Rapid identification of reproductive toxicants among environmental chemicals using an in vivo evaluation of gametogenesis in budding yeast Saccharomyces cerevisiae

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-06-19 DOI:10.1016/j.reprotox.2024.108630
Ravinder Kumar , Ashwini Oke , Beth Rockmill , Matthew de Cruz , Rafael Verduzco , Anura Shodhan , Xavier Woodruff-Madeira , Dimitri P. Abrahamsson , Julia Varshavsky , Juleen Lam , Joshua F. Robinson , Patrick Allard , Tracey J. Woodruff , Jennifer C. Fung
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Abstract

Infertility affects ∼12 % of couples, with environmental chemical exposure as a potential contributor. Of the chemicals that are actively manufactured, very few are assessed for reproductive health effects. Rodents are commonly used to evaluate reproductive effects, which is both costly and time consuming. Thus, there is a pressing need for rapid methods to test a broader range of chemicals. Here, we developed a strategy to evaluate large numbers of chemicals for reproductive toxicity via a yeast, S. cerevisiae high-throughput assay to assess gametogenesis as a potential new approach method (NAM). By simultaneously assessing chemicals for growth effects, we can distinguish if a chemical affects gametogenesis only, proliferative growth only or both. We identified a well-known mammalian reproductive toxicant, bisphenol A (BPA) and ranked 19 BPA analogs for reproductive harm. By testing mixtures of BPA and its analogs, we found that BPE and 17 β-estradiol each together with BPA showed synergistic effects that worsened reproductive outcome. We examined an additional 179 environmental chemicals including phthalates, pesticides, quaternary ammonium compounds and per- and polyfluoroalkyl substances and found 57 with reproductive effects. Many of the chemicals were found to be strong reproductive toxicants that have yet to be tested in mammals. Chemicals having affect before meiosis I division vs. meiosis II division were identified for 16 gametogenesis-specific chemicals. Finally, we demonstrate that in general yeast reproductive toxicity correlates well with published reproductive toxicity in mammals illustrating the promise of this NAM to quickly assess chemicals to prioritize the evaluation for human reproductive harm.

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利用对出芽酵母配子发生的体内评估,快速识别环境化学品中的生殖毒性物质。
不孕症影响着约 12% 的夫妇,环境中的化学品暴露是潜在的诱因之一。在目前生产的化学品中,很少有化学品会对生殖健康产生影响。通常使用啮齿动物来评估对生殖的影响,这既昂贵又耗时。因此,我们迫切需要快速方法来检测更广泛的化学品。在此,我们开发了一种策略,通过酵母菌(S. cerevisiae)高通量试验来评估大量化学品的生殖毒性,从而评估配子的发生,将其作为一种潜在的新方法(NAM)。通过同时评估化学物质对生长的影响,我们可以区分某种化学物质是只影响配子发生,还是只影响增殖生长,抑或是两者兼而有之。我们确定了一种众所周知的哺乳动物生殖毒性物质--双酚 A(BPA),并对 19 种双酚 A 类似物的生殖危害进行了排名。通过测试双酚 A 及其类似物的混合物,我们发现 BPE 和 17 β-雌二醇与双酚 A 在一起会产生协同效应,导致生殖结果恶化。我们还研究了另外 179 种环境化学物质,包括邻苯二甲酸盐、杀虫剂、季铵化合物以及全氟和多氟烷基物质,发现其中 57 种对生殖有影响。发现其中许多化学物质具有强烈的生殖毒性,但尚未在哺乳动物体内进行测试。在减数分裂 I 分裂与减数分裂 II 分裂之前,我们发现了 16 种对配子发生有特异性影响的化学物质。最后,我们证明,一般来说,酵母的生殖毒性与已公布的哺乳动物生殖毒性有很好的相关性,这说明这种 NAM 可以快速评估化学品,优先评估其对人类生殖的危害。
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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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