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Biology subjects

Venturelli, O. S.

Publications and source records attributed to Venturelli, O. S..

At least 19 recordsLinked to original sources

Decoding the role of microbial interspecies interactions on nitrogen fixation

Nitrogen fixation performed by rhizosphere bacteria has the potential to improve the sustainability of cereal crop cultivation. Deciphering the role of interspecies interactions on nitrogen fixation is crucial for devising strategies to enhance this process. To unravel the contributions of interspecies interactions, we constructed synthetic microbial communities from the bottom-up that contain diazotrophic bacteria that fix nitrogen and maize rhizosphere bacteria that do not have this capability. Interactions that impacted nitrogenase activity via growth-independent mechanisms were prevalent in the system. Nitrogenase activity increased and eventually saturated as a function of the number of inoculated diazotrophs. Using a tailored machine learning model for microbiome dynamics and explainable artificial intelligence, we deciphered species contributions on nitrogenase activity and diazotroph growth. We identified a community containing Klebsiella variicola, Herbaspirillum seropedicae, and Stutzerimonas stutzeri as a starting point for developing microbial inoculants for cereal crops. Taken together, these results provide insights into the role of interspecies interactions on nitrogenase activity.

systems biology↗

Mechanistic and machine learning models design human gut consortia that robustly inhibit Clostridioides difficile

Identifying design principles for robust inhibition of human pathogens is a major goal of microbiome engineering. By building synthetic microbial communities from the bottom-up guided by Bayesian active learning, we investigate the Clostridioides difficile growth landscape across thousands of species-metabolite conditions. Mechanistic consumer resource and machine learning models uncover significant interactions linking metabolites and species, and exhibit concordance with microbial interactions identified in human microbiome datasets. Guided by machine learning and mechanistic models, we elucidate microbial communities capable of robustly inhibiting C. difficile across diverse nutrient environments in vitro. Metabolomic profiling identified sorbitol, mannitol, and proline as key metabolites mediating community-driven C. difficile inhibition. Model-optimized communities significantly reduced C. difficile colonization in the murine gut whereas a model-designed non-inhibitory community did not exhibit this property. Communities display consistent metabolomic patterns in vitro and in vivo, suggesting that resource competition is a design principle of robust inhibition. Together, these findings establish an integrated experimental and computational framework for the rational design of microbial communities that robustly suppress pathogens across diverse environmental contexts.

systems biology↗

Physics-constrained neural ordinary differential equation models to discover and predict microbial community dynamics

Microbial communities play essential roles in shaping ecosystem functions and predictive modeling frameworks are crucial for understanding, controlling, and harnessing their properties. Competition and cross-feeding of metabolites drives microbiome dynamics and functions. Existing mechanistic models that capture metabolite-mediated interactions in microbial communities have limited flexibility due to rigid assumptions. While machine learning models provide flexibility, they require large datasets, are challenging to interpret, and can over-fit to experimental noise. To overcome these limitations, we develop a physics-constrained machine learning model, which we call the Neural Species Mediator (NSM), that combines a mechanistic model of metabolite dynamics with a machine learning component. The NSM is more accurate than mechanistic or machine learning components on experimental datasets and provides insights into direct biological interactions. In summary, embedding a neural network into a mechanistic model of microbial community dynamics improves prediction performance and interpretability compared to its constituent mechanistic or machine learning components. Significance statementMicrobial communities drive essential biological processes in every ecosystem. Predicting microbial community dynamics and functions and uncovering their interaction networks are challenging due to their complexity and emergent interactions. We develop a framework that combines biological knowledge with machine learning to accurately predict community and metabolite dynamics. This approach outperforms existing ecological and machine learning models by capturing environmentally mediated interactions while providing interpretable insights into microbe-metabolite interactions. Our framework enables the rational design and control of microbial communities for applications in medicine, agriculture and biotechnology

systems biology↗

Machine learning-guided design of human gut microbiome dynamics in response to dietary fibers

