Using environmental (e)DNA sequencing for aquatic biodiversity surveys: a beginner's guide

被引:41
作者
Shaw, Jennifer L. A. [1 ,2 ]
Weyrich, Laura [1 ]
Cooper, Alan [1 ]
机构
[1] Univ Adelaide, Australian Ctr Ancient DNA ACAD, Darling Bldg,North Terrace, Adelaide, SA 5000, Australia
[2] CSIRO, Land & Water Flagship, Prescott Bldg,Waite Rd, Urrbrae, SA 5064, Australia
关键词
metabarcoding; metagenomics; methods; monitoring; NGS; summary; FRESH-WATER BIODIVERSITY; DNA BARCODE; MICROBIAL DIVERSITY; COMMUNITY STRUCTURE; DEEP-SEA; BACTERIAL; RNA; EXTRACTION; ABUNDANCE; BIAS;
D O I
10.1071/MF15361
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Biological surveys are needed to monitor and assess the health of ecosystems and the species within them. However, morphology-based biodiversity surveys can be invasive, time consuming and financially expensive. Recently, environmental (e)DNA sequencing has been demonstrated as a potential alternative to morphological-based surveys because it enables the rapid and inexpensive detection of multiple taxa from DNA present in the environment. Numerous studies have shown that eDNA-based biodiversity surveys can provide considerable information about aquatic ecosystem function and health. Therefore, this molecular method has the potential to improve how current aquatic biological surveys are conducted. Currently, most eDNA literature is aimed at an audience with a moderate to advanced knowledge of DNA sequencing, creating a barrier for many ecologists who lack DNA sequencing expertise but wish to apply such methods to their research. The aim of this review is to provide guidance to non-geneticists regarding sequencing eDNA for aquatic biodiversity surveys and to highlight the requirements that need to be considered before the technique can be effectively incorporated into biomonitoring programs. Specifically, we provide details and recommendations on some of the major principles, from sample collection to bioinformatic analyses. For those areas where specific recommendations cannot be given, we have provided references to suitable literature.
引用
收藏
页码:20 / 33
页数:14
相关论文
共 117 条
[1]   Quantifying microbial communities with 454 pyrosequencing: does read abundance count? [J].
Amend, Anthony S. ;
Seifert, Keith A. ;
Bruns, Thomas D. .
MOLECULAR ECOLOGY, 2010, 19 (24) :5555-5565
[2]   Meta-barcoding of 'dirt' DNA from soil reflects vertebrate biodiversity [J].
Andersen, Kenneth ;
Bird, Karen Lise ;
Rasmussen, Morten ;
Haile, James ;
Breuning-Madsen, Henrik ;
Kjaer, Kurt H. ;
Orlando, Ludovic ;
Gilbert, M. Thomas P. ;
Willerslev, Eske .
MOLECULAR ECOLOGY, 2012, 21 (08) :1966-1979
[3]   Basic principles of real-time quantitative PCR [J].
Arya, M ;
Shergill, IS ;
Williamson, M ;
Gommersall, L ;
Arya, N ;
Patel, HRH .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (02) :209-219
[4]  
Awano T, 2009, P NATL ACAD SCI USA, V106, P2794, DOI [10.1073/pnas.0905845106, 10.1073/pnas.0812297106]
[5]   Biomonitoring 2.0: a new paradigm in ecosystem assessment made possible by next-generation DNA sequencing [J].
Baird, Donald J. ;
Hajibabaei, Mehrdad .
MOLECULAR ECOLOGY, 2012, 21 (08) :2039-2044
[6]   ITS as an environmental DNA barcode for fungi: an in silico approach reveals potential PCR biases [J].
Bellemain, Eva ;
Carlsen, Tor ;
Brochmann, Christian ;
Coissac, Eric ;
Taberlet, Pierre ;
Kauserud, Havard .
BMC MICROBIOLOGY, 2010, 10
[7]   Sequencing our way towards understanding global eukaryotic biodiversity [J].
Bik, Holly M. ;
Porazinska, Dorota L. ;
Creer, Simon ;
Caporaso, J. Gregory ;
Knight, Rob ;
Thomas, W. Kelley .
TRENDS IN ECOLOGY & EVOLUTION, 2012, 27 (04) :233-243
[8]   The Use of Coded PCR Primers Enables High-Throughput Sequencing of Multiple Homolog Amplification Products by 454 Parallel Sequencing [J].
Binladen, Jonas ;
Gilbert, M. Thomas P. ;
Bollback, Jonathan P. ;
Panitz, Frank ;
Bendixen, Christian ;
Nielsen, Rasmus ;
Willerslev, Eske .
PLOS ONE, 2007, 2 (02)
[9]  
Blankenberg Daniel, 2010, Curr Protoc Mol Biol, VChapter 19, DOI 10.1002/0471142727.mb1910s89
[10]  
Burger J, 1999, ELECTROPHORESIS, V20, P1722