Addressing Amazonian Fish Diversity Using Environmental DNA (eDNA): A First Glance

Larissa Matos Batista, Carolina Sousa De Sá-Leitão, Érica Martinha Silva de Souza, Carlos Henrique Dos Anjos-Santos, V. M. D. de Almeida-Val
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引用次数: 1

Abstract

Environmental DNA (eDNA) is considered to be an innovative method that can be used in the detection and identification of species present in aquatic environments, adding the advantage of describing the ichthyofauna without capturing the organisms. Out of the two possible approaches of eDNA, the metabarcoding approach aims to identify the diversity of a specific taxon and its composition using a universal DNA primer. This approach has grown considerably in recent years, although most studies focus on temperate regions, which causes a lack of clarity about the potential of the method in tropical regions since these have very distinct abiotic characteristics, as well as a higher diversity of fauna and flora. Therefore, as a way to verify the potential use of eDNA metabarcoding, this study focused on the Neotropical region, specifically the Amazon basin, a place with the highest ichthyofaunistic biodiversity in the world. As such, the goal of this study was to detect the composition of the main taxonomic groups of fish in the small stream Tarumã-Mirim, an acidic blackwater river that is located nearby Manaus city and is part of an environmental protection area near the city of Manaus, Brazil. For that, water samples of 6 L were collected along the river at 5 points (totaling 30 L). The water samples were stored in ice boxes and transported to the laboratory for filtration in fiberglass filters. Following the filtration and the extraction of eDNA, the samples were amplified in PCRs machines, using the universal primers MiFish developed by Miya et al., (2015). The next steps were: the construction of eDNA libraries, the sequencing on Illumina – Miseq platform, and a bioinformatic analysis. For the taxonomic identification of the eDNA sequences we used the sequences deposited in GenBank and the reference database developed specifically for Amazonian fish. The application and efficiency of eDNA metabarcoding for the samples, identified 42 molecular operational taxonomic units (MOTUs), which were grouped into six orders and eight families. A refined approach identified seven species and one genus. In addition, since eDNA samples were obtained along the entire river, it was possible to build a distribution map of fish species. Despite the limitation in identifying the abundance of all taxonomic groups present in the Tarumã-Mirim River, the metabarcoding approach for the eDNA was able to identify the species that have their contemporary distribution in the Amazonian rivers, as well as the detection of the three main groups of fish. Thus, the method may serve as a complement to ecological studies for the detection, identification and monitoring the Amazonian ichthyofauna. These results show that the eDNA approach needs to be optimized in tropical regions since the biotic and abiotic characteristics, which are peculiar to the tropics (acidic waters, high temperatures, etc.), may affect the adequate detection of the rich biodiversity of such sites
利用环境DNA (eDNA)解决亚马逊鱼类多样性:第一眼
环境DNA (Environmental DNA, eDNA)被认为是一种创新的方法,可以用于检测和鉴定存在于水生环境中的物种,增加了描述鱼类动物而不捕获生物的优势。在两种可能的eDNA方法中,元条形码方法旨在使用通用DNA引物识别特定分类单元的多样性及其组成。这种方法近年来有了很大的发展,尽管大多数研究集中在温带地区,这导致该方法在热带地区的潜力缺乏明确性,因为这些地区具有非常明显的非生物特征,以及更高的动植物多样性。因此,为了验证eDNA元条形码的潜在用途,本研究将重点放在新热带地区,特别是亚马逊流域,这是世界上鱼类生物多样性最高的地方。因此,本研究的目的是检测tarum - mirim小溪中主要分类类群的组成,这条酸性黑水河流位于马瑙斯市附近,是巴西马瑙斯市附近环境保护区的一部分。为此,沿河5点采集水样6升(共30升),水样保存在冰柜中,运至实验室用玻璃纤维过滤器过滤。在过滤和提取eDNA之后,使用Miya等人(2015)开发的通用引物MiFish在pcr机器中扩增样品。接下来的步骤是:构建eDNA文库,在Illumina - Miseq平台上测序,进行生物信息学分析。为了对eDNA序列进行分类鉴定,我们使用了储存在GenBank中的序列和专门为亚马逊鱼开发的参考数据库。eDNA元条形码技术在样品中的应用及效率分析表明,鉴定出42个分子操作分类单位(motu),隶属于6目8科。一种改进的方法鉴定出7种和1属。此外,由于沿整条河获得了eDNA样本,因此有可能建立鱼类分布图。尽管在识别tarum - mirim河中存在的所有分类群的丰度方面存在局限性,但eDNA的元条形码方法能够识别出在亚马逊河中具有当代分布的物种,以及三种主要鱼类的检测。因此,该方法可以作为生态学研究的补充,用于检测、鉴定和监测亚马逊鱼系动物。这些结果表明,eDNA方法需要在热带地区进行优化,因为热带地区特有的生物和非生物特征(酸性水域、高温等)可能会影响对这些地点丰富的生物多样性的充分检测
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