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Biology subjects

Eguiluz, V. M.

Publications and source records attributed to Eguiluz, V. M..

6 recordsLinked to original sources

Biodiversity dynamics with complex genotype-to-phenotype architecture in multilayer networks

2The genotype-to-phenotype architecture (GPA), defined by complex interactions such as pleiotropy, epistasis, and regulatory control, is a fundamental yet often overlooked driver of biodiversity dynamics. While empirical evidence suggests that traits mediating species interactions (biotic) and environmental responses (abiotic) are frequently correlated, most eco-evolutionary theories treat these traits as independent, leaving a gap in our understanding of how genomic architecture influences community-level outcomes. In this study, we contrast two distinct GPAs, modular (independent trait evolution) and correlated (integrated trait evolution), within a spatially explicit multilayer network framework. We evaluate their impact on biodiversity across varying regimes of selection, migration, and biotic and environmental filtering. Our results reveal a hierarchy of drivers: selection strength dictates the absolute magnitude of the architectural effect, while migration and context-dependent biotic and abiotic effects determine which architecture yields a diversity advantage. Correlated GPAs enhance species coexistence and diversity in low-migration landscapes characterized by strong selection and moderate, balanced biotic and abiotic pressures. In these contexts, trait integration serves as a buffer against selective noise. Conversely, modular GPAs support higher diversity under high migration and strong biotic interactions, where the decoupling of trait modules provides the adaptive flexibility necessary to navigate spatially conflicting selective pressures. Our findings demonstrate that genomic architecture acts as a critical filter for environmental perturbations. Integrating complex GPAs into multispecies models is essential for quantifying the co-evolutionary feedbacks among traits, population adaptation, and species persistence. Our framework provides a path for predicting how biodiversity emerges and persists across biological scales, from genomics to communities and food webs, under the accelerating pressures of global change. 1 ConclusionsO_LIWe integrate trait architecture to spatial biodiversity to show biodiversity patterns are not merely products of ecological interactions, but are fundamentally constrained by Genotype-to-Phenotype Architecture (GPA). By linking GPA to biodiversity we show the interplay between the complexity of an organism and community structure in determining diversity patterns. C_LIO_LIThe hierarchy of Eco-Evolutionary Drivers: We establish a new conceptual hierarchy where selection strength acts as the fundamental governor of architectural impact, while the specific architecture predicting higher diversity (Correlational vs. Modular) is dictated by the interplay of migration scales and context-dependent biotic and abiotic dynamics. C_LIO_LISelection-Migration contingency for coexistence: We provide a new hypothesis for species coexistence: Correlational selection serves as a stabilizing force under dispersal limitation, whereas Modular trait architecture provides the adaptive flexibility to maintain diversity in high-migration, spatially heterogeneous landscapes. C_LIO_LIAdaptive decoupling as a diversity engine: We propose that trait modularity functions as a "buffer" against extinction by decoupling phenotypic responses. This allows populations to navigate conflicting selective pressures, effectively facilitating evolutionary rescue in complex biotic environments. C_LIO_LIMethodological framework for empirical inference: To bridge the gap between theory and data, we provide a novel likelihood-based framework. This enables researchers to infer latent trait architectures from population genomic samplings, turning GPA from a theoretical construct into a measurable sampling variable in natural populations. C_LIO_LIWe define a new roadmap for the next generation of eco-evolutionary modeling. By identifying the gaps between existing simulation engines, we provide a conceptual "blueprint" for a digital ecosystem that fully integrates complex genetic architecture with global bio-diversity dynamics. C_LI

evolutionary biology↗

A syntax network morphospace reveals sudden transitions between discrete developmental stages during language acquisition

Syntax is an aspect of human language responsible for the hierarchical ordering of linguistic structures. Syntax can be summarized by dependency trees with words as nodes and edges reflecting syntactic subordination. By merging trees from several sentences, we obtain syntax graphs or networks, which display distinct shapes depending on whether the language capability is well-formed, still developing, or pathological. Such graphs make syntactic capacity quantifiable at a systemic level, revealing emerging patterns and universalities. What is the structure of syntax networks during ontogeny in typically developing (TD) children? Do cognitively challenged children develop language through alternative routes? Here we quantify and portray the typical development of syntax networks in Dutch, and find that children affected by Down syndrome, hearing impairment, and specific language impairment initially seem to follow the typical developmental path but eventually halt, culminating in a different linguistic phenotype. Our expanded data set (with almost 50 times more data than earlier studies) and increased mathematical dimensions to quantify network shape enable us to: (i) confirm and refine a proposed sharp transition in language development, (ii) correlate specific network traits with syntax maturation, and (iii) quantify the aspects that fall short in atypical development--suggesting potential diagnostic tools. We also find grounds to hypothesize a gap in syntax maturation, separating challenged children who nevertheless reach the latest stage from others systematically stuck, regardless of their condition. Our quantitative analysis enables a rigorous visualization of linguistic development trajectories, an old (yet mostly qualitative) theme in linguistics. Similar works should allow to test and propose specific hypotheses on solid grounds, as we do here. Future efforts should generalize to other languages and/or clinical conditions, seeking patterns that might point at universalities in language development.

