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Biology subjects

Wei, L.

Publications and source records attributed to Wei, L..

At least 55 records · Page 3Linked to original sources

scMomer: A modality-aware pretraining framework for single-cell multi-omics modeling under missing modality conditions

Foundation models offer new opportunities to capture cellular behavior from large-scale single-cell data. However, their development has been greatly constrained due to the limited availability of multi-omics profiles. Consequently, most models are designed for a single modality (e.g. scRNA-seq, or scATAC-seq, etc.), restricting their ability to capture the diversity of heterogeneous biological systems. Here, we introduce scMomer, a modality-aware pretraining framework designed for multi-modal representation learning under missing modality conditions. scMomer adopts a three-stage pretraining strategy that learns unimodal cell representations, models joint representations from multi-omics data, and distills multi-modal knowledge to enable multi-omics-like representations from unimodal input. Its modality-specific architecture and three-stage pretraining strategy enable effective learning under missing modality conditions and help capture cellular heterogeneity. Through extensive experiments, scMomer generates biologically meaningful embeddings and outperforms state-of-the-art unimodal approaches across diverse gene-level and cell-level downstream tasks, including cross-modality translation, gene function prediction, cell annotation, drug response prediction, and perturbation prediction. Overall, these results demonstrate that scMomer serves as a robust, generalizable, and scalable foundation for single-cell multi-modal analysis under missing modality conditions.

bioinformatics↗

Accurate detection and quantification of single-base m6A RNA modification using nanopore signals with multi-view deep learning

N6-methyladenosine (m6A) is a crucial epitranscriptomic mark. While Nanopore Direct RNA Sequencing (DRS) enables transcriptome-wide detection, most existing methods neglect or lack the capacity to effectively process the intrinsically variable-length raw signals generated by DRS reads.Here, we present MultiNano, a multi-view deep learning framework that converts variable-length raw signals into image-like feature representations, effectively resolving the length inconsistency problem. By integrating raw signal and basecalling features, MultiNano enables accurate and comprehensive transcriptome-wide detection of m6A modifications. Our model achieved state-of-the-art (SOTA) performance in various tasks, including site-level prediction, read-level prediction, cross-species transfer learning, and modification rate estimation. Furthermore, the false positive control strategy implemented in MultiNano significantly enhances the models robustness and predictive accuracy, offering a powerful alternative to traditional thresholding-based filtering algorithms. Collectively, our approach provides novel insights for the absolute quantification and single-base resolution of RNA modifications.

bioinformatics↗

DiffusionST: A deep generative diffusion model-based framework for enhancing spatial transcriptomics data quality and identifying spatial domains

Recent advancements in spatial transcriptomics technology have generated substantial volumes of spatial transcriptome data. However, the quality of this data is often compromised due to the limitations of current sequencing technologies. To address this issue, DiffusionST proposes a method for imputing spatial transcriptomics data and clustering the imputed data. The method employs a graph convolutional network (GCN) model combined with a newly designed loss function, denoising data using the zero-inflated negative binomial (ZINB) distribution, and data enhancement through a diffusion model to improve clustering accuracy. DiffusionST demonstrates superior clustering accuracy compared to six of the most popular spatial transcriptomics clustering algorithms. DiffusionST also excels in data imputation when compared to five single-cell RNA sequencing (scRNA-seq) imputation algorithms. Additionally, DiffusionSTs robustness against noise is quantitatively validated by manually introducing random dropout noise into the dataset, where our model significantly enhances the quality of spatial transcriptomic data. Moreover, DiffusionST is well-suited for high-resolution spatial transcriptomics data and has been demonstrated, through survival analysis and cell-cell communication studies, to dissect spatial domains within breast cancer tissues. These findings provide strong evidence of DiffusionSTs efficacy in handling spatial transcriptomic data especially with strong noise, making it a valuable tool in this field.

bioinformatics↗

Magellon - an extensible platform for cryo-EM data visualization, management, and processing

