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Bhattacharya, D.

Publications and source records attributed to Bhattacharya, D..

At least 19 recordsLinked to original sources

Root exudates enhance the ecological fitness of a non-native PGPR and reshape rhizosphere microbiome assembly

Root exudates play critical roles in rhizosphere microbiome assembly. Nevertheless, the molecular mechanisms by which plant growth-promoting rhizobacteria (PGPR) perceive these signals, adapt to the rhizosphere, and influence native microbial communities remain poorly understood. Here, using maize (Zea mays cv. Early Golden Bantam) and the rhizobacterium Priestia aryabhattai AB211, we took a multi-omics approach combining metabolomics, bacterial transcriptomics and proteomics, and rhizosphere metagenomics to elucidate the mechanism underlying this process. Maize root exudates were enriched in diverse carbon and nitrogen metabolites that promoted bacterial growth and induced extensive molecular reprogramming of pathways involved in nutrient acquisition, chemotaxis, motility, stress adaptation, and plant growth promotion, thereby enhancing rhizosphere competence. In field-conditioned soil, AB211 persisted as a core member of the maize rhizosphere microbiome, promoted early seedling growth, and reshaped microbial community composition and function. Root exudates-primed (RE-primed) AB211 further enhanced the enrichment of microbial functions associated with nutrient cycling, quorum sensing, plant growth promotion, and rhizosphere fitness, highlighting the role of root exudates in modulating the rhizosphere-adaptative potential of beneficial bacteria. These findings establish a mechanistic framework linking root exudates composition with PGPR adaptation and microbiome assembly, providing a foundation for engineering ecologically adapted microbial inoculants to improve crop productivity and sustainable agriculture.

microbiology↗

Transcriptional networks underlying tumour plasticity in small-cell lung cancer

Across human malignancies, the ability of cancer cells to switch states (plasticity) drives progression, metastasis, and therapy resistance 1-3. Here we investigated the transcriptional and epigenetic basis of plasticity in small-cell lung cancer (SCLC), an aggressive, treatment-refractory cancer 4, 5. SCLC tumours display plasticity along a neuroendocrine (NE) to nonNE axis; however, the trajectories of lineage transition and the gene regulatory network underlying it, remain poorly defined 6. Using single-cell multi-omics, we resolved distinct transcriptional SCLC cell states, including a previously unrecognised Intermediate state comprised of low-identity immunogenic SCLC cells that serve as an obligatory route in NE to nonNE lineage transition. Using single-cell gene expression and chromatin accessibility data, we next developed a Boolean Bayes model for transcription factor networks (BoBa-T) to predict regulators of SCLC cell states. We validated RORB as a novel gatekeeper of the NE state that represses the nonNE identity in SCLC. RORB inactivation drives NE cells into the Intermediate state, upregulates immunogenic programs, and inhibits tumour growth in immunocompetent hosts. Our work identifies a plastic, immunogenic waypoint for SCLC lineage switching and reveals strategies to target it therapeutically.

cancer biology↗

Genomic characterization reveals high clonal redundancy in two Acropora cervicornis nurseries in the Dominican Republic

Acropora cervicornis is often propagated through fragmentation (i.e., clonal propagation), a common practice implemented by restoration projects. Known as asexual propagation, this strategy may rapidly increase coral cover but reduces genetic variation. We used 2b-RAD sequencing to characterize multilocus genotypic variation among 45 A. cervicornis colonies maintained in two in-situ nurseries (Cap Cana, Acuario) in Punta Cana, Dominican Republic. After reference-based SNP discovery and filtering, 2,515 high-quality SNPs were retained in the dataset. Principal coordinate analysis (PCoA), hierarchical clustering, identity-by-state (IBS) distances, and relatedness estimates identified only three multilocus genets among the 45 colonies (AC1, AC2, and AC3). Of these, AC2 was the most abundant (n = 23; 51.1%), followed by AC3 (n = 14; 31.1%) and lastly AC1 (n = 8; 17.8%). Within-genet IBS distances (0.153-0.227) did not overlap with between-genet distances (0.406-0.497). AC1 and AC2 were detected in both nurseries, whereas AC3 was limited to Acuario. These results reveal substantial clonal redundancy among sampled nursery colonies that determines local reef conservation efforts. These data highlight the value of incorporating genotype identification in nursery-based coral restoration projects.

