Transcriptome Analysis Reveals MAPK/AMPK as a Key Regulator of the Inflammatory Response in PST Detoxification in Mytilus galloprovincialis and Argopecten irradians

Toxins (Basel). 2022 Jul 28;14(8):516. doi: 10.3390/toxins14080516.

Abstract

Paralytic shellfish toxins (PSTs) are an increasingly important source of pollution. Bivalves, as the main transmission medium, accumulate and metabolize PSTs while protecting themselves from damage. At present, the resistance mechanism of bivalves to PSTs is unclear. In this study, Mytilus galloprovincialis and Argopecten irradians were used as experimental shellfish species for in situ monitoring. We compared the inflammatory-related gene responses of the two shellfish during PSTs exposure by using transcriptomes. The results showed that the accumulation and metabolism rate of PSTs in M. galloprovincialis was five-fold higher than that in A. irradians. The inflammatory balance mechanism of M. galloprovincialis involved the co-regulation of the MAPK-based and AMPK-based anti-inflammatory pathways. A. irradians bore a higher risk of death because it did not have the balance system, and the regulation of apoptosis-related pathways such as the PI3K-AKT signaling pathway were upregulated. Taken together, the regulation of the inflammatory balance coincides with the ability of bivalves to cope with PSTs. Inflammation is an important factor that affects the metabolic pattern of PSTs in bivalves. This study provides new evidence to support the studies on the resistance mechanism of bivalves to PSTs.

Keywords: Argopecten irradians; Mytilus galloprovincialis; inflammatory balance; oxidative stress; paralytic shellfish toxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Dinoflagellida* / metabolism
  • Gene Expression Profiling
  • Marine Toxins / metabolism
  • Mytilus* / genetics
  • Mytilus* / metabolism
  • Pectinidae* / genetics
  • Pectinidae* / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Shellfish Poisoning* / metabolism

Substances

  • Marine Toxins
  • AMP-Activated Protein Kinases

Grants and funding

This work was funded by the National Key R&D Program of China (No. 2017YFC1600701), the National Natural Science Foundation of China (No. 32072329, 31772075), and Central Public-interest Scientific Institution Basal Research Fund, CAFS (No. 2020TD71). We thank LetPub (www.letpub.com) for its linguistic assistance during the preparation of this manuscript.