Single particle cryo-electron microscopy (cryo-EM) has revolutionized structural biology by enabling high-resolution determination of macromolecular structures. However, the field faces challenges in data management, processing workflow integration, and software extensibility. We present Magellon, an innovative cryo-EM software platform that addresses these challenges through a modern microservices architecture. Magellon consists of an extensible backend with a web-based front end that we call Magellon Viewer. Together, these combine high-performance computing capabilities with an intuitive user interface, enabling researchers to efficiently process and analyze cryo-EM data. The platforms distinguishing features include a plugin-based architecture, distributed processing capabilities, comprehensive monitoring systems, and a novel approach to data organization and visualization. A key philosophy of the approach is that the Magellon backend provides a platform that uses robust industry-standard libraries to orchestrate computational tasks while offering users and developers flexibility in selecting the computational resources for performing calculations. Magellon represents a significant advancement in cryo-EM software infrastructure, offering flexibility, scalability, and extensibility while maintaining ease of use.

biophysics↗

Conformal Bioprinting of Bi-phasic Jammed Bioinks, Independent of Gravity, Orientation, and Curvature

Rapid in situ bioprinting on complex, human-scale anatomical surfaces remain a key challenge for clinical translation. Here, we present a gravity-independent, conformal bioprinting strategy using bi-phasic granular bioink and multinozzle printheads capable of adapting to arbitrary surface curvatures. The bioink comprised of jammed gelatin microgels suspended in a fibrinogen matrix exhibits yield-stress behavior to maintain shape fidelity after extrusion while supporting cell viability and proliferation. Two monolithic multinozzle printhead architectures with identical bioink delivery networks were evaluated: (1) a rigid configuration for handheld bioprinting and (2) a soft robotic variant capable of real-time curvature adaptation via pneumatic actuation. Microgravity experiments aboard a parabolic flight confirmed successful bioink deposition under [~]0 g conditions. A ladder-rung microfluidic architecture ensured uniform bioink delivery across printhead nozzles, improving deposition consistency. In situ bioprinting on anatomical facial phantoms confirmed conformal, high-throughput (deposition at 20 mm{middle dot}s-1) deposition of bioink over physiologically relevant curvatures, both with and without cells. Cell-laden constructs retained >85% cell viability post-printing and supported proliferation. This work introduces a scalable bioprinting platform suitable for clinical, remote, and deep-space environments, enabling autonomous tissue fabrication. The curvature-adaptive printhead advances current in situ bioprinting capabilities, facilitating the generation of personalized grafts with complex anatomical geometries.

bioengineering↗

GFP-Free Live-Neuron Quantitative Imaging Reveals Compartmentalization and Growth Dynamics of PolyQ Aggregates

Huntingtons Disease (HD), the most prevalent polyglutamine (polyQ) neurodegenerative disorder, features brain aggregates induced by mutant huntingtin (mHtt) proteins harboring expanded polyQ tracts. Despite extensive efforts, molecular mechanisms of polyQ aggregates remain elusive. Here we establish quantitative stimulated Raman scattering imaging of polyQ aggregates (q-aggSRS) for non-invasive investigations in live neuronal co-cultures using deuterated glutamine labeling. Q-aggSRS allows for specific visualization by targeting the distinct Raman peak from carbon-deuterium bonds, eliminating the need for bulky GFP tagging. Coupled with analysis from aggregate-tailored expansion microscopy, newly designed two-color imaging, and pulse-chase visualization, we comprehensively quantified the mHtt and non-mHtt proteins within the same aggregates across varying sizes, cell types, mHtt constructs, and subcellular locations. Our findings demonstrate a two-phase aggregate growth model with a distinct core-shell spatial organization, reveal significant heterogeneity in nucleus/cytoplasm compartmentalization specific to neurons, and identify previously unrecognized "gel-like" aggregates specifically in neuronal nuclei. These insights should advance our understanding of native polyQ aggregates and our proposed interaction coefficients may offer new quantitative parameters for developing effective HD therapies.

