Development of an assay for the detection of the federally threatened Florida eastern indigo snake (Drymarchon couperi) using soil eDNA

IF 2.8 2区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION
Carlos A. Santamaria, Emily Galbraith, Alison M. Gainsbury
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Abstract

Accurate information on species range contraction is the cornerstone of effective biodiversity conservation. The eastern indigo snake (Drymarchon couperi) is an apex predator in Florida and, similar to many species native to Florida, is threatened by widespread habitat destruction. Environmental deoxyribonucleic acid (eDNA) monitoring of this elusive snake would provide a non-invasive approach to improve our knowledge of the species' range and distribution. We designed and tested an eDNA assay that can detect the presence of D. couperi from soil samples from their natural scrub habitat in Florida. We validated our assay in silico, in vitro, and in situ. Furthermore, we investigated the influence of temperature and humidity on the degradation rate of eDNA over time. We successfully amplified the cytochrome b gene for D. couperi at concentrations as low as 3 × 10−3 ng/μL and successfully detected the presence of D. couperi in 2 of 30 in situ field soil samples. The degradation experiment resulted in detectable DNA for 10 days. Interestingly, temperature and humidity had no effect on the degradation rate of eDNA in our experimental conditions. This study provides support for soil eDNA applications to detect the presence of a federally threatened species in their natural environment bolstering our ability to monitor the conservation and management of imperiled species. Environmental DNA provides an additional conservation tool to quickly and effectively monitor species range shifts driven by multiple anthropogenic stressors to promote the persistence of imperiled species.

Abstract Image

利用土壤 eDNA 开发检测受联邦威胁的佛罗里达东部靛蓝蛇(Drymarchon couperi)的方法
物种分布范围缩小的准确信息是有效保护生物多样性的基石。东部靛青蛇(Drymarchon couperi)是佛罗里达州的一种顶级掠食者,与许多原产于佛罗里达州的物种类似,受到广泛栖息地破坏的威胁。对这种难以捉摸的蛇类进行环境脱氧核糖核酸(eDNA)监测将提供一种非侵入性方法,以提高我们对该物种的分布范围和分布情况的了解。我们设计并测试了一种 eDNA 检测方法,该方法可以从佛罗里达州库珀蛇自然灌丛栖息地的土壤样本中检测到库珀蛇的存在。我们在硅学、体外和原位验证了我们的检测方法。此外,我们还研究了温度和湿度对 eDNA 随着时间推移的降解率的影响。我们在低至 3 × 10-3 纳克/微升的浓度下成功扩增了库伯鱼的细胞色素 b 基因,并在 30 份现场土壤样本中的 2 份样本中成功检测到库伯鱼的存在。降解实验的结果是,10 天内都能检测到 DNA。有趣的是,在我们的实验条件下,温度和湿度对 eDNA 的降解率没有影响。这项研究为应用土壤 eDNA 检测自然环境中是否存在联邦濒危物种提供了支持,增强了我们监测濒危物种保护和管理的能力。环境 DNA 提供了另一种保护工具,可快速有效地监测多种人为压力因素导致的物种分布范围变化,从而促进濒危物种的生存。
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来源期刊
Conservation Science and Practice
Conservation Science and Practice BIODIVERSITY CONSERVATION-
CiteScore
5.50
自引率
6.50%
发文量
240
审稿时长
10 weeks
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