In situ hybridisation with digoxigenin-labelled DNA probes for detection of viral genomes.

Abstract:

:The applicability of a recently developed non-radioactive DNA labelling and detection method, which uses the digoxigenin (DIG) enzyme linked immunosorbent assay (ELISA) system, for the detection of viral infections in pathology specimens by in situ hybridisation, was examined. Its efficacy was compared with that of biotin and radioisotope labelling methods. Three cases of progressive multifocal leucoencephalopathy, two of verruca vulgaris, and seven cases of laryngeal papilloma were studied. The sensitivity of the DIG labelled probe was almost the same as that of a 35S-labelled probe in the dot-blot hybridisation test. Using in situ hybridisation with 35S-labelled and DIG labelled probes, the levels of the hybridised signals detected were similar. The biotin labelled probe was less sensitive, particularly in the cases of laryngeal papilloma. The DIG labelling and detection method was highly sensitive and applicable to the detection of viral infection by ISH, and is preferable to a radiolabelled probe, especially when in situ hybridisation is done in the pathology laboratory.

journal_name

J Clin Pathol

authors

Furuta Y,Shinohara T,Sano K,Meguro M,Nagashima K

doi

10.1136/jcp.43.10.806

subject

Has Abstract

pub_date

1990-10-01 00:00:00

pages

806-9

issue

10

eissn

0021-9746

issn

1472-4146

journal_volume

43

pub_type

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