Christopher Keneally, Virginie Gaget, Stephen P. Kidd, Justin D. Brookes
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This study evaluates environmental nucleic acid (eNA) sampling methods across salinity gradients in aquatic ecosystems, focusing on the impact of preservation techniques on environmental DNA (eDNA) yield and environmental RNA (eRNA) yield and quality. Fieldwork was conducted at three sites within the Coorong estuary system in South Australia, representing low salinity, marine, and hypersaline conditions. Snap freezing and <i>LifeGuard</i> preservation solution treatments were applied in situ to compare their effects on nucleic acid yields and eRNA integrity. Snap freezing enhanced eDNA yield in low salinity sediments but negatively impacted eRNA integrity in marine and hypersaline conditions. Conversely, treatment with preservation solution consistently improved both eDNA and eRNA recovery across all salinity levels, which makes this approach a good candidate for preserving eNA molecules across environmental gradients. 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引用次数: 0
摘要
基于环境核酸的评估是了解微生物生态学和水生环境退化的有力工具。这种方法对于指导河口(世界上一些退化最严重的生态系统)的恢复尤其有用。随着这种方法的普及,应用方法的多样性也在不断增加。该领域存在一系列最佳实践方法,可根据环境因素(如物理化学梯度、产量最大化以及研究区域内不同地点的核酸采样质量)进行选择。研究区内核酸采样的一致方法还能确保这些地点之间的准确比较。本研究评估了水生生态系统中不同盐度梯度的环境核酸(ENA)采样方法,重点关注保存技术对环境 DNA(eDNA)产量和环境 RNA(eRNA)产量及质量的影响。实地考察在南澳大利亚库龙河口系统的三个地点进行,分别代表低盐度、海洋和高盐度条件。研究人员在现场采用了速冻和 LifeGuard 保存液处理方法,以比较它们对核酸产量和 eRNA 完整性的影响。快速冷冻提高了低盐度沉积物中的 eDNA 产量,但对海洋和高盐度条件下的 eRNA 完整性产生了负面影响。相反,在所有盐度水平下,用保存液处理都能持续提高 eDNA 和 eRNA 的回收率,这使得这种方法成为跨越环境梯度保存 eNA 分子的良好候选方法。这项研究强调了根据特定环境条件调整样本保存方法的必要性,以便对沿岸生态系统中基于 eNA 的微生物群落进行准确评估。这些发现有助于为不同盐度条件下的底栖生物群落制定稳健的 eNA 采样方案。
Sample Preservation Solution Increases Nucleic Acid Yield and Environmental RNA Quality in Sediments Across an Estuarine Salinity Gradient
Environmental nucleic acid-based assessments are powerful tools for understanding microbial ecology, and environmental degradation in aquatic environments. This approach is particularly useful in guiding restoration in estuaries, some of the most degraded ecosystems in the world. The recent popularity of this approach has been accompanied by a parallel increase in the diversity of applied methods. A range of best practice methods exist across the field that can be employed and are selected based on environmental considerations such as physicochemical gradients, maximizing yield, and quality of nucleic acids sampled across sites within a study area. A consistent approach to intra-study nucleic acid sampling also ensures accurate comparison between those sites. This study evaluates environmental nucleic acid (eNA) sampling methods across salinity gradients in aquatic ecosystems, focusing on the impact of preservation techniques on environmental DNA (eDNA) yield and environmental RNA (eRNA) yield and quality. Fieldwork was conducted at three sites within the Coorong estuary system in South Australia, representing low salinity, marine, and hypersaline conditions. Snap freezing and LifeGuard preservation solution treatments were applied in situ to compare their effects on nucleic acid yields and eRNA integrity. Snap freezing enhanced eDNA yield in low salinity sediments but negatively impacted eRNA integrity in marine and hypersaline conditions. Conversely, treatment with preservation solution consistently improved both eDNA and eRNA recovery across all salinity levels, which makes this approach a good candidate for preserving eNA molecules across environmental gradients. The study underscores the necessity of tailoring sample preservation methods to specific environmental conditions for accurate eNA-based microbial community assessments in coastal ecosystems. These findings contribute to the development of robust eNA sampling protocols for benthic communities under varying salinity conditions.