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Andrea Y. Weiße

Publications and source records attributed to Andrea Y. Weiße.

2 recordsLinked to original sources

Network memory in the movement of hospital patients carrying drug-resistant bacteria

Hospitals constitute highly interconnected systems that bring into contact an abundance of infectious pathogens and susceptible individuals, thus making infection outbreaks both common and challenging. In recent years, there has been a sharp incidence of antimicrobial-resistance amongst healthcare-associated infections, a situation now considered endemic in many countries. Here we present network-based analyses of a data set capturing the movement of patients harbouring drug-resistant bacteria across three large London hospitals. We show that there are substantial memory effects in the movement of hospital patients colonised with drug-resistant bacteria. Such memory effects break first-order Markovian transitive assumptions and substantially alter the conclusions from the analysis, specifically on node rankings and the evolution of diffusive processes. We capture variable length memory effects by constructing a lumped-state memory network, which we then use to identify overlapping communities of wards. We find that these communities of wards display a quasi-hierarchical structure at different levels of granularity which is consistent with different aspects of patient flows related to hospital locations and medical specialties.

physics.soc-ph↗

Prediction of cellular burden with host-circuit models

Heterologous gene expression draws resources from host cells. These resources include vital components to sustain growth and replication, and the resulting cellular burden is a widely recognised bottleneck in the design of robust circuits. In this tutorial we discuss the use of computational models that integrate gene circuits and the physiology of host cells. Through various use cases, we illustrate the power of host-circuit models to predict the impact of design parameters on both burden and circuit functionality. Our approach relies on a new generation of computational models for microbial growth that can flexibly accommodate resource bottlenecks encountered in gene circuit design. Adoption of this modelling paradigm can facilitate fast and robust design cycles in synthetic biology.

q-bio.MN↗