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在罗氏沼虾虹彩病毒(MrNV)和传染性皮下及造血组织坏死病毒(XSV)感染性克隆的实验挑战中,单独的 MrNV 就能导致淡水虾(罗氏沼虾)死亡。

In experimental challenge with infectious clones of Macrobrachium rosenbergii nodavirus (MrNV) and extra small virus (XSV), MrNV alone can cause mortality in freshwater prawn (Macrobrachium rosenbergii).

机构信息

Center of Excellence for Shrimp Molecular Biology and Biotechnology (Centex Shrimp), Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand; National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Klong 1, Klong Luang, Pratum Thani, 12120, Thailand.

Center of Excellence for Shrimp Molecular Biology and Biotechnology (Centex Shrimp), Faculty of Science, Mahidol University, Rama 6 Road, Bangkok, 10400, Thailand.

出版信息

Virology. 2020 Jan 15;540:30-37. doi: 10.1016/j.virol.2019.11.004. Epub 2019 Nov 5.

Abstract

To overcome the lack of immortal shrimp cell lines for shrimp viral research, we constructed and tested DNA infectious clones of Macrobrachium rosenbergii nodavirus (MrNV) and extra small virus (XSV) often found together in freshwater prawn (M. rosenbergii) exhibiting white tail disease (WTD). Full-length cDNAs of MrNV and XSV genomic RNA were individually inserted into the baculovirus pFastBacDUAL shuttle vector. Individual Sf9 (insect cell line) transfection resulted in production of RNA (RT-PCR) and capsid proteins (immunofluorescence) for both viruses. Presence of respective virions was confirmed by density gradient purification followed by RT-PCR and transmission electron microscopy. Infectivity was by tested in immersion-challenge tests with M. rosenbergii post-larvae (PL) using both semi-purified viruses, individually or combined, and confirmed by histological analysis (morphology and immunofluorescence) and quantitative RT-PCR. Mortality accompanied by WTD lesions occurred with MrNV alone or in combination with XSV but not with XSV alone, despite its replication.

摘要

为了克服虾类病毒研究中缺乏永生虾细胞系的问题,我们构建并测试了淡水虾(罗氏沼虾)中常见的白斑综合征病毒(MrNV)和极微小病毒(XSV)的 DNA 感染性克隆,这些虾表现出白尾病(WTD)。MrNV 和 XSV 基因组 RNA 的全长 cDNA 分别插入杆状病毒 pFastBacDUAL 穿梭载体。单个 Sf9(昆虫细胞系)转染导致两种病毒的 RNA(RT-PCR)和衣壳蛋白(免疫荧光)产生。通过密度梯度纯化,然后进行 RT-PCR 和透射电子显微镜检查,证实了相应病毒粒子的存在。使用半纯化的病毒单独或组合进行浸浴挑战试验,用罗氏沼虾幼体(PL)进行感染性测试,并通过组织学分析(形态和免疫荧光)和定量 RT-PCR 进行确认。单独使用 MrNV 或与 XSV 一起使用会导致 WTD 病变和死亡率,但 XSV 单独使用时不会,尽管它可以复制。

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