ecology↗

Proteomic analysis of Stony Coral Tissue Loss Disease demonstrates coral-algal dysbiosis during disease progression

Stony Coral Tissue Loss Disease (SCTLD) has devastated Caribbean reefs, yet the host molecular response to infection is poorly understood. Previous gene expression studies of diseased corals identified shifts in the immune response, apoptosis, and coral-algal dysbiosis. Here, we characterized the proteomic response of Diploria labyrinthiformis to SCTLD by comparing protein abundance in healthy tissue from uninfected colonies and apparently healthy and neighboring diseased tissue from infected colonies. These results were compared with existing metagenomic data from the same samples that previously demonstrated significant shifts in the coral microbiome due to SCTLD. We identified 480 differentially abundant proteins when comparing diseased lesion and healthy tissues, but only 12 between apparently healthy and healthy tissues. Pathway-level analysis provides evidence of immune suppression in apparently healthy tissue, suggesting that host molecular responses precede visible disease progression. Diseased lesion tissues showed wound-healing responses combined with a decreased abundance of proteins involved in symbiosome maintenance and increased oxidative stress responses, consistent with host-algal dysbiosis. This result correlates with the previous metagenomic analysis of these samples which found that infected colonies exhibit distinct algal symbiont communities dominated by Symbiodinium necroappetens, whereas healthy colonies are dominated by Durusdinium trenchii and Breviolum spp. Comparison with existing transcriptomic studies revealed both shared and distinct molecular responses, underscoring the importance of integrating multi-omics approaches to understand coral diseases. Our results suggest that SCTLD in D. labyrinthiformis is associated with early immune suppression, coral-algal dysbiosis, oxidative stress, and subsequent wound-healing responses.

ecology↗

A Dual-Function Guanidinium Scaffold that Couples Copper Sequestration with Redox Protection in Wilson disease

Wilson disease (WD) is caused due to mutations in the copper ATPase gene ATP7B, that result in accumulation of labile copper pools and the consequent disruption of cellular redox homeostasis through uncontrolled copper-mediated reactive oxygen species generation. Current therapies mainly depend on high-affinity copper chelation to lower metal burden which sometimes also strip copper from cuproproteins and may disturb physiological copper-dependent processes. It also does not directly suppress pathological copper reactivity i.e., free radical generation, a major driver of WD progression. To overcome these limitations, we have rationally designed Gua-Cu-3, a C-symmetric guanidinium-based molecule that can chelate labile copper without metal stripping from cuproproteins due to moderate binding affinity and it has intrinsic antioxidant activity within a single nanosheet-forming supramolecular self-assembly. Spectroscopic, calorimetric, and computational analyses revealed controlled multivalent copper coordination (Kd = 95.4 M) while radical-scavenging and hydroxyl-radical inhibition assays further revealed potent redox-regulatory activity. In cellular models of copper overload, Gua-Cu-3 treatment reduces ATP7B trafficking from trans-Golgi network, confirming effective intracellular copper sequestration. This was accompanied by a marked reduction in oxidative stress, reduction of translocation of Nrf2 in nucleus and of HO-1 expression, thereby limiting lipid peroxidation which leads to restoration of cellular homeostasis, including improved lysosomal integrity, reduced endoplasmic reticulum stress, decreased mitochondrial superoxide levels, and diminished apoptosis. Importantly, the protective effects extended, beyond cultured cells, Gua-Cu-3 attenuates oxidative stress in ATP7B-homolog-deficient C. elegans and rescues copper-induced developmental defects in zebrafish, outperforming D-penicillamine, which is currently in use for Wilson disease management. These findings establish Gua-Cu-3 as a molecularly designed supramolecular copper-reactivity buffer that couples-controlled copper sequestration with redox regulation which is distinct from conventional copper depletion and provides a framework for treating Wilson disease and other disorders associated with metal dyshomeostasis and oxidative stress.

