A polymerase chain reaction (PCR) assay for the rapid detection and typing of molluscum contagiosum virus (MCV) was developed. The target DNA was a 393 base pair (bp) segment, which is present in the coding region of the MCV p43K gene product. Release of MCV DNA from skin lesions was performed by us
Simple procedure for discrimination and typing of enteric adenoviruses after detection by polymerase chain reaction
✍ Scribed by Annika Allard; Adriana Kajon; Göran Wadell
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 567 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
A procedure was developed for specific discrimination and typing of the enteric human adenoviruses, Ad40 and Ad41, after polymerase chain reaction (PCR) amplification of a sequence in the hexon gene highly conserved among all 47 sero‐types recognised. By Taq I restriction of the 300 bp amplimers, subgenus F DNA could be discriminated from DNAs of adenoviruses belonging to all other subgenera. Discrimination between Ad40 and Ad41 was subsequently achieved by cleavage with either Cfo I, HinP I, Mae III, Mvn I, and/or Rsa I. Thus, PCR detection of viral DNA combined with restriction analysis of amplified products provides a valuable tool for use in epidemiological studies of diarrhoea of adenoviral aetiology. © 1994 Wiley‐Liss, inc.
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