bioRxiv Science⌕ Search

bioRxiv · 10.1101/2024.11.11.623027

Unraveling Keystone Taxa: Interactions Within Microbial Networks and Environmental Dynamics in Lake Mendota

Abstract

Microbial communities in freshwater ecosystems drive critical biogeochemical cycles, nutrient transformations, and energy flows essential for ecosystem stability. Yet, in the face of accelerating environmental changes, the responses of these microbial networks to spatial and temporal shifts remain underexplored, particularly with rising anoxia. We investigated the microbial ecosystems of Lake Mendota, Wisconsin, USA, through comprehensive metagenomic and metatranscriptomic analyses to elucidate their adaptations to environmental fluctuations across temporal and spatial dimensions. Employing tools like Sparse Inverse Covariance Estimation for Ecological Association Inference (SPIEC-EASI) and Conditional Auto-Regressive Least Absolute Shrinkage and Selection Operator (CARlasso), we identified key microbial taxa and their interactions with environmental parameters such as depth, temperature, pH, and dissolved oxygen. Our findings reveal that biological interactions more than environmental variables shape microbial community assembly and function. Specifically, keystone taxa from the phylum Bacteroidota emerged as pivotal in nutrient cycling and organic matter decomposition, processes crucial for sustaining water quality. Notably, these keystone taxa demonstrate dynamic adaptability, suggesting that microbial networks can rapidly adjust to changes in composition, a trait essential for resilience in the face of warming temperatures and altered precipitation patterns. This study provides critical insights into the resilience and adaptability of freshwater microbiomes, highlighting the role of microbial interactions in maintaining ecosystem health. By understanding how these microbial networks respond to environmental pressures, we can better predict shifts in microbial dynamics and anticipate the broader ecological impacts of climate change on freshwater systems. ImportanceThis research underscores the critical role of keystone taxa in freshwater ecosystems, highlighting how these organisms maintain water quality and contribute to the stability of aquatic environments. Understanding the ecological roles of these taxa is essential for developing strategies to manage ecosystems and conserve freshwater resources, particularly in the face of ongoing environmental challenges like climate change. The insights provided by this study not only enhance our comprehension of microbial interactions but also support effective ecosystem management and conservation efforts.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yang, Q., Aghdam, R., Tran, P. Q., Anantharaman, K., Solis-Lemus, C.. 2024-11-11. Unraveling Keystone Taxa: Interactions Within Microbial Networks and Environmental Dynamics in Lake Mendota. https://doi.org/10.1101/2024.11.11.623027

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Matrix-controlled emergence of biofilm architecture shapes antimicrobial survival

Biofilms are structured microbial communities whose extracellular matrix is widely regarded as a basis of their protection against antimicrobial compounds. Yet how matrix production by individual bacteria gives rise to collective architecture and antimicrobial protection remains poorly understood. Here, we systematically varied expression of the master biofilm regulator csgD in Salmonella enterica and found that increasing matrix production reorganizes biofilms from dense, isotropic packings into sparse, nematically aligned communities by altering cell-cell interactions. By combining experimentally measured biofilm architectures with reaction-diffusion modeling, we show that these structural changes produce distinct patterns of antimicrobial killing, ranging from preferential killing near the liquid-biofilm interface to more uniform killing throughout the community. Consequently, increasing matrix production unexpectedly reduces antimicrobial survival by shifting the biofilm into different transport regimes, while strain-specific physiological differences further modulate antimicrobial depletion. Rather than acting as a passive barrier, EPS therefore shapes antimicrobial susceptibility by reorganizing biofilm architecture and its transport properties. EPS thus provides a physical link between molecular regulation, collective architecture and antimicrobial survival, providing a quantitative framework for understanding how cellular matrix production generates emergent biofilm function.

microbiology↗

Mapping virulence-associated protein interaction networks reveals regulators of thermotolerance in Cryptococcus neoformans

Protein-protein interactions (PPIs) influence critical biological processes in pathogenic microorganisms, such as the human fungal pathogen, Cryptococcus neoformans. Fungal thermotolerance and stress response pathways are key virulence determinants that directly impact pathogen adaptation and survival and the infection process. To establish a comprehensive baseline of PPIs in C. neoformans and explore these interactions to infer functional roles for uncharacterized proteins, we applied size exclusion chromatography coupled with mass spectrometry to the secreted and cellular proteomes of the fungi. As a result, 216 and 1699 unique proteins were identified across 24 secretome and proteome fractions, respectively. The predicted secretome networks included expected proteins associated with vesicles and virulence, indicating a role in extracellular defense. Whereas the cryptococcal proteome highlighted interactions among proteins with defined roles in fungal virulence for protein stability and thermotolerance, including two previously uncharacterized proteins, CNAG_00287 and CNAG_05199, putatively involved in complex formation with heat-shock proteins (HSP). Based on sequence and structure homology, we propose that CNAG_00287 is a tetratricopeptide repeat-containing co-chaperone that modulates Hsp 70 activity and CNAG_05199 functions as a Hsp70. We validated the thermotolerance role of CNAG_00287 in heat-related stress, as its absence significantly impaired fungal growth in nutrient-limited media at 37 {degrees}C. Together, this work resolves virulence-associated PPIs within C. neoformans and reveals new molecular regulators of thermotolerance that underpin fungal pathogenicity.

microbiology↗

Environmental filtering and host identity collectively shape root-associated microbiomes of Ericaceae and ectomycorrhizal plants in fumarole fields

Background Symbiosis with microbes is a key strategy that has enabled plants to colonize extreme environments. Since the benefits conferred by root-associated microbes depend on both environmental conditions and host-microbe combinations, plant adaptation to harsh environments is closely linked to the assembly of root microbial communities. Understanding how environmental and host filtering jointly shape these communities is therefore fundamental to elucidating the mechanisms underlying plant adaptation to extreme environments. Results In this study, we investigated the differentiation of root-associated prokaryotic and fungal communities and individual operational taxonomic units (OTUs) across two contrasting habitats surrounding fumaroles, solfatara-field and forest-edge habitats, and six dominant Ericaceae and ectomycorrhizal plant taxa. Prokaryotic and fungal OTUs rarely exhibited strong preferences for both habitat and host identity. Instead, many of prokaryotic and fungal OTUs specialized to one of these niches, collectively generating root microbial communities differentiated by both factors. Nonetheless, striking specializations in habitat and host niches were observed in the fungal family Hyaloscyphaceae (Helotiales). To gain insight into the evolutionary basis of microbial specialization, we examined phylogenetic signals in preference phenotypes. The resulting weak phylogenetic signals in these preference phenotypes further suggest that this fungal clade has undergone substantial ecological divergence. Conclusion Overall, our findings indicate that root-associated microbial communities in extreme environments are assembled through the accumulation of microbial taxa specialized to either habitat or host, and that strong ecological specialization in fungi can arise with little phylogenetic constraint.

microbiology↗