Dietary fibers are key modulators of human gut microbiome dynamics and functions, yet we lack the ability to predict community dynamics and functions in response to fibers. We integrate machine learning, Bayesian optimization, and high-throughput community construction to investigate how dietary fibers shape health-relevant functions of human gut microbial communities. To efficiently navigate the landscape of fiber-microbiome interactions, we implemented a design-test-learn cycle to identify fiber-species combinations that maximize a multi-objective function capturing beneficial community properties. Our model-guided approach revealed a highly butyrogenic and robust ecological motif characterized by the copresence of inulin, Bacteroides uniformis, and Anaerostipes caccae and a higher-order interaction with Prevotella copri. In germ-free mice, model-designed species-fiber combinations impacted colonization, community diversity and short-chain fatty acid profiles. In sum, our work establishes a novel framework for designing microbial communities with desired functions in response to key nutrients such as dietary fibers.

systems biology↗

A data-driven modeling framework for mapping genotypes to synthetic microbial community functions

Microbial communities play a central role in transforming environments across Earth, driving both physical and chemical changes. By harnessing these capabilities, synthetic microbial communities, assembled from the bottom up, offer valuable insights into the mechanisms that govern community functions. These communities can also be tailored to produce desired outcomes, such as the synthesis of health-related metabolites or nitrogen fixation to improve plant productivity. Widely used computational models predict synthetic community functions using species abundances as inputs, making it impossible to predict the effects of species not included in the training data. We bridge this gap using a data-driven community genotype function (dCGF) model. By lifting the representation of each species to a high-dimensional genetic feature space, dCGF learns a mapping from community genetic feature matrices to community functions. We demonstrate that dCGF can accurately predict communities in a fixed environmental context that are composed in part or entirely from new species with known genetic features. In addition, dCGF facilitates the identification of species roles for a community function and hypotheses about how specific genetic features influence community functions. In sum, dCGF provides a new data-driven avenue for modeling synthetic microbial communities using genetic information, which could empower model-driven design of microbial communities.

systems biology↗

Human gut microbiota interactions shape the long-term growth dynamics and evolutionary adaptations of Clostridioides difficile

Clostridioides difficile can transiently or persistently colonize the human gut, posing a risk factor for infections. This colonization is influenced by complex molecular and ecological interactions with human gut microbiota. By investigating C. difficile dynamics in human gut communities over hundreds of generations, we show patterns of stable coexistence, instability, or competitive exclusion. Lowering carbohydrate concentration shifted a community containing C. difficile and the prevalent human gut symbiont Phocaeicola vulgatus from competitive exclusion to coexistence, facilitated by increased cross-feeding. In this environment, C. difficile adapted via single-point mutations in key metabolic genes, altering its metabolic niche from proline to glucose utilization. These metabolic changes substantially impacted inter-species interactions and reduced disease severity in the mammalian gut. In sum, human gut microbiota interactions are crucial in shaping the long-term growth dynamics and evolutionary adaptations of C. difficile, offering key insights for developing anti-C. difficile strategies.

systems biology↗

Engineered lysins to modulate human gut microbiome communities

The ability to precisely control the human gut microbiomes composition, metabolic networks, and host interactions would revolutionize medicine and how we treat human disease. Microbiome remodeling approaches such as probiotics, prebiotics, antibiotics, and fecal microbiota transplantation are global perturbations with consequences that are difficult to predict. Lysins are enzymes produced by bacteriophages and bacteria that have exceptional specificity to lyse bacterial cells and could be applied for targeted microbiome remodeling. In this work we demonstrate the ability of lysins to target diverse human gut commensal bacteria, how domain recombination can give rise to chimeric lysins with altered species preferences, and how engineered lysins can directly remodel the structure and function of synthetic human gut microbiomes. Lysins represent a general platform that can be rapidly tailored through protein engineering to control complex microbial ecosystems.

synthetic biology↗

Elucidating human gut microbiota interactions that robustly inhibit diverse Clostridioides difficile strains across different nutrient landscapes

