A PCR based DNA hybridisation capture system for the detection of human cytomegalovirus. A comparative study with other identification methods.

Abstract:

:A simple, sensitive and specific colourimetric hybridisation method for the detection of HCMV DNA in clinical specimens is described. This method combines a PCR assay with a sensitive sandwich hybridisation assay. It relies on the use of a specific capture probe linked covalently to polystyrene microplates and a specific polybiotinylated detection probe. Amplified DNA fragments, sandwiched between these two probes, are detected by an enzymatic colour reaction. This PCR-based colourimetric hybridisation method was compared with other known HCMV detection methods. Clinical specimens (n = 145, corresponding to 106 patients) were tested by both a nested PCR assay and this colourimetric hybridisation method; and by either the culture method or the pp65 antigenaemia test depending on the type of sample used. The results showed that the PCR-based hybridisation method has a specificity similar to tissue culture, known as the conventional gold standard method, and could be used for the examination of the clinical specimens.

journal_name

J Virol Methods

authors

Mansy F,Brancart F,Liesnard C,Bollen A,Godfroid E

doi

10.1016/s0166-0934(99)00023-3

subject

Has Abstract

pub_date

1999-07-01 00:00:00

pages

113-22

issue

2

eissn

0166-0934

issn

1879-0984

pii

S0166093499000233

journal_volume

80

pub_type

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