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利用甲藻亚历山大藻的细胞或培养滤液去除两种致病性盾纤毛虫 Miamiensis avidus 和 Miamiensis sp.。

Removal of two pathogenic scuticociliates Miamiensis avidus and Miamiensis sp. using cells or culture filtrates of the dinoflagellate Alexandrium andersonii.

机构信息

School of Earth and Environmental Sciences, College of Natural Sciences, Seoul National University, Seoul 08826, Republic of Korea.

School of Earth and Environmental Sciences, College of Natural Sciences, Seoul National University, Seoul 08826, Republic of Korea; Advanced Institutes of Convergence Technology, Suwon, Gyeonggi-do 16229, Republic of Korea.

出版信息

Harmful Algae. 2017 Mar;63:133-145. doi: 10.1016/j.hal.2017.02.002. Epub 2017 Feb 27.

Abstract

Scuticociliatosis, which is caused by parasitic protistan pathogens known as scuticociliates, is one of the most serious diseases in marine aquaculture worldwide. Thus, elimination of these ciliates is a primary concern for scientists and managers in the aquaculture industry. To date, formalin and other toxic chemicals have been used as anti-scuticociliate agents, but issues regarding their secondary effects often arise. Consequently, development of safer methods is necessary. To find out a safe method of controlling scuticociliate populations in aqua-tanks or small-scale natural environments, cultures of 14 phototrophic dinoflagellates were tested to determine whether they were able to control populations of the common scuticociliates Miamiensis avidus and Miamiensis sp. isolated from Korean waters. Among the dinoflagellates tested, both cells and culture filtrates of Alexandrium andersonii effectively killed M. avidus and Miamiensis sp. The minimal concentration of cells and equivalent culture filtrates of A. andersonii to kill all M. avidus cells within 48h of incubation was ca. 2500 and 4500 cells ml, respectively; whereas those needed to kill all Miamiensis sp. cells were ca. 1000 and 4500 cells ml, respectively. It was estimated that 1m of the stock culture containing 20,000A. andersonii cells ml could eliminate all M. avidus cells in 7m of waters within the aqua-tanks on land and all Miamiensis sp. cells in 19m of waters within 48h. None of the brine shrimp Artemia salina nauplii incubated with concentrations of 50-4500A. andersonii cells ml for 24h was dead. Furthermore, none of the flounder Paralichthys olivaceus juveniles incubated with a mean concentration of ca. 2280A. andersonii cells ml for 96h was dead. Therefore, A. andersonii cultures may be used as a safe biological method for controlling populations of scuticociliates and can replace toxic formalin. The results of this study provided the basis for developing the method to control scuticociliate populations and understanding interactions between scuticociliates and phototrophic dinoflagellates in marine ecosystems.

摘要

旋口虫病是由一种名为旋口纤毛虫的寄生原生动物病原体引起的,是世界范围内水产养殖中最严重的疾病之一。因此,消除这些纤毛虫是水产养殖业科学家和管理者的首要关注点。迄今为止,福尔马林和其他有毒化学品已被用作抗旋口纤毛虫剂,但它们的副作用问题经常出现。因此,有必要开发更安全的方法。为了在水产养殖池或小规模自然环境中找到控制旋口纤毛虫种群的安全方法,测试了 14 种光养鞭毛藻的培养物,以确定它们是否能够控制从韩国水域分离出来的常见旋口纤毛虫 Miamiensis avidus 和 Miamiensis sp. 的种群。在测试的鞭毛藻中,亚历山大藻的细胞和培养液滤液都能有效地杀死 M. avidus 和 Miamiensis sp. 。在孵育 48 小时内,杀死所有 M. avidus 细胞所需的亚历山大藻细胞和等效培养液滤液的最小浓度分别约为 2500 和 4500 个细胞/ml;而杀死所有 Miamiensis sp. 细胞所需的浓度分别约为 1000 和 4500 个细胞/ml。据估计,含有 20,000 个亚历山大藻细胞/ml 的储备培养物 1m 可以在陆地上的水产养殖池中的 7m 水中在 48 小时内消除所有 M. avidus 细胞,以及在 48 小时内消除所有 Miamiensis sp. 细胞在 19m 的水中。用浓度为 50-4500 个亚历山大藻细胞/ml 孵育 24 小时的盐水虾 Artemia salina 无节幼体无一死亡。此外,用约 2280 个亚历山大藻细胞/ml 的平均浓度孵育 96 小时的牙鲆幼鱼无一死亡。因此,亚历山大藻培养物可作为一种安全的生物方法用于控制旋口纤毛虫种群,并可替代有毒的福尔马林。本研究结果为开发控制旋口纤毛虫种群的方法和了解海洋生态系统中旋口纤毛虫和光养鞭毛藻之间的相互作用提供了依据。

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