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Flori, S.

Publications and source records attributed to Flori, S..

7 recordsLinked to original sources

Thylakoid plasticity primes photoprotection in diatoms

For many millions of years, diatoms have been major primary producers in marine ecosystems, supporting food webs and contributing to carbon sequestration through the export of photosynthetically fixed carbon to the deep ocean, mitigating atmospheric carbon dioxide levels and global climate. A key factor in their ecological success is their ability to rapidly adapt to fluctuating light, balancing efficient light harvesting under dim conditions with energy dissipation under excess light. However, the mechanisms behind this regulation have not been fully elucidated. This study shows that several processes contribute to dissipating excess excitation energy in diatoms exposed to light stress: (i) the detachment of the oxygen-evolving complex proteins from the PSII core, leading to energy dissipation via charge recombination, (ii) Non-Photochemical Quenching (NPQ) in the antenna, i.e., thermal dissipation of excited states and (iii) excitation energy transfer from PSII to PSI via energy spillover. The latter process is observed in parallel with high light-induced topological changes of the thylakoids that may favor transient interactions between the photosystems. Along with the accumulation of light-stress-protecting carotenoids on longer time-scales, this ensemble of photoprotective mechanisms provides a dynamic and flexible response to the light challenges expected in coastal marine habitats.

biochemistry↗

An Advanced Mobile Laboratory to enable field-based microbial ecology and cell biology across scales

Microbial biodiversity is central to ecosystem function, yet mechanistic insights into the cell biology of environmental organisms remain limited. The underlying challenges are twofold: most microbes remain uncultivable, and a persistent gap exists between field sampling and laboratory analyses. Here, we introduce the Advanced Mobile Laboratory (AML), a field-deployable platform that integrates confocal microscopy, image-enabled cell sorting, and cryo-preparation for expansion and electron microscopy. This setup enables immediate, standardized processing and analysis of environmental communities directly at the sampling site. We demonstrate its capability using marine eukaryotic plankton, showing how the AML enables multiscale investigations, from live imaging of natural communities to enabling ultrastructural and single-cell omics analyses, while minimizing sample degradation and enabling on-site experimentation. By bringing high-end sample preparation and analytical capacity into the field, the AML enables studying life in its natural context to mechanistically understand lifes diversity in the environment.

cell biology↗

MorphoLearn: A morphology-driven workflow to decipher 3D electron microscopy segmentation in diatoms

Three-dimensional electron microscopy (3D EM) enables the quantitative analysis of cellular ultrastructure. However, large-scale segmentation of whole-cell volumes poses a significant challenge, especially in biologically diverse systems. Unlike medical and animal cell imaging, which often benefit from temporal redundancy and relatively uniform morphology, studies of microbial and microalgal biodiversity must rely on static snapshots. These snapshots exhibit high variability in cell shape, organelle organisation, and image contrast. Consequently, robust AI-assisted segmentation in this context requires models that learn directly from morphological features and can adapt to heterogeneous sample preparation. In this paper, we present a systematic framework for AI-assisted segmentation of Focused Ion Beam-Scanning Electron Microscopy (FIB-SEM) datasets. This framework is specifically designed to address the challenges posed by morphological diversity and contrast variability while remaining within realistic computational constraints. We evaluate multiple lightweight 3D encoder-decoder architectures and identify VNet as the best option for balancing computational efficiency and volumetric accuracy in whole-cell segmentation. Using datasets from two strains of Phaeodactylum tricornutum and extending our analysis to cross-species comparisons, we demonstrate that training on specific regions of interest can lead to an overestimation of model performance. In contrast, performing whole-cell segmentation uncovers significant differences in architectural robustness. Moreover, we show that transfer learning and contrast-aware hybrid strategies allow for efficient adaptation to previously unseen datasets with minimal annotation. The incorporation of boundary-aware loss functions significantly enhances the delineation of closely associated organelles, such as chloroplasts and mitochondria, in multi-class segmentation tasks. Together, these findings establish a scalable, reproducible, and biologically informed AI framework for 3D FIB-SEM segmentation. This framework enables high-throughput analysis of cellular ultrastructure across diverse species and imaging conditions. Author SummaryCells exhibit a wide range of shapes, sizes, and internal structures, particularly among various microbial species. These morphological differences are not arbitrary; they indicate how cells adapt to their environments and manage essential biological functions. Modern three-dimensional electron microscopy can capture this structural diversity at the nanometre scale, but analysing the resulting data is often slow. This is due to the time-consuming process of manually outlining cellular structures, which also requires expert knowledge. Artificial intelligence (AI) has made significant advances in accelerating image analysis in medical and animal cell studies, typically by learning from repeated observations over time. However, studies focusing on microbial and microalgal biodiversity often rely on single snapshots of diverse cells prepared under varying imaging conditions. This complicates automated analysis since AI systems must learn from morphology directly rather than from temporal repetition. In this study, we developed and evaluated an AI-assisted segmentation framework specifically for whole-cell 3D electron microscopy data. By systematically comparing efficient neural network architectures and incorporating transfer learning and contrast-aware strategies, we demonstrate that accurate segmentation can be achieved even with limited training data and standard computing resources. Our approach facilitates faster, scalable, and reproducible analysis of cellular ultrastructure, paving the way for large-scale investigations into cell morphology, adaptation, and diversity across species. Significance statementQuantitative analysis of cellular ultrastructure across species is currently limited by challenges in segmenting large three-dimensional electron microscopy datasets. Unlike medical imaging, which often benefits from artificial intelligence due to its use of temporal repetition and consistent morphology, studies of microbial biodiversity depend on single snapshots that display extreme variations in cell shape and image contrast. This work presents a scalable, morphology-driven AI framework for whole-cell 3D segmentation that is resilient to biological diversity and variations in sample preparation. By enabling accurate analysis with minimal annotations and standard computational resources, this approach enhances access to high-throughput ultrastructural studies and facilitates comparative investigations of cellular adaptation across different species.