The human gut pathogen Clostridioides difficile displays extreme genetic variability and confronts a changeable nutrient landscape in the gut. We mapped gut microbiota inter-species interactions impacting the growth and toxin production of diverse C. difficile strains in different nutrient environments. Although negative interactions impacting C. difficile are prevalent in environments promoting resource competition, they are sparse in an environment containing C. difficile-preferred carbohydrates. C. difficile strains display differences in interactions with Clostridium scindens and the ability to compete for proline. C. difficile toxin production displays substantial community-context dependent variation and does not trend with growth-mediated inter-species interactions. C. difficile shows substantial differences in transcriptional profiles in the presence of the closely related species C. hiranonis or C. scindens. In co-culture with C. hiranonis, C. difficile exhibits massive alterations in metabolism and other cellular processes, consistent with their high metabolic overlap. Further, Clostridium hiranonis inhibits the growth and toxin production of diverse C. difficile strains across different nutrient environments and ameliorates the disease severity of a C. difficile challenge in a murine model. In sum, strain-level variability and nutrient environments are major variables shaping gut microbiota interactions with C. difficile.

systems biology↗

The arginine dihydrolase pathway shapes human gut microbial community assembly, functions, and mammalian host colonization

The arginine dihydrolase pathway (arc operon) present in a subset of diverse human gut species enables arginine catabolism. This specialized metabolic pathway can alter environmental pH and nitrogen availability, which in turn could shape gut microbiota inter-species interactions. By exploiting synthetic control of gene expression, we investigated the role of the arc operon in probiotic Escherichia coli Nissle 1917 on human gut community assembly and health-relevant metabolite profiles in vitro and in the murine gut. By stabilizing environmental pH, the arc operon reduced variability in community composition across different initial pH perturbations. The abundance of butyrate producing bacteria were altered in response to arc operon activity and butyrate production was enhanced in a physiologically relevant pH range. While the presence of the arc operon altered community dynamics, it did not impact production of short chain fatty acids. Dynamic computational modeling of pH-mediated interactions reveals the quantitative contribution of this mechanism to community assembly. In sum, our framework to quantify the contribution of molecular pathways and mechanism modalities on microbial community dynamics and functions could be applied more broadly.

systems biology↗

Massively parallel single-cell sequencing of genetic loci in diverse microbial populations

Single cell genetic heterogeneity is ubiquitous in microbial populations and an important aspect of microbial biology. However, we lack a broadly applicable and accessible method to study this heterogeneity at the single cell level. Here, we introduce a simple, robust, and generalizable platform for quantitative and massively parallel single cell sequencing of target genetic loci in microbes using ultrahigh-throughput droplet microfluidics (Droplet Targeted Amplicon Sequencing or DoTA-seq). Using DoTA-seq, we elucidate the highly diverse single cell ON/OFF states of the phase-variable capsule synthesis operons in the prevalent human gut species Bacteroides fragilis. In addition, we quantify the shifts in antibiotic resistance gene abundances in different species in a 25 member human gut microbial community in response to antibiotics. By sequencing tens of thousands of single-cells derived from a human fecal sample, we identify links between plasmid replicons and the taxonomic lineages of their associated hosts. In sum, DoTA-seq is an accessible and broadly applicable tool for profiling single-cell genetic variation in microbiomes.

microbiology↗

Integrating a tailored recurrent neural network with Bayesian experimental design to optimize microbial community functions

Microbiomes interact dynamically with their environment to perform exploitable functions such as production of valuable metabolites and degradation of toxic metabolites for a wide range of applications in human health, agriculture, and environmental cleanup. Developing computational models to predict the key bacterial species and environmental factors to build and optimize such functions are crucial to accelerate microbial community engineering. However, there is an unknown web of interactions that determine the highly complex and dynamic behaviors of these systems, which precludes the development of models based on known mechanisms. By contrast, entirely data-driven machine learning models can produce physically unrealistic predictions and often require significant amounts of experimental data to learn system behavior. We develop a physically constrained recurrent neural network that preserves model flexibility but is constrained to produce physically consistent predictions and show that it outperforms existing machine learning methods in the prediction of experimentally measured species abundance and metabolite concentrations. Further, we present an experimental design algorithm to select a set of experimental conditions that simultaneously maximize the expected gain in information and target microbial community functions. Using a bioreactor case study, we demonstrate how the proposed framework can be used to efficiently navigate a large design space to identify optimal operating conditions. The proposed methodology offers a flexible machine learning approach specifically tailored to optimize microbiome target functions through the sequential design of informative experiments that seek to explore and exploit community functions. 1 Author summaryThe functions performed by microbiomes hold tremendous promise to address grand challenges facing society ranging from improving human health to promoting plant growth. To design their properties, flexible computational models that can predict the temporally changing behaviors of microbiomes in response to key environmental parameters are needed. When considering bottom-up design of microbiomes, the number of possible communities grows exponentially with the number of organisms and environmental factors, which makes it challenging to navigate the microbiome function landscape. To overcome these challenges, we present a physically constrained machine learning model for microbiomes and a Bayesian experimental design framework to efficiently navigate the space of possible communities and environmental factors.

