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Development of a multiplex real-time qPCR assay for simultaneous enumeration of up to four marine toxic bloom-forming microalgal species.
Abstract
Harmful algal blooms (HAB) pose serious economic and health risks worldwide. Current methods of identification require high levels of taxonomic skill and can be highly time-consuming thus limiting sample throughput. So, new rapid and reliable methods for detection and enumeration of HAB species are required. Here we describe a high-throughput, multiplex-qPCR (M-qPCR) method using hydrolysis probe technology for the simultaneous detection of four HAB species commonly found in many coastal areas worldwide: Alexandrium tamarense, Karenia mikimotoi, Karlodinium veneficum and Prymnesium parvum. Primers and probes were species-specific and highly efficient when tested in simplex. Species were then added in succession and the assay conditions adjusted until all four species could be quantitatively evaluated simultaneously. Enumeration accuracy of the M-qPCR assay as a monitoring tool was evaluated using spiked natural environmental samples from Danish coastal waters. Comparison of estimates of cell abundances obtained by the M-qPCR technique with those obtained by light microscopy (Sedgwick Rafter technique) showed no statistically significant difference across a range of concentrations. We were also able to identify and enumerate target cells that would be below the detection limit of light microscopy making this a suitable method for early bloom detection or for low biomass species. With the development of molecular probes for a greater number of algal species M-qPCR will be of great benefit to phytoplankton monitoring programmes and the aquaculture industry worldwide.
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“Numerous studies have shown the utility and statistical rigor of determining cell concentrations using qPCR compared to other visual detection methods for the HAB species presented here (e.g., Handy et al., 2008;Eckford-Soper and Daugbjerg, 2015;Lee et al., 2017;Vandersea et al., 2017).”
From Current and Future Remote Sensing of Harmful Algal Blooms in the Chesapeake Bay to Support the Shellfish Industry (2020) · cites this paper as Eckford-Soper and Daugbjerg, 2015
Citations
Cites
Harmful algal blooms and eutrophication: nutrient sources, composition, and consequences
Anderson, D. M., Glibert, P. M., & Burkholder, J. M. (2002) · Estuaries · doi:10.1007/bf02804901 · Cited by 2,965
Research works printed but not linked: 28
- Al-Tebrineh, 2012, A multiplex qPCR targeting hepato- and neurotoxicgenic cyanobacteria of global significance, Harmful Algae, 25, 19, 10.1016/j.hal.2011.11.001 · DOI
- Anderson, 1994, Red tides, Sci. Am., 271, 62, 10.1038/scientificamerican0894-62 · DOI
- Anderson, 2012, Progress in understanding harmful algal blooms: paradigm shifts and new technologies for research, monitoring, and management, Ann. Rev. Mar. Sci., 4, 143, 10.1146/annurev-marine-120308-081121 · DOI · Paper page
- Bertozzini, 2005, Development of new procedures for the isolation of phytoplankton DNA from fixed samples, J. Appl. Phycol., 17, 223, 10.1007/s10811-005-2130-5 · DOI
- Bresnan, 2008, Monitoring PSP toxicty and Alexandrium hotspots in Scottish waters
- Collins, 2009, Evaluation of quantitative real-time TaqMan PCRs for detection and quantification of Alexandrium species in Scottish waters, 1
- Dittami, 2013, Molecular probes for the detection and identification of ichthyotoxic marine microalgae of the genus Pseudochattonella (Dictyochophyceae, Ochrophyta), Environ. Sci. Pollut. Res. Int., 20, 6824, 10.1007/s11356-012-1402-2 · DOI
- Eckford-Soper, 2015, Examination of six commonly used laboratory fixatives in HAB monitoring programs for their use in quantitative PCR based on Taqman probe technology, Harmful Algae, 42, 52, 10.1016/j.hal.2014.12.007 · DOI
- Eckford-Soper, 2013, Identification and quantification of toxic and nontoxic strains of the harmful dinoflagellate Alexandrium tamarense using fluorescence in situ hybridization and flow cytometry, Limnol. Oceanogr. Methods, 11, 540, 10.4319/lom.2013.11.540 · DOI
- Erdner, 2010, A quantitative real-time PCR assay for the identification and enumeration of Alexandrium cysts in marine sediments, Deep. Sea. Res. Part 2. Top. Stud. Oceanogr., 57, 279, 10.1016/j.dsr2.2009.09.006 · DOI
- Galluzzi, 2008, Detection and quantification of Prymnesium parvum (Haptophyceae) by real-time PCR, Lett. Appl. Microbiol., 46, 261, 10.1111/j.1472-765X.2007.02294.x · DOI
