Zhou Sheng-Yu, Liu Yan-Meng, Zhang Qi-Zhong, Fu Yao-Wu, Lin De-Jie
Engineering Research Center of Tropical and Subtropical Aquatic Ecological Engineering, Ministry of Education, Key Laboratory of Aquatic Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, Institute of Hydrobiology, Jinan University, West 601 Huangpu Avenue, Tianhe District, Guangzhou 510632, China.
Engineering Research Center of Tropical and Subtropical Aquatic Ecological Engineering, Ministry of Education, Key Laboratory of Aquatic Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, Institute of Hydrobiology, Jinan University, West 601 Huangpu Avenue, Tianhe District, Guangzhou 510632, China.
Vet Parasitol. 2018 Apr 15;253:22-25. doi: 10.1016/j.vetpar.2018.02.005. Epub 2018 Feb 6.
Ichthyophthirius multifiliis is a ciliated parasite that infests almost all freshwater fish species and causes great economic losses to the aquaculture industry. In this study, a compound with anti-I. multifiliis activity was isolated from Polygonum cuspidatum and identified as emodin. In vitro anti-I. multifiliis results showed that emodin at 1 mg/L killed all I. multifiliis theronts for 96.0 min, and at 0.5 mg/L or lower concentrations could not kill all I. multifiliis theronts, but could significantly reduce the infectivity of theronts after pretreatment with emodin at the low concentrations mentioned above for 2 h. Additionally, emodin at 1 mg/L and 2 mg/L completely terminated the reproduction of nonencysted and encysted tomonts, respectively. In vivo tests, emodin at 0.5 mg/L could cure infected grass carp and protect naive fish from I. multifiliis infection by continuous adding emodin for 10 days. The 96 h median lethal concentration (LC) of emodin to grass carp was 3.15 mg/L, which were approximately 18 and 7 times the median effective concentration (EC) of emodin for killing theronts (0.18 mg/L) and nonencysted tomonts (0.45 mg/L), respectively. On the basis of these results, emodin is an effective compound for the development of a new drug against I. multifiliis.
多子小瓜虫是一种纤毛虫寄生虫,几乎感染所有淡水鱼类品种,给水产养殖业造成巨大经济损失。在本研究中,从虎杖中分离出一种具有抗多子小瓜虫活性的化合物,并鉴定为大黄素。体外抗多子小瓜虫结果表明,1mg/L的大黄素在96.0分钟内可杀死所有多子小瓜虫幼虫,而在0.5mg/L或更低浓度下不能杀死所有多子小瓜虫幼虫,但在上述低浓度大黄素预处理2小时后,可显著降低幼虫的感染性。此外,1mg/L和2mg/L的大黄素分别完全终止了非包囊期和包囊期滋养体的繁殖。在体内试验中,0.5mg/L的大黄素通过连续添加10天可治愈感染的草鱼,并保护未感染的鱼免受多子小瓜虫感染。大黄素对草鱼的96小时半数致死浓度(LC)为3.15mg/L,分别约为大黄素杀死幼虫(0.18mg/L)和非包囊期滋养体(0.45mg/L)的半数有效浓度(EC)的18倍和7倍。基于这些结果,大黄素是开发抗多子小瓜虫新药的有效化合物。