The role of structure in the interaction between bacteria, mammary epithelial cells and milk fat globules from raw or "cultured" milk.

Food Chem

Animal Science Department, The faculty of Agriculture, Food and Environmental Sciences, The Hebrew University of Jerusalem, Israel. Electronic address:

Published: March 2025

AI Article Synopsis

  • The study investigates how the structural properties of milk fat globules (MFG) influence their interaction with both harmful and beneficial bacteria, focusing on MFG from mammary gland epithelial cells (MEC) and raw milk.
  • Results show that smaller MFG promote the growth of beneficial bacteria like B.subtilis, while larger MFG encourage biofilm formation, while pathogenic bacteria like E. coli are not affected by MFG size.
  • The findings suggest that the structure of MFG is crucial for its interactions with bacteria, indicating that MFG size variations might help beneficial bacteria thrive and offer protection against harmful ones.

Article Abstract

The study aimed to distinguish between the role played by the structural properties of MFG from its chemical composition in modulating its interaction with pathogenic and commensal bacteria. MFG from mammary gland epithelial cells (MEC) or raw milk was tested. Small MFG from both sources promoted growth of B.subtilis while large MFG triggered biofilm formation. Metabolomic profiles supported these findings for MEC-derived MFG. In contrast, pathogenic bacteria like E. coli weren't affected by MFG size from both sources. Using lipid mixture formulated to mimic the chemical composition of small MFG did not induce growth of the bacteria. Results validate that (i) milk components secreted by MEC share some structural-functional properties with raw MFG and (ii) the structure of the MFG plays a pivotal role in modulating the interaction between milk fat and bacteria. Taken together, MFG size variations may provide a competitive advantage to commensal bacteria as a protective mechanism.

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Source
http://dx.doi.org/10.1016/j.foodchem.2024.142244DOI Listing

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