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通过泛病毒微阵列检测仓鸮(Tyto alba)中的一种新型禽呼肠孤病毒。

Detection of a new avian bornavirus in barn owl (Tyto alba) by pan-viral microarray.

机构信息

Centro de Investigación en Sanidad Animal (CISA-INIA), CSIC, 28130 Valdeolmos, Spain.

QlifeAps, Industriparken 39-41, DK-2750 Ballerup, Denmark; Virus Research & Development Laboratory Statens Serum Institut, Copenhagen, Denmark.

出版信息

Vet Microbiol. 2024 Feb;289:109959. doi: 10.1016/j.vetmic.2023.109959. Epub 2023 Dec 19.

DOI:10.1016/j.vetmic.2023.109959
PMID:38134487
Abstract

A barn owl (Tyto alba) died with neurological signs compatible with a viral infection. After discarding other possible infections caused by circulating viruses in the area, analysis of the central nervous system using a pan-viral microarray revealed hybridization to canary bornavirus 2 (CnBV-2). Subsequent sequence analysis confirmed the presence of a virus sharing more than 83% identity with CnBV-2. Surprisingly, the new sequence corresponds to a new virus, here named Barn owl Bornavirus 1 (BoBV-1), within the Orthobornavirus serini species. Moreover, it is the first member of this species that has been detected in a non-passerine bird, indicating that Orthobornavirus serini species comprises viruses with a wider range of hosts than previously presumed. The use of this microarray has proven to be an excellent tool for viral detection in clinical samples, with capacity to detect new viral variants. This allows the diagnosis of a great range of viruses, which can cause similar disease symptoms and which identification by PCR methods might be tedious, probably unsuccessful and, in the long run, expensive. This platform is highly useful for a fast and precise viral detection, contributing to the improvement of diagnostic methods.

摘要

一只仓鸮(Tyto alba)出现与病毒感染相一致的神经症状后死亡。在排除了该地区循环病毒引起的其他可能感染后,使用泛病毒微阵列对中枢神经系统进行分析,结果显示与金丝雀 bornavirus 2(CnBV-2)发生杂交。随后的序列分析证实存在与 CnBV-2 相似度超过 83%的病毒。令人惊讶的是,新序列与 Orthobornavirus serini 种内的一种新病毒 Barn owl Bornavirus 1(BoBV-1)相对应。此外,这是首次在非雀形目鸟类中检测到该种病毒,表明 Orthobornavirus serini 种包含宿主范围比以前认为的更广的病毒。该微阵列的使用已被证明是临床样本中病毒检测的出色工具,具有检测新病毒变体的能力。这使得能够诊断出大量可能引起类似疾病症状的病毒,而通过 PCR 方法进行鉴定可能繁琐、可能不成功,并且从长远来看成本高昂。该平台对于快速准确的病毒检测非常有用,有助于改进诊断方法。

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