Cell Biology↗

ORIGAMI: Orientation-Aware Graph Neural Network for Assessing Multimeric Interfaces of Protein Complex Structures

Deep learning-based protein structure prediction methods have led to a paradigm-shift in computational structural biology, yet reliably assessing the quality of computationally predicted multimeric structures remains challenging. Recent methods have demonstrated benefits of employing graph neural networks for assessing multimeric interfaces of protein complexes, but ignore geometric orientational features naturally occurring in 3-dimensional protein conformational space and act only on scalar weights. We present ORIGAMI, an orientation-aware graph neural network for assessing multimeric interfaces of protein complex structures that leverages both scalar and 3D vector node representations to perform symmetry-aware geometric operations while maintaining SO(3)-equivariance by capturing fine-grained orientational relationships between residues across protein-protein interfaces to estimate the interface Local Distance Difference Test (iLDDT) score. Tested on targets from multiple rounds of Critical Assessment of Structure Prediction (CASP) challenges, ORIGAMI achieves superior performance across multiple interface quality assessment benchmarks, with particularly strong gains in the expanded CASP16 interface-level evaluation and in controlled comparisons against both non-equivariant and equivariant graph neural network baselines. It also demonstrates robust cross-metric generalization by reproducing superposition-based DockQ scores with high fidelity, despite being trained only to estimate the superposition-free iLDDT score. ORIGAMI is freely available at https://github.com/Bhattacharya-Lab/ORIGAMI.

bioinformatics↗

Multi-omics data of a weedy coral species from Ulithi Atoll (Micronesia) to investigate the impact of human disturbance on coral health and resilience

BackgroundCoral reefs are among the most biodiverse ecosystems on Earth yet face an increasing risk of collapse under climate change and intensifying anthropogenic pressures. Although there is strong evidence that stressors such as overfishing, sedimentation, and wastewater runoff can drive shifts in coral community structure, few studies have investigated the molecular mechanisms underlying these shifts. Integrating data across multiple layers of biological organization, from the genome to the proteome and metabolome, offers a powerful approach to understanding how coral physiology and resilience are impacted by human activities. FindingsHere, we present high-coverage whole genome sequencing (Montipora only) together with untargeted metabolomic and proteomic datasets from three coral genera (Acropora, Pocillopora, and Montipora) that inhabit Ulithi Atoll, Yap State, FSM. Ulithi Atoll is an ideal system for investigating how anthropogenic pressures influence coral molecular ecology and adaptation, with extensive historical ecological data available through the long-term research program of the One People One Reef collaborative to connect multi-omics data with macroecological trends. Following data cleaning and quality control, all datasets exhibited minimal technical variation among samples, providing a comprehensive baseline for future research on coral resilience across a mosaic of natural and anthropogenic stressors. ConclusionsThese data provide a resource for examining how anthropogenic pressures influence coral physiology and resilience across environmental gradients. They also allow the identification of biomarkers of chronic stress that may inform the development of point-of-care diagnostic tools for coral health and contribute to evidence-based reef conservation and management strategies.