biophysics↗

Single-Cell Metabolic Imaging Reveals Glycogen Driven-Adaptations in Endothelial Cells

Endothelial dysfunction (ED) is a defining feature of diabetes mellitus (DM) and a key contributor to many metabolic and cardiovascular diseases. Endothelial cells (ECs) are known to be highly glycolytic and primarily rely on glucose to meet their energy demands. However, the role of glycogen metabolism in ECs remains poorly characterized due to a lack of suitable tools. Here, we utilize stimulated Raman scattering (SRS) microscopy to investigate subcellular glycogen metabolism in live ECs under stress conditions associated with highly prevalent diabetes and diabetic complications. We demonstrate that ECs exposed to a diabetes-mimicking milieu- high glucose and tumor necrosis factor (TNF-)- divert excess glucose toward subcellular glycogen storage, and that this storage capacity is significantly enhanced by the inhibition of glycogen synthase kinase 3 (GSK3). Pulse-chase experiments uncover glycogen dynamics and reveal that glycogen is rapidly mobilized under glucose starvation, highlighting its role as an immediate energy reserve in ECs. We further extend the capabilities of SRS metabolic imaging to visualize glutamine and lactate metabolism for the first time, directly showcasing the reliance of ECs on these alternative carbon substrates during glucose deprivation. Our results indicate that ECs containing glycogen exhibit a reduced immediate metabolic demand for these gluconeogenic substrates in the absence of extracellular glucose. These findings suggest that glycogen may play a broader role beyond energy reserves in ECs by modulating stress-responsive metabolic adaptations and may offer potential therapeutic opportunities to address diabetes-induced ED and related cardiometabolic diseases.

cell biology↗

Endothelial AGO1 Drives Vascular Inflammation and Atherosclerosis via a Non-Canonical Nuclear Mechanism

BACKGROUNDEndothelial cell (EC) dysfunction is a cause and consequence of vascular inflammation and lipid dysregulation in atherosclerosis, yet the molecular drivers linking EC dysfunction to systemic metabolic derangements remain incompletely understood. Moreover, whether inhibiting an endogenous gene in ECs can impact liver function, lipid profile, and the vascular inflammation in the context of atherosclerosis has not been demonstrated. We previously identified Argonaute 1 (AGO1), a component of the RNA-induced silencing complex, as a regulator of EC function in angiogenesis and obesity. However, the role of endothelial AGO1 in vascular inflammation and liver function in the context of hyperlipidemia and atherosclerosis is unknown. METHODSEC-conditional AGO1 knockout (EC-AGO1-KO) and wildtype mice were subjected to pro-atherosclerotic models induced by AAV9-PCSK9 coupled with a Western diet or partial carotid ligation. Metabolic and vascular phenotype and gene expression were analyzed. In human liver sinusoidal and aortic ECs, AGO1 was knocked down using antisense oligonucleotides (ASO), followed by assessment of inflammatory responses (qPCR, RNA-seq, ELISA, and monocyte adhesion assays). To identify the molecular mechanisms linking AGO1 and EC inflammation, Cut&Tag sequencing, chromatin immunoprecipitation, immunofluorescence, proximal ligation assay, and co-immunoprecipitation were performed. The therapeutic effect of AGO1 inhibition was assessed using ASO-delivered via lipid nanoparticle (LNP) for systemic distribution and monocyte membrane-coated nanoparticles (MoNP) to target the inflamed endothelium. RESULTSEC-AGO1-KO mice exhibited improved plasma lipid profiles, reduced hepatic steatosis, inflammation, and fibrosis, and decreased aortic atherosclerotic burden. AGO1 knockdown in ECs attenuated inflammatory responses. Mechanistically, AGO1 interacted with NF-{kappa}B p65 and promoted p65 nuclear translocation and the transcriptional activation of pro-inflammatory genes, including ICAM1 and THBS1. AGO1-ASO delivered through LNP or MoNP achieved the anti-inflammatory, anti-hyperlipidemic, and anti-atherosclerotic effects, recapitulating the phenotypes observed with EC-AGO1-KO. CONCLUSIONSEndothelial AGO1 promotes vascular inflammation and liver dysfunction in the context of hyperlipidemia and atherosclerosis, in part through a non-canonical nuclear action of AGO1 as an NF-{kappa}B coactivator. Inhibition of endothelial AGO1 provides the dual benefits of ameliorating lipid dysregulation and suppressing vascular inflammation. These results highlight EC-AGO1 as a possible therapeutic target for atherosclerosis and cardiometabolic diseases.

