多种全氟辛烷磺酸会产生与斑马鱼发育毒性有关的独特转录组变化

IF 3.6 Q2 TOXICOLOGY Frontiers in toxicology Pub Date : 2024-07-22 DOI:10.3389/ftox.2024.1425537
Yvonne Rericha, Lindsey St. Mary, Lisa Truong, Ryan McClure, J. K. Martin, Scott W. Leonard, Preethi Thunga, Michael T. Simonich, Katrina M. Waters, Jennifer A. Field, R. Tanguay
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引用次数: 0

摘要

全氟烷基和多氟烷基物质(PFAS)是一类广泛存在且具有持久性的污染物,对环境和人类健康造成了重大影响。目前还缺乏对结构各异的全氟烷基化合物毒性作用模式的全面了解。为了满足这一需求,我们最近报告了我们应用斑马鱼来评估大量 PFAS 的发育毒性。在本研究中,我们优先选择了 15 种能诱导显著形态学效应的生物活性全氟辛烷磺酸,并在早期发育暴露(受精后 8 小时)后的单一时间点(受精后 48 小时)进行了 RNA 序列分析,以确定早期转录反应的特征。在受精后 24-120 小时之间的多个时间点,从汇集的全鱼样本中测定了 15 种 PFAS 中 5 种的内部浓度,并在多个时间点(受精后 48-96 小时)对 Nafion 副产品 2 进行了额外的时间转录组学研究。在各种全氟辛烷磺酸暴露中发现了大量差异表达基因。大多数引起强大转录组变化的 PFAS 影响了大脑和神经系统发育的生物过程。虽然全氟辛烷磺酸破坏了独特的过程,但我们也发现,全氟辛烷磺酸的某些功能头组的相似性与相似基因组表达的破坏有关。在发育早期接触特定磺酸类全氟辛烷磺酸(包括纳菲昂副产物2)后,体内负荷在受精后24-96小时采样时间点增加,且高于链长相似的磺酰胺类全氟辛烷磺酸。与此同时,Nafion 副产品 2 诱导的转录反应在施肥后 48 至 96 小时内也有所增加。基于毒性、转录组效应和作用模式的全氟辛烷磺酸特性将有助于进一步确定全氟辛烷磺酸结构的优先次序,以便进行测试和知情危害评估。
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Diverse PFAS produce unique transcriptomic changes linked to developmental toxicity in zebrafish
Per- and polyfluoroalkyl substances (PFAS) are a widespread and persistent class of contaminants posing significant environmental and human health concerns. Comprehensive understanding of the modes of action underlying toxicity among structurally diverse PFAS is mostly lacking. To address this need, we recently reported on our application of developing zebrafish to evaluate a large library of PFAS for developmental toxicity. In the present study, we prioritized 15 bioactive PFAS that induced significant morphological effects and performed RNA-sequencing to characterize early transcriptional responses at a single timepoint (48 h post fertilization) after early developmental exposures (8 h post fertilization). Internal concentrations of 5 of the 15 PFAS were measured from pooled whole fish samples across multiple timepoints between 24–120 h post fertilization, and additional temporal transcriptomics at several timepoints (48–96 h post fertilization) were conducted for Nafion byproduct 2. A broad range of differentially expressed gene counts were identified across the PFAS exposures. Most PFAS that elicited robust transcriptomic changes affected biological processes of the brain and nervous system development. While PFAS disrupted unique processes, we also found that similarities in some functional head groups of PFAS were associated with the disruption in expression of similar gene sets. Body burdens after early developmental exposures to select sulfonic acid PFAS, including Nafion byproduct 2, increased from the 24–96 h post fertilization sampling timepoints and were greater than those of sulfonamide PFAS of similar chain lengths. In parallel, the Nafion byproduct 2-induced transcriptional responses increased between 48 and 96 h post fertilization. PFAS characteristics based on toxicity, transcriptomic effects, and modes of action will contribute to further prioritization of PFAS structures for testing and informed hazard assessment.
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