Development of an In Situ Hybridization Method for Detection of Akabane Virus

Nihat Toplu, T. Ç. Oğuzoğlu, A. Akkoç
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Abstract

Akabane virus (AKAV) is an arbovirus belonging to the family Bunyaviridae, genus Orthobunyavirus. AKAV consists of three-segment (L, M, and S RNA segments), negative single-stranded RNA. The aim of this study was to investigate an in situ hybridization method (ISH) in a Vero E6 cell line infected with Akabane virus. The 320 base pair amplicon was obtained by RT-PCR with a primer pair and labeled with digoxigenin. Akabane virus RNAs were seen as a granular pattern in the cytoplasm of infected cells. As a result, the expression of the particular Akabane virus gene area was successfully disclosed in the current investigation using the ISH method with a digoxigenin-labeled probe.
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开发用于检测赤羽病毒的原位杂交方法
赤羽病毒(AKAV)是一种虫媒病毒,属于布尼亚病毒科、正布尼亚病毒属。AKAV 由三段(L、M 和 S RNA 段)阴性单链 RNA 组成。本研究的目的是在感染赤羽病毒的 Vero E6 细胞系中研究一种原位杂交方法(ISH)。使用引物对通过 RT-PCR 获得 320 碱基对扩增片段,并用地高辛标记。在感染细胞的细胞质中,可以看到赤羽病毒 RNA 呈颗粒状。因此,在本次研究中,使用地高辛标记探针的 ISH 方法成功地揭示了赤羽病毒特定基因区域的表达。
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