Tedesco Perla, Beraldo Paola, Massimo Michela, Fioravanti Maria Letizia, Volpatti Donatella, Dirks Ron, Galuppi Roberta
Department of Veterinary Medical Sciences, Alma Mater Studiorum-University of Bologna, Bologna, Italy.
Department of Agricultural, Food, Environmental and Animal Sciences, University of Udine, Udine, Italy.
Front Vet Sci. 2020 Feb 21;7:83. doi: 10.3389/fvets.2020.00083. eCollection 2020.
The fish parasites spp. (Oomycota) and (Dinophyceae) cause important losses in freshwater and marine aquaculture industry, respectively. The possible adverse effects of compounds used to control these parasites in aquaculture resulted in increased interest on the search for natural products with antiparasitic activity. In this work, eighteen plant-derived compounds (2',4'-Dihydroxychalcone; 7-Hydroxyflavone; Artemisinin; Camphor (1R); Diallyl sulfide; Esculetin; Eucalyptol; Garlicin 80%; Harmalol hydrochloride dihydrate; Palmatine chloride; Piperine; Plumbagin; Resveratrol; Rosmarinic acid; Sclareolide; Tomatine, Umbelliferone, and Usnic Acid) have been tested . Sixteen of these were used to determine their effects on the gill cell line G1B (ATCC®CRL-2536™) and on the motility of viable dinospores of , and thirteen were screened for inhibitory activity against spp. The cytotoxicity results on G1B cells determined that only two compounds (2',4'-Dihydroxychalcone and Tomatine) exhibited dose-dependent toxic effects. The highest surveyed concentrations (0.1 and 0.01 mM) reduced cell viability by 80%. Upon lowering the compound concentration the percentage of dead cells was lower than 20%. The same two compounds revealed to be potential antiparasitics by reducing in a dose-dependent manner the motility of dinospores up to 100%. With respect to , a Minimum Inhibitory Concentration was found for Tomatine (0.1 mM), Piperine and Plumbagin (0.25 mM), while 2',4'-Dihydroxychalcone considerably slowed down mycelial growth for 24 h at a concentration of 0.1 mM. Therefore, this research allowed to identify two compounds, Tomatine and 2',4'-Dihydroxychalcone, effective against both parasites. These compounds could represent promising candidates for the treatment of amyloodiniosis and saprolegniosis in aquaculture. Nevertheless, further and tests are required in order to determine concentrations that are effective against the considered pathogens but at the same time safe for hosts, environment and consumers.
鱼类寄生虫水霉属(卵菌纲)和锥体虫属(甲藻纲)分别给淡水和海水养殖业造成了重大损失。水产养殖中用于控制这些寄生虫的化合物可能产生的不利影响,使得人们对寻找具有抗寄生虫活性的天然产物的兴趣日益增加。在这项研究中,对18种植物源化合物(2',4'-二羟基查耳酮;7-羟基黄酮;青蒿素;樟脑(1R);二烯丙基硫醚;七叶亭;桉叶油醇;80%大蒜素;盐酸去氢骆驼蓬碱二水合物;氯化巴马汀;胡椒碱;白花丹素;白藜芦醇;迷迭香酸;硬尾醇内酯;番茄碱、伞形花内酯和松萝酸)进行了测试。其中16种用于测定它们对鳃细胞系G1B(ATCC®CRL-2536™)以及锥体虫属活游动孢子运动性的影响,13种用于筛选对水霉属的抑制活性。对G1B细胞的细胞毒性结果表明,只有两种化合物(2',4'-二羟基查耳酮和番茄碱)表现出剂量依赖性毒性作用。所检测的最高浓度(0.1和0.01 mM)使细胞活力降低了80%。降低化合物浓度后,死细胞百分比低于20%。同样这两种化合物通过以剂量依赖性方式将锥体虫属游动孢子的运动性降低达100%,显示出潜在的抗寄生虫作用。对于水霉属,发现番茄碱(0.1 mM)、胡椒碱和白花丹素(0.25 mM)有最低抑菌浓度,而2',4'-二羟基查耳酮在浓度为0.1 mM时可使菌丝体生长在24小时内显著减缓。因此,这项研究得以鉴定出两种对两种寄生虫均有效的化合物,即番茄碱和2',4'-二羟基查耳酮。这些化合物可能是水产养殖中治疗淀粉卵涡鞭虫病和水霉病的有前景的候选药物。然而,为了确定对所考虑病原体有效但同时对宿主、环境和消费者安全的浓度,还需要进一步的体内和体外试验。