Gut Pathogens · 2019 · 36 citations · 53 references
Life SciencesInfectious DiseasesMicrobiologyMedical MicrobiologyMicrobial EcologyMicrobial PathogenesisGut MicrobiotaLactic Acid BacteriaPrebioticsProbioticsProbiotics In FoodsProtozoal InfectionsAxenic Culture EstablishmentAxenic Culture MaintenanceEscherichia ColiLactic Acid Bacteria InteractionsLactic Acid Bacteria ProbioticsProbiotic Effects On Gut MicrobiotaProbiotic MicroorganismsProtozoan Proliferation Assays
Blastocystis subtype 3 is an intestinal protist present in humans throughout the world with a controversial pathogenic potential. It has been suggested that probiotic bacteria inhibit the multiplication of gut protozoans, while others are beneficial for their development. This study aimed to evaluate the efficacy of the lactic acid bacteria Lactobacillus rhamnosus , Lactococcus lactis and Enterococcus faecium in Blastocystis ST3 eradication and the relevance of the intestinal microorganisms Escherichia coli , Candida albicans and Candida glabrata in protozoan proliferation. Blastocystis xenic and axenic culture was co-incubated with the above-mentioned microorganisms and their cell free supernatants at different concentrations in vitro. The number of protozoan cells was counted every day. Both experiments, with xenic and axenic cultures, showed Blastocystis inhibition by L. rhamnosus and L. lactis and their supernatants from the 2nd day of co-incubation. Furthermore, co-incubation with both E. faecium and E. coli showed a beneficial influence on Blastocystis during the first 2 days. Only after 3 days did the above-mentioned bacteria start to inhibit Blastocystis growth in both cultures. The supernatant containing the metabolites of E. coli was effective to a lesser degree. Compared to the control samples, co-incubation with both C. albicans and C. glabrata showed a faster decrease in Blastocystis proliferation, but this was not statistically significant. This study has shown the potential of using L. rhamnosus and L. lactis , as well as E. faecium as a prophylactic treatment against Blastocystis colonization or as an additional treatment regimen in combination with standard drugs.
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Erwin G. Zoetendal, A.D.L. Akkermans, Willem M. de Vos · Applied and Environmental Microbiology · 1998 · 1.4K citations · Full text
Life Sciences, Biology, Microbiology +14
Candidalysin is a fungal peptide toxin critical for mucosal infection
David L. Moyes, Duncan Wilson, Jonathan P. Richardson et al. · Nature · 2016 · 899 citations · Full text
Jens Walter, Christian Hertel, Gerald W. Tannock et al. · Applied and Environmental Microbiology · 2001 · 795 citations · Full text