genomics↗

Somatic mutations reveal the ontogeny of human microglia

Microglia are the resident hematopoietic cells of the central nervous system1. In mice, microglia seed the brain during embryogenesis and can be maintained throughout life with minimal input from adult hematopoiesis2-4. The origins of human microglia are less clear, but recent evidence suggests that marrow-derived cells may be able to supplement the human microglial pool in certain individuals5,6. Here, to investigate the ontogeny of human microglia, we develop a method that uses the collection of accumulated somatic mutations which uniquely labels each clone of cells to track the infiltration of marrow-derived cells into the human brain. Applying this method to 20 aged individuals, we find evidence of an influx of marrow-derived cells into the brain in all examined individuals. Single cell analysis, including single cell lineage tracing using mitochondrial DNA variants, demonstrates that these infiltrating cells are nearly identical to microglia and can comprise a large fraction of the microglial pool. Analysis of large-scale sequencing cohorts demonstrates a protective association between most types of clonal hematopoiesis and Alzheimers disease. In sum, this work uncovers a widespread influx of myeloid cells into the healthy human brain which serves to reinforce the pool of human microglia and becomes common with aging.

immunology↗

Copper-transporting ATPase ATP7B and the lysosomal exocytosis pathway synergise to detoxify cadmium

Cadmium, being a highly toxic metal, perturbs cellular homeostasis by forming stable complexes with numerous thiol-active proteins, ultimately leading to severe liver and lung damage. Despite its well-documented toxicity, the molecular mechanisms governing cadmium export remain poorly understood. Given the chemical similarity between cadmium and copper, we investigated whether the canonical copper-exporting ATPases, ATP7A and ATP7B participate in cadmium handling. Upon Cd treatment in hepatocytes, ATP7B undergoes trafficking to lysosomes via the retromer complex, as also observed in the case of elevated copper, accompanied by the upregulation of acidic lysosomal populations. In contrast, ATP7A expressed in lung adenocarcinoma cells, though exhibit vesicular redistribution upon Cd exposure, does not mediate lysosomal sequestration, suggesting distinct deployment of late secretory pathways by the two copper ATPases in response to cadmium. We have also observed that ATP7B-/- hepatocytes exhibit increased sensitivity to Cd exposure compared to wild-type cells. Whereas, overexpressing the ATP7B amino-terminal copper-binding domain in bacteria alleviates cadmium-induced stress, indicating its capacity to sequester Cd. Caenorhabditis elegans lacking copper-ATPase cua-1, displayed increased Cd sensitivity, while mutants (glo-1-/-), deficient in lysosome-related organelles (LRO), and (lmp-1-/-), deficient in lysosomal membrane glycoprotein, showed reduced resistance to cadmium toxicity. Treatment of the worm with cadmium increases the abundance of lysosomes marked by elevation in lysosomal biogenesis and functional genes, reinforcing the importance of lysosomal pathways in cadmium detoxification. To summarise, we delineated the non-canonical role of copper ATPases and lysosomes in cadmium-induced cellular toxicity.

cell biology↗

PFAS triggers a SpoT-associated metabolic switch that promotes persister-like phenotype in Salmonella Typhi

Per- and polyfluoroalkyl substances (PFAS) are new pollutants in the environment whose effects on bacterias physiology is not well understood. In this study, we show that exposure to PFAS causes membrane depolarization in Salmonella enterica serovar Typhi. This works as a metabolic uncoupler that breaks down proton motive force without immediately killing the cells. This disturbance results in a significant elevation of intracellular NADH and NAD levels while preserving redox equilibrium, signifying an augmented metabolic flux. At the same time, we see that {beta}-oxidation pathways are turned on, which suggests that the cells are shifting toward breaking down fats to make up for the lack of energy. Even though there are more reducing equivalents, ATP levels go down, which is what happens when respiration is uncoupled. This puts the cells in a state of "pseudo-starvation." This metabolic stress triggers the SpoT-dependent stringent response, leading to the accumulation of (p)ppGpp. Genetic analysis employing {Delta}relA and {Delta}relA{Delta}spoT mutants confirm that SpoT is necessary for this adaptive response. Functionally, PFAS-treated populations show an enhanced proportion of persister-like cells, which connects exposure to environmental pollutant in the environment to antibiotic tolerance. Our findings reveal a previously unidentified mechanism by which PFAS alters bacterial metabolism and stress responses, facilitating persistence through membrane depolarization, metabolic reconfiguration, and stringent response activation. This study underscores the potential influence of environmental pollutants on bacterial survival mechanisms and antibiotic resistance.

