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Wang, T.

Publications and source records attributed to Wang, T..

At least 145 records · Page 8Linked to original sources

Decoding Prokaryotic Whole Genomes with a Product-Contextualized Large Language Model

Genomes encode the instructions for life, yet their interpretation requires models capable of capturing long-range genome-wide functional context at scale. Existing genomic foundation models have primarily focused on sequence-level representations, providing powerful tools for biological prediction while leaving complementary opportunities for function-level genome modeling. Here, we present GenSyntax, a function-level genome representation learning framework that models prokaryotic genomes as ordered sequences of gene-product descriptors. By treating gene products as semantic units, GenSyntax transforms annotated replicons into interpretable "genetic paragraphs" that capture genome-wide functional context. We trained GenSyntax on 49,250 annotated prokaryotic genomes and evaluated its ability across genome-scale tasks, including plasmid host prediction, gene-product disambiguation, genome contig ordering and gene essentiality prediction. Compared with general-purpose large language models and representative genomic foundation models, GenSyntax achieved competitive performance across multiple benchmarks, with independent external evaluations supporting its generalization beyond the original training datasets. GenSyntax embeddings also captured signals associated with microbial phenotypes, and gene essentiality predictions enabled exploratory design of minimal genomes. Together with the lightweight GenSyntax-Tiny model, GenSyntax provides a complementary, post-annotation framework for function-level analysis of prokaryotic genomes.

genomics↗

FAK inhibitor treatment systemically regulates the glioblastoma immune environment via blocking monocyte trafficking

Glioblastoma (GBM) is the most common primary malignant brain tumour in adults with dismal survival rates, and current therapies, including most immunotherapies, are not efficacious due to the highly immunosuppressive microenvironment. Studies in other solid cancers report that impairment of the integrin effector pathway involving focal adhesion kinase (FAK) can promote anti-tumour immune responses. Therefore, we set out to address whether, and if so how, suppressing FAK function may influence GBM by using both tumour cell-specific FAK gene deletion and systemic delivery of a clinically relevant FAK kinase inhibitor (FAKi) VS-4718 in an orthotopic murine stem cell model of GBM. We found that treatment with the FAKi, but not tumour cell-specific FAK gene deletion, resulted in GBM clearance and improved survival. This was dependent on adaptive immunity, and tumour-infiltrating T cells in FAKi-treated tumours displayed increased cytotoxic potential and reduced exhaustion. We also found a significant reduction in immuno-suppressive peripherally-derived macrophages and FAKi treatment caused sequestration of inflammatory monocytes within the bone marrow, resulting in impaired monocyte trafficking to tumours as judged by adoptive transfer. This is due to suppression of key adhesion and migration signalling through 4{beta}1 integrin and CX3CR1 in peripheral monocytes. Our work here describes a previously unidentified role for FAK in trafficking of peripheral suppressive macrophages to GBM tumours, reducing T cell exhaustion and promoting anti-tumour immunity. This highlights a new way in which systemic FAK inhibitors can be used to provide a beneficial immune modulatory strategy for the treatment of GBM.

immunology↗

Graded Hair Cell Ablation Reveals Functional Redundancy in the Mature Mouse Vestibular System

Inner ear hair cells are mechanoreceptors critical for hearing and balance. Damage to vestibular hair cells causes balance impairment, yet it is unclear whether hair cell loss correlates with vestibular dysfunction. In this study, we ablated hair cells in Pou4f3DTR/+ mice with diphtheria toxin (DT), and found a dose-dependent decrease in hair cell survival in both the macula and crista ampullaris, including loss of type I and II hair cells in the striolar/central and extrastriolar/peripheral regions. Responses to linear acceleration, measured by the translational vestibulo-ocular reflex (tVOR) and vestibular sensory evoked potential (VsEP), were intact with 25% or more hair cell survival in the macula, and diminished only when hair cell survival decreased further. By contrast, rotational vestibulo-ocular reflex (rVOR) responses were significantly reduced with [~]31% hair cell survival in the cristae. Further, single-unit recordings of vestibular afferents from cristae and maculae showed more irregular and reduced firing rates, but only those corresponding to cristae displayed reduced sensitivity to head rotation. Limited hair cell regeneration was observed in the extrastriolar/peripheral regions of both maculae and cristae 6 months post ablation, although no significant recovery of the VORs was observed. Thus, the adult mouse vestibular end organs display different degrees of redundancy, demonstrating robust responses to head rotation and linear acceleration despite loss of most hair cells.

neuroscience↗

Preserved Neural Dynamics across Arm- and Brain-controlled Movements

The neural activity for motor control is complex and dynamic; it has been found to dramatically transit from planning to executing movements. As brain-machine interfaces (BMIs) can directly connect the brain and the external world by yielding comparable motor outcomes with artificial apparatus, a central question is whether the BMI-controlled movements share neural dynamics or underlying mechanism with natural movements. To enable a systematic comparison, we developed a feedforward BMI framework with distinct planning and executing epochs that enables ballistic cursor control to intercept moving targets. This BMI allowed monkeys to voluntarily initiate neural states which controlled the direction and timing to launch a ballistic movement, like skeet shooting. Based on this, we found similar neural representations and computational structures across arm- and brain-controlled conditions. Notably, in addition to resembling the rotational structure in natural reaching, the neural population dynamics during open-loop BMI also shared preserved manifolds with those during reaching arm movements. These findings suggest a fundamental principle, and reveal a set of basic computational motifs for the neural control of movement in an abstract hierarchy in the absence of constraints from actuators. This study thus has the potential to reshape the consideration of how BMIs assist paralyzed patients in interacting with dynamic environments, and to promote next-generation BMI systems.

