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Stone, H.

Publications and source records attributed to Stone, H..

5 recordsLinked to original sources

Phylogenies as graphs: structured neural networks improve host origin predictions from paramyxovirus sequences

Accurately identifying the host of a virus from its genome sequence is a task with important applications in zoonotic disease surveillance and filling data gaps for metagenomic sampling. Machine learning approaches have seen broad application in making host predictions directly from viral genome sequences. However, most host prediction models do not incorporate information on viral phylogeny, which is strongly correlated with both genome composition and host. We apply a novel graph neural network (GNN) approach which explicitly represents viral phylogeny in model architecture to predict hosts of origin within the paramyxoviruses. We conduct rigorous benchmarking against non-structured neural networks and predictions made using phylogeny alone, showing that GNNs carry distinct advantages over other methods when making predictions where training data is sparse. Validation across different phylogenetic scales shows that simple phylogenetic prediction is effective in many applications and that phylogeny contributes a large proportion of the predictive power of host prediction models, with genome compositional features providing additional power only for specific predictions outside the range of the training data. This novel modelling approach and model validation framework are flexible and can be applied to other viral families.

evolutionary biology↗

DENcode: A model for haplotype-informed transmission probability of dengue virus

Dengue virus transmission networks are often only partially resolved, due to gaps in sampling, unobserved mosquito-mediated transmission, and using methods (phylogenetics) that describe evolutionary relatedness but not explicit, probabilistic transmission links between individual infections. We developed DENcode, a framework to estimate the relative likelihood of vector-mediated transmission between pairs of dengue cases by combining a temperature- and time-modulated epidemiological kernel, which captures the extrinsic incubation period and human infectiousness, with a phylogenetically informed genetic similarity kernel derived from patristic distances between viral haplotypes or consensus sequences. Validation with a real-life dataset of 90 dengue infections sampled from Colombo, Sri Lanka between 2017 - 2020 and sequenced to resolve within-host haplotypes, DENcode estimates were stable across 100 Monte Carlo iterations, yielding narrow credible intervals (median width <0.001) and consistent top-ranked transmission pairs. Sensitivity analyses using ablation experiments showed that removing either the genetic or epidemiological component substantially altered the distribution of linkage probabilities, indicating that both contribute meaningfully to the inferred transmission structure. Serotype-specific transmission networks constructed from pairwise linkage probabilities from DENcode were analysed using degree- and path-based centrality measures at probability thresholds of 0.1 and 0.5, revealing relative importance of cases to disease transmission within the community. Haplotype-derived networks were more informative than consensus-based networks (x 3.6 and x 1.6 times more edges for DENV2 and 3 respectively). DENcode is a robust framework to explore dengue transmission within a community that provides an output of network of transmission probabilities informed by pathogen genetic similarity and clinical epidemiological parameters. Author summaryTracing epidemics of dengue in setting where dengue transmission happens continuously poses many challenges especially with limited availability of genomic surveillance. Here we introduce a model that uses genomic data together with time and location data to calculate a probability of two cases of dengue being related to each other. Using data from the Colombo dengue study, from 2017 to 2020, Sri Lanka, we evaluated the model. We used haplotype level sequences that correspond to the viral variation within the human host and consensus level sequences that average the data from a single human host into a single sequence. We constructed transmission probability networks for each dengue serotype and were able to identify patients who played key roles in the corresponding networks. We were able to show that this model is robust and will be a valuable tool in the context of dengue control.

bioinformatics↗

Room Temperature Aerosol Dehydration of Green Fluorescence Protein

Rapid Room-Temperature Aerosol Dehydration (RTAD) is a novel, scalable drying technology for powderization and thermal stabilization of pharmaceutical drug products. Compared to conventional spray drying, RTAD utilizes sub-20 {micro}m droplets that evaporate rapidly at room temperature, thereby reducing drying-induced stresses for thermally sensitive biologics. In this study, we employed Green Fluorescent Protein (GFP) as a model biological molecule to optimize the RTAD system design and process parameters. We investigated the effects of droplet size, multiphase flow patterns in the drying chamber, and usage of polysorbate 20 as a model surfactant on GFP fluorescence after drying and powder reconstitution. The experiments demonstrated that the presence of polysorbate 20 in the formulation significantly influenced GFP fluorescence intensity, especially for smaller droplets. The numerical studies using Computational Fluid Dynamics simulations revealed that the intensity of GFP fluorescence in the produced dry powders was dependent on the patterns of multiphase flow in the drying chamber. Non-axisymmetric flows and closed circulating streamlines near the drying gas inlet negatively impacted the GFP fluorescence intensity. Through iterative optimization of chamber design, process parameters, and feedstock formulation, we achieved the recovery (compared to the initial samples) of GFP fluorescence intensity exceeding 96% in the obtained dry powders. This work establishes GFP as a sensitive model biologic and its fluorescence intensity as a powerful tool for rapidly assessing bioactivity following dehydration. The insights gained from this study have broad implications for the design and scale-up of room-temperature drying technologies, which can potentially transform the production of dry powder biopharmaceuticals.

pharmacology and toxicology↗

Live imaging of SARS-CoV-2 infection in mice reveals neutralizing antibodies require Fc function for optimal efficacy

Neutralizing antibodies (NAbs) are effective in treating COVID-19 but the mechanism of immune protection is not fully understood. Here, we applied live bioluminescence imaging (BLI) to monitor the real-time effects of NAb treatment in prophylaxis and therapy of K18-hACE2 mice intranasally infected with SARS-CoV-2-nanoluciferase. We could visualize virus spread sequentially from the nasal cavity to the lungs and thereafter systemically to various organs including the brain, which culminated in death. Highly potent NAbs from a COVID-19 convalescent subject prevented, and also effectively resolved, established infection when administered within three days. In addition to direct Fab-mediated neutralization, Fc effector interactions of NAbs with monocytes, neutrophils and natural killer cells were required to effectively dampen inflammatory responses and limit immunopathology. Our study highlights that both Fab and Fc effector functions of NAbs are essential for optimal in vivo efficacy against SARS-CoV-2.

immunology↗

Sailing in rough waters: examining volatility of fMRI noise

BackgroundThe assumption that functional magnetic resonance imaging (fMRI) noise has constant volatility has recently been challenged by studies examining heteroscedasticity arising from head motion and physiological noise. The present study builds on this work using latest methods from the field of financial mathematics to model fMRI noise volatility. MethodsMulti-echo nd human fMRI scans were used and realised volatility was estimated. The Hurst parameter H [isin] (0, 1), which governs the roughness/irregularity of realised volatility time series, was estimated. Calibration of H was performed pathwise, using well-established neural network calibration tools. ResultsIn all experiments the volatility calibrated to values within the rough case, H < 0.5, and on average fMRI noise was very rough with 0.03 < H < 0.05. Some edge effects were also observed, whereby H was larger near the edges of the phantoms. DiscussionThe findings suggest that fMRI volatility is not only non-constant, but also substantially more irregular than a standard Brownian motion. Thus, further research is needed to examine the impact such pronounced oscillations in the volatility of fMRI noise have on data analyses.

neuroscience↗