Ruiz Eliot, Leprieur Fabien, Sposito Gérard, Lüthi Martina, Schmidlin Michel, Panfili Jacques, Pellissier Loïc, Albouy Camille
MARBEC, Univ Montpellier, IRD, IFREMER, CNRS Montpellier France.
Mediterranean Coastal Environment Station University of Montpellier Sète France.
Ecol Evol. 2025 Feb 12;15(2):e70645. doi: 10.1002/ece3.70645. eCollection 2025 Feb.
While acquiring age information is crucial for efficient stock management and biodiversity conservation, traditional aging methods fail to offer a universal, non-invasive, and precise way of estimating a wild animal's age. DNA methylation from tissue DNA (tDNA) was recently proposed as a method to overcome these issues and showed more accurate results than telomere-length-based age assessments. Here, we used environmental DNA (eDNA) for the first time as a template for age estimation, focusing on the larval phase (10-24 days post-hatch) of cultured (seabass), a species of major economic and conservation interest. Using third-generation sequencing, we were able to directly detect various modification types (e.g., cytosine and adenosine methylation in all contexts) across the whole genome using amplification-free nanopore sequencing. However, aging sites were only present in the mitogenome, which could be a specific feature of eDNA methylation or the consequence of better DNA protection within mitochondria. By considering qualitative and quantitative information about aging sites according to an objective model selection framework, our epigenetic clock reached a cross-validated accuracy of 2.6 days (Median Absolute Error). Such performances are higher than those of previous clocks, notably for adult seabass even when scaling MAE to the age range, which could be linked to a more dynamic epigenome during early life stages. Overall, our pilot study proposes new methods to determine the potential of eDNA for simultaneous age and biodiversity assessments, although robust validation of our preliminary results along with methodological developments are needed before field applications can be envisaged.
虽然获取年龄信息对于高效的种群管理和生物多样性保护至关重要,但传统的年龄鉴定方法无法提供一种通用、非侵入性且精确的估算野生动物年龄的方法。最近,基于组织DNA(tDNA)的DNA甲基化被提出作为一种克服这些问题的方法,并且比基于端粒长度的年龄评估显示出更准确的结果。在这里,我们首次使用环境DNA(eDNA)作为年龄估计的模板,重点关注养殖海鲈(一种具有重要经济和保护价值的物种)的幼体阶段(孵化后10 - 24天)。使用第三代测序技术,我们能够通过无扩增纳米孔测序直接检测全基因组中的各种修饰类型(例如,所有背景下的胞嘧啶和腺苷甲基化)。然而,衰老位点仅存在于线粒体基因组中,这可能是eDNA甲基化的一个特定特征,或者是线粒体内更好的DNA保护的结果。根据一个客观的模型选择框架,通过考虑衰老位点的定性和定量信息,我们的表观遗传时钟达到了2.6天的交叉验证准确率(平均绝对误差)。这样的性能高于以前的时钟,特别是对于成年海鲈,即使将平均绝对误差按年龄范围进行缩放时也是如此,这可能与生命早期阶段更动态的表观基因组有关。总体而言,我们的初步研究提出了新的方法来确定eDNA在同时进行年龄和生物多样性评估方面的潜力,尽管在考虑实际应用之前,需要对我们的初步结果进行有力的验证以及方法学的进一步发展。