pathology↗

GeST: Towards Building A Generative Pretrained Transformer for Learning Cellular Spatial Context

Learning spatial context of cells through pretraining on spatial transcriptomics (ST) data may empower us to systematically decipher tissue organization and cellular interactions. Yet, transformer-based generative models often focus on modeling individual cells, neglecting the intricate spatial relationships within them. We develop GeST, a deep transformer model that is pretrained by a novel spatially informed generation task: Predict cellular expression profile of a given location based on the information from its neighboring cells. We propose a spatial attention mechanism for efficient pretraining, a flexible serialization strategy for converting ST data into sequences, and a cell tokenization method for quantizing gene expression profiles. We pretrained GeST on large-scale ST datasets of different ST technologies and demonstrated its superior performance in generating unseen spatial cells. Our results also show that GeST can extract spatial niche embeddings in a zero-shot way and can be further fine-tuned for spatial annotation tasks. Furthermore, GeST can simulate gene expression changes in response to perturbations of cells within spatial context, closely matching existing experimental results. Overall, GeST offers a powerful generative pre-training framework for learning spatial contexts in spatial transcriptomics.

bioinformatics↗

The multiomics landscape of small peptides encoded by long non-coding RNA-derived sORFs in rice

Long non-coding RNAs (lncRNAs), representing the non-coding RNA regions, constitute a significant portion of the genomes in complex organisms. Recent studies suggest that some lncRNAs have the capability to encode peptides. However, the presence of the lncRNA-derived sORFs-encoded polypeotides (LSEPs) in plants is not well understood. In this study, we developed a multi-omics approach that encompasses transcriptomics, translatomics (Ribo-seq), and proteomics to identify of LSEPs in rice. Among the 2764 identified lncRNAs, 42.69% were found to be bound by the ribosome, indicating a potential for encoding. Optimized small peptide extraction protocol was further developed, and the small peptides from rice leaves were extracted and subjected to LC-MS/MS analysis, leading to the identification of a total of 403 LSEPs across four constructed search databases. This work confirms the peptide-coding ability of lncRNAs in plants. Collectively, our study establishes an efficient multi-omics method for identifiying small peptides encoded by lncRNAs, which may be valuable for large-scare screening of LSEPs in plants.

plant biology↗

Identifying Key Cells for Fibrosis by Systematically Calling Cell Type-Phenotype Associations across Massive Heterogenous Datasets

Fibrotic diseases pose a significant burden on health care, yet the key pathogenic fibroblasts involved remain unclear. We developed the fibrotic disease fibroblast atlas (FDFA), which comprises 394 single-cell and 38 spatial transcriptomic samples from 11 common fibrotic diseases. To perform a cell-type phenotype association study in large-scale heterogeneous datasets, we developed the single-cell phenotype association research kit for large-scale dataset exploration (SPARKLE). SPARKLE handles heterogeneity by incorporating confounding information into its generalized linear mixed models (GLMMs). The application of SPARKLE to FDFA revealed that matrix fibroblasts (MTFs) constitute a crucial pathogenic cell group in fibrosis. Their increased proportion correlate with the fibrotic process. MTFs also synergize with MYO-Fs, increasing their degree of fibrosis. Based on MTF, we identified 25 potential antifibrotic targets for broad-spectrum antifibrotic therapies. This study enhances our understanding of fibrosis and provides a reliable framework for large-scale cell type-phenotype association research. HighlightsO_LIA cross-tissue, multidisease fibrotic disease fibroblast atlas (FDFA) reveals diverse fibroblast subtypes in fibrosis diseases. C_LIO_LIA new toolkit, SPARKLE, is introduced for detecting robust cell type-phenotype associations in large-scale heterogeneous datasets. C_LIO_LIMultiple pathogenic fibroblasts associated with common fibrosis disease (MTF) onset and progression have been identified, suggesting potential cell-specific therapeutic strategies for fibrosis-related diseases. C_LI

bioinformatics↗

High throughput identification of genetic regulators of microglial inflammatory processes in Alzheimer's disease

