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Hassan, C.

Publications and source records attributed to Hassan, C..

3 recordsLinked to original sources

Effects of sexual dimorphism and estrous cycle on C. difficile infections prophylaxis in two rodent models

Clostridioides difficile infection (CDI) is responsible for the majority of identifiable hospital-related antibiotic-associated diarrhea. Susceptibility to CDI and severity of disease varies depending on a variety of factors such as aggressive use of broad-spectrum antibiotics, age, and immune status. Epidemiological studies have consistently shown that female patients are more at risk for CDI than their male counterparts. C. difficile is spread by spores which can persist in the environment and in the intestines of patients. Spores do not cause disease but germinate in the antibiotic-altered gut of patients to generate toxin producing vegetative cells. The germination of C. difficile spores is mediated by the composition of bile salts in the gut with taurocholate facilitating germination and chenodeoxycholate inhibiting it.

microbiology↗

Predicting animal movement with deepSSF: a deep learning step selection framework

O_LIPredictions of animal movement are vital for understanding and managing wild populations. However, the fine-scale, complex decision-making of animals can pose challenges for the accurate prediction of trajectories. Step selection functions (SSFs), a common tool for inferring relationships between animal movement and the environment, are also increasingly used to simulate animal trajectories for prediction. Although admitting a lot of flexibility, the SSF framework is limited to its reliance on pre-defined functional forms for fitting to data, and SSFs that involve complex functional forms to model detailed processes can be prohibitively difficult to fit and interpret. C_LIO_LIHere, we present deepSSF, an approach to fit and predict animal movement data using deep learning. Whilst not specific to any particular model, we denote the deepSSF approach as building and training a neural network architecture that receives multiple environmental layers and scalar values as inputs, and outputs a single layer representing the next-step probability. To demonstrate a deepSSF model, we build a model in PyTorch that has distinct but interacting habitat selection and movement subnetworks, which allows for explicit representation of both processes and interpretable intermediate outputs. We apply our model to GPS data of introduced water buffalo (Bubalus bubalis) in the tropical savannas of Northern Australia. C_LIO_LIOur deepSSF model was able to learn features that are present in the habitat covariate layers, such as linear features (rivers, forest edges), and the composition of certain habitat areas, without having to specify them pre-emptively within the SSF framework. It was also able to capture the complex interactions between the habitat covariates as well as temporal dynamics across time of day and year. C_LIO_LIWe expect that the deepSSF approach will generate accurate and informative animal movement trajectories, which can be used for deepening our understanding of animal-environment systems and for the practical management of species. Considering the wide range of deep learning tools, the deepSSF approach could be extended to represent memory and social dynamic processes, with the potential for integrating non-spatial data sources such as accelerometers and physiological sensors. C_LI

ecology↗

Effects of sexual dimorphism and estrous cycle on C. difficile infections in rodent models

Clostridioides difficile infection (CDI) is responsible for the majority of identifiable antibiotic-associated diarrhea. Women are more susceptible to CDI than men. In this study, we show that female mice developed more severe CDI than males. Furthermore, females in estrus developed only mild CDI 1-2 days later, while females in proestrus developed deadly disease. Mirroring the delayed effect of the estrous cycle, pre-infection prolactin levels formed a complex network with immunoglobulins and cytokines that affected early CDI severity one day after challenge. Similarly, pre-infection progesterone and luteinizing hormone formed a network that affected CDI two days after challenge. As expected, immune effectors early in the infection formed a hormone-independent network that concurrently correlated with CDI severity. Interestingly, early infection follicular stimulating hormone levels created a network that affected the CDI recovery phase. In summary, murine sexual hormones affect CDI progression by affecting the immune system both before and during disease progression.

microbiology↗