systems biology↗

Single-cell bacterial sequencing of invertible loci reveals promoter inversion rates as a strong determinant of population heterogeneity

Population heterogeneity can promote bacterial fitness in response to unpredictable environmental conditions. Human gut symbiont Bacteroides spp., displays variability in single cell surface architectures by combinatorial regulation of promoter inversions that drive expression of capsular polysaccharides (CPS). Using high-throughput single-cell sequencing, we reveal population heterogeneity generated through combinatorial promoter inversion and show that B. fragilis populations can access diverse CPS promoter states. Combining our data with stochastic computational modeling, we demonstrate that the rates of promoter inversion regulated by a broadly conserved serine recombinase are a major mechanism shaping population heterogeneity. Exploiting control over the expression of the recombinase, we devise a method for creating phase-locked variants and show that populations with different initial compositions converge to a similar steady-state composition over time. Our approach can be used to interrogate single-cell phase variable states of diverse microbes including bacterial pathogens. Summary sentenceHigh-throughput single cell sequencing of phase variation reveals regulation as a major driver of population diversification

systems biology↗

Microbial Community Interactions on a Chip

Multispecies microbial communities drive most ecosystems on Earth. Chemical and biological interactions within these communities can affect survival of individual members and the entire community. However, the prohibitively high number of possible interactions within a microbial community has made the characterization of factors that influence community development challenging. Here we report a Microbial Community Interaction (CI) device to advance the systematic study of chemical and biological interactions within a microbial community. The CI creates a combinatorial landscape made up of an array of triangular wells interconnected with circular wells, which each contains either a different chemical or microbial strain, generating chemical gradients and revealing biological interactions. Bacillus cereus UW85 containing GFP provided the "target" readout in the triangular wells, and antibiotics or microorganisms in adjacent circular wells are designated the "variables". The CI device revealed that gentamicin and vancomycin are antagonistic to each other in inhibiting the target B. cereus UW85, displaying weaker inhibitory activity when used in combination than alone. We identified three-member communities constructed with isolates from the plant rhizosphere that increased or decreased growth of B. cereus. The CI device enables both strain-level and community-level insight. The scalable geometric design of the CI device enables experiments with high combinatorial efficiency, thereby providing a simple, scalable platform for systematic interrogation of three-factor interactions that influence microorganisms in solitary or community life.

microbiology↗

Microbial interactions impact the growth response of Clostridioides difficile to antibiotics

In the human gut, the growth of Clostridioides difficile is impacted by a complex web of inter-species interactions with members of human gut microbiota. We investigate the contribution of inter-species interactions on the antibiotic response of C. difficile to clinically relevant antibiotics using bottom-up assembly of human gut communities. We discover two classes of microbial interactions that alter C. difficiles antibiotic susceptibility: infrequent increases in tolerance at high antibiotic concentrations and frequent growth enhancements at low antibiotic concentrations. Based on genome-wide transcriptional profiling data, we demonstrate that metal sequestration due to hydrogen sulfide production by the prevalent gut species Desulfovibrio piger increases metronidazole tolerance of C. difficile. Competition with species that display higher sensitivity to the antibiotic than C. difficile leads to enhanced growth of C. difficile at low antibiotic concentrations. A dynamic computational model identifies the ecological design principles driving this effect. Our results provide a deeper understanding of ecological and molecular principles shaping C. difficiles response to antibiotics, which could inform therapeutic interventions.

