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Goodman, A.

Publications and source records attributed to Goodman, A..

20 records · Page 2Linked to original sources

Evolution Of Hierarchy In Bacterial Metabolic Networks

BackgroundIn self-organized systems, the concept of flow hierarchy is a useful way to characterize the movement of information throughout a network. Hierarchical network organizations are shown to arise when there is a cost of maintaining links in the network. A similar constraint exists in metabolic networks, where costs come from reduced efficiency of nonspecific enzymes or from producing unnecessary enzymes. Previous analyses of bacterial metabolic networks have been used to predict the minimal nutrients that a bacterium needs to grow, its mutualistic relationships with other bacteria, and its major ecological niche. Using flow hierarchy, we can also infer the tradeoffs between growth rate and metabolic efficiency that bacteria make given their environmental constraints.\n\nResultsUsing a comparative approach on 2,935 bacterial metabolic networks, we show that flow hierarchy in bacterial metabolic networks tracks a fundamental tradeoff between growth rate and biomass production, and reflects a bacteriums realized ecological strategy. Additionally, by inferring the ancestral metabolic networks, we find that hierarchy decreases with distance from the root of the tree, suggesting the important pressure of increased growth rate relative to efficiency in the face of competition.\n\nConclusionsJust as hierarchical character is an important structural property in efficiently engineered systems, it also evolves in self-organized bacterial metabolic networks, reflects the life-history strategies of those bacteria, and plays an important role in network organization and efficiency.

evolutionary biology↗

The Landscape Of Type VI Secretion Across Human Gut Microbiomes Reveals Its Role In Community Composition

While the composition of the human gut microbiome has been well defined, the forces governing its assembly are poorly understood. Recently, prominent members of this community from the order Bacteroidales were shown to possess the type VI secretion system (T6SS), which mediates contact-dependent antagonism between Gram-negative bacteria. However, the distribution of the T6SS in human gut microbiomes and its role have not yet been characterized. To address this challenge, we construct an extensive catalog of T6SS effector/immunity (E-I) genes from three genetic architectures (GA1-3) found in Bacteroidales genomes. We then use metagenomic analysis to assess the abundances of these genes across a large set of gut microbiome samples. We find that despite E-I diversity across reference strains, each individual microbiome harbors a limited set of E-I genes representing a single E-I genotype. Importantly, for GA1-2, these genotypes are not associated with a specific species, suggesting selection for compatibility. GA3, in contrast, is restricted to B. fragilis, and its low diversity reflects a single B. fragilis strain per sample. We further show that in infant microbiomes GA3 is enriched and B. fragilis strains are replaced over time, suggesting competition for dominance in developing microbiomes. Finally, we find a strong association between the presence of GA3 and increased abundance of Bacteroides, indicating that this system confers a selective advantage in vivo in Bacteroides rich ecosystems. Combined, our findings provide the first comprehensive characterization of the T6SS landscape in the human microbiome, implicating it in both intra- and inter-species interactions.

microbiology↗