AI Article Synopsis

  • The study analyzed paralytic shellfish toxins in the digestive glands of the cockle Cerastoderma edule over a 25-day period following exposure to the harmful algal bloom Gymnodinium catenatum.
  • The findings showed that the main toxins present were C1+2, B1, and dcGTX2+3, with the ratio of C1+2 to B1 decreasing over time, suggesting B1 is eliminated more slowly.
  • Different patterns in toxin reduction were observed across sub-cellular fractions, particularly a notable increase in B1 within lysosomes after eight days, likely due to conversions from other toxins during digestion.

Article Abstract

Concentrations of paralytic shellfish toxins (C1+2, B1, dcGTX2+3, dcSTX, GTX2+3 and STX) were determined by LC-FLD in composite samples of digestive glands of the cockle Cerastoderma edule and in each sub-cellular particulate fractions obtained after differential centrifugation (nuclei+debris, mitochondria, lysosomes and microsomes). The specimens were sampled during the exposure to a bloom of Gymnodinium catenatum (day 0) and in the subsequent 8, 12, 14, 19, 21 and 25 days under natural depuration conditions. Toxin profiles of digestive glands were dominated by C1+2 followed by B1 and dcGTX2+3, although the proportion between C1+2 and B1 contents decreased with the time, indicating a slower elimination of B1. All toxins, except GTX2+3 and STX, were quantified in the four sub-cellular fractions. The content of the quantified toxins decreased most markedly in nuclei+debris and microsomal fractions, during the first eight and 12 days, respectively. Conversely, different patterns were observed among toxins in mitochondrial and lysosomal fractions. The less accentuated decreases of dcGTX2+3 and dcSTX contents in the mitochondrial fraction may have resulted from the conversion of other toxins, like C1+2 and B1, associated with enzymatic activities in that fraction. The largest discrepancy was registered in lysosomal fraction for B1, since its content increased after eight days of post-bloom conditions. Input of B1 may come from the conversion of other toxins, like the abundant B2 and C1+2. These transformations are associated to the major role of lysosomes in the intra-cellular digestive process of materials acquired through vesicular transport.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ecoenv.2014.02.011DOI Listing

Publication Analysis

Top Keywords

paralytic shellfish
8
shellfish toxins
8
sub-cellular fractions
8
cockle cerastoderma
8
cerastoderma edule
8
toxins c1+2
8
c1+2 dcgtx2+3
8
dcgtx2+3 dcstx
8
gtx2+3 stx
8
digestive glands
8

Similar Publications

In New Zealand, the frequency and intensity of marine heatwaves (MHWs) and blooms of the harmful algal species, Alexandrium pacificum, are increasing in areas where there are natural reefs and commercial farms of the mussel, Perna canaliculus. In this study, we assessed the whole organism, tissue and molecular-level response of juvenile (spat) P. canaliculus exposed to these abiotic and biotic stressors, alone and together.

View Article and Find Full Text PDF

The development of rapid detection techniques for Alexandrium catenella.

Environ Sci Pollut Res Int

January 2025

College of the Environment and Ecology, Xiamen University, Xiamen, 361102, Fujian, People's Republic of China.

Alexandrium catenella is an important toxic algal species in the Alexandrium genus, which can form toxic red tides in large numbers. The paralytic shellfish poisoning (PSP) produced by Alexandrium catenella can seriously endanger human health and threaten the production and development of the aquaculture and fishery industries. Therefore, it is important to explore and develop effective detection and early warning methods for toxic red tides.

View Article and Find Full Text PDF

The rapid, sensitive, and accurate detection of paralytic shellfish toxins (PSTs), such as saxitoxin (STX), is critical for protecting human health due to the frequent occurrence of toxic red tides. In this work, to address the low affinity of traditional mouse monoclonal antibodies (m-mAbs), rabbit monoclonal antibodies (r-mAbs) against STX were produced by a single B-cell sorting culture and a cross-selection strategy. The r-mAbs showed 100-fold improvement in sensitivity (IC = 0.

View Article and Find Full Text PDF

Understanding the Molecular Mechanisms of Pyrene in Governing the Critical Metabolic Circuits of .

Environ Sci Technol

January 2025

Key Laboratory of Eutrophication and Red Tide Prevention of Guangdong Higher Education Institutes, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.

Pyrene, a representative polycyclic aromatic hydrocarbon, frequently occurs in aquatic environments and is associated with lethal impacts on humans and wildlife. This study examined the impact of pyrene on , a dinoflagellate responsible for harmful algal blooms, and their capability to bioremove pyrene. In a 96 h exposure experiment, effectively reduced the pyrene concentration in seawater to 50, 100, and 200 μg/L, with a combined removal efficiency of 96% in seawater.

View Article and Find Full Text PDF

The DnaJ-Hsp70-Hsp90 co-chaperon networks in scallops under toxic Alexandrium dinoflagellates exposure.

Ecotoxicol Environ Saf

January 2025

MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences (Qingdao 266003), and Key Laboratory of Tropical Aquatic Germplasm of Hainan Province, Sanya Oceanographic Institution (Sanya 572024), Ocean University of China, China. Electronic address:

Heat shock proteins (Hsps) are highly conserved molecular chaperones with essential roles against biotic and abiotic stressors. A large set of co-chaperons comprising J-domain proteins (DnaJs) regulate the ATPase cycle of Hsp70s with Hsp90s, together constituting a dynamic and functionally versatile network for protein folding/unfolding and regulation. Marine bivalves could accumulate and tolerate paralytic shellfish toxins (PSTs), the well-noted neurotoxins generated during harmful algal blooms.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!