systems biology↗

NAc-DBS selectively enhances memory updating without effect on retrieval

Deep brain stimulation (DBS) has emerged as a widely used therapeutic option when pharmacological treatments prove ineffective or refractory for psychiatric patients. The nucleus accumbens (NAc) represents a frequently targeted site in DBS interventions due to its demonstrated safety profile and therapeutic efficacy in obsessive-compulsive disorder, major depression, and anorexia nervosa. However, limited mechanistic understanding hampers its broader clinical applicability. This study sought to delineate the distinct behavioural dimensions modulated by NAc-DBS, its impact on distinct facets of memory, and to elucidate the underlying brain-network mechanism of action. We developed a novel spatial navigation task for rats and employed a high-dimensional behavioural analysis complemented by fMRI to dissect the cognitive, behavioural and neurobiological effects of NAc-DBS. Active NAc-DBS produced a selective enhancement of long-term memory encoding without affecting memory recall or working memory. We found no effect of NAc-DBS on motor, appetitive or stress-related behaviours. Sustained neuronal activation in the NAc, septum, entorhinal and insular cortex demonstrated no desensitization to chronic NAc-DBS, which triggered a functional reorganization among dopaminergic-related structures. These findings suggest that NAc-DBS induces a functional reorganization in the mesocorticolimbic system, potentially mimicking a dopaminergic novelty signal to enhance memory updating. This provides a mechanistic basis for the therapeutic use of NAc-DBS, particularly in improving cognitive flexibility in psychiatric disorders.

neuroscience↗

The architecture of multifunctional ecological networks

Understanding how biotic interactions affect ecosystem functioning has been a research priority in natural sciences due to their critical role in bolstering ecological resilience1-3. Yet, traditional assessment of ecological complexity typically focus on species-species effective interactions that mediate a particular function (e.g. pollination4 or seed dispersal5), overlooking the synergistic effect of multiple functions that further underpin species-function and function-function interactions in multifunctional ecosystems. At the same time, while ecological network theory holds a potential to quantify the relationship between biodiversity and ecosystem multifunctionality6, 7, its connection has been done mainly conceptually, due to challenges measuring different interactions and establishing their relevance across multiple niche dimensions8, 9. Such lack of quantitative studies therefore limits our ability to determine which species and interactions are important to maintain the multiple functions of ecosystems10. Here we develop a framework -derived from a resource-consumer-function tensor analysis-that bridges these gaps by framing biodiversity-ecosystem multifunctionality in terms of multilayer ecological network theory. Its application to recently collected ecological data -- reporting weighted interactions between plants, animals and fungi across multiple function types--allows to (i) unveil and quantify the existence of both (multi-functional) keystone species and a dual function keystoneness pattern, and (ii) project plants and functions into a similarity space where clear clusters emerge and the importance of weak links is manifested. This dual insight from species and functional perspectives will better guide conservation efforts to reduce biodiversity loss.

ecology↗

Rapid Evolution of SARS-CoV-2 Challenges Human Defenses

Evolutionary ecology theory provides an avenue to anticipate the future behavior of SARS-CoV-2. Here we quantify the accelerating evolution of SARS-CoV-2 by tracking the SARS-CoV-2 mutation globally, with a focus on the Receptor Binding Domain (RBD) of the spike protein believed to determine infectivity. We estimate that 384 million people were infected by March 1st, 2021, producing up to 1021 copies of the virus, with one new RBD variant appearing for every 600,000 human infections, resulting in approximately three new effective RBD variants produced daily. Doubling the number of RBD variants every 71.67 days followed by selection of the most infective variants challenges our defenses and calls for a shift to anticipatory, rather than reactive tactics. One-Sentence SummaryAccelerating evolution of SARS-CoV-2 demands formulating universal vaccines and treatments based on big-data simulations of possible new variants.

evolutionary biology↗

Meta-analysis reveals host-dependent nitrogen recycling as a mechanism of symbiont control in Aiptasia

The metabolic symbiosis with photosynthetic algae of the genus Symbiodinium allows corals to thrive in the oligotrophic environments of tropical seas. Many aspects of this relationship have been investigated using transcriptomic analyses in the emerging model organism Aiptasia. However, previous studies identified thousands of putatively symbiosis-related genes, making it difficult to disentangle symbiosis-induced responses from undesired experimental parameters. Using a meta-analysis approach, we identified a core set of 731 high-confidence symbiosis-associated genes that reveal host-dependent recycling of waste ammonium and amino acid synthesis as central processes in this relationship. Combining transcriptomic and metabolomic analyses, we show that symbiont-derived carbon enables host recycling of ammonium into nonessential amino acids. We propose that this provides a regulatory mechanism to control symbiont growth through a carbon-dependent negative feedback of nitrogen availability to the symbiont. The dependence of this mechanism on symbiont-derived carbon highlights the susceptibility of this symbiosis to changes in carbon translocation, as imposed by environmental stress.

genomics↗