microbiology↗

Modeling human B cell development with pluripotent stem cells

The ability to generate functional B cells from human pluripotent stem cells (hPSCs) would open new opportunities to develop novel B cell-based therapies to treat a range of human diseases and disorders. Towards this goal, we established a protocol that promotes the efficient development of B lineage cells from definitive hematopoietic progenitors generated from different hPSC lines. Flow cytometric and multi-omic scRNA-seq analyses revealed that B cell development from hPSCs transitions through the well-established pro-B, pre-B and naive B cell stages, accurately recapitulating B lymphopoiesis in the human adult bone marrow. Importantly, the naive B cells generated with this approach could be induced to mature into plasma cells that secrete antibodies and undergo class switching. Analyses of signaling pathways that regulate B lymphopoiesis in these cultures uncovered a potent inhibitory effect of IL-7 on functional IgH rearrangement, resulting in the development of abnormal cells that failed to undergo pre-B cell maturation. Finally, analysis of the different hPSC-derived hematopoietic programs revealed that both definitive and yolk sac progenitors display B cell potential, indicating that there are distinct developmental sources of human B lineage cells. Taken together, these findings demonstrate the efficient generation of B cells from hPSCs and, in doing so, provide a system for further investigating the earliest stages of human B lymphopoiesis and a source of appropriately staged plasma cells for future therapeutic applications.

developmental biology↗

Distinct complexes of RAD51 paralogs participate in different fork protection pathways

Error-free genome duplication is critical for cellular homeostasis and genome maintenance. Stalled forks undergo remodeling during replication stress, and unprotected forks undergo degradation by nucleases. RAD51 paralogs are evolutionarily conserved essential proteins for genome maintenance with diverse roles ranging from homologous recombination (HR) to replication stress responses. However, the mechanisms underlying their participation in fork maintenance remain unclear. Here, we demonstrate that the RAD51 paralogs do not participate in the canonical SMARCAL1-BRCA2 axis of fork protection. Instead, RAD51D-XRCC2 (DX2) and RAD51C-XRCC3 (CX3) complexes protect forks remodeled by the FBH1 helicase, whereas the RAD51B-RAD51C (BC) subcomplex but not BRCA2 safeguards forks remodeled by the FANCM translocase, revealing a new FANCM-mediated pathway of fork remodeling which is protected by the BC sub-complex. Mechanistically, we show that FANCM-mediated fork reversal is RAD51-dependent and generates substrates for MRE11-, EXO1-, and DNA2-mediated degradation in the absence of RAD51B/C. Our findings establish the participation of the RAD51 paralogs in multiple fork protection pathways in a fork-remodeler-specific manner, highlighting the existence of several independent fork remodeling and protection mechanisms for maintaining genomic stability under replication stress.

cell biology↗

The Landscape of Stop Codon-Free Regions in Primates: A Reservoir of Proto-Genes

Gene duplication has long been viewed as the primary source of new genes, yet growing evidence suggests that de novo emergence from non-coding DNA may be more common than previously assumed, requiring unbiased genome-wide strategies to identify its structural precursors. New protein-coding genes can arise from non-coding DNA, but the sequence features enabling this transition remain unclear. Here, we systematically identify and characterise stop-codon-free regions (SCFRs) across telomere-to-telomere assemblies of human and six other primates. Short SCFRs are abundant and widely distributed, whereas long SCFRs are rare and increasingly associated with coding overlap, moderate GC enrichment, and structured exon-intron contexts. We define exon shadows as in-frame SCFR extensions beyond annotated exon boundaries that lack stop codons, revealing latent coding-compatible sequence adjacent to established exons. We also detect introns fully spanned by single SCFRs, consistent with exitron-like architectures. Repeat composition, codon usage, and Fourier spectral analyses show that length filtering enriches for gene-like features and identifies a subset of long SCFRs with codon-scale periodicity. Together, these findings provide a framework for identifying extended ORF-like regions that may serve as substrates for de novo gene emergence in primates.

genomics↗

Integrated single cell multiomic profiling and functional validation reveal distinct cellular routes to human plasma cell differentiation.

