台北荣民总医院1977 ~ 1993年临床资料中流感病毒的分离与鉴定。

W T Liu, H Y Wei, S T Hu, C H Tsai, S R Chern, H C Wang
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引用次数: 0

摘要

本研究于一九七七年至一九九三年,在台北退伍军人总医院临床病毒学实验室,收集了15,189份咽拭子样本,以分离及鉴定流感病毒。大部分样本来自儿科。经鉴定的流感病毒毒株有634种;分离成功率平均为4.17% /年。其中56.3%(357/634)为B型流感;甲型H1N1流感占12.1%(77/634),甲型H3N2流感占28.1%(178/634)。约3.5%(22/634)被归类为流感样药物,因为与现有的单克隆抗体无反应。近年来,建立了逆转录聚合酶链反应(RT-PCR)来重新评估这些病毒库。该方法可为甲型H1N1流感、甲型H3N2流感和乙型流感提供快速诊断方法,并可通过RT-PCR方法和扩增DNA测序来了解台北地区再循环或再次出现的病毒分离株的变异情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and identification of influenza viruses from clinical materials in 1977-1993 at Veterans General Hospital-Taipei.

From 1977 to 1993, 15,189 throat swab samples were received for isolation and identification of influenza virus in the Clinical Virology Laboratory, Veterans General Hospital-Taipei. Most of the samples came from the Pediatric Department. There were 634 identified strains of the influenza virus; the successful isolation rate was 4.17% in average/year. Among these isolates, 56.3% (357/634) were influenza B; 12.1% (77/634) were influenza A/H1N1 and 28.1% (178/634) were influenza A/H3N2. About 3.5% (22/634) were classified as flu-like agents because of no reaction with available monoclonal antibodies. In recent years, reverse transcriptase polymerase chain reaction (RT-PCR) was established here to re-evaluate these virus stocks. This method can provide rapid diagnosis method to identify influenza A/H1N1, A/H3N2 and B. Further, the RT-PCR method and sequencing of amplified DNA could be used to see the variation of virus isolates which were recirculated or which reappeared in the Taipei area.

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