Restoration ofandCaused the Elimination ofsp. in a Model of Antibiotic-Induced Dysbiosis.

Abstract

Inflammatory bowel disease (IBD) is a multifactorial disease involving the interaction of the gut microbiota, genes, host immunity, and environmental factors. Dysbiosis in IBD is associated with pathobiont proliferation, so targeted antibiotic therapy is a rational strategy. When restoring the microbiota with probiotics, it is necessary to take into account the mutual influence of co-cultivated microorganisms, as the microbiota is a dynamic community of species that mediates homeostasis and physiological processes in the intestine. The aim of our study was to investigate the recovery efficacy of two potential probiotic bacteria,and, inmice with impaired mucosal layer. Two approaches were used to determine the efficacy of probiotic supplementation in mice with dysbiosis caused by mucin-2 deficiency: bacterial seeding on selective media and real-time PCR analysis. The recovery time and the type of probiotic bacteria relocated affected only the number of. A significant positive correlation was found between colony-forming unit (CFU) and the amount ofDNA in the group that was replanted with probiotic. As for, it could be restored to its original level even without any additional bacteria supplementation after two weeks. Interestingly, the treatment of mice withcaused a decrease in the amount of. Furthermore, eitherortreatment eliminated protozoan overgrowth caused by antibiotic administration.