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一种用于快速对罗非鱼传染性脾肾坏死病毒(ISKNV)进行全基因组测序的多重、平铺式 PCR 方法。

A Multiplexed, Tiled PCR Method for Rapid Whole-Genome Sequencing of Infectious Spleen and Kidney Necrosis Virus (ISKNV) in Tilapia.

机构信息

Department of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.

Centre for Environment, Fisheries and Aquaculture Science (Cefas), The Nothe, Barrack Road, Weymouth DT4 8UB, UK.

出版信息

Viruses. 2023 Apr 14;15(4):965. doi: 10.3390/v15040965.

Abstract

Tilapia farming is one of the most important sectors in aquaculture worldwide and of major importance to global food security. Infectious spleen and kidney necrosis virus (ISKNV) has been identified as an agent of high morbidity and mortality, threatening tilapia aquaculture. ISKNV was detected in Lake Volta, Ghana, in September 2018 and spread rapidly, with mortality rates between 60 and 90% and losses of more than 10 tonnes of fish per day. Understanding the spread and evolution of viral pathogens is important for control strategies. Here, we developed a tiled-PCR sequencing approach for the whole-genome sequencing of ISKNV, using long read sequencing to enable field-based, real-time genomic surveillance. This work represents the first use of tiled-PCR for whole genome recovery of viruses in aquaculture, with the longest genome target (>110 kb dsDNA) to date. Our protocol was applied to field samples collected from the ISKNV outbreaks from four intensive tilapia cage culture systems across Lake Volta, between October 2018 and May 2022. Despite the low mutation rate of dsDNA viruses, 20 single nucleotide polymorphisms accumulated during the sampling period. Droplet digital PCR identified a minimum requirement of template in a sample to recover 50% of an ISKNV genome at 275 femtograms (2410 viral templates per 5 µL sequencing reaction). Overall, tiled-PCR sequencing of ISKNV provides an informative tool to assist in disease control in aquaculture.

摘要

罗非鱼养殖是全球水产养殖中最重要的领域之一,对全球粮食安全具有重要意义。传染性脾肾坏死病毒 (ISKNV) 已被确定为高发病率和死亡率的病原体,对罗非鱼养殖业构成威胁。ISKNV 于 2018 年 9 月在加纳的沃尔特湖被检测到,并迅速传播,死亡率在 60%至 90%之间,每天损失超过 10 吨鱼。了解病毒病原体的传播和进化对于控制策略很重要。在这里,我们使用长读测序开发了一种用于 ISKNV 全基因组测序的拼接 PCR 测序方法,用于现场实时基因组监测。这是拼接 PCR 首次用于水产养殖中病毒的全基因组回收,目标基因组最长 (>110 kb dsDNA)。我们的方案应用于 2018 年 10 月至 2022 年 5 月期间从沃尔特湖上四个集约化罗非鱼网箱养殖系统中采集的 ISKNV 暴发的现场样本。尽管 dsDNA 病毒的突变率较低,但在采样期间积累了 20 个单核苷酸多态性。微滴数字 PCR 确定了从样本中恢复 50%ISKNV 基因组所需的模板的最低要求,其模板量为 275 飞克(5 µL 测序反应中 2410 个病毒模板)。总体而言,ISKNV 的拼接 PCR 测序为水产养殖疾病控制提供了一种有用的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ea/10145788/29b00085391a/viruses-15-00965-g001.jpg

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