Biology subjects

Bastien, E.

Publications and source records attributed to Bastien, E..

3 recordsLinked to original sources

bioRxiv2025

Transient volume stabilization reveals the key role a PM permeability in pyroptotic cell swelling.

Pyroptosis, an inflammatory form of cell death, is characterized by massive cell swelling and plasma membrane rupture. Although swelling was recently shown to occur in two steps, the molecular and biophysical mechanisms driving this process remained unclear. Using fast quantitative microscopy, we reveal that between the two swelling phases, cell volume transiently stabilizes despite sustained plasma membrane permeability to ions and small molecules. From a biophysical perspective, the existence of such a plateau is puzzling, as ion pumps should not be able to regulate cell volume under these conditions. To address this, we developed a physical model based on an ion pump and leak framework that incorporates the dynamics of non-selective pore formation. Experimentally, we demonstrate that the plateau phase is controlled by the dynamics of the GSDMD pore enlargement, which is modulated by Ninj1 activation, possibly through intracellular calcium. Ninj1-mediated lesions are also required for the second swelling phase. We further show that fully opened GSDMD pores display an effective hydrodynamic radius slightly above 1.9 nm, providing an insitu upper bound for pore size. Together, our findings demonstrate that pyroptotic volume dysregulation emerges from the successive and interdependent actions of GSDMD and Ninj1, each imparting distinct permeability regimes associated with increased water filtration and decreased ion selectivity due to pore opening. These insights bridge molecular and biophysical perspectives on lytic cell death and may inform the broader understanding of membrane rupture in inflammatory and pathological contexts. Significance StatementAmong programmed modes of lytic cell death, pyroptosis mediated by gasdermin D (GSDMD) and ninjurin-1 (Ninj1) involves dramatic changes in cell shape and large volume fluctuations, fundamentally altering the cells physical properties. By combining optogenetics, quantitative microscopy, and modeling, we show that a progressive increase in plasma membrane pore size drives cell swelling and membrane lysis through successive and interdependent actions of GSDMD and Ninj1, each imparting distinct permeability regimes associated with increased water filtration and decreased ion selectivity. A deeper understanding of these dynamic cell modifications will shed light on the molecular and biophysical mechanisms driving different forms of cell death.

biophysics↗

bioRxiv2024

Tracking Microcystis viruses and infection dynamics across distinct phases of a Microcystis-dominated bloom

Given the impact of viruses on microbial community composition and function, viruses have the potential to play a significant role in the fate of freshwater cyanobacterial harmful algal blooms (cHABs). Yet the role of viruses in cHABs remains poorly understood. We sought to address this knowledge gap with a metagenomic analysis of viruses of bloom-forming Microcystis aeruginosa across cHAB phases in the western basin of Lake Erie. Size-fractionation of the water allowed us to identify significant fraction-specific trends in viral diversity, which corresponded with Microcystis genetic diversity. Using a new machine-learning model, we predicted infections between viral and microbial host populations. We predicted hundreds of viral populations with infection histories including Microcystis and non-Microcystis hosts, suggesting extensive interconnectivity and the potential for virus-mediated cross-species exchange of genetic material within cHABs communities. Infection predictions revealed a broad host range for Lake Erie Microcystis viruses, challenging previous notions of "narrow" host-virus interactions in cHABs. Abundant viral genes belonging to predicted Microcystis viruses revealed their potential role in key metabolic pathways and adaptation to environmental changes. We observed significant turnover of predicted Microcystis virus populations across time. Viral diversity was highest in the viral fraction and lowest in the colony-associated fraction, suggesting that Microcystis colony formation and growth during cHABs leads to bottlenecks in viral diversity. These findings advance our understanding of uncultivated Microcystis virus diversity, their potential effects on host metabolism, potential influence on species interactions, and potential coevolutionary processes between microbial hosts and their viral predators within Microcystis-dominated cHABs. ImportanceUnderstanding interactions between viruses, their hosts, and environmental parameters may be key to identifying the mechanisms underlying the persistence and demise of cyanobacterial harmful algal blooms (cHABs). In this study we describe the viral diversity and host ranges of viruses predicted to infect Microcystis, describing the distribution of these properties across time, space, and different bloom-associated size fractions. Additionally, the study highlights abundant genes belonging to predicted Microcystis viruses and their potential roles in key metabolic pathways and adaptation to environmental changes. The observed turnover of Microcystis virus populations, with the highest diversity in viral fractions and the lowest in colony-associated fractions, suggests that Microcystis colony formation during blooms plays an important role in shaping viral diversity and community turnover. These findings contribute to a better understanding of the interplay between viruses, Microcystis, and their accompanying bacterial communities, shedding light on mechanisms driving bloom dynamics, species interactions, and coevolutionary processes.

microbiology↗

bioRxiv2023

An optogenetic approach to control and monitor inflammasome activation.

Inflammasomes are multiprotein platforms which control caspase-1 activation, leading to the processing of proinflammatory cytokines into mature and active cytokines IL-1{beta} and IL-18, and to pyroptosis through the cleavage of gasdermin-D (GSDMD). Inflammasomes assemble upon activation of specific cytosolic pattern recognition receptors (PRRs) by damage-associated molecular patterns (DAMPs) or pathogen-associated molecular patterns (PAMPs). They converge to the nucleation of apoptosis-associated speck-like containing a caspase activation and recruitment domain (ASC) to form hetero-oligomers with caspase-1. Studying inflammasome encoding activities remains challenging because PAMPs and DAMPs are sensed by a large diversity of cytosolic and membranous PRRs. To bypass the different signals required to activate the inflammasome, we designed an optogenetic approach to temporally and quantitatively manipulate ASC assembly (i.e. in a PAMP- or DAMP-independent manner). We reveal that controlling light-sensitive oligomerization of ASC is sufficient to recapitulate the classical features of inflammasomes within minutes, and enabled us to decipher the complexity of volume regulation and pore opening during pyroptosis. Overall, this approach offers interesting perspective to decipher PRR signaling pathways in the field of innate immunity.

immunology↗