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Published on: October 29, 2014
A human flora-associated rat model of the breast-fed infant gut
Christine A Edwards1, C Rumney, M Davies
1Department of Human Nutrition, Glasgow University, Yorkhill Hospitals, Glasgow, UK. caeln@clinmed.gla.ac.uk
Insights
A novel infant rat model effectively mimics the gut bacteria of breast-fed infants, validating its use for studying diet
Area of Science:
- Microbiology
- Gastroenterology
- Pediatrics
Background:
- Infant gut microbiota plays a crucial role in the development of gastrointestinal, respiratory, and allergic diseases.
- Early diet significantly shapes the gut microflora composition and function.
- Investigating the interplay between diet, gut flora, and mucosal immunity in human infants is challenging.
Purpose of the Study:
- To develop and validate an infant human flora-associated (IHFA) rat model.
- To enable the study of diet, gut microbiota, and mucosal interactions in early life.
Main Methods:
- Germ-free infant rats were colonized with fecal bacteria from exclusively breast-fed infants.
- Rats were fed a modified infant formula for 8 weeks.
- Fecal and cecal contents were analyzed for bacterial populations, metabolites, enzymes, and pathogen adhesion inhibition.
Main Results:
- The IHFA rat gut microbiota composition, dominated by lactic acid bacteria, Bifidobacterium, and lactobacilli, mirrored that of breast-fed infants.
- Fecal short-chain fatty acid profiles, particularly acetic and lactic acid, were similar to human infant samples.
- Rat intestinal samples demonstrated pathogen adhesion inhibition, though less effectively than human samples.
Conclusions:
- The IHFA rat model accurately represents the intestinal flora of breast-fed infants.
- This model is a valid tool for investigating the impact of diet on bacterial colonization and metabolism in early life.
Objectives:
Bacterial colonization of the infant gut may have important influences on the development of gastrointestinal, respiratory, and allergic disease. Early diet is a major determinant of the gut microflora. It is very difficult to carry out studies in human infants that can investigate the interaction of diet, flora, and mucosa. In this study we have developed an infant human flora-associated (IHFA) rat model to allow such investigation.
Methods:
Germ-free infant rats were infected with fecal bacteria from exclusively breast-fed infants and were maintained on a modified infant formula for 8 weeks. The fecal and cecal contents were collected and compared with feces of breast-fed infants for bacterial populations, bacterial metabolites, and enzymes and for the ability to inhibit adhesion of pathogenic bacteria to human mucosal cells.
Results:
The IHFA cecum and feces were dominated by lactic acid bacteria, Bifidobacterium, and lactobacilli, which were representative of the infant feces. The fecal short-chain fatty acid profile was dominated by acetic and lactic acid in a similar manner to human infant feces. Other bacterial metabolites were similar to those of the human infant. Rat intestinal samples were able to inhibit the adhesion of pathogens to mucosal cells, but to a lesser extent than the human samples.
Conclusions:
This IHFA infant model of the intestinal flora of the breast-fed infant is considered valid for studying the effect of diet on bacterial colonization and metabolism.
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