- Godhe, 2007, Intercalibration of classical and molecular techniques for identification of Alexandrium fundyense (Dinophyceae) and estimation of cell densities, Harmful Algae, 6, 56, 10.1016/j.hal.2006.06.002 · DOI
- Handy, 2008, Using quantitative real-time PCR to study competition and community dynamics among Delaware Inland Bays harmful algae in field and laboratory studies, Harmful Algae, 7, 599, 10.1016/j.hal.2007.12.018 · DOI · Paper page
- Handy, 2006, Simultaneous enumeration of multiple raphidophyte species by quantitative real-time PCR: capabilities and limitations, Limnol. Oceanogr. Methods, 4, 193, 10.4319/lom.2006.4.193 · DOI
- Jakobsen, 2002, Discovery of the toxic dinoflagellate Pfiesteria in northern European waters, Proc. Biol. Sci., 269, 211, 10.1098/rspb.2001.1852 · DOI
- Karlen, 2007, Statistical significance of quantitative PCR, BMC Bioinform., 8, 131, 10.1186/1471-2105-8-131 · DOI · Paper page
- Main, 2014, Effects of growth phase, diel cycle and macronutrient stress on the quantification of Heterosigma akashiwo using qPCR and SHA, Harmful Algae, 37, 92, 10.1016/j.hal.2014.05.014 · DOI
- Medlin, 2013, Molecular tools for monitoring harmful algal blooms, Environ. Sci. Pollut. Res., 20, 6683, 10.1007/s11356-012-1195-3 · DOI
- Ogino, 2001, A method to compensate for different amplification efficiencies, J. Mol. Diagn., 3, 189, 10.1016/S1525-1578(10)60671-X · DOI
- Park, 2009, Development of a SYTO9 based real-time PCR probe for detection and quantification of toxic dinoflagellate Karlodinium veneficum (Dinophyceae) in environmental samples, Phycologia, 48, 32, 10.2216/08-52.1 · DOI
- Penna, 2007, Monitoring of HAB species in the Mediterranean Sea through molecular methods, J. Plankton Res., 29, 19, 10.1093/plankt/fbl053 · DOI
- Penna, 2013, The quantitative real-time PCR applications in the monitoring of marine harmful algal bloom (HAB) species, Environ. Sci. Pollut. Res. Int., 20, 6851, 10.1007/s11356-013-1519-y · DOI
- Schmittgen, 2000, Quantitative reverse transcription-polymerase chain reaction to study mRNA decay: comparison of endpoint and real-time methods, Anal. Biochem., 285, 194, 10.1006/abio.2000.4753 · DOI
- Toebe, 2013, Molecular discrimination of toxic and non-toxic Alexandrium species (Dinophyta) in natural phytoplankton assemblages from the Scottish coast of the North Sea, Eur. J. Phycol., 10.1080/09670262.2012.752870 · DOI
- Touzet, 2010, Co-occurrence of the West European (Gr.III) and North American (Gr.I) Ribotypes of Alexandrium tamarense (Dinophyceae) in Shetland, Scotland, Protist, 161, 370, 10.1016/j.protis.2009.12.001 · DOI
- Utermöl, 1958, Zur Vervollkommnung der quantitativen Phytoplankton-Methodik, Mitt. Int. Ver. Theor. Angew. Limnol, 1
- Yuan, 2012, Development of a rapid detection and quantification method of Karenia mikimotoi by real-time quantitative PCR, Harmful Algae, 17, 83, 10.1016/j.hal.2012.03.004 · DOI
- Zhong, 2011, Multiplex digital PCR: breaking the one target per color barrier of quantitative PCR, Lab Chip, 11, 2167, 10.1039/c1lc20126c · DOI
Cited by
Sorted by citations
Wolny, J. L., Tomlinson, M. C., Schollaert Uz, S., Egerton, T. A., McKay, J. R., Meredith, A., Reece, K. S., Scott, G. P., & Stumpf, R. P. (2020) · Frontiers in Marine Science · doi:10.3389/fmars.2020.00337 · Cited by 80
Metadata
- Authors
- Eckford-Soper, L. K., & Daugbjerg, N.
- Affiliations
- University of Copenhagen (DK)
- Corresponding author
- Eckford-Soper, Lisa K.
- Venue
- Harmful Algae
- Publisher
- Elsevier BV
- Published
- 2015-09
- Volume
- 48
- Pages
- 37-43
- ISSN
- 1568-9883 (ISSN-L)
- OpenAlex
- W990580484
- Cited by
- 49
- References
- 1
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 3 · 2023: 1 · 2022: 8 · 2021: 8 · 2020: 3 · 2019: 9 · 2018: 7 · 2016: 2
- FWCI
- 2.21
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Harmful Algae (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- Danish Council for Strategic Research (11-116169)
- Topics
- Physical Sciences › Environmental Science › Environmental Chemistry › Marine Toxins and Detection Methods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Molecular Biology Techniques and Applications
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Marine Plankton and Biogeochemistry
- Keywords
- harmful algal blooms, Alexandrium tamarense, Karenia mikimotoi, Karlodinium veneficum, Prymnesium parvum, TaqMan probes, phytoplankton monitoring, aquaculture, coastal waters, light microscopy comparison
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