Visualizing Bacterial Physiology at High Resolution using Single-Molecule Tracking and Lattice-Light Sheet Microscopy

Seminar Details
Thursday, February 13, 2020 - 4:00pm to 5:30pm


Andreas Gahlmann, Ph.D.
Assistant Professor
Department of Chemistry
Department of Molecular Physiology & Biological Physics
Center for Cell and Membrane Physiology
University of Virginia


Chemistry Dow Lab 1640

Sponsoring Department(s)

Our lab develops new imaging approaches for visualizing bacterial physiology in relevant contexts: We use live-cell single-molecule localization microscopy and lattice-light sheet microscopy to access 3D spatial and temporal information with high resolution. At molecular and cellular length scales, our research focuses on understanding how Gram-negative bacterial pathogens inject effector proteins into the cytosol of eukaryotic host cells using the Type 3 Secretion System (T3SS) â a 7 MDa multi-protein complex that spans two, and sometimes three cellular membranes. Type 3 secretion is a major virulence mechanism used by prominent bacterial pathogens that results in more than 1 million human deaths each year. At cellular and super-cellular length scales, our research focuses on visualizing the behaviors of individual bacteria inside tissue-like microbial communities, called biofilms. As a major component of bacterial biomass on earth, biofilms have substantial impacts on the biogeochemistry of our planet and on the biochemistry of higher living organisms.
In the first part of my talk, I will describe how single-molecule localization and tracking microscopy in different genetic backgrounds provides a path towards investigating the molecular mechanism(s) of type 3 secretion in living cells. Through computational aberration correction and numerical modeling, we determine the 3D subcellular localization and diffusive states of individual, fluorescently labeled T3SS proteins. Our results to date indicate that T3SS proteins pre-assemble into freely diffusing cytosolic complexes prior to binding to the membrane-spanning multi-protein complex. Determining to what extent cytosolic proteins assemble with each other in living cells provides key insights into the dynamic regulatory network that controls type 3 secretion.
In the second part of my talk, I will describe how lattice light-sheet microscopy enables non-invasive 3D imaging of microbial biofilms at single-cell resolution. Analyzing the resulting 3D images using a combination of computer vision and machine learning approaches enables multi-cell tracking of cell motions, cell morphologies, and cellular gene expression over time. Our goal now is to apply these new imaging and image analysis approaches to understand the emerging functional capabilities of bacterial biofilms in terms of the behavioral phenotypes of individual cells. Such knowledge can help inform new strategies for controlling biofilm growth and harness the metabolic potential of the microbial world in biotechnological applications.