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Assessing the Viability of a Synthetic Bacterial Consortium on the In Vitro Gut Host-microbe Interface
Published on: July 4, 2018
Insights from genomes of representatives of the human gut commensal Bifidobacterium bifidum
Sabrina Duranti1, Christian Milani1, Gabriele Andrea Lugli1
1Laboratory of Probiogenomics, Department of Life Sciences, University of Parma, Parma, Italy.
Insights
Bifidobacterium bifidum possesses unique genes enabling it to metabolize host glycans, crucial for infant gut microbiota adaptation. This adaptation highlights the evolutionary impact of nutrient access on bacterial genomes.
Area of Science:
- Microbiology
- Genomics
- Human Microbiome
Background:
- Bifidobacteria are gut bacteria influencing host physiology.
- Bifidobacterium bifidum is a key member of the infant gut microbiota.
- Molecular mechanisms of B. bifidum adaptation are not well understood.
Purpose of the Study:
- To investigate the genetic basis of B. bifidum adaptation to the human infant gut.
- To identify unique genetic features related to nutrient acquisition in B. bifidum.
Main Methods:
- Pan-genome analysis of 15 B. bifidum strains.
- In silico identification of conserved genes.
- Growth experiments and transcriptomic analysis.
- Metagenomic dataset interrogation.
Main Results:
- A conserved gene unique to B. bifidum was identified, targeting host-derived glycans like mucin.
- Experimental data confirmed B. bifidum's ability to break down host glycans.
- Genetic features for glycan breakdown are widespread in B. bifidum.
Conclusions:
- Metabolic access to host glycans is a significant evolutionary driver for B. bifidum.
- These specialized metabolic capabilities shape the infant intestinal microbiota ecology.
Abstract:
Bifidobacteria are bacterial gut commensals of mammals, birds and social insects that are perceived to influence the metabolism/physiology of their host. In this context, members of the Bifidobacterium bifidum species are believed to significantly contribute to the overall microbiota of the human gut at infant stage. However, the molecular reasons for their adaptation to this environment are poorly understood. In this study, we analysed the pan-genome of B. bifidum species by decoding genomes of 15 B. bifidum strains, which highlighted the existence of a conserved gene uniquely present in this bifidobacterial taxon, underscoring a nutrient acquisition strategy that targets host-derived glycans, such as those present in mucin. Growth experiments and corresponding transcriptomic analyses confirmed the in silico data and supported these intriguing and unique host glycan-specific saccharolytic features. The ubiquity of the genetic features of B. bifidum for the breakdown of host glycans was confirmed by interrogating metagenomic datasets, thereby supporting the notion that metabolic access to host-derived glycans is a potent evolutionary force that has shaped B. bifidum genomes and consequently the ecology of the infant intestinal microbiota.
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