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Updated: Nov 25, 2025

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
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.
Abstract:
The protozoan parasite Cryptosporidium sp. is a leading cause of diarrheal disease in those with compromised or underdeveloped immune systems, particularly infants and toddlers in resource-poor localities. As an enteric pathogen, Cryptosporidium sp. invades the apical surface of intestinal epithelial cells, where it resides in close proximity to metabolites in the intestinal lumen. However, the effect of gut metabolites on susceptibility to Cryptosporidium infection remains largely unstudied. Here, we first identified which gut metabolites are prevalent in neonatal mice when they are most susceptible to Cryptosporidium parvum infection and then tested the isolated effects of these metabolites on C. parvum invasion and growth in intestinal epithelial cells. Our findings demonstrate that medium or long-chain saturated fatty acids inhibit C. parvum growth, perhaps by negatively affecting the streamlined metabolism in C. parvum, which is unable to synthesize fatty acids. Conversely, long-chain unsaturated fatty acids enhanced C. parvum invasion, possibly by modulating membrane fluidity. Hence, gut metabolites, either from diet or produced by the microbiota, influence C. parvum growth in vitro and may also contribute to the early susceptibility to cryptosporidiosis seen in young animals.IMPORTANCECryptosporidium sp. occupies a unique intracellular niche that exposes the parasite to both host cell contents and the intestinal lumen, including metabolites from the diet and produced by the microbiota. Both dietary and microbial products change over the course of early development and could contribute to the changes seen in susceptibility to cryptosporidiosis in humans and mice. Consistent with this model, we show that the immature gut metabolome influenced the growth of Cryptosporidium parvumin vitro Interestingly, metabolites that significantly altered parasite growth were fatty acids, a class of molecules that Cryptosporidium sp. is unable to synthesize de novo The enhancing effects of polyunsaturated fatty acids and the inhibitory effects of saturated fatty acids presented in this study may provide a framework for future studies into this enteric parasite's interactions with exogenous fatty acids during the initial stages of infection.
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.

