Biology subjects

Morris, M. M.

Publications and source records attributed to Morris, M. M..

3 recordsLinked to original sources

bioRxiv2026

Single-Cell Atlas of Dorsal Root Ganglion Remodeling After Neuroma-Forming Nerve Injury Reveals Intervention-Specific Glial and Immune Programs

Peripheral nerve injury, whether caused by a cut, crush, or excessive stretch, can cause disordered regeneration and formation of a painful neuroma at the injury site. Regrowing axons may end in a swelling, hypersensitive nerve stump, producing pain along the affected nerve distribution that may outweigh sensory or motor deficits. Although neuromas are common, treatment outcomes are inconsistent and the mechanisms that initiate and sustain neuroma-associated pain remain poorly defined. Many surgical and non-surgical approaches (excision with transposition, capping, sclerosis, cryoablation) are used, yet comparative studies have not identified a superior technique, highlighting biological heterogeneity and knowledge gaps. A proximal nerve crush (axonotmetic injury) performed upstream of a neuroma or transection is proposed to reshape axonal growth and interrupt retrograde injury signaling, potentially shifting the system toward a more regenerative, pain-resolving state. However, how proximal crush remodels long-term programs in the dorsal root ganglion (DRG), and how these changes relate to neuroma-like outcomes, are unclear. Here, we build a single-cell atlas of DRG remodeling after neuroma-forming injury and compare it with two interventions- proximal nerve crush and nerve resection, using scRNA-seq. By resolving transcriptional responses across sensory neurons, satellite glial cells, Schwann cells, and macrophages, we identify intervention-specific glial and immune programs that distinguish permissive regeneration from persistent, pain-associated states and nominate pathways for mechanism-guided neuroma therapies.

neuroscience↗

bioRxiv2024

A toxic environment selects for specialist microbiome in poison frogs

Shifts in microbiome community composition can have large effects on host health. It is therefore important to understand how perturbations, like those caused by the introduction of exogenous chemicals, modulate microbiome community composition. In poison frogs within the family Dendrobatidae, the skin microbiome is exposed to the alkaloids that the frogs sequester from their diet and use for defense. Given the demonstrated antimicrobial effects of these poison frog alkaloids, these compounds may be structuring the skin microbial community. To test this, we first characterized microbial communities from chemically defended and closely related non-defended frogs from Ecuador. Then we conducted a laboratory experiment to monitor the effect of the alkaloid decahydroquinoline (DHQ) on the microbiome of a single frog species. In both the field and lab experiments, we found that alkaloid-exposed microbiomes are more species rich and phylogenetically diverse, with an increase in rare taxa. To better understand the strain-specific behavior in response to alkaloids, we cultured microbial strains from poison frog skin and found the majority of strains exhibited either enhanced growth or were not impacted by the addition of DHQ. Additionally, stable isotope tracing coupled to nanoSIMS suggests that some of these strains are able to metabolize DHQ. Taken together, these data suggest that poison frog chemical defenses open new niches for skin-associated microbes with specific adaptations, including the likely metabolism of alkaloids, that enable their survival in this toxic environment. This work helps expand our understanding of how exposure to exogenous compounds like alkaloids can impact host microbiomes.

microbiology↗

bioRxiv2022

Single cell carbon and nitrogen incorporation and remineralization profiles are uncoupled from phylogenetic groupings of diatom-associated bacteria

Bacterial remineralization of algal organic matter is thought to fuel algal growth, but this has not been quantified. Consequently, we cannot currently predict whether some bacterial taxa may provide more remineralized nutrients to algae than others, nor whether this is linked their incorporation. We quantified bacterial incorporation of algal-derived complex dissolved organic C (DOC) and N (DON) and net algal incorporation of remineralized C and N at the single cell level using isotope tracing and NanoSIMS for fifteen bacterial co-cultures growing with the diatom Phaeodactylum tricornutum. We found unexpected variability in the net C and N fluxes between algae and bacteria, including non-ubiquitous complex DON utilization and remineralization. We identified three distinct functional categories of metabolic interactions, which we termed macromolecule remineralizers, macromolecule users, and small-molecule users, the latter exhibiting efficient growth under low carbon availability. The functional categories were not linked to phylogeny and could not be elucidated strictly from metabolic capacity as predicted by comparative genomics. Using comparative proteogenomic analyses, we show that a complex DON incorporating strain expressed proteins related to growth and peptide transport, and a non-incorporator prioritized reactive oxygen species scavenging and inorganic nutrient uptake. Our analysis suggests that phylogeny does not predict the extent of algae-bacteria metabolite exchange, and activity-based measurements are indispensable to classify the high diversity of microbes into functional groups. These categorizations are useful for conceptual understanding and mechanistic numerical modeling to ultimately predict the fate of elemental cycles in response to environmental change.

microbiology↗