Genome-wide association studies (GWAS) have identified over a hundred genetic risk factors for Alzheimers disease (AD), many of which are predominantly expressed in microglia. However, the pathogenic role for most of them remains unclear. To systematically investigate how AD GWAS variants influence human microglial inflammatory responses, we conducted CRISPR inhibition (CRISPRi) screens targeting 119 AD GWAS hits in hiPSC-derived microglia (iMGLs) and used the production of reactive oxygen species (ROS) in response to the viral mimic poly(I:C) as a functional readout. Top hits whose knockdown either increased or decreased ROS levels in response to poly(I:C) were further analyzed using CROP-seq to integrate CRISPRi with single-cell RNA sequencing (scRNA-seq). This analysis identified 9 unique microglial clusters, including a poly(I:C)-driven inflammatory cluster 2. Emerging evidence supports a pathogenic role of viral infections in AD and cross comparison of our scRNA-seq data with iMGLs xenotransplanted into an AD mouse model shows significant overlap between our clusters and AD-relevant microglial clusters. Knockdown of MS4A6A and EED, which resulted in elevated ROS production in the presence of poly(I:C), increased the proportion of cluster 2 cells and induced functionally related changes in gene expression. In addition, KD of MS4A6 led to a reduction in the proportion of iMGLs in the DAM (disease associated microglia) cluster under all conditions, suggesting that this gene may modulate the DAM response. In contrast, KD of INPP5D or RAPEP1 which lead to low levels of ROS in the presence of poly(I:C), did not significantly affect the proportion of cells in cluster 2 but rather shaped the inflammatory response. This included the upregulation of an HLA-associated inflammatory cluster (cluster 6) by INPP5D knockdown under all conditions, independent of poly(I:C) stimulation. Importantly, KD of INPP5D or RAPEP1 had many shared differentially expressed genes (DEGs) under both vehicle and poly(I:C) treated conditions. Overall, our findings demonstrate that despite the diverse biological functions of AD GWAS variants, they converge functionally to regulate human microglial states and shape inflammatory responses relevant to AD pathology.

neuroscience↗

Multi-modal Diffusion Model with Dual-Cross-Attention for Multi-Omics Data Generation and Translation

Single-cell multi-omics technologies offer unprecedented opportunities to decipher complex cellular mechanisms. To overcome experimental limitations in scale, cost, and coverage, powerful computational methods are essential for integrating diverse data modalities and generating high-fidelity in-silico data. In this paper, we present scDiffusion-X, a latent diffusion model specifically designed for this purpose. The core innovation is a Dual-Cross-Attention (DCA) module that adaptively learns intricate, hidden relationships between different molecular modalities, offering a more flexible and interpretable approach than traditional integration strategies. Extensive benchmarking experiments demonstrate that scDiffusion-X excels at generating realistic multi-omics data, preserving cellular heterogeneity and global data structures with excellent scalability. Distinct from existing multi-omics simulators, scDiffusion-X uniquely enables high-fidelity modality translation by predicting one molecular modality from another and provides robust uncertainty quantification. Beyond data generation, we designed a gradient-based interpretation framework to transform DCA module into a discovery tool, enabling inference of comprehensive cell-type-specific heterogeneous gene regulatory networks (GRNs). By integrating state-of-the-art generative modeling with deep biological interpretability, scDiffusion-X serves as a powerful tool for dissecting regulatory relationships, predicting perturbation responses, poised to accelerate discovery in single-cell multi-omics research.