cell biology↗

Diatom ultrastructural diversity across controlled and natural environments

Diatoms are ubiquitous aquatic microalgae critical to our planet, that were amongst the pioneer model organisms in cell biology for their large and transparent cell structure. However, their robust silica cell wall renders diatoms impermeable to many dyes and antibodies, and complicates the intracellular delivery of gene editing tools - driving in part the eventual decline of diatoms as mainstream model species despite their unique cellular physiology and remarkable ecological success. Here, we demonstrate that cryo-fixation combined with ultrastructural expansion microscopy (cryo-ExM) can overcome the silica barrier across diverse diatom species spanning over 80 million years of evolutionary time. We illustrate the potential of cryo-ExM to provide scalable, cost-effective volumetric imaging of diatom ultrastructure in laboratory cultures, as well as field-collected samples from the pan-European TREC expedition. We first reveal striking similarities in interphase microtubule organization across diverse diatom species by characterizing cytoskeletal arrangements throughout cell cycles and populations, uniting both pennate and centric morphologies under shared principles. We further unveil diatom photosynthetic diversity through qualitative and quantitative comparative analysis of chloroplast and pyrenoid morphologies, demonstrating that each diatom species architects unique photosynthetic machinery. Using cryo-ExM on environmental samples further exposes intricate diatom symbioses, revealing tight spatial organisation of ecological interactions. This methodology makes diatoms more accessible for modern and comparative cell biology research, providing new opportunities to investigate the cellular mechanisms of one of Earths most successful photosynthetic groups. HighlightsO_LICryo-ExM successfully overcomes diatom frustule barriers to achieve consistent, high-resolution immunofluorescence across evolutionarily diverse species - allowing for comparative cell biology in one of the most important phytoplankton groups on the planet. C_LIO_LICharacterizing microtubule organisation in asynchronously cycling single cells and colonial chains, reveals core features of interphase microtubule organisation across multiple pennate and centric diatom species. C_LIO_LIComparative analysis of chloroplast and pyrenoid morphologies across species provides qualitative and quantitative insights on photosynthetic diversity, suggesting that photosynthetic architectures are unique to each diatom. C_LIO_LIApplied to environmental samples, cryo-ExM provides detailed insight on spatial organisation of diatom symbioses. C_LI

cell biology↗

Diatom pyrenoids are encased in a protein shell that enables efficient CO2 fixation

