Exposure to okadaic acid could disrupt the colonic microenvironment in rats

Yang Liu1, Tian-Qing Yuan2, Jian-Wei Zheng2

  • 1Obstetrics and Gynecology, The First Affiliated Hospital of Jinan University, Guangzhou, China; Key Laboratory of Aquatic Eutrophication and Control of Harmful Algal Blooms of Guangdong Higher Education Institute, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.

Insights

Okadaic acid (OA) damages the gut lining and alters gut bacteria. Opportunistic pathogens may contribute to OA

Area of Science:

  • Marine Toxinology
  • Gastroenterology
  • Microbiology

Background:

  • Okadaic acid (OA) is a prevalent marine phycotoxin causing gastrointestinal distress.
  • The precise toxic mechanism of OA, particularly its impact on the digestive tract, remains unclear.

Purpose of the Study:

  • To investigate the effects of OA exposure on the epithelial microenvironment, focusing on the epithelial barrier and gut microbiota.
  • To elucidate the role of gut bacteria in OA-induced toxicity.

Main Methods:

  • Exposure of rats to Okadaic Acid (OA).
  • Assessment of epithelial barrier integrity, including cell junctions and mucus layer.
  • Analysis of gut bacterial composition using metagenomics.
  • Correlation analysis between bacterial abundance and animal body weight.

Main Results:

  • OA exposure led to impaired epithelial cell junctions, mucus layer destruction, and increased bacterial invasion in rat colons.
  • A shift in gut microbiota was observed, with decreased beneficial bacteria and increased pathogenic bacteria (e.g., Escherichia/Shigella).
  • A significant negative correlation was found between pathogenic bacteria abundance and animal body weight.

Conclusions:

  • Okadaic acid (OA) disrupts the intestinal epithelial barrier and alters gut microbiota composition.
  • Opportunistic pathogens, such as Escherichia coli and Shigella, may play a role in OA-induced cytoskeletal remodeling and mucosal damage.
  • These findings suggest opportunistic pathogens might contribute to the complex toxicity of OA during epithelial barrier damage.

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