Study of the In Vitro Antagonistic Activity of Various Single-Strain and Multi-Strain Probiotics against .

Int J Environ Res Public Health

Faculty of Medicine, Institute of Microbiology and Immunology, University of Ljubljana, Zaloška 4, 1000 Ljubljana, Slovenia.

Published: July 2018

is an important commensal of our gut, however, many pathogenic strains exist, causing various severe infections in the gut or beyond. Due to several antibiotic resistance patterns of , research of alternative treatments or adjuvant therapy is important. One of these is the use of probiotics as antagonistic agents against . Most published studies investigate only one strain of and single-strain probiotics. The objectives of this study were to evaluate the antagonistic activity of selected single-strain and multi-strain probiotic supplements against selected clinical pathotypes using the in vitro agar spot test and the co-culturing method. Molecular methods were used to determine the presence of the genus lactobacilli and bifidobacteria as well as certain selected strains in the probiotic supplements. The agar-spot test showed that the multi-strain probiotics were more effective than the single-strain probiotics. On the other hand, the co-culturing method showed the opposite result, indicating that results are importantly influenced by the chosen method. The most effective single-strain probiotics against strains were subsp. BB-12 and DSM 17938. The most effective multi-strain probiotics contained lactobacilli, bifidobacteria and enterococci strains, thus proving that most effective probiotics against strains are the lactic acid bacteria and bifidobacteria. The overall results from both in vitro tests reveal that all selected probiotics exhibited an antagonistic activity against all strains. From a public health perspective probiotics have thus proved to be successful in inhibiting the growth of and could therefore be used as adjuvant therapy or alternative therapy in infections.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069398PMC
http://dx.doi.org/10.3390/ijerph15071539DOI Listing

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