Bifidobacteria-Insight into clinical outcomes and mechanisms of its probiotic action

被引:110
|
作者
Sarkar, Amrita [1 ]
Mandal, Santanu
机构
[1] Univ Manchester, Sch Chem, 131 Princess St, Manchester M1 7DN, Lancs, England
关键词
Gut microbiome; Pathogen protection; Clinical application; Adverse effects; Immunomodulatory effect; Combinatorial therapy; IRRITABLE-BOWEL-SYNDROME; IN-VITRO EVALUATION; CHAIN FATTY-ACIDS; LIPOTEICHOIC ACID; DOUBLE-BLIND; ADHESION PROPERTIES; ATOPIC-DERMATITIS; BIFIDUM PRL2010; ANTIMICROBIAL ACTIVITY; ULCERATIVE-COLITIS;
D O I
10.1016/j.micres.2016.07.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The invasion of pathogens causes a disruption of the gut homeostasis. Innate immune responses and those triggered by endogenous microbiota form the first line of defence in our body. Pathogens often successfully overcome the resistances offered, calling for therapeutic intervention. Conventional strategy involving antibiotics might eradicate pathogens, but often leave the gut uncolonised and susceptible to recurrences. Probiotic supplements are useful alternatives. Bifidobacterium is one of widely studied probiotic genus, effective in restoring gut homeostasis. Mechanisms of probiotic action of bifidobacteria are several, often with strain-specificity. Analysis of streamlined literature reports reveal that although most studies report the probiotic aspect of bifidobacteria, sporadic documented contradictory results exist, challenging its therapeutic application and prompting studies to unambiguously establish the strain-associated probiotic activity and negate adverse effects prior to its clinical administration. Multi-strain/combinatorial therapy possibly relies on a combination of underlying operating mechanisms, each contributing towards enhanced probiotic efficacy, understanding which could help in developing customised formulations against targeted pathogens. Bifidogenic activity is also mediated by surface-associated structural components such as exopolysaccharides, lipoteichoic acids along with metabolites and bifidocins. This highlights scope for developing advanced structural therapeutic strategy which might be pivotal in replacing intact cell probiotics therapy. (C) 2016 Elsevier GmbH. All rights reserved.
引用
收藏
页码:159 / 171
页数:13
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