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从病毒学角度看:大西洋鲑(Salmo salar)感染过程中的传染性鲑鱼贫血病毒(ISAV)转录组。

From the viral perspective: infectious salmon anemia virus (ISAV) transcriptome during the infective process in Atlantic salmon (Salmo salar).

作者信息

Valenzuela-Miranda Diego, Cabrejos María Eugenia, Yañez José Manuel, Gallardo-Escárate Cristian

机构信息

Laboratory of Biotechnology and Aquatic Genomics, Interdisciplinary Center for Aquaculture Research (INCAR), University of Concepción, P.O. Box 160-C, Concepción, Chile; Aquainnovo, Casilla 30B, Puerto Montt 5503032, Chile.

Facultad de Ciencias Agronómicas, Universidad de Chile, Av Santa Rosa 11315, La Pintana, Santiago 8820808, Chile.

出版信息

Mar Genomics. 2015 Apr;20:39-43. doi: 10.1016/j.margen.2014.12.007. Epub 2015 Jan 2.

Abstract

The infectious salmon anemia virus (ISAV) is a severe disease that mainly affects the Atlantic salmon (Salmo salar) aquaculture industry. Although several transcriptional studies have aimed to understand Salmon-ISAV interaction through the evaluation of host-gene transcription, none of them has focused their attention upon the viral transcriptional dynamics. For this purpose, RNA-Seq and RT-qPCR analyses were conducted in gills, liver and head-kidney of S. salar challenged by cohabitation with ISAV. Results evidence the time and tissue transcript patterns involved in the viral expression and how the transcription levels of ISAV segments are directly linked with the protein abundance found in other virus of the Orthomyxoviridae family. In addition, RT-qPCR result evidenced that quantification of ISAV through amplification of segment 3 would result in a more sensitive approach for detection and quantification of ISAV. This study offers a more comprehensive approach regarding the ISAV infective process and gives novel knowledge for its molecular detection.

摘要

传染性鲑鱼贫血病毒(ISAV)是一种严重疾病,主要影响大西洋鲑(Salmo salar)养殖业。尽管有几项转录研究旨在通过评估宿主基因转录来了解鲑鱼与ISAV的相互作用,但它们都没有将注意力集中在病毒转录动力学上。为此,对与ISAV同居感染的大西洋鲑的鳃、肝脏和头肾进行了RNA测序(RNA-Seq)和逆转录定量聚合酶链反应(RT-qPCR)分析。结果证明了病毒表达所涉及的时间和组织转录模式,以及ISAV各片段的转录水平如何与正粘病毒科其他病毒中发现的蛋白质丰度直接相关。此外,RT-qPCR结果证明,通过扩增第3片段对ISAV进行定量,将产生一种更灵敏的ISAV检测和定量方法。本研究为ISAV感染过程提供了更全面的方法,并为其分子检测提供了新知识。

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