Delivery of E. coli Nissle to the mouse gut by mucoadhesive microcontainers does not improve its competitive ability against strains linked to ulcerative colitis

Author:

Bondegaard Pi Westi1,Torp Anders Meyer1,Guerra Priscila1,Kristensen Katja Ann1,Christfort Juliane Fjelrad2,Krogfelt Karen Angeliki3,Nielsen Line Hagner2,Zor Kinga2,Boisen Anja2,Mortensen Martin Steen1,Bahl Martin Iain1ORCID,Licht Tine Rask1ORCID

Affiliation:

1. National Food Institute, Technical University of Denmark , Kgs. Lyngby, 2800 , Denmark

2. Department of Health Technology, Technical University of Denmark , Kgs. Lyngby, 2800 , Denmark

3. Department of Science and Environment, Molecular and Medical Biology, Roskilde University , Roskilde, 4000 , Denmark

Abstract

Abstract For patients with ulcerative colitis (UC), administration of the probiotic E. coli Nissle (EcN) holds promise for alleviation of disease symptoms. The mechanisms are unclear, but it has been hypothesised that a capacity of the probiotic to outcompete potentially detrimental UC-associated E. coli strains plays an important role. However, this could previously not be confirmed in a mouse model of competition between EcN and two UC-associated strains, as reported by Petersen et al. 2011. In the present study, we re-evaluated the idea, hypothesising that delivery of EcN by a micro device dosing system (microcontainers), designed for delivery into the intestinal mucus, could support colonisation and confer a competition advantage compared to classical oral dosing. Six groups of mice were pre-colonised with one of two UC-associated E. coli strains followed by oral delivery of EcN, either in capsules containing microcontainers with freeze-dried EcN powder, capsules containing freeze-dried EcN powder, or as a fresh sucrose suspension. Co-colonisation between the probiotic and the disease-associated strains was observed regardless of dosing method, and no competition advantages linked to microcontainer delivery were identified within this setup. Other approaches are thus needed if the competitive capacity of EcN in the gut should be improved.

Funder

Novo Nordisk Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Microbiology

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