Lipopolysaccharide and lipoteichoic acid influence milk production ability via different early responses in bovine mammary epithelial cells.

Exp Cell Res

Laboratory of Cell and Tissue Biology, Research Faculty of Agriculture, Hokkaido University, North 9, West 9, 060-8589, Sapporo, Japan. Electronic address:

Published: March 2021

AI Article Synopsis

  • Lipopolysaccharide (LPS) and lipoteichoic acid (LTA) are components from E. coli and S. aureus, which cause different types of mastitis, but the reasons for varying symptoms remain unclear.
  • The study examined how LPS and LTA impact lactating bovine mammary epithelial cells (BMECs), revealing that LPS reduced secretion of key milk components while LTA increased lactoferrin production without affecting β-casein.
  • LPS and LTA activated different immune pathways and influenced gene expression related to milk fat synthesis, suggesting that the unique responses of BMECs to each toxin could explain the differing symptoms from these pathogens.

Article Abstract

Lipopolysaccharide (LPS) and lipoteichoic acid (LTA) are cell wall components of Escherichia coli and Staphylococcus aureus, which cause clinical and subclinical mastitis, respectively. However, the reason of the difference in symptoms by pathogen type remains unclear. In this study, the influence of LPS and LTA on early response and milk production in lactating bovine mammary epithelial cells (BMECs) was comparatively investigated. The results showed that LPS decreased the secretion of β-casein, lactose, and triglycerides, whereas LTA decreased the secretion of lactose and triglycerides but increased lactoferrin production without any influence on β-casein secretion. In addition, the influence of milk lipid droplet size in BMECs and gene expression related to milk fat synthesis was different between LPS and LTA. LPS increased the gene expression of interleukin (IL)-1β, tumor necrosis factor-α, and IL-8 through the activation of the nuclear factor-κB (NF-κB), p38, and c-Jun N-terminal kinase pathways, whereas LTA increased IL-1β and CC chemokine ligand 5 expression through the activation of the NF-κB pathway. Moreover, these cytokines and chemokines differently affected the milk production ability of BMECs. These results suggested that the pathogen-specific symptoms may be related to the differences in the early response of BMECs to bacterial toxins.

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Source
http://dx.doi.org/10.1016/j.yexcr.2021.112472DOI Listing

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