𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genomic typing of BK virus in clinical specimens by direct sequencing of polymerase chain reaction products

✍ Scribed by Li Jin; Patricia E. Gibson; James C. Booth; Jonathan P. Clewley


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
636 KB
Volume
41
Category
Article
ISSN
0146-6615

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Two hundred and twelve urine specimens, from several clinical groups, were examined for BK virus (BKV) using the polymerase chain reaction (PCR) to detect the VP1 region of BKV DNA. Positive results were obtained on 14 specimens from 44 post‐transplant patients (31.8%), 10 specimens from 39 pregnant women (25.6%), and 5 specimens from 100 children (5%) but not on any specimens from 29 laboratory staff. Twentyeight of the amplified BKV genomes, 19 from urine specimens, eight from culture fluid of inoculated tissue, and also one from a throat washing were directly sequenced from single‐stranded templates immobilized via a biotinylated primer; it was possible to assign all to one of the four subtypes of BKV which had previously been identified on the basis of variation in nucleotide sequence of the VP1 region. Serological subgroup classification correlated with the genomic subtyping results in 21 of the isolates. The distribution of the BKV subtypes and the clinical status of the infected individuals are discussed.


πŸ“œ SIMILAR VOLUMES


Identification and typing of molluscum c
✍ Thompson, Carol H. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 319 KB πŸ‘ 1 views

A polymerase chain reaction (PCR) which enables the detection of molluscum contagiosum virus (MCV) genomes in either fresh or formalinfixed clinical specimens is described. The primers used were designed to amplify a 167 bp region of the 3.8kbp HindIII fragment K of the MCV 1 genome. The ability of

Typing of hepatitis B virus genomes by a
✍ Helene Norder; Berit Hammas; Lars O. Magnius πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 710 KB

## Abstract The amplification of hepatitis B virus (HBV) DNA sequences in sera for molecular epidemiology of HBV is an important application of the polymerase chain reaction (PCR) with regard to HBV. To simplify the PCR for this purpose, the optimal concentrations of SDS and detergents for carrying

Nested polymerase chain reaction for det
✍ Maurizio Zazzi; Laura Romano; Agostina Brasini; Pier Egisto Valensin πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 345 KB

## Abstract A highly sensitive two‐step polymerase chain reaction (PCR) method was evaluated for detection of human immunodeficiency virus type 1 (HIV‐1) DNA in clinical specimens. The product resulting from the first amplification reaction is used as the template for the second PCR with an interna

Evaluation of a multiple peptide assay f
✍ Zhu-Xu Zhang; Zhi-Bing Yun; Margaret Chen; Anders SΓΆnnerborg; Matti SΓ€llberg πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 628 KB

A panel of 16 type-specific synthetic peptides corresponding to variable antigenic regions within the hepatitis C virus (HCV) core, nonstruc-tural4 (NS4), and NS5 proteins was synthesised. The peptide panel was used to develop an enzyme immunoassay (EIA) for the detection of antibodies directed to H

Detection of human immunodeficiency viru
✍ Patrizia Bagnarelli; Stefano Menzo; Aldo Manzin; Mauro Giacca; Pietro Emanuele V πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 762 KB

An application of the polymerase chain reaction (PCR) to the direct detection of human immunodeficiency virus type 1 (HIV-1) viremia is described. The amplification of specific HIV-1 sequences of gag and env viral genes was carried out after the reverse-transcription of plasma samples (plasma RT-PCR