Upon activation, B cells undergo profound transcriptional, epigenetic, and metabolic reprogramming to form antibody secreting plasma cells bearing little resemblance to their progenitors. Here, we used single cell RNA and ATAC sequencing of primary and in vitro differentiating human B cells to identify multiple distinct plasma cell subsets and differentiation routes depending on the starting cell type. In primary tonsils, we observed two distinct plasma cell subsets distinguished by expression of CD44 variant 9 (CD44v9), CD38, CD31, and CD10. A transient and rare CD30+ intermediate was identified both in primary tonsils and in vitro. CD40, TLR9, and cytokine stimulation of naive and memory B cells yielded CD30+ cells, which then formed plasma cells that were exclusively CD44v9+. CD30+ intermediates were not generated from primary germinal center B cells as they differentiated into plasma cells, which mostly lacked expression of CD44v9. Analysis of single cell multiomic data and pharmacological inhibition experiments demonstrated that the CD30+ intermediate was promoted by the transcription factor MEF2C. BAFF and APRIL promoted further maturation of these cells to CD44v9+ plasma cells. These data suggest that human germinal center-independent and -dependent ontogenies are biased towards distinct differentiation routes and terminal plasma cells.

immunology↗

T CELLS promote the growth of small-cell lung carcinoma via an IL-6/CD74 axis

A central challenge in immuno-oncology is overcoming the limited efficacy and durability of immune checkpoint inhibition (ICI). This is particularly true in small-cell lung cancer (SCLC), where chemotherapy plus ICI is standard of care but rarely curative. Here, we found that T cells are surprisingly both necessary and sufficient for optimal tumor growth in mouse models of SCLC. These pro-tumoral effects are mediated by interleukin-6 (IL-6) production, which induces the pro-survival factor CD74 in SCLC cells. Notably, T cells within human SCLC tumors express IL-6, and low IL-6 signaling correlates with improved survival following chemotherapy plus ICI in patients. Accordingly, IL-6 blockade synergizes with ICI to inhibit SCLC growth in vivo. These findings reveal a paradoxical role for T cells in SCLC, uncovering an unexpected T cell-IL-6-CD74 axis that promotes tumor survival, and identify IL-6 as a promising target to help unleash the full potential of immunotherapy in this aggressive cancer.

cancer biology↗

TFEB activation ameliorates listeriolysin O-mediated subversion of lysosomal and LC3 function during Listeria monocytogenes infection

