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During cooperative growth, microbes often experience higher fitness by sharing resources via metabolite exchange. How competitive species evolve to cooperate is, however, not known. Moreover, existing models (based on optimization of steady-state resources or fluxes) are often unable to explain the growth advantage for the cooperating species, even for simple reciprocally cross-feeding auxotrophic pairs. We present here an abstract model of cell growth that considers the stochastic burst-like gene expression of biosynthetic pathways of limiting biomass precursor metabolites and directly connect the amount of metabolite produced to cell growth and division, using a "metabolic sizer/adder" rule. Our model recapitulates Monod's law and yields the experimentally observed right-skewed long-tailed distribution of cell doubling times. The model further predicts the growth effect of secretion and uptake of metabolites by linking it to changes in the internal metabolite levels. The model also explains why auxotrophs may grow faster when supplied with the metabolite they cannot produce and why two reciprocally cross-feeding auxotrophs can grow faster than prototrophs. Overall, our framework allows us to predict the growth effect of metabolic interactions in independent microbes and microbial communities, setting up the stage to study the evolution of these interactions. Cooperative behaviors are highly prevalent in the wild, but their evolution is not understood. Metabolic flux models can demonstrate the viability of metabolic exchange as cooperative interactions, but steady-state growth models cannot explain why cooperators grow faster. We present a stochastic model that connects growth to the cell's internal metabolite levels and quantifies the growth effect of metabolite exchange and auxotrophy. We show that a reduction in gene expression noise can explain why cells that import metabolites or become auxotrophs can grow faster and why reciprocal cross-feeding of metabolites between complementary auxotrophs allows them to grow faster. Furthermore, our framework can simulate the growth of interacting cells, which will enable us to understand the possible trajectories of the evolution of cooperation .
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http://dx.doi.org/10.1128/mSystems.00448-21 | DOI Listing |
Unlabelled: Viruses can rapidly adapt and evolve to new, unfavorable environments due to their decreased replication fidelity, large reproductive index, and short life cycle. Often these adaptations that enable increased fitness in a new, specialized environment comes with a trade-off of decreased fitness in a standard, general environment. Understanding the tradeoffs of generalist and specialist viruses has provided important insight into vaccine development, mechanism of action of antivirals, and function of viral proteins.
View Article and Find Full Text PDFMol Biol Cell
September 2025
Cytogenetics Laboratory, Department of Zoology, Institute of Science, Banaras Hindu University, Varanasi-221005.
Cell size is strongly correlated with several biological processes, including the cell cycle and growth. Here, we investigated the regulation of stem cell size during central nervous system (CNS) development and its association with cell fate. We note that neural stem cells (NSCs) in different regions of the ventral nerve cord increase their size at different rates.
View Article and Find Full Text PDFJ Phys Chem B
August 2025
William A. Brookshire Department of Chemical and Biomolecular Engineering, University of Houston, 4226 Martin L. King Blvd., Houston, Texas 77204-4004, United States.
The aggregation pathways of Aβ42 peptides are complex and can lead to both amyloids and nonamyloid aggregates. We use atomic force microscopy imaging to monitor the assembly of aggregate structures and their dynamics. Two aggregation pathways emerge, one leading to amyloid fibrils and a second one that includes the formation of oligomers and apparently amorphous aggregates, which we identify as nonamyloid.
View Article and Find Full Text PDFJ Exp Biol
August 2025
McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB, Canada.
Bone fracture repair is a unique form of scarless tissue regeneration in mammals that recapitulates many aspects of endochondral ossification seen in developing long bones. For example, transgenic mouse studies have shown that many development-related genes involved in endochondral ossification (EO), which involves transformation of transient cartilaginous tissue into bone, are also redeployed during the bone repair process. While there is an expanding appreciation for the mechanistic overlap between bone development and repair, little is known about the relationship between rates of bone growth and bone repair in natural populations.
View Article and Find Full Text PDFAnimals (Basel)
July 2025
Department of Livestock Management, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan.
This study investigated the association between temperament and retrospective growth rates in 84 Nili Ravi buffalo heifers aged 18 to 24 months. Temperament was assessed using chute score and exit velocity, measured twice at a seven-day interval, and classified as calm (≤3) or nervous (>3). Retrospective average daily weight gain data were retrieved from farm records, and blood samples were collected to measure cortisol levels.
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