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一种用于监测野生鸟类甲型流感病毒的实时聚合酶链反应检测法。

A real-time PCR assay for the monitoring of influenza A virus in wild birds.

作者信息

Karlsson Malin, Wallensten Anders, Lundkvist Ake, Olsen Björn, Brytting Maria

机构信息

Swedish Institute for Infectious Disease Control, SE-171 82 Stockholm, Sweden.

出版信息

J Virol Methods. 2007 Sep;144(1-2):27-31. doi: 10.1016/j.jviromet.2007.03.013. Epub 2007 May 7.

Abstract

A screening system including a new real-time PCR assay for the monitoring of influenza A virus in wild birds was developed. The real-time PCR assay uses SYBR green chemistry and the primers are targeting the matrix gene of influenza A virus. The performance of the assay was compared with two other assays, one assay also using SYBR green chemistry and one assay using TaqMan chemistry, i.e. a specific probe. A total of 45 fecal bird samples were analysed for influenza A virus in three different PCR reactions. Overall, 26 samples were positive in at least one of the three real-time PCR assays. Of the 26 samples, 18 were positive by all three reactions. Eight samples were found positive exclusively by the two SYBR green reactions, six of which were detected by both SYBR green reactions. Of the 26 positive samples, 15 samples were verified as positive either by virus isolation or influenza A M2-gene PCR. The results showed that the two SYBR green systems had a higher performance regarding the detection of influenza A as compared to the PCR reaction using a specific probe.

摘要

开发了一种筛查系统,该系统包括一种用于监测野生鸟类甲型流感病毒的新型实时荧光定量聚合酶链反应(PCR)检测方法。该实时荧光定量PCR检测方法采用SYBR Green化学法,引物靶向甲型流感病毒的基质基因。将该检测方法的性能与另外两种检测方法进行了比较,一种检测方法也采用SYBR Green化学法,另一种检测方法采用TaqMan化学法,即一种特异性探针。在三种不同的PCR反应中,共对45份鸟类粪便样本进行了甲型流感病毒分析。总体而言,在三种实时荧光定量PCR检测方法中,至少有一种检测方法呈阳性的样本有26份。在这26份样本中,有18份在所有三种反应中均呈阳性。有8份样本仅在两种SYBR Green反应中呈阳性,其中6份在两种SYBR Green反应中均被检测到。在26份阳性样本中,有15份样本通过病毒分离或甲型流感M2基因PCR被确认为阳性。结果表明,与使用特异性探针的PCR反应相比,两种SYBR Green系统在检测甲型流感方面具有更高的性能。

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