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利用聚合酶链反应诊断猕猴血液中的D型猿猴逆转录病毒感染

Use of polymerase chain reaction for diagnosis of type D simian retrovirus infection in macaque blood.

作者信息

Wang Y, Thouless M E

机构信息

Regional Primate Research Center, University of Washington, Seattle 98195-7238, USA.

出版信息

Lab Anim Sci. 1996 Apr;46(2):187-92.

PMID:8723235
Abstract

We developed a simple and specific polymerase chain reaction (PCR) method for the detection of type D simian retrovirus (SRV) infection (SRV-1, SRV-2, and SRV-3) using whole blood samples from macaques. Each pair of primers for the three serotypes of SRV was highly specific for its respective envelope proviral DNA and was sensitive enough to easily detect about five copies of the SRV-2 proviral genome. The PCR products were confirmed by Southern blot hybridization with digoxigenin-labeled internal oligonucleotide probes. For diagnostic purposes the three sets of primers were mixed together. The molecular weight of the PCR product for each of the three serotypes differed. Serotypes were confirmed by hybridization with a mixture of SRV-2 and SRV-1 and -3 internal probes. The PCR analysis of 39 whole blood samples correctly identified five SRV-1 and nine SRV-2 culture-positive samples. It also detected SRV-2 in two culture-negative blood samples from monkeys from which SRV had been previously isolated.

摘要

我们开发了一种简单且特异的聚合酶链反应(PCR)方法,用于使用猕猴的全血样本检测D型猴逆转录病毒(SRV)感染(SRV-1、SRV-2和SRV-3)。针对SRV三种血清型的每对引物对其各自的包膜前病毒DNA具有高度特异性,并且灵敏度足以轻松检测到约五个拷贝的SRV-2前病毒基因组。PCR产物通过与地高辛标记的内部寡核苷酸探针进行Southern印迹杂交来确认。为了诊断目的,将三组引物混合在一起。三种血清型的PCR产物的分子量不同。通过与SRV-2以及SRV-1和-3内部探针的混合物杂交来确认血清型。对39份全血样本进行的PCR分析正确鉴定出5份SRV-1培养阳性样本和9份SRV-2培养阳性样本。它还在先前已分离出SRV的两只猴子的两份培养阴性血样中检测到了SRV-2。

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