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通过新开发的多重TaqMan检测法对属于辛布血清群谱系1的虫媒病毒进行广谱检测以及对赤羽、爱诺和佩顿病毒进行特异性检测。

Broad-range detection of arboviruses belonging to Simbu serogroup lineage 1 and specific detection of Akabane, Aino and Peaton viruses by newly developed multiple TaqMan assays.

作者信息

Shirafuji Hiroaki, Yazaki Ryu, Shuto Yozo, Yanase Tohru, Kato Tomoko, Ishikura Youji, Sakaguchi Zenjiro, Suzuki Moemi, Yamakawa Makoto

机构信息

Kyushu Research Station, National Institute of Animal Health (NIAH), National Agriculture and Food Research Organization (NARO), Japan.

Kusu Livestock Hygiene Service Center, Oita Prefectural Government, Japan.

出版信息

J Virol Methods. 2015 Dec 1;225:9-15. doi: 10.1016/j.jviromet.2015.08.021. Epub 2015 Sep 2.

Abstract

TaqMan assays were developed for the broad-range detection of arboviruses belonging to Simbu serogroup lineage 1 in the genus Orthobunyavirus and also for the specific detection of three viruses in the lineage, Akabane, Aino and Peaton viruses (AKAV, AINOV and PEAV, respectively). A primer and probe set was designed for the broad-range detection of Simbu serogroup lineage 1 (Pan-Simbu1 set) mainly targeting AKAV, AINOV, PEAV, Sathuperi and Shamonda viruses (SATV and SHAV), and the forward and reverse primers of the Pan-Simbu1 set were also used for the specific detection of AKAV with another probe (AKAV-specific set). In addition, two more primer and probe sets were designed for AINOV- and PEAV-specific detection, respectively (AINOV- and PEAV-specific sets). All of the four primer and probe sets successfully detected targeted viruses, and thus broad-range and specific detection of all the targeted viruses can be achieved by using two multiplex assays and a single assay in a dual (two-color) assay format when another primer and probe set for a bovine β-actin control is also used. The assays had an analytical sensitivity of 10 copies/tube for AKAV, at least 100 copies/tube for AINOV, 100 copies/tube for PEAV, one copy/tube for SATV and at least 10 copies/tube for SHAV, respectively. Diagnostic sensitivity of the assays was tested with field-collected bovine samples, and the results suggested that the sensitivity was higher than that of a conventional RT-PCR. These data indicate that the newly developed TaqMan assays will be useful tools for the diagnosis and screening of field-collected samples for infections of AKAV and several other arboviruses belonging to the Simbu serogroup lineage 1.

摘要

TaqMan检测法用于广泛检测正布尼亚病毒属中辛布血清群谱系1的虫媒病毒,也用于特异性检测该谱系中的三种病毒,即赤羽病毒、爱诺病毒和皮顿病毒(分别为AKAV、AINOV和PEAV)。设计了一组引物和探针用于广泛检测辛布血清群谱系1(泛辛布1组),主要针对AKAV、AINOV、PEAV、萨图佩里病毒和沙蒙达病毒(SATV和SHAV),泛辛布1组的正向和反向引物也用于用另一种探针特异性检测AKAV(AKAV特异性组)。此外,还分别设计了另外两组引物和探针用于AINOV和PEAV的特异性检测(AINOV特异性组和PEAV特异性组)。所有这四组引物和探针均成功检测到目标病毒,因此,当还使用一组用于牛β-肌动蛋白对照的引物和探针时,通过在双(双色)检测形式中使用两种多重检测和一种单一检测,可以实现对所有目标病毒进行广泛和特异性检测。这些检测方法对AKAV的分析灵敏度为每管10个拷贝,对AINOV至少为每管100个拷贝,对PEAV为每管100个拷贝,对SATV为每管1个拷贝,对SHAV至少为每管10个拷贝。用现场采集的牛样本测试了这些检测方法的诊断灵敏度,结果表明其灵敏度高于传统的RT-PCR。这些数据表明,新开发的TaqMan检测法将成为诊断和筛查现场采集样本中AKAV及其他几种属于辛布血清群谱系1的虫媒病毒感染的有用工具。

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