Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Ministry of Education, Shanghai Ocean University, Shanghai 201306, China.
International Research Center for Marine Biosciences, Ministry of Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
Viruses. 2022 Apr 18;14(4):840. doi: 10.3390/v14040840.
PCR-based DNA amplification has been one of the major methods in aquaculture research for decades, although its use outside the modern laboratory environment is limited due to the relatively complex methods and high costs. To this end, we investigated a swabbing and disc protocol for the collection of DNA samples from fish which could extract DNA from fish skin mucus by a non-invasion technique costing only $0.02 (USD) and requiring less than 30 seconds. The disc method that we chose could use the cheap filter paper to extract DNA from above 10 crucian carp blood cells, which is comparable to the commercial kit. By using skin mucus swabbing and the disc method, we can obtain amplification-ready DNA from mucus to distinguish different species from our smallest fish (medaka, ~2.5 cm and crucian carp, ~7 cm) to our biggest fish (tilapia, ~15 cm). Furthermore, the viral pathogen herpesvirus (CaHV) of crucian carp was detected using our method, which would make performing molecular diagnostic assays achievable in limited-resource settings including aquafarms and aqua stores outside the laboratory environment.
基于聚合酶链式反应(PCR)的 DNA 扩增技术已经成为水产养殖研究中的主要方法之一,尽管由于方法相对复杂且成本较高,其在现代实验室环境之外的应用受到限制。为此,我们研究了一种从鱼类采集 DNA 样本的擦拭和圆盘法,该方法采用非侵入性技术,仅需花费 0.02 美元(USD)且耗时不到 30 秒,即可从鱼类皮肤黏液中提取 DNA。我们选择的圆盘法可以使用廉价的滤纸从超过 10 个鲫鱼血细胞中提取 DNA,与商用试剂盒相当。通过使用皮肤黏液擦拭和圆盘法,我们可以从黏液中获得可用于扩增的 DNA,从而能够区分从最小的鱼类(如 2.5 厘米长的青鳉鱼和 7 厘米长的鲫鱼)到最大的鱼类(15 厘米长的罗非鱼)的不同物种。此外,我们的方法还可以检测鲫鱼的疱疹病毒(CaHV)等病毒病原体,这使得在包括水产养殖场和水产商店在内的资源有限的环境中进行分子诊断检测成为可能。