Environmentally relevant concentrations of thiamethoxam cause cytotoxic and genotoxic damage in bullfrog (Lithobates catesbeianus) tadpoles.

IF 2.7 4区 环境科学与生态学 Q2 ECOLOGY
Aline Arantes De Oliveira, Miller Caldas Barradas, Acácio Arlem Tomaz, Diego da Silva Lima, João Victor Borges Assis, Andréa Rodrigues Chaves, Thiago Bernardi Vieira, Marta Sofia Monteiro, Renato Almeida Sarmento, Althiéris de Souza Saraiva, Daniela De Melo E Silva
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Abstract

Neonicotinoids are emerging pollutants of major concern due to their widespread use and potential risks to biodiversity, yet their genetic and lethal toxicity, key parameters in environmental risk assessment, are still poorly explored in anurans. In this study, we evaluated the acute toxicity of thiamethoxam (96 h) in Lithobates catesbeianus tadpoles, determining lethal concentrations (LC10-96 h, 50-96 h, 90-96 h) and assessing subindividual effects, including genotoxicity (Comet assay), mutagenicity (Micronucleus test), and cytotoxicity, at environmentally relevant concentrations (lethal: 14.40-3516 µg a.i./L; subindividual: 9.4-59 µg a.i./L). The LC10-96 h, 50-96 h, 90-96 h were defined as 624.44, 1070.13, and 1833.03 µg a.i./L, confidence interval 95%, respectively. Subindividual exposure induced significant genotoxic effects at a concentration of 31 µg a.i./L, and mutagenic responses with an increased frequency of lobed nuclei, nuclear budding, and anucleated cells, especially at a concentration of 59 µg a.i./L. A positive correlation was observed between Comet assay parameters and nuclear abnormalities. Taken together, these findings demonstrate dose-dependent genomic damage and suggest links between distinct cellular alterations. Integrated with the lethal toxicity data, the results indicate that thiamethoxam disrupts essential cellular processes in amphibians, highlighting L. catesbeianus as a sensitive bioindicator, reinforcing the relevance of genotoxic and mutagenic biomarkers in assessing the impacts of neonicotinoids on aquatic ecosystems.

环境相关浓度的噻虫嗪对牛蛙蝌蚪造成细胞毒性和基因毒性损害。
新烟碱类化合物因其广泛使用和对生物多样性的潜在危害而成为备受关注的新兴污染物,但其遗传毒性和致死毒性作为环境风险评估的关键参数在无尾动物中的研究仍甚少。在这项研究中,我们评估了噻虫嗪(96 h)对斑岩蝌蚪的急性毒性,测定了致死浓度(LC10-96 h, 50-96 h, 90-96 h),并评估了亚个体效应,包括遗传毒性(Comet试验)、致突变性(微核试验)和细胞毒性,在环境相关浓度下(致死:14.40-3516 μ g a.i./L;亚个体:9.4-59 μ g a.i./L)。LC10-96 h、50-96 h、90-96 h分别定义为624.44、1070.13和1833.03µg a.i./L,置信区间为95%。在浓度为31 μ g a.i./L时,亚个体暴露诱导了显著的基因毒性效应,并且随着分叶细胞核、核出芽和无核细胞的频率增加而发生诱变反应,特别是在浓度为59 μ g a.i./L时。彗星试验参数与核异常呈正相关。综上所述,这些发现证明了剂量依赖性基因组损伤,并提示了不同细胞改变之间的联系。结合致死毒性数据,结果表明噻虫嗪破坏两栖动物的基本细胞过程,突出了L. catesbeianus作为敏感的生物指标,加强了基因毒性和诱变生物标志物在评估新烟碱类对水生生态系统影响中的相关性。
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来源期刊
Ecotoxicology
Ecotoxicology 环境科学-毒理学
CiteScore
5.30
自引率
3.70%
发文量
107
审稿时长
4.7 months
期刊介绍: Ecotoxicology is an international journal devoted to the publication of fundamental research on the effects of toxic chemicals on populations, communities and terrestrial, freshwater and marine ecosystems. It aims to elucidate mechanisms and processes whereby chemicals exert their effects on ecosystems and the impact caused at the population or community level. The journal is not biased with respect to taxon or biome, and papers that indicate possible new approaches to regulation and control of toxic chemicals and those aiding in formulating ways of conserving threatened species are particularly welcome. Studies on individuals should demonstrate linkage to population effects in clear and quantitative ways. Laboratory studies must show a clear linkage to specific field situations. The journal includes not only original research papers but technical notes and review articles, both invited and submitted. A strong, broadly based editorial board ensures as wide an international coverage as possible.
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