Molecular methods for cost-efficient monitoring of HAB (harmful algal bloom) dinoflagellate resting cysts

Mar Pollut Bull. 2019 Oct:147:209-218. doi: 10.1016/j.marpolbul.2018.06.013. Epub 2018 Jun 15.

Abstract

Cyst abundance and identity are essential for understanding and predicting blooms, and for assessing the dispersal of toxic target dinoflagellate species by natural or human mediated ways, as with ballast waters. The aim of this study was to apply rapid, specific and sensitive qPCR assays to enumerate toxic dinoflagellate cysts in sediment samples collected from Adriatic harbours. The molecular standard curves of various target species allowed obtaining the rDNA copy number per cyst. The analytical sensitivity for specific standard curves was determined to be 2 or 10 rDNA copies per reaction. The abundance varied in the range of 1-747 dinoflagellate cysts g-1 dry weight. The assays showed greater sensitivity as compared to counts by light microscopy. This qPCR method revealed a powerful tool for the quantification of cysts from toxic dinoflagellate resting stages in sediment samples from Adriatic ports.

Keywords: Adriatic Sea; Cysts; HAB species; Microscopy; Quantitative PCR; Sediments.

MeSH terms

  • Biological Monitoring / methods*
  • DNA Copy Number Variations
  • DNA, Ribosomal / genetics
  • Dinoflagellida / genetics*
  • Dinoflagellida / physiology
  • Geologic Sediments / microbiology
  • Harmful Algal Bloom*
  • Mediterranean Sea
  • Plasmids
  • Real-Time Polymerase Chain Reaction / methods*
  • Reproducibility of Results
  • Seasons
  • Sensitivity and Specificity
  • Ships

Substances

  • DNA, Ribosomal