bioinformatics↗

HGCPep: A Hypergraph-based Deep Learning Model for Enhancing Representation of Peptide Features in Cancer-associated ncPEPs Identification

The emergence of non-coding RNA-encoded small peptides (ncPEPs) has sparked significant interest within the realm of cancer immunotherapy, owing to their potential as valuable therapeutic targets and biomarkers. The identification and characterization of cancer-associated ncPEPs assume a crucial role in propelling cancer research forward and augmenting our comprehension of immune-related processes. However, prevailing methods for cancer-associated ncPEPs identification primarily rely on sequence order, neglecting the latent relationships between peptides. As widely acknowledged in the central dogma, peptides are translated from RNA via a many-to-many mapping. In this study, we capitalize on the translation relationship and introduce a hypergraph-based model called HGCPep to enhance the representation of peptide features. Specifically, RNA is regarded as a hyperedge connecting the peptides that are translated from it. Our experimental results validate that the HGCPep approach, leveraging the strengths of hypergraph and convolutional neural networks, outperforms alternative methodologies in the recognition of ncPEPs. Additionally, employing a reduction tool, we visualize the results of multi-label classification within a 2D latent space, shedding light on how multi-label classification task influence the representation of peptides. The dataset and source code of our proposed method can be found via https://github.com/Longwt123/HGCPep_Github.

bioinformatics↗

A poly(A) polymerase and oligo(dT)-dependent method for the purification of engineering circular RNAs that enhances protein expression in eukaryotic cells

Circular RNA (circRNA) has garnered significant attention as a promising therapeutic tool due to its remarkable stability and resistance to exonuclease degradation. However, the development of scalable and efficient purification methods remains a critical challenge. In this study, we propose and evaluate a novel purification strategy for engineered circular RNA (PAPdt), which leverages poly(A) polymerase and oligo(dT) affinity chromatography. Using poly(A) polymerase, we add poly(A) tails of over 200 nucleotides to the 3-OH ends of all linear RNA impurities in a circular RNA preparation. These linear RNAs are then separated from the circular RNA via oligo(dT) affinity chromatography. The linear impurities, bearing longer poly(A) tails, exhibit extended retention on the oligo(dT) column, whereas the circular RNA, with a shorter poly(A) sequence, elutes more quickly. By stepwise elution with ultrapure water, we effectively separate the circular RNA from the linear contaminants. This method offers a fundamental solution to the purification of circular RNA, combining high efficiency, purity, and cost-effectiveness.

bioengineering↗

Benchmarking AI Models for In Silico Gene Perturbation of Cells

Understanding perturbations at the single-cell level is essential for unraveling cellular mechanisms and their implications in health and disease. The growing availability of biological data has driven the development of a variety of in silico perturbation methods designed for single-cell analysis, which offer a means to address many inherent limitations of experimental approaches. However, these computational methods are often tailored to specific scenarios and validated on limited datasets and metrics, making their evaluation and comparison challenging. In this work, we introduce a comprehensive benchmarking framework to systematically evaluate in silico perturbation methods across four key scenarios: predicting effects of unseen perturbations in known cell types, predicting effects of observed perturbations in unseen cell types, zero-shot transfer to bulk RNA-seq of cell lines, and application to real-world biological cases. For each scenario, we curated diverse and abundant datasets, standardizing them into flexible formats to enable efficient analysis. Additionally, we developed multiple metrics tailored to each scenario, facilitating a thorough and comparative evaluation of these methods. Our benchmarking study assessed 10 methods, ranging from linear baselines to advanced machine learning approaches, across these scenarios. While some methods demonstrated surprising efficacy in specific contexts, significant challenges remain, particularly in zero-shot predictions and the modeling of complex biological processes. This work provides a valuable resource for evaluating and improving in silico perturbation methods, serving as a foundation for bridging computational predictions with experimental validation and real-world biological applications.

bioinformatics↗

The fermented cabbage metabolome and its protection against cytokine-induced intestinal barrier disruption of Caco-2 monolayers

