Search bioRxiv⌕ Search

Biology subjects

Augustin, C.

Publications and source records attributed to Augustin, C..

3 recordsLinked to original sources

Drivers of host-infectious agent community associations in seabirds from sub-Antarctic oceanic islands

Understanding the patterns and drivers of infectious disease dynamics at different levels of life organization is a fundamental disease ecology challenge. In this study, we performed a multi-infectious agents (IA) screening of 1,983 individuals belonging to 18 seabird species, sampled between 2017 and 2022 across five sub-Antarctic islands in the Southern Indian and Atlantic Oceans. Our aim was to identify the drivers of IA community in these seabirds by considering intrinsic and extrinsic factors on three dimensions: distance between seabird metapopulations and within-island sites, macro-community (host functional traits based on feeding and breeding features) and intra-host IA community composition. Samples were screened for 24 DNA-based IAs using a high-throughput real-time PCR method, followed by subsequent hierarchical modelling of species communities. Campylobacter lari, Escherichia coli, Pasteurella multocida, Chlamydiaceae and Mycobacterium spp. were found to be present on all islands in some, but not all, species. However, only E. coli was detected in all species. According to our modelling results, the influence of year and within-island site had limited influence on IA presence/absence, accounting respectively for an average of 1.0% and 1.8% of the variation in IA community. Including host species as a response variable produced a better model fit than including host species functional traits, highlighting the difficulty in simplifying systems by focusing on high-level functional categories. Model outputs show how each species influences IA distribution depending on IA traits, but no clear trend has emerged. Interestingly, burrowing species were less frequently infected with directly transmitted IAs, probably due to the low frequency of transmission events associated with their breeding features and limited social contacts. Our findings pave the way for further multi-dimension studies that would combine complementary approaches to disentangle the complex processes at play in the dynamics of hosts and IAs interactions.

ecology↗

Patient-specific multi-physics simulations of fibrotic changes in left atrial tissue mechanics impact on hemodynamics

Stroke is a leading cause of death and disability worldwide. Atrial myopathy, including fibrosis, is associated with an increased risk of ischemic stroke, but the mechanisms underlying this association are poorly understood. Fibrosis modifies myocardial structure, impairing electrical propagation and tissue biomechanics, and creating stagnant flow regions where clots could form. Fibrosis can be mapped non-invasively using late gadolinium enhancement magnetic resonance imaging (LGE-MRI). However, fibrosis maps are not currently incorporated into stroke risk calculations or computational electro-mechano-fluidic models. We present multi-physics simulations of left atrial (LA) myocardial motion and hemodynamics using patient-specific anatomies and fibrotic maps from LGE-MRI. We modify tissue stiffness and active tension generation in fibrotic regions and investigate how these changes affect LA flow for different fibrotic burdens. We find that fibrotic regions and, to a lesser extent, non-fibrotic regions experience reduced myocardial strain, resulting in decreased LA emptying fraction consistent with clinical observations. Both fibrotic tissue stiffening and hypocontractility independently reduce LA function, but together, these two alterations cause more pronounced effects than either one alone. Fibrosis significantly alters flow patterns throughout the atrial chamber, and particularly, the filling and emptying jets of the left atrial appendage (LAA). The effects of fibrosis in LA flow are largely captured by the concomitant changes in LA emptying fraction except inside the LAA, where a multi-factorial behavior is observed. This work illustrates how high-fidelity, multi-physics models can be used to study thrombogenesis mechanisms in patient-specific anatomies, shedding light onto the links between atrial fibrosis and ischemic stroke. Key pointsO_LILeft atrial (LA) fibrosis is associated with arrhythmogenesis and increased risk of ischemic stroke; its extent and pattern can be quantified on a patient-specific basis using late gadolinium enhancement magnetic resonance imaging. C_LIO_LICurrent stroke risk prediction tools have limited personalization, and their accuracy could be improved by incorporating patient-specific information like fibrotic maps and hemodynamic patterns. C_LIO_LIWe present the first electro-mechano-fluidic multi-physics computational simulations of LA flow, including fibrosis and anatomies from medical imaging. C_LIO_LIMechanical changes in fibrotic tissue impair global LA motion, decreasing LA and left atrial appendage (LAA) emptying fractions, especially in subjects with higher fibrosis burdens. C_LIO_LIFibrotic-mediated LA motion impairment alters LA and LAA flow near the endocardium and the whole cavity, ultimately leading to more stagnant blood regions in the LAA. C_LI

bioengineering↗

The openCARP Simulation Environment for Cardiac Electrophysiology

Background and ObjectiveCardiac electrophysiology is a medical specialty with a long and rich tradition of computational modeling. Nevertheless, no community standard for cardiac electrophysiology simulation software has evolved yet. Here, we present the openCARP simulation environment as one solution that could foster the needs of large parts of this community. Methods and ResultsopenCARP and the Python-based carputils framework allow developing and sharing simulation pipelines which automate in silico experiments including all modeling and simulation steps to increase reproducibility and productivity. The continuously expanding openCARP user community is supported by tailored infrastructure. Documentation and training material facilitate access to this complementary research tool for new users. After a brief historic review, this paper summarizes requirements for a high-usability electrophysiology simulator and describes how openCARP fulfills them. We introduce the openCARP modeling workflow in a multi-scale example of atrial fibrillation simulations on single cell, tissue, organ and body level and finally outline future development potential. ConclusionAs an open simulator, openCARP can advance the computational cardiac electrophysiology field by making state-of-the-art simulations accessible. In combination with the carputils framework, it offers a tailored software solution for the scientific community and contributes towards increasing use, transparency, standardization and reproducibility of in silico experiments.

bioinformatics↗