Dayeh Vivian R, Solhaug Anita, Hamilton Mark E, Linton Laura E, Lee Lucy E J, Bols Niels C
Department of Biology, University of Waterloo, Waterloo, ON, N2L 3G1, Canada.
Norwegian Veterinary Institute, 1433, Ås, Norway.
In Vitro Cell Dev Biol Anim. 2025 Feb 3. doi: 10.1007/s11626-025-01014-5.
Mycotoxins in aquatic feeds and their effects on fish are becoming more important in aquaculture, as fishmeal and fish oil in feeds are being replaced with more sustainable plant protein. Here, we investigated the potential of the mycotoxin, beauvericin (BEA), to impact the rainbow trout (RT) intestine by using cultures of the epithelial cell line, RTgutGC. BEA was dosed in different ways and exposed at temperatures ranging from 4 to 26 °C before being evaluated for cell viability by the metabolic reduction of Alamar Blue, by the accumulation of Neutral Red (lysosomal activity), cytotoxicity (CellTox Green), and for wound healing. BEA induces cell death in RTgutGC cells. The lysosomes are the main target (Neutral Red assay is the most sensitive) while cytotoxicity and plasma membrane rupture (CellTox Green) occur at considerably higher concentrations. BEA caused a dose-dependent decline in Neutral Red reading at all tested temperatures but Alamar Blue readings did not decline at 4 °C. Under these conditions, BEA appears to impair only lysosomal activity. Wound healing was reduced at 4, 10, and 26 °C compared to 18 °C. Also BEA treatment, at non-cytotoxic concentrations, reduced wound healing, but the temperature had little influence on this. Different carrier vehicles (methanol, DMSO) and exposure methods (passive or active dispersal) for BEA exposure were also studied. Here, methanol and passive dispersal gave comparable results to exposure with DMSO and active dispersal. In contrast, when DMSO was dosed with passive dispersal, immediate cytotoxicity in combination with BEA was induced.
随着水产饲料中的鱼粉和鱼油被更具可持续性的植物蛋白所取代,水产饲料中的霉菌毒素及其对鱼类的影响在水产养殖中变得愈发重要。在此,我们通过使用虹鳟鱼(RT)肠道上皮细胞系RTgutGC培养物,研究了霉菌毒素白僵菌素(BEA)对虹鳟鱼肠道的潜在影响。BEA采用不同方式给药,并在4至26°C的温度范围内进行暴露,然后通过Alamar Blue的代谢还原、中性红的积累(溶酶体活性)、细胞毒性(CellTox Green)以及伤口愈合情况来评估细胞活力。BEA可诱导RTgutGC细胞死亡。溶酶体是主要靶点(中性红测定最为敏感),而细胞毒性和质膜破裂(CellTox Green)则在相当高的浓度下才会出现。在所有测试温度下,BEA都会导致中性红读数呈剂量依赖性下降,但在4°C时Alamar Blue读数并未下降。在这些条件下,BEA似乎仅损害溶酶体活性。与18°C相比,在4°C、10°C和26°C时伤口愈合能力下降。此外,在非细胞毒性浓度下,BEA处理也会降低伤口愈合能力,但温度对此影响不大。还研究了BEA暴露的不同载体(甲醇、二甲基亚砜)和暴露方法(被动或主动分散)。在此,甲醇和被动分散与二甲基亚砜和主动分散暴露的结果相当。相比之下,当二甲基亚砜采用被动分散给药时,会诱导与BEA相关的即时细胞毒性。