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利用数字 PCR 对水产养殖中的优先细菌进行绝对定量。

Absolute quantification of priority bacteria in aquaculture using digital PCR.

机构信息

SINTEF Ocean, Brattørkaia 17C, Trondheim 7010, Norway.

SINTEF Ocean, Brattørkaia 17C, Trondheim 7010, Norway.

出版信息

J Microbiol Methods. 2021 Apr;183:106171. doi: 10.1016/j.mimet.2021.106171. Epub 2021 Feb 19.

DOI:10.1016/j.mimet.2021.106171
PMID:33610596
Abstract

Modern aquaculture systems are designed for intensive rearing of fish or other species. Both land-based and offshore systems typically contain high loads of biomass and the water quality in these systems is of paramount importance for fish health and production. Microorganisms play a crucial role in removal of organic matter and nitrogen-recycling, production of toxic hydrogen sulfide (HS), and can affect fish health directly if pathogenic for fish or exerting probiotic properties. Methods currently used in aquaculture for monitoring certain bacteria species numbers still have typically low precision, specificity, sensitivity and are time-consuming. Here, we demonstrate the use of Digital PCR as a powerful tool for absolute quantification of sulfate-reducing bacteria (SRB) and major pathogens in salmon aquaculture, Moritella viscosa, Yersinia ruckeri and Flavobacterium psychrophilum. In addition, an assay for quantification of Listeria monocytogenes, which is a human pathogen bacterium and relevant target associated with salmonid cultivation in recirculating systems and salmon processing, has been assessed. Sudden mass mortality incidents caused by HS produced by SRB have become of major concern in closed aquaculture systems. An ultra-sensitive assay for quantification of SRB has been established using Desulfovibrio desulfuricans as reference strain. The use of TaqMan® probe technology allowed for the development of multi-plex assays capable of simultaneous quantification of these aquaculture priority bacteria. In single-plex assays, limit of detection was found to be at around 20 fg DNA for M. viscosa, Y. ruckeri and F. psychrophilum, and as low as 2 fg DNA for L. monocytogenes and D. desulfuricans.

摘要

现代水产养殖系统旨在集约化养殖鱼类或其他物种。陆基和近海系统通常都含有大量的生物量,这些系统的水质对鱼类的健康和生产至关重要。微生物在去除有机物和氮循环、产生有毒的硫化氢(HS)方面发挥着关键作用,如果对鱼类具有致病性或具有益生菌特性,它们会直接影响鱼类的健康。水产养殖中目前用于监测某些细菌数量的方法通常精度、特异性、灵敏度较低,且耗时。在这里,我们展示了数字 PCR 作为一种强大工具在鲑鱼养殖中硫酸盐还原菌(SRB)和主要病原体(粘质莫拉氏菌、鲁氏耶尔森菌和嗜冷黄杆菌)绝对定量中的应用。此外,还评估了一种用于定量检测单核细胞增生李斯特菌(一种人类病原体细菌,与循环系统中鲑鱼养殖和鲑鱼加工相关的目标)的检测方法。由 SRB 产生的 HS 引起的突然大规模死亡事件已成为封闭水产养殖系统的主要关注点。已经建立了一种超灵敏的用于定量检测 SRB 的方法,使用脱硫脱硫弧菌作为参考菌株。TaqMan®探针技术的使用允许开发能够同时定量这些水产养殖优先细菌的多重检测方法。在单重检测中,我们发现粘质莫拉氏菌、鲁氏耶尔森菌和嗜冷黄杆菌的检测限约为 20 fg DNA,单核细胞增生李斯特菌和脱硫脱硫弧菌的检测限低至 2 fg DNA。

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