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使用一步法逆转录聚合酶链反应(RT-PCR)检测石蜡包埋人体组织中的辛诺柏病毒RNA并进行序列确认。

Detection and sequence confirmation of Sin Nombre virus RNA in paraffin-embedded human tissues using one-step RT-PCR.

作者信息

Schwarz T F, Zaki S R, Morzunov S, Peters C J, Nichol S T

机构信息

Special Pathogens Branch, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.

出版信息

J Virol Methods. 1995 Feb;51(2-3):349-56. doi: 10.1016/0166-0934(94)00142-4.

Abstract

Sin Nombre virus (SNV) is the causative agent of hantavirus pulmonary syndrome (HPS). SNV RNA can be detected in fresh or frozen autopsy tissue samples by reverse transcriptase polymerase chain reaction (RT-PCR), and virus antigens can be identified by immunohistochemistry. A method was developed for demonstration of SNV RNA in formalin-fixed, paraffin-embedded tissues by RT-PCR. Virus genomes were detected in 8 of 12 (66.7%) fixed human tissue samples that were positive by immunohistochemistry, and RT-PCR prior to tissue fixation. By comparison with nucleotide sequences determined previously in fresh or frozen tissues of the same patients, identical genomic sequences were obtained, proving the authenticity of the PCR products. The study demonstrates that detection of SNV RNA in formalin-fixed, paraffin-embedded archival tissue by RT-PCR is feasible. This method allows retrospective studies on the phylogenetic epidemiology of SNV in North America.

摘要

辛诺柏病毒(SNV)是汉坦病毒肺综合征(HPS)的病原体。通过逆转录聚合酶链反应(RT-PCR)可在新鲜或冷冻的尸检组织样本中检测到SNV RNA,并且可通过免疫组织化学鉴定病毒抗原。已开发出一种通过RT-PCR在福尔马林固定、石蜡包埋组织中检测SNV RNA的方法。在12份经免疫组织化学检测为阳性且在组织固定前经RT-PCR检测的固定人体组织样本中,有8份(66.7%)检测到病毒基因组。通过与先前在同一患者的新鲜或冷冻组织中确定的核苷酸序列进行比较,获得了相同的基因组序列,证明了PCR产物的真实性。该研究表明,通过RT-PCR在福尔马林固定、石蜡包埋的存档组织中检测SNV RNA是可行的。这种方法有助于对北美的SNV进行系统发育流行病学的回顾性研究。

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