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通过聚合酶链反应产物的直接测序对临床标本中的BK病毒进行基因分型。

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

作者信息

Jin L, Gibson P E, Booth J C, Clewley J P

机构信息

Virus Reference Division, Central Public Health Laboratory, London, England.

出版信息

J Med Virol. 1993 Sep;41(1):11-7. doi: 10.1002/jmv.1890410104.

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. Twenty-eight 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.

摘要

使用聚合酶链反应(PCR)检测BK病毒(BKV)的VP1区域,对来自几个临床组的212份尿液标本进行了检测。44名移植后患者的14份标本(31.8%)、39名孕妇的10份标本(25.6%)和100名儿童的5份标本(5%)检测结果呈阳性,而29名实验室工作人员的任何标本检测结果均为阴性。对28个扩增的BKV基因组进行了直接测序,其中19个来自尿液标本,8个来自接种组织的培养液,还有1个来自咽洗液,这些基因组通过生物素化引物固定在单链模板上;可以将所有这些基因组归为先前根据VP1区域核苷酸序列变异确定的BKV四种亚型之一。21株分离株的血清学亚组分类与基因组亚型分析结果相关。本文讨论了BKV亚型的分布以及受感染个体的临床状况。

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