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Epprecht, T.

Publications and source records attributed to Epprecht, T..

2 recordsLinked to original sources

Chlamydia trachomatis deploys sphingolipids for genome organisation

Chlamydia trachomatis is an obligate intracellular bacterial pathogen and a leading cause of sexually transmitted infections worldwide. During its biphasic developmental cycle, infectious, non-replicative elementary bodies alternate with replicative reticulate bodies within a membrane-bound intracellular niche known as the inclusion. C. trachomatis relies heavily on host-derived metabolites, including sphingolipids, which are essential for inclusion integrity, bacterial growth and production of infectious progeny. Here, using expansion microscopy, we uncover an unexpected localization of sphingolipid derivatives within the highly condensed DNA nucleoids of elementary bodies. These sphingolipids are released from nucleoids prior to DNA decondensation during the elementary-to-reticulate body transition, the earliest phenotypic event in the complex developmental cycle of these bacteria. Thereafter, nucleoids undergo a characteristic DNA decondensation process that we visualized by expansion microscopy. By combining super-resolution imaging with a FRET-based metabolic tracking approach and lipidomics, we identified sphingomyelin derived from the sphingolipid analogues as the sphingolipid species predominantly associated with the condensing nucleoids of elementary bodies. Notably, reticulate bodies arrested in their developmental stage fail to accumulate sphingomyelin, suggesting a role for this lipid in stage-specific DNA condensation. Together, our findings suggest an unanticipated role for sphingolipids in bacterial DNA organization and developmental regulation in C. trachomatis.

microbiology↗

A simplified High-Pressure Freezing Workflow in Autogrids

Cryo-electron tomography (cryo-ET) is a powerful method for studying biological structures in near-native states, yet vitrification of thick and complex specimens remains a major limitation. High-pressure freezing (HPF) allows vitrification of up to [~]200 {micro}m thick samples, but its seamless integration into cryo-electron microscopy (cryo-EM) workflows is hindered by planchettes that are not optimized for EM grids, resulting in extensive handling, reliance on user experience, and frequent grid damage. Here, we present a streamlined HPF workflow based on newly designed planchettes that directly accommodate clipped EM Autogrids. Combined with interchangeable lids for controlling sample thickness, this system enables robust vitrification of diverse specimens, including single-celled eukaryotes and tissue biopsies, while minimizing post-freezing handling. Integration with plasma-focused ion beam milling supports both on-grid lamella preparation and lift-out approaches. We demonstrate reliable preservation of cellular ultrastructure and macromolecular integrity by cryo-ET and subtomogram averaging. This resource provides a practical and scalable solution for integrating HPF into modern cryo-ET pipelines, expanding access to structurally complex biological systems and supporting future clinical applications.

cell biology↗