Antimicrobial Activities of Alginate and Chitosan Oligosaccharides Against Staphylococcus aureus and Group B Streptococcus
Asadpoor, Mostafa; Ithakisiou, Georgia-Nefeli; van Putten, Jos P M; Pieters, Roland J; Folkerts, Gert; Braber, Saskia
(2021) Frontiers in Microbiology, volume 12, pp. 1 - 15
(Article)
Abstract
The bacterial pathogens Streptococcus agalactiae (GBS) and Staphylococcus aureus (S. aureus) cause serious infections in humans and animals. The emergence of antibiotic-resistant isolates and bacterial biofilm formation entails the urge of novel treatment strategies. Recently, there is a profound scientific interest in the capabilities of non-digestible oligosaccharides as antimicrobial and
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anti-biofilm agents as well as adjuvants in antibiotic combination therapies. In this study, we investigated the potential of alginate oligosaccharides (AOS) and chitosan oligosaccharides (COS) as alternative for, or in combination with antibiotic treatment. AOS (2-16%) significantly decreased GBS V growth by determining the minimum inhibitory concentration. Both AOS (8 and 16%) and COS (2-16%) were able to prevent biofilm formation by S. aureus wood 46. A checkerboard biofilm formation assay demonstrated a synergistic effect of COS and clindamycin on the S. aureus biofilm formation, while AOS (2 and 4%) were found to sensitize GBS V to trimethoprim. In conclusion, AOS and COS affect the growth of GBS V and S. aureus wood 46 and can function as anti-biofilm agents. The promising effects of AOS and COS in combination with different antibiotics may offer new opportunities to combat antimicrobial resistance.
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Keywords: Staphylococcus aureus, alginate oligosaccharides, anti-biofilm, bacterial growth, chitosan oligosaccharides, group B Streptococcus, sensitization, synergy, Microbiology, Microbiology (medical)
ISSN: 1664-302X
Publisher: Frontiers Media S.A.
Note: Funding Information: We would like to acknowledge Suzan Rooijakkers and Nina Van Sorge from Department of Medical Microbiology, Utrecht Medical Center, Netherlands, for their generous gift of pathogens and Lisanne de Vor from the same department for her technical assistance with the biofilm formation assay. We appreciated the help that we received from Soheil Varasteh in designing the experiments. We would also like to thank Ebrahim Rezazadeh Zarandi from Immunology of Infectious Diseases Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran, for his assistance during the data analysis of the checkerboard biofilm formation assay. Publisher Copyright: © Copyright © 2021 Asadpoor, Ithakisiou, van Putten, Pieters, Folkerts and Braber.
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