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利用逆转录聚合酶链反应(RT-PCR)检测对虾传染性肌肉坏死病毒(IMNV)

Detection of infectious myonecrosis virus (IMNV) of penaeid shrimp by reverse-transcriptase polymerase chain reaction (RT-PCR).

作者信息

Poulos Bonnie T, Lightner Donald V

机构信息

The University of Arizona, Aquaculture Pathology Laboratory, Department of Veterinary Science and Microbiology, 1117 East Lowell Street, Tucson, Arizona 85721, USA.

出版信息

Dis Aquat Organ. 2006 Nov 21;73(1):69-72. doi: 10.3354/dao073069.

Abstract

Infectious myonecrosis virus (IMNV) infecting cultured Litopenaeus vannamei in Brazil is a double-stranded RNA virus that causes a slowly progressive disease with cumulative mortalities of up to 70%. The disease is currently diagnosed using a combination of gross signs (primarily skeletal tail muscle necrosis with white opaque discoloration), histopathology, and in situ hybridization with a digoxigenin-labeled gene probe. A rapid and sensitive method for definitive diagnosis of the disease was developed using reverse-transcriptase polymerase chain reaction (RT-PCR). Two primer sets were used to detect 328 and 139 bp amplicons in a nested RT-PCR assay. Using RNA extracted from purified virions, the first step reaction detected 100 copies of the IMNV viral genome whereas the nested step detected 10 copies. The primers were shown to be specific for IMNV and no amplicons were detected using RNA extracted from shrimp infected with other penaeid shrimp viruses (Taura syndrome virus [TSV], yellowhead virus [YHV], infectious hypodermal hematopoietic necrosis virus [IHHNV] and white spot syndrome virus [WSSV]).

摘要

感染巴西养殖凡纳滨对虾的传染性肌肉坏死病毒(IMNV)是一种双链RNA病毒,可引发一种缓慢进展的疾病,累计死亡率高达70%。目前,该病通过综合大体症状(主要是尾部骨骼肌坏死并伴有白色不透明变色)、组织病理学以及使用地高辛标记基因探针的原位杂交技术进行诊断。利用逆转录聚合酶链反应(RT-PCR)开发了一种用于该疾病确诊的快速灵敏方法。在巢式RT-PCR检测中,使用两组引物来检测328和139 bp的扩增子。使用从纯化病毒粒子中提取的RNA,第一步反应可检测到100个IMNV病毒基因组拷贝,而巢式步骤可检测到10个拷贝。这些引物对IMNV具有特异性,使用感染其他对虾病毒(桃拉综合征病毒[TSV]、黄头病毒[YHV]、传染性皮下和造血组织坏死病毒[IHHNV]以及白斑综合征病毒[WSSV])的对虾提取的RNA未检测到扩增子。

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