Pyrenoids are subcompartments of algal chloroplasts that concentrate Rubisco enzymes and their CO2 substrate, thereby increasing the efficiency of carbon fixation. Diatoms perform up to 20% of global CO2 fixation, but their pyrenoids remain poorly characterized at a molecular level. Here, we used in vivo photo-crosslinking to catalogue components of diatom pyrenoids and identified a pyrenoid shell (PyShell) protein, which we localized to the pyrenoid periphery of both the pennate diatom, Pheaodactylum tricornutum, and the centric diatom, Thalassiosira pseudonana. In situ cryo-electron tomography (cryo-ET) revealed that the pyrenoids of both diatom species are encased in a lattice-like protein sheath. Disruption of PyShell expression in T. pseudonana resulted in the absence of this protein sheath, altered pyrenoid morphology, and a high-CO2 requiring phenotype, with impaired growth and reduced carbon fixation efficiency under standard atmospheric conditions. Pyrenoids in mutant cells were fragmented and lacked the thylakoid membranes that normally traverse the Rubisco matrix, demonstrating how the PyShell plays a guiding role in establishing pyrenoid architecture. Recombinant PyShell proteins self-assembled into helical tubes, enabling us to determine a 3.0 [A]-resolution PyShell structure. We then fit this in vitro structure into an in situ subtomogram average of the pyrenoids protein sheath, yielding a putative atomic model of the PyShell within diatom cells. The structure and function of the diatom PyShell provides a new molecular view of how CO2 is assimilated in the ocean, a crucial biome that is on the front lines of climate change.

cell biology↗

Distinct physiological responses of Coccolithus braarudii life cycle phases to light intensity and nutrient availability

Coccolithophores feature a haplo-diplontic life cycle comprised of diploid cells producing heterococcoliths and haploid cells producing morphologically different holococcoliths. These life cycle phases of each species appear to have distinct spatial and temporal distributions in the oceans, with the heavily-calcified heterococcolithophores (HET) often more prevalent in winter and at greater depths, whilst the lightly-calcified holococcolithophores (HOL) are more abundant in summer and in shallower waters. The haplo-diplontic life cycle may therefore allow coccolithophores to expand their ecological niche, switching between life cycle phases to exploit conditions that are more favourable. However, coccolithophore life cycles remain poorly understood and fundamental information on the physiological differences between life cycle phases is required if we are to better understand the ecophysiology of coccolithophores. In this study, we have examined the physiology of HET and HOL phases of the coccolithophore Coccolithus braarudii in response to changes in light and nutrient availability. We found that the HOL phase was more tolerant to high light than the HET phase, which exhibited defects in calcification at high irradiances. The HET phase exhibited defects in coccolith formation under both nitrate (N) and phosphate (P) limitation, whilst no defects in calcification were detected in the HOL phase. The HOL phase grew to a higher cell density under P-limitation than N-limitation, whereas no difference was observed in the maximum cell density reached by the HET phase at these nutrient concentrations. HET cells grown under a light:dark cycle divided primarily in the dark and early part of the light phase, whereas HOL cells continued to divide throughout the 24 h period. The physiological differences may contribute to the distinct biogeographical distributions observed between life cycle phases, with the HOL phase potentially better adapted to high light, low nutrient regimes, such as those found in seasonally stratified surface waters. HighlightsO_LICoccolithus braarudii life cycle phases exhibit different physiological responses. C_LIO_LIThe heavily-calcified heterococcolithophores (HET) life cycle phase is more sensitive to high light. C_LIO_LIThe lightly-calcified holococcolithophores (HOL) life cycle phase may be better suited to growth under low phosphate availability. C_LI

microbiology↗

Photoprotection is regulated by light-independent CO2 availability

Photosynthetic algae have evolved mechanisms to cope with suboptimal light and CO2 conditions. When light energy exceeds CO2 fixation capacity, Chlamydomonas reinhardtii activates photoprotection, mediated by LHCSR1/3 and PSBS, and the CO2 Concentrating Mechanism (CCM). How light and CO2 signals converge to regulate these processes remains unclear. Here, we show that excess light activates photoprotection- and CCM-related genes by altering intracellular CO2 concentrations and that depletion of CO2 drives these responses, even in total darkness. High CO2 levels, derived from respiration or impaired photosynthetic fixation, repress LHCSR3/CCM genes while stabilizing the LHCSR1 protein. Finally, we show that the CCM regulator CIA5 also regulates photoprotection, controlling LHCSR3 and PSBS transcript accumulation while inhibiting LHCSR1 protein accumulation. This work has allowed us to dissect the effect of CO2 and light on CCM and photoprotection, demonstrating that light often indirectly affects these processes by impacting intracellular CO2 levels.

plant biology↗