Latent space-driven quantification of biofilm formation using time-resolved droplet microfluidics published in Microchemical Journal

Automated segnmentation of bacterial structures within a droplet. The image shows a bright-field microscopy view where a large biofilm region (green, outlined in blue) has been segmented from surrounding features. Small aggregates (yellow contours) are also highlighted. This segmentation enables structural differentiation of biofilm components for downstream quantitative analysis. (Image by D. Pérez Guerrero.)
Latent space-driven quantification of biofilm formation using time-resolved droplet microfluidics
Daniela Pérez Guerrero, Jesús Manuel Antúnez Domínguez, Aurélie Vigne, Daniel Midtvedt, Wylie Ahmed, Lisa D. Muiznieks, Giovanni Volpe, Caroline Beck Adiels
Microchemical Journal 225, 117685 (2026)
arXiv: 2507.07632
DOI: 10.1016/j.microc.2026.117685

Bacterial biofilms play crucial roles across diverse contexts, from public health risks to beneficial applications in bioremediation, biodegradation, and wastewater treatment. However, tools that enable high-resolution, dynamic analysis of their responses to environmental cues and collective cellular behaviors remain limited. Here, we present a droplet-based microfluidic platform that combines continuous in situ microscopy with subsequent unsupervised deep learning for quantitative analysis of biofilm development. In our setup, Bacillus subtilis cells are encapsulated in monodisperse aqueous microdroplets containing Lysogeny Broth, suspended in an oil phase and immobilized within microfabricated traps, providing continuous optical access throughout biofilm formation at the water–oil interface. The platform supports both fluorescence and bright-field imaging, enabling high-throughput, time-resolved monitoring of thousands of droplets under controlled conditions. To extract quantitative information from these large datasets, we developed an automated analysis pipeline based on a Variational Autoencoder (VAE) trained directly on microscopy images from our experiments. This unsupervised model enables segmentation and latent-space representation of bacterial structures without manual annotation or synthetic training data. Post-segmentation size thresholding enables classification of bacterial aggregates and larger biofilm-like clusters, including quantification of biofilm porosity, thereby supporting detailed morphological and temporal analyses across droplets and conditions. By integrating droplet microfluidics with unsupervised deep learning, our platform provides a scalable, robust, and rapid approach for high-throughput quantitative studies of biofilm behavior. It resolves complex structural biofilm patterns, bypasses the need for manual annotation, and opens new opportunities to probe environmental determinants of biofilm formation. Departing from earlier methods, our framework fuses biological training data with unsupervised models to quantify microbial community dynamics across scales, offering a generalizable platform for future high-resolution microbiology.

Seminar by W. Ahmed on 13 March 2024

A schematic of a passive particle immersed in an active bath experiencing non-equilibrium fluctuations. (Illustration by W. Ahmed)
Emergent behavior in active biological matter
Wylie Ahmed
Laboratoire de Physique Theorique, Toulouse (France) and California State University, Fullerton (USA)

13 March 2024, 12:30, Nexus

Motivated by nucleus centering in mouse oocytes, we explore a different type of biological active matter. We investigate the stochastic force fluctuations of micro swimmers in two scenarios: (1) a single swimmer navigating through a passive fluid; (2) a dense suspension of swimmers surrounding a passive tracer. By direct force measurement using optical tweezers we show that the force trajectory of an individual micro swimmer exhibits rich oscillatory dynamics that vary in time. Interestingly, when these highly fluctuating force dynamics are analyzed using the framework of stochastic thermodynamics we recover energy dissipation rates in agreement with time-averaged fluid dynamics studies. For a dense suspension of swimmers serving as an active bath for a passive tracer we observe both shear thinning and thickening, which depends on Peclet number, and enhanced diffusion of our tracer by a factor of 2. We estimate the energy transfer rate from the active bath to the passive tracer. These two scenarios allow us to explore energy exchange between an active swimmer in a passive bath and a passive tracer in an active bath.

Wylie Ahmed visits the Soft Matter Lab. Welcome!

(Photo by A. Ciarlo)
Wylie Ahmed is a Visiting Professor from the Laboratoire de Physique Theorique in Toulouse, France. He is also an associate professor (on leave) at California State University, Fullerton where he leads the Laboratory for Soft, Living, and Active Matter (SLAMLab). His visiting position is financed through the CNRS with partial support from the Soft Matter Lab.
He will visit us for 5 months from March 1, 2024, to July 31, 2024.

He completed his Ph.D. at the University of Illinois at Urbana-Champaign, and was a Marie Skłodowska-Curie Research Fellow at the Institut Curie in Paris, France. He started his group in 2016 in California and is now moving his research activities to Toulouse France. His research interests are in cellular biophysics, soft and active matter physics, and bio-inspired materials with a theme towards understanding emergent behavior.