Di Paolo Carolina, Groh Ksenia J, Zennegg Markus, Vermeirssen Etiënne L M, Murk Albertinka J, Eggen Rik I L, Hollert Henner, Werner Inge, Schirmer Kristin
Swiss Centre for Applied Ecotoxicology Eawag-EPFL, 8600, Dübendorf, Switzerland; Department of Ecosystem Analysis, Institute for Environmental Research, RWTH Aachen University, 52074, Aachen, Germany.
Eawag, Swiss Federal Institute of Aquatic Science and Technology, 8600, Dübendorf, Switzerland; ETH Zürich, Department of Chemistry and Applied Biosciences, 8093 Zürich, Switzerland.
Aquat Toxicol. 2015 Dec;169:168-78. doi: 10.1016/j.aquatox.2015.10.014. Epub 2015 Oct 28.
The occurrence of chronic or delayed toxicity resulting from the exposure to sublethal chemical concentrations is an increasing concern in environmental risk assessment. The Fish Embryo Toxicity (FET) test with zebrafish provides a reliable prediction of acute toxicity in adult fish, but it cannot yet be applied to predict the occurrence of chronic or delayed toxicity. Identification of sublethal FET endpoints that can assist in predicting the occurrence of chronic or delayed toxicity would be advantageous. The present study characterized the occurrence of delayed toxicity in zebrafish larvae following early exposure to PCB126, previously described to cause delayed effects in the common sole. The first aim was to investigate the occurrence and temporal profiles of delayed toxicity during zebrafish larval development and compare them to those previously described for sole to evaluate the suitability of zebrafish as a model fish species for delayed toxicity assessment. The second aim was to examine the correlation between the sublethal endpoints assessed during embryonal and early larval development and the delayed effects observed during later larval development. After exposure to PCB126 (3-3000ng/L) until 5 days post fertilization (dpf), larvae were reared in clean water until 14 or 28 dpf. Mortality and sublethal morphological and behavioural endpoints were recorded daily, and growth was assessed at 28 dpf. Early life exposure to PCB126 caused delayed mortality (300 ng/L and 3000 ng/L) as well as growth impairment and delayed development (100 ng/L) during the clean water period. Effects on swim bladder inflation and cartilaginous tissues within 5 dpf were the most promising for predicting delayed mortality and sublethal effects, such as decreased standard length, delayed metamorphosis, reduced inflation of swim bladder and column malformations. The EC50 value for swim bladder inflation at 5 dpf (169 ng/L) was similar to the LC50 value at 8 dpf (188 and 202 ng/L in two experiments). Interestingly, the patterns of delayed mortality and delayed effects on growth and development were similar between sole and zebrafish. This indicates the comparability of critical developmental stages across divergent fish species such as a cold water marine flatfish and a tropical freshwater cyprinid. Additionally, sublethal effects in early embryo-larval stages were found promising for predicting delayed lethal and sublethal effects of PCB126. Therefore, the proposed method with zebrafish is expected to provide valuable information on delayed mortality and delayed sublethal effects of chemicals and environmental samples that may be extrapolated to other species.
在环境风险评估中,因暴露于亚致死化学物质浓度而导致的慢性或延迟毒性的发生日益受到关注。斑马鱼胚胎毒性(FET)试验能可靠预测成年鱼的急性毒性,但尚不能用于预测慢性或延迟毒性的发生。识别有助于预测慢性或延迟毒性发生的亚致死FET终点将具有重要意义。本研究描述了斑马鱼幼体在早期暴露于多氯联苯126(PCB126)后延迟毒性的发生情况,此前已报道PCB126会在欧洲鳎中引起延迟效应。第一个目标是研究斑马鱼幼体发育过程中延迟毒性的发生情况和时间模式,并将其与先前描述的欧洲鳎的情况进行比较,以评估斑马鱼作为延迟毒性评估模型鱼类的适用性。第二个目标是研究胚胎期和幼体早期发育阶段评估的亚致死终点与幼体后期发育阶段观察到的延迟效应之间的相关性。在受精后5天(dpf)之前暴露于PCB126(3 - 3000 ng/L)后,幼体在清洁水中饲养至14或28 dpf。每天记录死亡率以及亚致死形态和行为终点,并在28 dpf时评估生长情况。早期暴露于PCB126会导致清洁水期出现延迟死亡(300 ng/L和3000 ng/L)以及生长受损和发育延迟(100 ng/L)。在5 dpf内对鳔充气和软骨组织的影响对于预测延迟死亡和亚致死效应(如标准体长减小、变态延迟、鳔充气减少和柱状畸形)最具潜力。5 dpf时鳔充气的半数效应浓度(EC50)值(169 ng/L)与8 dpf时的半数致死浓度(LC50)值(两个实验中分别为188和202 ng/L)相似。有趣的是,欧洲鳎和斑马鱼之间延迟死亡以及对生长和发育的延迟效应模式相似。这表明不同鱼类物种(如冷水海洋比目鱼和热带淡水鲤科鱼)关键发育阶段具有可比性。此外,发现胚胎 - 幼体早期阶段的亚致死效应对于预测PCB126的延迟致死和亚致死效应很有前景。因此,所提出的斑马鱼方法有望提供有关化学物质和环境样品延迟死亡及延迟亚致死效应的有价值信息,这些信息可能外推至其他物种。