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应用环境DNA检测野生濒危海鳐物种。

Application of environmental DNA to detect an endangered marine skate species in the wild.

作者信息

Weltz Kay, Lyle Jeremy M, Ovenden Jennifer, Morgan Jessica A T, Moreno David A, Semmens Jayson M

机构信息

Fisheries and Aquaculture Centre, Institute for Marine and Antarctic Studies, University of Tasmania, Hobart, Tasmania, Australia.

Molecular Fisheries Laboratory, School of Biomedical Sciences, University of Queensland, Brisbane, Queensland, Australia.

出版信息

PLoS One. 2017 Jun 7;12(6):e0178124. doi: 10.1371/journal.pone.0178124. eCollection 2017.

Abstract

Environmental DNA (eDNA) techniques have only recently been applied in the marine environment to detect the presence of marine species. Species-specific primers and probes were designed to detect the eDNA of the endangered Maugean skate (Zearaja maugeana) from as little as 1 L of water collected at depth (10-15 m) in Macquarie Harbour (MH), Tasmania. The identity of the eDNA was confirmed as Z. maugeana by sequencing the qPCR products and aligning these with the target sequence for a 100% match. This result has validated the use of this eDNA technique for detecting a rare species, Z. maugeana, in the wild. Being able to investigate the presence, and possibly the abundance, of Z. maugeana in MH and Bathurst harbour (BH), would be addressing a conservation imperative for the endangered Z. maugeana. For future application of this technique in the field, the rate of decay was determined for Z. maugeana eDNA under ambient dissolved oxygen (DO) levels (55% saturation) and lower DO (20% saturation) levels, revealing that the eDNA can be detected for 4 and 16 hours respectively, after which eDNA concentration drops below the detection threshold of the assay. With the rate of decay being influenced by starting eDNA concentrations, it is recommended that samples be filtered as soon as possible after collection to minimize further loss of eDNA prior to and during sample processing.

摘要

环境DNA(eDNA)技术直到最近才应用于海洋环境中以检测海洋物种的存在。设计了物种特异性引物和探针,用于从塔斯马尼亚州麦夸里港(MH)深度为10至15米处采集的仅1升水样中检测濒危的莫氏鳐(Zearaja maugeana)的eDNA。通过对qPCR产物进行测序并将其与目标序列比对以实现100%匹配,确认了该eDNA为莫氏鳐。这一结果验证了这种eDNA技术在野外检测珍稀物种莫氏鳐的用途。能够调查莫氏鳐在麦夸里港和巴瑟斯特港(BH)的存在情况以及可能的数量,将满足濒危物种莫氏鳐的保护需求。对于该技术在野外的未来应用,测定了莫氏鳐eDNA在环境溶解氧(DO)水平(55%饱和度)和较低DO(20%饱和度)水平下的衰减率,结果表明,eDNA分别可在4小时和16小时内被检测到,之后eDNA浓度降至检测阈值以下。由于衰减率受起始eDNA浓度影响,建议在采集后尽快对样品进行过滤,以尽量减少样品处理前及处理过程中eDNA的进一步损失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f49/5462358/934c9021b28d/pone.0178124.g001.jpg

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