Nucleic acids-based tools for ballast water surveillance, monitoring, and research

被引:27
作者
Darling, John A. [1 ]
Frederick, Raymond M. [2 ]
机构
[1] US EPA, Natl Exposure Res Lab, Res Triangle Pk, NC 27711 USA
[2] US EPA, Natl Risk Management Res Lab, Edison, NJ USA
关键词
Ballast water; Monitoring; Nucleic acids; PCR; High throughput sequencing; Compliance; ENVIRONMENTAL DNA; GREAT-LAKES; BIODIVERSITY ASSESSMENT; ESCHERICHIA-COLI; UV DISINFECTION; FLOW-CYTOMETRY; PHYTOPLANKTON; PERFORMANCE; DIVERSITY; SHIPS;
D O I
10.1016/j.seares.2017.02.005
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Understanding the risks of biological invasion posed by ballast water-whether in the context of compliance testing, routine monitoring, or basic research-is fundamentally an exercise in biodiversity assessment, and as such should take advantage of the best tools available for tackling that problem. The past several decades have seen growing application of genetic methods for the study of biodiversity, driven in large part by dramatic technological advances in nucleic acids analysis. Monitoring approaches based on such methods have the potential to increase dramatically sampling throughput for biodiversity assessments, and to improve on the sensitivity, specificity, and taxonomic accuracy of traditional approaches. The application of targeted detection tools (largely focused on PCR but increasingly incorporating novel probe-based methodologies) has led to a paradigm shift in rare species monitoring, and such tools have already been applied for early detection in the context of ballast water surveillance. Rapid improvements in community profiling approaches based on high throughput sequencing (HTS) could similarly impact broader efforts to catalogue biodiversity present in ballast tanks, and could provide novel opportunities to better understand the risks of biotic exchange posed by ballast water transport-and the effectiveness of attempts to mitigate those risks. These various approaches still face considerable challenges to effective implementation, depending on particular management or research needs. Compliance testing, for instance, remains dependent on accurate quantification of viable target organisms; while tools based on RNA detection show promise in this context, the demands of such testing require considerable additional investment in methods development. In general surveillance and research contexts, both targeted and community-based approaches are still limited by various factors: quantification remains a challenge (especially for taxa in larger size classes), gaps in nucleic acids reference databases are still considerable, uncertainties in taxonomic assignment methods persist, and many applications have not yet matured sufficiently to offer standardized methods capable of meeting rigorous quality assurance standards. Nevertheless, the potential value of these tools, their growing utilization in biodiversity monitoring, and the rapid methodological advances over the past decade all suggest that they should be seriously considered for inclusion in the ballast water surveillance toolkit. Published by Elsevier B.V.
引用
收藏
页码:43 / 52
页数:10
相关论文
共 96 条
  • [1] Evaluating the response of freshwater organisms to vital staining
    Adams, Jennifer K.
    Briski, Elizabeta
    Ram, Jeffrey L.
    Bailey, Sarah A.
    [J]. MANAGEMENT OF BIOLOGICAL INVASIONS, 2014, 5 (03): : 197 - 208
  • [2] [Anonymous], 2012, Federal Register, V77, P17254
  • [3] Environmental DNA evidence of transfer of North Sea molluscs across tropical waters through ballast water
    Ardura, Alba
    Zaiko, Anastasija
    Martinez, Jose L.
    Samuiloviene, Aurelija
    Borrell, Yaisel
    Garcia-Vazquez, Eva
    [J]. JOURNAL OF MOLLUSCAN STUDIES, 2015, 81 : 495 - 501
  • [4] Multiplex PCR allows simultaneous detection of pathogens in ships' ballast water
    Aridgides, LJ
    Doblin, MA
    Berke, T
    Dobbs, FC
    Matson, DO
    Drake, LA
    [J]. MARINE POLLUTION BULLETIN, 2004, 48 (11-12) : 1096 - 1101
  • [5] The ecology of environmental DNA and implications for conservation genetics
    Barnes, Matthew A.
    Turner, Cameron R.
    [J]. CONSERVATION GENETICS, 2016, 17 (01) : 1 - 17
  • [6] Ballast water risk assessment: principles, processes, and methods
    Barry, Simon C.
    Hayes, Keith R.
    Hewitt, Chad L.
    Behrens, Hanna L.
    Dragsund, Egil
    Bakke, Siri M.
    [J]. ICES JOURNAL OF MARINE SCIENCE, 2008, 65 (02) : 121 - 131
  • [7] DNA barcoding of parasites and invertebrate disease vectors: what you don't know can hurt you
    Besansky, NJ
    Severson, DW
    Ferdig, MT
    [J]. TRENDS IN PARASITOLOGY, 2003, 19 (12) : 545 - 546
  • [8] Sequencing our way towards understanding global eukaryotic biodiversity
    Bik, Holly M.
    Porazinska, Dorota L.
    Creer, Simon
    Caporaso, J. Gregory
    Knight, Rob
    Thomas, W. Kelley
    [J]. TRENDS IN ECOLOGY & EVOLUTION, 2012, 27 (04) : 233 - 243
  • [9] The use of molecular tools in invasion biology: an emphasis on freshwater ecosystems
    Blanchet, S.
    [J]. FISHERIES MANAGEMENT AND ECOLOGY, 2012, 19 (02) : 120 - 132
  • [10] Environmental DNA for wildlife biology and biodiversity monitoring
    Bohmann, Kristine
    Evans, Alice
    Gilbert, M. Thomas P.
    Carvalho, Gary R.
    Creer, Simon
    Knapp, Michael
    Yu, Douglas W.
    de Bruyn, Mark
    [J]. TRENDS IN ECOLOGY & EVOLUTION, 2014, 29 (06) : 358 - 367