Fermented vegetables, such as fermented cabbage (sauerkraut), have garnered growing interest for their associations with a myriad of health benefits. However, the mechanistic details underlying the outcomes of consuming these foods require further investigation. This study examined the capacity of soluble metabolites in laboratory-scale and commercial fermented cabbage to protect against disruption of polarized Caco-2 monolayers by IFN-{gamma} and TNF-. Laboratory-scale ferments (LSF) were prepared with and without the addition of Lactiplantibacillus plantarum NCIMB8826R (LP8826R) and sampled after 7- and 14-days of incubation. Trans-epithelial electrical resistance (TER) and paracellular permeability to fluorescein isothiocyanate-dextran (FITC) revealed that fermented cabbage, but not raw cabbage or brine, protected against cytokine-induced damage to the Caco-2 monolayers. Barrier-protective effects occurred despite increased IL-8 production following cytokine exposure. Metabolomic analyses performed using gas and liquid chromatography resulted in the identification of 149 and 333 metabolites, respectively. Significant differences were found between raw and fermented cabbage. LSF metabolomes changed over time and the profiles of LSF with LP8826R best resembled the commercial product. Overall, fermentation resulted in lower carbohydrate and increased lactic acid, lipid, amino acid derivative (including D-phenyl-lactate (D-PLA), indole-3-lactate (ILA), and {gamma}-aminobutyric acid (GABA)), and phenolic compound concentrations. Lactate, D-PLA, and ILA tested individually and combined only partially protected against cytokine-induced TER reductions and increases in paracellular permeability of Caco-2 monolayers. The findings show that intestinal barrier-protective compounds are consistently enriched during cabbage fermentations, irrespective of scale or microbial additions, that may contribute to the health-promoting potential of these foods. ImportanceFermented vegetables are increasingly associated with health benefits. However, the importance of microbial transformations to foods during the fermentation process remain to be determined. We found that the metabolites in spontaneously fermented cabbage protected polarized intestinal epithelial cells against damage induced by proinflammatory cytokines. Cabbage fermentations resulted in consistent metabolome profiles enriched in bioactive compounds known to be made by beneficial members of the human gut microbiome, including D-phenyl-lactate (D-PLA) and indole-3-lactate (ILA). The metabolomes were distinct from raw cabbage and further differentiated based on sampling time, addition of an exogenous Lactiplantibacillus plantarum strain, and source. Because only partial protection against intestinal barrier disruption was found when individual metabolites (D-PLA, ILA, lactate) were applied, the findings indicate that the complex mixture of metabolites in a cabbage fermentation offer advantages over single metabolites to benefit intestinal health.

microbiology↗

A high-quality genome of the mass-blooming desert plant Cistanthe longiscapa and its photosynthetic behavior related to drought and life history

O_LICrassulacean acid metabolism (CAM) photosynthesis has independently evolved many times in arid-adapted plant lineages. Cistanthe longiscapa (Montiaceae), a desert mass-blooming annual, can upregulate CAM facultatively upon stress such as drought. Few studies, however, consider life history stages when measuring CAM activity or its facultative onset. C_LIO_LITo test the effect of drought and flowering on photosynthetic activity, we assayed Cistanthe individuals in fully-watered and drought conditions, as well as fully-watered individuals at pre-flowering and flowering life stages. We assembled and annotated a chromosome-scale genome of C. longiscapa and compared it with the genome of Portulaca amilis and analyzed differential gene expression. C_LIO_LIResults show significantly upregulated CAM in drought conditions as compared to fully-watered conditions; furthermore, flowering individuals showed slightly higher CAM activity as compared to pre-flowering plants, even when fully-watered. Differential gene expression analyses provide preliminary support for the possible co-regulation of CAM expression and reproduction. C_LIO_LIWe emphasize the potentially missed significance of life history in the CAM literature, and consider how the CAM biochemical module could become co-opted into other plant behaviors and responses, such as the shift to reproduction or flowering in annuals. C_LI

plant biology↗