systems biology↗

Growth limitation via chemically complex carbohydrates reduces sensitivity of synthetic human gut communities to perturbations

Dietary fiber affects the composition and functions of microbial communities that reside in the human gut. However, we lack a detailed and quantitative understanding of how these nutrients shape microbial community dynamics, interaction networks and systems-level properties. Using synthetic human gut communities coupled to computational modeling, we dissect the effects of varied fiber types or their constituent sugars on community assembly and sensitivity to perturbations. By quantifying carbohydrate chemical complexity, we demonstrate that microbial growth decreases as a function of complexity. We further demonstrate that the balance of species occupying distinct metabolic niches is altered by the presence of chemically complex carbohydrates. The frequency of negative inter-species interactions is reduced in the presence of complex carbohydrates. Communities grown in complex carbohydrates reproducibly assemble from a wide range of initial species abundances and display reduced sensitivity to invasion. Resource competition is identified as a key mechanism influencing the response of communities to perturbations. The strength of resource competition can promote sensitivity of community assembly to variations in initial species proportions and impact community resistance to invasion. By limiting microbial growth, complex carbohydrates promote the expansion of species occupying niches beyond carbohydrate utilization, shape the distribution of inter-species interactions, which in turn determines the communitys response to perturbations.

ecology↗

Model-guided design of the diversity of a synthetic human gut community

Microbial communities have tremendous potential as therapeutics. However, a major bottleneck is manufacturing high-diversity microbial communities with desired species compositions. We develop a two-stage, model-guided framework to produce microbial communities with target species compositions. We apply this method to optimize the diversity of a synthetic human gut community. The first stage exploits media components to enable uniform growth responses of individual species and the second stage uses a design-test-learn cycle with initial species abundance as a control point to manipulate community composition. Our designed culture conditions yield 91% of the maximum possible diversity. Leveraging these data, we construct a dynamic ecological model to guide the design of lower-order communities with desired temporal properties over a longer timescale. In sum, a deeper understanding of how microbial community assembly responds to changes in environmental factors, initial species abundances, and inter-species interactions can enable the predictable design of community dynamics.

systems biology↗

Programming bacteria to sense environmental DNA for multiplexed pathogen detection

DNA is a universal and programmable signal of living organisms. Here we developed cell-based DNA sensors by engineering the naturally competent bacterium Bacillus subtilis (B. subtilis) to detect specific DNA sequences in the environment. The DNA sensor strains can identify diverse bacterial species including major human pathogens with high specificity and sensitivity. Multiplexed detection of genomic DNA from different species in complex samples can be achieved by coupling the sensing mechanism to orthogonal fluorescent reporters. We also demonstrate that the DNA sensors can detect the presence of species in the complex samples without requiring DNA extraction. The modularity of the living cell-based DNA sensing mechanism and simple detection procedure could enable programmable DNA sensing for broad applications.

synthetic biology↗

Deep Learning Enables Design of Multifunctional Synthetic Human Gut Microbiome Dynamics

Predicting the dynamics and functions of microbiomes constructed from the bottom-up is a key challenge in exploiting them to our benefit. Current ordinary differential equation-based models fail to capture complex behaviors that fall outside of a predetermined ecological theory and do not scale well with increasing community complexity and in considering multiple functions. We develop and apply a long short-term memory (LSTM) framework to advance our understanding of community assembly and health-relevant metabolite production using a synthetic human gut community. A mainstay of deep learning, the LSTM learns a high dimensional data-driven non-linear dynamical system model used to design communities with desired metabolite profiles. We show that the LSTM model can outperform the widely used generalized Lotka-Volterra model. We build methods decipher microbe-microbe and microbe-metabolite interactions from an otherwise black-box model. These methods highlight that Actinobacteria, Firmicutes and Proteobacteria are significant drivers of metabolite production whereas Bacteroides shape community dynamics. We use the LSTM model to navigate a large multidimensional functional landscape to identify communities with unique health-relevant metabolite profiles and temporal behaviors. In sum, the accuracy of the LSTM model can be exploited for experimental planning and to guide the design of synthetic microbiomes with target dynamic functions.

systems biology↗