Xenophagy is a crucial innate subcellular defense mechanism, functioning as a selective autophagy pathway that captures intracellular pathogens within xenophagosomes for subsequent lysosomal degradation. However, many pathogens have evolved strategies to subvert this process, ensuring their intracellular replication and survival within the host cell. Despite its significance, the precise mechanisms by which intracellularly motile xenophagy cargo like Listeria monocytogenes (Lm) circumvent this selective autophagy pathway are not yet completely understood. In this study, we identify a previously unrecognized function of the secreted virulence factor listeriolysin (LLO) in orchestrating a multi-layered disruption of host autophagy-lysosomal machinery. While LLO is classically known for its role in mediating vacuolar escape, our findings reveal that it also contains a functional LIR motif which enables LLO to directly bind LC3 in the cytosol, rendering it unavailable for xenophagosome formation. Concurrently, LLO impairs lysosomal function by reducing its hydrolytic capacity and suppresses nuclear translocation of TFEB, a key transcription factor that governs autophagy and lysosome biogenesis, further compromising host degradative pathways. Using various Lm mutant strains, we show that actin-based motility is dispensable for xenophagy evasion. Instead, the intracellular persistence of Lm primarily stems from two factors: LLO-mediated LC3 binding, which diverts LC3 from its xenophagic functions, and the inhibition of TFEB nuclear translocation. Importantly, pharmacological activation of TFEB or genetic disruption of the LLO-LC3 interaction restores xenophagy and substantially reduces bacterial load. Collectively, our findings position LLO as a multifaceted virulence determinant that employs previously uncharacterized mechanisms to subvert host cell-autonomous defense. This study deepens mechanistic insight into the pathogenesis of Lm and highlights LC3 and TFEB as promising therapeutic targets for host-directed therapies against intracellular infections. Highlights{blacksquare} Listeria monocytogenes (Lm) evades xenophagy independently of its host-actin polymerization ability {blacksquare}Listeriolysin O (LLO) impairs lysosomal degradative potential and suppresses TFEB nuclear translocation {blacksquare}LLO binds LC3 through its LC3-interacting region (LIR) motif, effectively limiting LC3 availability for xenophagosome formation {blacksquare}Restoring LC3 and TFEB function enables intracellular clearance of Lm Graphical abstractThe graphical abstract illustrates how vacuolar ({Delta}hlyA), and cytosolic (WT and {Delta}actA) Listeria monocytogenes differentially engage with host-degradative pathways. Listeriolysin O (LLO), a critical virulence factor, is highlighted as the linchpin determining whether these bacteria get targeted for degradation or successfully evade the host response. In {Delta}hlyA strain infected cells, where LLO is absent, (1) the bacteria remain confined within the phagosome. (2 - 4) The phagosomal compartment then fuse with lysosome, to form phagolysosome that is both acidified and hydrolytically active, enabling effective bacterial degradation while sustaining autophagy flux. (5) This process coincides with nuclear translocation of the master transcription regulator, TFEB, which enhances lysosomal biogenesis and function, boosting bacterial clearance. On the other hand, both WT and {Delta}actA strains produce LLO, (1, 2) which allows them to escape from the phagosome into the host cytosol. (3) WT strain induces polymerization of host cell actin, leading to the formation of actin clouds that mature into actin tails, facilitating bacterial mobility and cell to cell spread. (4) The {Delta}actA strain, despite lacking the ability to interact with host actin, still replicates in the cytosol. LLO plays a multifaceted role in evading host defenses. (5 - 6) It limits LC3 availability for nascent xenophagosome formation by binding to LC3, reducing bacterial capture by the xenophagy machinery. (7 - 8) Furthermore, even when a few bacteria are successfully sequestered within phagosome or xenophagosome, LLO-mediated lysosomal dysfunction impair their maturation into degradative phagolysosome and xenolysosome. (9) Compounding this, LLO suppresses nuclear translocation of TFEB, thereby dampening transcriptional activation of autophagy-lysosomal pathways. Collectively, these mechanisms compromise the host degradative capacity, allowing cytosolic bacteria to replicate and evade clearance. Several unanswered questions remain regarding the structural and mechanistic aspects of the interaction of LLO with LC3. It is still unclear whether LC3 conjugation occurs on single or double membrane vesicles, and whether these vesicular structures are fully sealed. Additionally, it is not yet determined if LLO binds LC3 specifically at sites of omegasome or phagophore formation. The aggregation behavior of LLO also raises intriguing possibilities: could these aggregates play a protective role in shielding LLO from its degradation? Furthermore, it remains to be clarified whether LLO exists freely in the cytosol or is associated with specific membrane-bound compartments. Finally, the precise mechanism by which LLO interferes with TFEB nuclear translocation is another critical open question requiring further investigation. O_FIG O_LINKSMALLFIG WIDTH=165 HEIGHT=200 SRC="FIGDIR/small/691302v1_ufig1.gif" ALT="Figure 1"> View larger version (50K): org.highwire.dtl.DTLVardef@21c235org.highwire.dtl.DTLVardef@553714org.highwire.dtl.DTLVardef@932e53org.highwire.dtl.DTLVardef@c686ef_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Staying in the loop to make ends meet: roles and regulation of GlmR in Bacillus subtilis

