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采用多重实时 PCR 检测法对天花、猴痘、牛痘和痘苗病毒进行种特异性鉴定。

Species-specific identification of variola, monkeypox, cowpox, and vaccinia viruses by multiplex real-time PCR assay.

机构信息

State Research Center of Virology and Biotechnology VECTOR, Koltsovo, Novosibirsk Region 630559, Russia.

出版信息

J Virol Methods. 2011 Aug;175(2):163-9. doi: 10.1016/j.jviromet.2011.05.002. Epub 2011 May 27.

Abstract

A method of one-stage rapid identification of variola (VARV), monkeypox (MPXV), cowpox (CPXV), and vaccinia (VACV) viruses, pathogenic for humans, utilizing multiplex real-time TaqMan PCR (MuRT-PCR) assay was developed. Four pairs of oligonucleotide primers and four hybridization probes with various fluorescent dyes and the corresponding fluorescence quenchers were concurrently used for MuRT-PCR assay. The hybridization probe specific for the VARV sequence contained FAM/BHQ1 as a dye/quencher pair; MPXV-specific, TAMRA/BHQ2; CPXV-specific, JOE/BHQ1; VACV-specific, Cy5/BHQ3. The specificity and sensitivity of the developed method were assessed by analyzing DNA of 29 strains belonging to six orthopoxvirus species as well as the DNA samples isolated from archive clinical specimens of human smallpox cases and experimental specimens isolated from CPXV-infected mice and MPXV-infected marmot.

摘要

一种用于快速鉴定人类致病的天花(VARV)、猴痘(MPXV)、牛痘(CPXV)和牛痘(VACV)病毒的一步法,利用多重实时 TaqMan PCR(MuRT-PCR)检测方法。MuRT-PCR 检测方法同时使用了四对寡核苷酸引物和四种带有不同荧光染料和相应荧光淬灭剂的杂交探针。针对 VARV 序列的杂交探针包含 FAM/BHQ1 作为染料/淬灭剂对;针对 MPXV 的是 TAMRA/BHQ2;针对 CPXV 的是 JOE/BHQ1;针对 VACV 的是 Cy5/BHQ3。通过分析属于六个正痘病毒属的 29 株病毒的 DNA 以及从小天花病例的存档临床标本和从 CPXV 感染的小鼠和 MPXV 感染的土拨鼠中分离的实验标本中分离的 DNA 样本,评估了所开发方法的特异性和敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ab/9628778/efa782aead96/gr1.jpg

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