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Schwartzman, J.

Publications and source records attributed to Schwartzman, J..

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Modular assembly of polysaccharide-degrading microbial communities in the ocean

Many complex biological systems such as metabolic networks can be divided into functional and organizational subunits, called modules, which provide the flexibility to assemble novel multi-functional hierarchies by a mix and match of simpler components. Here we show that polysaccharide-degrading microbial communities in the ocean can also assemble in a modular fashion. Using synthetic particles made of a variety of polysaccharides commonly found in the ocean, we showed that the particle colonization dynamics of natural bacterioplankton assemblages can be understood as the aggregation of species modules of two main types: a first module type made of narrow niche-range primary degraders, whose dynamics are controlled by particle polysaccharide composition, and a second module type containing broad niche-range, substrate-independent taxa whose dynamics are controlled by interspecific interactions, in particular cross-feeding via organic acids, amino acids and other metabolic byproducts. As a consequence of this modular logic, communities can be predicted to assemble by a sum of substrate-specific primary degrader modules, one for each complex polysaccharide in the particle, connected to a single broad-niche range consumer module. We validate this model by showing that a linear combination of the communities on single-polysaccharide particles accurately predicts community composition on mixed-polysaccharide particles. Our results suggest thus that the assembly of heterotrophic communities that degrade complex organic materials follow simple design principles that can be exploited to engineer heterotrophic microbiomes.

microbiology

Pseudomonas aeruginosa Can Inhibit Growth of Streptococcal Species via Iron Sequestration

Cystic Fibrosis (CF) is a genetic disease that causes patients to accumulate thick, dehydrated mucus in the lung and develop chronic, polymicrobial infections due to reduced mucociliary clearance. These chronic polymicrobial infections and subsequent decline in lung function are significant factors in the morbidity and mortality of CF. Pseudomonas aeruginosa and Streptococcus spp. are among the most prevalent organisms in the CF lung; the presence of P. aeruginosa correlates with lung function decline and the Streptococcus milleri group (SMG), a subgroup of the viridans streptococci, is associated with exacerbations in patients with CF. Here we characterize the interspecies interactions that occur between these two genera. We demonstrated that multiple P. aeruginosa laboratory strains and clinical CF isolates promote the growth of multiple SMG strains and oral streptococci in an in vitro coculture system. We investigated the mechanism by which P. aeruginosa enhances growth of streptococci by screening for mutants of P. aeruginosa PA14 unable to enhance Streptococcus growth, and we identified the P. aeruginosa pqsL::TnM mutant, which failed to promote growth of S. constellatus and S. sanguinis. Characterization of the P. aeruginosa {Delta}pqsL mutant revealed that this strain cannot promote Streptococcus growth. Our genetic data and growth studies support a model whereby the P. aeruginosa {Delta}pqsL mutant overproduces siderophores, and thus likely outcompetes Streptococcus sanguinis for limited iron. We propose a model whereby competition for iron represents one important means of interaction between P. aeruginosa and Streptococcus spp.\n\nImportanceCystic fibrosis (CF) lung infections are increasingly recognized for their polymicrobial nature. These polymicrobial infections may alter the biology of the organisms involved in CF-related infections, leading to changes in growth, virulence and/or antibiotic tolerance, and could thereby affect patient health and response to treatment. In this study, we demonstrate interactions between P. aeruginosa and streptococci using a coculture model, and show that one interaction between these microbes is likely competition for iron. Thus, these data indicate that one CF pathogen may influence the growth of another and add to our limited knowledge of polymicrobial interactions in the CF airway.

microbiology