Galacto-oligosaccharides as an anti-bacterial and anti-invasive agent in lung infections
Publication date
2022-04
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Abstract
Emerging antimicrobial resistance in infections asks for novel intervention strategies. Galacto-oligosaccharides (GOS) might be attractive alternatives to antibiotics due to their anti-inflammatory and anti-adhesive properties. Mannheimia haemolytica is one of the major Pasteurellaceae associated with bovine lung infections. Using M. haemolytica, we demonstrated that GOS have the capacity to reduce bacterial viability and can be used as adjuvant to improve antibiotic efficacy. Using M. haemolytica-treated primary bronchial epithelial cells (PBECs) of calves, we identified the anti-adhesive and anti-invasive activities of GOS. The observed inhibition of cytokine/chemokine release and the prevention of airway epithelial barrier dysfunction in M. haemolytica-treated PBECs by GOS might be related to the downregulation of "toll-like receptor 4/nuclear factor-κB" pathway and the anti-invasive and anti-adhesive properties of GOS. Particularly, GOS lowered lipopolysaccharides- but not flagellin-induced cytokine/chemokine release in calf and human airway epithelial cells. Finally, we performed in vivo experiments in calves and demonstrated for the first time that intranasal application of GOS can relieve lung infections/inflammation and lower M. haemolytica positivity in the lungs without affecting clinical performance. These findings not only shed light on the anti-inflammatory mechanisms of GOS during lung infections, but GOS might also be a promising anti-bacterial agent for preventing (lung) infections.
Keywords
Airway inflammation, Antibiotic adjuvant, Bactericidal effect, Carbohydrate-based biomaterials, Intranasal drug delivery, Respiratory pathogens, Biophysics, Bioengineering, Ceramics and Composites, Biomaterials, Mechanics of Materials
Citation
Cai, Y, van Putten, J P M, Gilbert, M S, Gerrits, W J J, Folkerts, G & Braber, S 2022, 'Galacto-oligosaccharides as an anti-bacterial and anti-invasive agent in lung infections', Biomaterials, vol. 283, 121461, pp. 1-18. https://doi.org/10.1016/j.biomaterials.2022.121461