Molecular tools for phytoplankton monitoring samples

HABs can have severe impacts in fisheries or human health by the consumption of contaminated bivalves. Monitoring assessment (quantitative and qualitative identification) of these organisms, is routinely accomplished by microscopic identification and counting of these organisms. Nonetheless, molecular biology techniques are gaining relevance, once these approaches can easily identify phytoplankton organisms at species level and even cell number quantifications. This work tests 12 methods/kits for genomic DNA extraction and seven DNA polymerases to determine which is the best method for routinely use in a common molecular laboratory, for phytoplankton monitoring samples analyses. From our work, Direct PCR master mix for tissue samples, proved to be the most adequate by its velocity of processivity, practicability, reproducibility, sensitiveness and robustness. However, brands such as Omega Biotek, GRISP, Qiagen and MP Biomedicals also showed good results for conventional DNA extraction as well as all the Taq brands tested (GRISP, GE Healthcare Life Sciences, ThermoFisher Scientific and Promega). Lugol’s solution, with our tested kits did not show negative interference in DNA amplification. The same can be said about mechanical digestion, with no significant differences among kits with or without this homogenization step.

[1]  A. Kremp,et al.  Sample Preservation, DNA or RNA Extraction and Data Analysis for High-Throughput Phytoplankton Community Sequencing , 2017, Front. Microbiol..

[2]  D. Anderson,et al.  Paralytic shellfish toxin production by the dinoflagellate Alexandrium pacificum (Chinhae Bay, Korea) in axenic, nutrient-limited chemostat cultures and nutrient-enriched batch cultures. , 2016, Marine pollution bulletin.

[3]  R. S. Reis,et al.  Use of different Taq DNA polymerases for detection of Chlamydia trachomatis in cervical samples , 2015 .

[4]  Senjie Lin,et al.  An Improved DNA Extraction Method for Efficient and Quantitative Recovery of Phytoplankton Diversity in Natural Assemblages , 2015, PloS one.

[5]  Young-Tae Park,et al.  Monitoring and trends in harmful algal blooms and red tides in Korean coastal waters, with emphasis on Cochlodinium polykrikoides , 2013 .

[6]  Yoshito Fujii,et al.  COMPARISON OF SIX COMMERCIALLY-AVAILABLE DNA POLYMERASES FOR DIRECT PCR , 2013, Revista do Instituto de Medicina Tropical de Sao Paulo.

[7]  Philippe Delahaut,et al.  Multiplex biotoxin surface plasmon resonance method for marine biotoxins in algal and seawater samples , 2013, Environmental Science and Pollution Research.

[8]  M. Bastianini,et al.  Toxic Pseudo-nitzschia spp. in the northwestern Adriatic Sea: characterization of species composition by genetic and molecular quantitative analyses , 2013 .

[9]  A. Penna,et al.  The quantitative real-time PCR applications in the monitoring of marine harmful algal bloom (HAB) species. , 2013, Environmental science and pollution research international.

[10]  C. Schrader,et al.  PCR inhibitors – occurrence, properties and removal , 2012, Journal of applied microbiology.

[11]  Lucy E. Eland,et al.  Evaluation of DNA extraction methods for freshwater eukaryotic microalgae. , 2012, Water research.

[12]  M. Magnani,et al.  Analysis of rRNA gene content in the Mediterranean dinoflagellate Alexandrium catenella and Alexandrium taylori: implications for the quantitative real-time PCR-based monitoring methods , 2010, Journal of Applied Phycology.

[13]  M. Frischer,et al.  Evaluation of DNA extraction and handling procedures for PCR-based copepod feeding studies , 2009 .

[14]  H. Jeong,et al.  Identification of the dinoflagellate community during Cochlodinium polykrikoides (Dinophyceae) blooms using amplified rDNA melting curve analysis and real-time PCR probes , 2009 .

[15]  Katherine Hubbard,et al.  INTER‐ AND INTRASPECIFIC COMMUNITY STRUCTURE WITHIN THE DIATOM GENUS PSEUDO‐NITZSCHIA (BACILLARIOPHYCEAE) 1 , 2008, Journal of phycology.

[16]  J. Boenigk,et al.  Improved Methodology for Identification of Protists and Microalgae from Plankton Samples Preserved in Lugol's Iodine Solution: Combining Microscopic Analysis with Single-Cell PCR , 2008, Applied and Environmental Microbiology.

[17]  S. M. McDonald,et al.  Identifying Pseudo-nitzschia species in natural samples using genus-specific PCR primers and clone libraries , 2007 .

[18]  M. Magnani,et al.  Monitoring of HAB species in the Mediterranean Sea through molecular methods , 2006 .

[19]  W. Pepiński,et al.  Efficiency comparison of seven different Taq polymerases used in hemogenetics , 2006 .

[20]  M. Magnani,et al.  Development of new procedures for the isolation of phytoplankton DNA from fixed samples , 2005, Journal of Applied Phycology.

[21]  K. Goodwin,et al.  A DNA hybridization assay to identify toxic dinoflagellates in coastal waters: detection of Karenia brevis in the Rookery Bay National Estuarine Research Reserve , 2005 .

[22]  Katja Metfies,et al.  Electrochemical detection of the toxic dinoflagellate Alexandrium ostenfeldii with a DNA-biosensor. , 2005, Biosensors & bioelectronics.

[23]  Mauro Magnani,et al.  Development of a Real-Time PCR Assay for Rapid Detection and Quantification of Alexandrium minutum (a Dinoflagellate) , 2004, Applied and Environmental Microbiology.

[24]  H. Hogrefe,et al.  Amplification efficiency of thermostable DNA polymerases. , 2003, Analytical biochemistry.

[25]  D. Anderson,et al.  Molecular quantification of toxic Alexandrium fundyense in the Gulf of Maine. , 2003, The Biological bulletin.

[26]  D. Anderson,et al.  Identification of Alexandrium affine and A. margalefii (Dinophyceae) using DNA sequencing and LSU rDNA-based RFLP-PCR assays , 2003 .

[27]  D. Anderson,et al.  PCR amplification of microalgal DNA for sequencing and species identification: studies on fixatives and algal growth stages , 2002 .

[28]  P. Gentien,et al.  Genetic diversity and molecular detection of three toxic dinoflagellate genera (Alexandrium, Dinophysis, and Karenia) from French coasts. , 2002, Protist.

[29]  Junchao Huang,et al.  Modified CTAB protocol using a silica matrix for isolation of plant genomic DNA. , 2000, BioTechniques.

[30]  B. Rether,et al.  Isolation of polysaccharide-free DNA from plants , 1993, Plant Molecular Biology Reporter.

[31]  R. Guillard,et al.  Culture of Phytoplankton for Feeding Marine Invertebrates , 1975 .