to monitor the kinetics of viral proliferation and the response to
treatment. We demonstrate that, in immunosuppressed patients with
invasive virus infections, surveillance by the assays described may
permit detection of increasing viral load several days to weeks prior
to the onset of clinical symptoms. In virus infections for which
specific treatment is available, the quantitative PCR assays presented
provide reliable diagnostic tools for timely initiation of appropriate
therapy and for rapid assessment of the efficacy of antiviral treatment
strategies.
Publisher
American Society for Microbiology
Cited by
262 articles.
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