Toxin production, growth kinetics and molecular characterization of Ostreopsis cf. ovata isolated from Todos os Santos Bay, tropical southwestern Atlantic

Toxicon. 2017 Nov:138:18-30. doi: 10.1016/j.toxicon.2017.08.007. Epub 2017 Aug 8.

Abstract

The toxin profile and hemolytic activity of a strain of Ostreopsis cf. ovata (UFBA013) isolated from Todos os Santos Bay (northeastern Brazil) were evaluated under different levels of N and P. Phylogenetic analyses based on ITS rDNA region (ITS1-5.8S-ITS2) placed UFBA013 within the Atlantic/Mediterranean/Pacific clade of O. cf. ovata. Growth experiments were conducted in f/2 medium modified by adding N and P (P: 0-36 μM; N: 0-882 μM). The growth kinetics was adequately described by logistic equations. The best growth (highest Gm) was recorded under levels of N/P = 0/18, 129/5 and 441/36, while one of the lowest Gm was obtained under P-depletion. The maximum and specific maximum growth rates (as vm; cells mL-1 d-1 and μm; d-1) were achieved with N limitation (N/P = 441/36) and P-limitation/depletion (753/5.3 and 441/0) and are the highest values reported in the literature, most similar to isolates from Pacific and Mediterranean areas. The control experiment (N/P = 441/18) also yielded similar values to those from some Mediterranean isolates, but higher than formerly reported for Brazilian isolates. In all conditions assayed, no palytoxin (PLTX) was detected. The ovatoxins (OVTXs) a, b, c, d and e did not show significant differences in cell quota between exponential and stationary phases. A significant relationship was detected between OVTXs concentration and hemolytic activity.

Keywords: Growth; Hemolytic assay; N; Ovatoxins; P; Phylogenetic analysis.

MeSH terms

  • Animals
  • Brazil
  • DNA, Ribosomal
  • Dinoflagellida / classification
  • Dinoflagellida / growth & development*
  • Dinoflagellida / metabolism*
  • Harmful Algal Bloom
  • Hemolysis
  • Marine Toxins / metabolism*
  • Nitrogen / metabolism
  • Phosphorus / metabolism
  • Phylogeny
  • Seawater / chemistry
  • Sequence Analysis, DNA
  • Sheep

Substances

  • DNA, Ribosomal
  • Marine Toxins
  • Phosphorus
  • Nitrogen