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The ability to adhere to mucus and epithelial cells is considered an important selection criterion for potential probiotic strains. The adhesion of probiotic strains varies among strains, depending on the cell surface properties such as hydrophobicity and extracellular protein profile. Auto-aggregation and co-aggregation of bacteria are two important interactions leading to flocculation formation in natural and engineered systems. In these systems, bacteria form flocs either by aggregating with genetically identical cells (auto-aggregation) or with genetically distinct cells (co-aggregation). Since they are species-dependent, the process of flocculation formation through auto-aggregation and co-aggregation is more predictable if there is sufficient knowledge of the interaction relationships between bacterial cells. Auto-aggregation and co-aggregation of microorganisms leading to the formation of biofilms or flocs are widespread in natural systems. The specific cell-cell interactions were determined using auto-aggregation assay and co-aggregation assay.
Auto-aggregation appears to be the first step in the adhesion process, allowing bacteria to form a barrier and prevent the adhesion of undesirable bacteria. Auto-aggregation of bacteria refers to the process by which bacteria interact in a static liquid suspension and settle to the bottom. Auto-aggregation is a widely studied phenomenon that leads to the formation of a community structure that facilitates interaction and communication between cells, gene exchange, adhesion, and colonization in different environments. The ability of auto-aggregation has been associated with adhesion. To achieve the desired benefit of probiotic bacteria, they need to form sufficiently large biomass through aggregation. The identified triggers of auto-aggregation include gut, nutritional, chemical, and oxidative stress, temperature changes, and nutrient availability.
The ability of probiotic strains to co-aggregate is central to forming biofilms and competing with pathogens for binding sites. Co-aggregation interactions are thought to contribute to biofilm development through two pathways.
Any culturable probiotic or other microorganisms. For example, Lactobacillus, Bifidobacterium, Streptococcus, and so on.
E. coli, Staphylococcus aureus, Salmonella, or other pathogens.
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For Research Use Only. Not intended for use in food manufacturing or medical procedures (diagnostics or therapeutics). Do Not Use in Humans.
For Research Use Only. Not intended for use in food manufacturing or medical procedures (diagnostics or therapeutics). Do Not Use in Humans.
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