Neonatal Mouse Gut Metabolites Influence Cryptosporidium parvum Infection in Intestinal Epithelial Cells

Kelli L VanDussen1, Lisa J Funkhouser-Jones2, Marianna E Akey2

  • 1Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.

Mbio
|December 16, 2020
PubMed

Insights

Gut metabolites significantly impact Cryptosporidium parvum infection. Saturated fatty acids inhibit parasite growth, while unsaturated fatty acids enhance invasion, influencing cryptosporidiosis susceptibility in young animals.

Area of Science:

  • Microbiology
  • Parasitology
  • Host-Pathogen Interactions

Background:

  • Cryptosporidium sp. is a major cause of diarrheal disease, especially in immunocompromised individuals.
  • This enteric pathogen infects intestinal cells, interacting with gut metabolites.
  • The influence of gut metabolites on Cryptosporidium susceptibility is poorly understood.

Purpose of the Study:

  • Identify prevalent gut metabolites in neonatal mice susceptible to Cryptosporidium parvum.
  • Investigate the effects of these metabolites on C. parvum invasion and growth in vitro.
  • Elucidate the role of gut metabolites in early-life susceptibility to cryptosporidiosis.

Main Methods:

  • Metabolomic analysis of neonatal mouse gut contents.
  • In vitro assays testing metabolite effects on C. parvum invasion of intestinal cells.
  • In vitro assays assessing metabolite effects on C. parvum growth.

Main Results:

  • Medium and long-chain saturated fatty acids inhibited C. parvum growth.
  • Long-chain unsaturated fatty acids enhanced C. parvum invasion.
  • Fatty acids, which Cryptosporidium cannot synthesize, significantly altered parasite growth.

Conclusions:

  • Gut metabolites, including fatty acids, influence Cryptosporidium parvum growth and invasion in vitro.
  • Dietary and microbial metabolites may contribute to the age-dependent susceptibility to cryptosporidiosis.
  • Fatty acid profiles could be a target for understanding and potentially managing cryptosporidiosis.

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