The metabolic networks of most life forms integrate cost-benefit analysis to properly budget carbon and other essential nutrients through continuous assessment of nutrient availability and environmental threats. Bacillus subtilis is a Gram-positive model bacterium found in diverse ecological niches such as soil, marine environments, and the human gut. As such, B. subtilis cells finetune metabolic pathways by monitoring signals indicating the presence of nutrients and stressors. A highly conserved protein, GlmR, is a key player in rationing carbon for the production of cell envelope precursors. This function of GlmR can be attributed to its role in cell shape regulation and antibiotic resistance. Given its central position in carbon utilization, GlmR is under post-translational regulation by phosphorylation and UDP-N-acetylglucosamine (UDP-GlcNAc) binding. GlmR is also linked to cyclic-di-AMP (c-di-AMP), a nucleotide second messenger involved in stress response. In this study, we probed the importance of GlmR in cell morphogenesis, c-di-AMP signaling, and investigated the physiological significance of post-translational regulation. Our results reveal that cells lacking glmR exhibit: (i) increased susceptibility to tunicamycin, a cell envelope targeting antibiotic; (ii) impaired division site positioning; and (iii) elevated intracellular c-di-AMP concentration. Furthermore, we show that the function of GlmR is finetuned by UDP-GlcNAc binding, phosphorylation, and acetylation. Additionally, we provide evidence showing that the recently discovered enzymatic activity of GlmR is integral for its function. We show that GlmR is a cell width determinant and propose a model suggesting close cooperation with an actin-like protein, MreB. Overall, our studies highlight that GlmR is at the crux of carbon flux with an important role in maintaining cell envelope integrity. IMPORTANCEBacteria must integrate feedback from multiple metabolic processes to efficiently allocate carbon to produce essential building blocks such as nucleotides, amino acids, and cell wall precursors to support life. GlmR is a critical metabolic factor involved in the making of cell envelope precursors in diverse bacterial phyla. In Bacillus subtilis, cells lacking GlmR are deformed and hypersensitive to cell wall targeting antibiotics. As siphoning off too much carbon from other essential processes is detrimental to cell viability, GlmR activity is tightly regulated. Here we report that absence of GlmR leads to aberrant placement of cytokinetic machinery and an increase in the levels of cyclic-di-AMP, a nucleotide second messenger that assists in the cell wall stress response. We also show that GlmR function is post-translationally finetuned by phosphorylation and acetylation. Furthermore, our data reveals that the catalytic activity of GlmR is required for its function. Thus, the activity of GlmR is tightly calibrated through multiple means for efficient carbon utilization.

microbiology↗

PARSEbp: Pairwise Agreement-based RNA Scoring with Emphasis on Base Pairings

MotivationHigh-fidelity scoring of RNA 3D structures remains a major challenge in RNA structure prediction and conformational sampling. While single-model methods for scoring RNA structures can capture individual structural features, they fail to capture the broader structural consensus within a conformational ensemble, limiting their effectiveness in ranking and model selection. ResultsWe present PARSEbp, a fast and effective multi-model RNA scoring method that integrates pairwise structural agreement across the conformational ensemble with base pairing consistency. By leveraging both alignment-based global structural agreement at the 3D level and base pairing consistency at the 2D level, PARSEbp efficiently constructs a consensus similarity matrix from which per-structure accuracy scores are computed. Tested on 16th Critical Assessment of Structure Prediction (CASP16) RNA targets, PARSEbp significantly outperforms existing single- and multi-model RNA scoring functions, including traditional statistical potentials, state-of-the-art deep learning methods, and consensus-based approaches, as well as a baseline variant of PARSEbp without the emphasis on base pairings, across a wide range of complementary assessment metrics. AvailabilityPARSEbp is freely available at https://github.com/Bhattacharya-Lab/PARSEbp.

bioinformatics↗