neuroscience↗

Full-length structure of CPR-containing self-sufficient cytochrome P450

Cytochrome P450 (P450s) are heme-thiolate monooxygenases that exploit electrons sourced from pyridine nucleotide to reduce the oxygen and heme iron to catalyze hydroxylation of inactivated C-H bond1-4. Self-sufficient P450s that contain the substrate-binding heme-domain and the electron-donating NADPH:cytochrome P450 reductase (CPR) domain in the same polypeptide chain are highly effective and have been engineered to catalyze various challenging reactions. The high efficacy attributes to the effective electron transfer rate, but how the electrons travel among the redox centers remains elusive owing to the lack of structural information of the full-length protein. Here, we report the structure of a homologue of the most extensively studied P450BM3 from Shimazuella soli (SoP450) resolved by single particle cryo-electron microscopy (cryo-EM) and X-ray crystallography. SoP450 primarily exists as a homodimer formed via the intertwined CPR-domains. The spatial alignment of the heme-domain that is linked via an extensive loop was also determined. Notably, a class of structure that lacks one heme-domain was identified from the cryo-EM analyses, indicating that the heme-domain is mobile. We suspected that the heme-domain could move to reach the CPR-domain for electron acquisition and built a model of putative catalytic state to reveal how the electrons are relayed from NADPH to heme. These results are of fundamental importance to understand the catalytic reaction of CPR-containing self-sufficient P450s, which shall provide critical information to the engineering and applications of these enzymes.

synthetic biology↗

ABA-responsive transcription factor CbNAC63 is involved in modulating biosynthesis of triterpenoid saponins in Conyza blinii

Conyza blinii, a traditional Chinese medicinal herb, accumulates triterpenoid saponins. NAC transcription factors (TFs) are pivotal for plant stress responses and hormone-mediated secondary metabolism, while abscisic acid (ABA) regulates terpenoid biosynthesis in medicinal plants. However, how NAC TFs mediate ABA-regulated triterpenoid saponin synthesis in C. blinii remains unclear. In order to address this gap, the focus was directed towards CbNAC63--a NAC TF identified from the nocturnal low-temperature transcriptome of C. blinii. Phylogenetic and motif analyses showed it belongs to the stress-responsive NAC subclade with conserved domains. Y2H assays revealed its self-interaction, enhancing transcriptional activity; subcellular localization confirmed nuclear localization. RT-qPCR results indicated CbNAC63 exhibits tissue-specific expression under nocturnal low-temperature stress, accompanied by increased triterpenoid saponin accumulation. ABA signaling primarily regulates this process: exogenous ABA enhanced CbNAC63 expression and saponin content, while fluridone suppressed both. Overexpression (OE) and virus-induced gene silencing (VIGS) demonstrated CbNAC63 positively regulates saponin biosynthesis. Y1H and dual-luciferase reporter assays confirmed CbNAC63 directly binds to the promoters of Cb{beta}AS and CbHMGR and activates their transcription. In summary, the study shows CbNAC63 integrates ABA and low-temperature signals, activating MVA pathway genes to regulate saponin synthesis. This unveils a novel "ABA-CbNAC63-MVA" module, enriches the classic regulatory network, and provides a target for improving medicinal plant quality. HighlightsIdentifies CbNAC63 as a novel regulator that integrates ABA and cold signals to boost saponin production in medicinal plants.

plant biology↗

Fluctuating flooding motivates the facilitation of a wetland invader: a probe into the stress gradient hypothesis

Stress gradient hypothesis proposes that the plant interaction tends to convert from competition to facilitation when facing accelerating stress. The present study aims to explore the interaction between two co-existing wetland plant invaders - Alternanthera philoxeroides and Myriophyllum aquaticum with exposure to flooding stress. Different plant assemblages including monospecific (single individual per species), homospecific (two individuals of same species) and heterospecific (two individuals of different species) treatments were subjected to different flooding regimes including mesic habitat, constant flooding and fluctuating flooding. The plant interaction was evaluated by biomass accumulation, biomass allocation and relative competition intensity index (RCI). We found that the biomass accumulation and allocation of A. philoxeroides were consistent across different treatments of community assemblage and flooding regime, while the root mass, biomass and root mass allocation of M. aquaticum significantly increased at the presence of A. philoxeroides. Moreover, the RCI of M. aquaticum decreased at the presence of A. philoxeroides. Especially, the RCI of M. aquaticum was 0.06 in the homospecific community, while that of M. aquaticum was -0.82 in the heterospecific treatment under fluctuating flooding condition. Overall, Alternanthera philoxeroides facilitated M. aquaticum, especially under fluctuating flooding condition, which complies with the stress gradient hypothesis. The water level drawdown can benefit the impedance of the growth of M. aquaticum and the deceleration of the co-invasion of A. philoxeroides and M. aquaticum.

ecology↗

Form and function of actin impacts actin health and aging.

The actin cytoskeleton is a fundamental and highly conserved structure that functions in diverse cellular processes, yet its direct contribution to organismal aging remains unclear. Here, we systematically interrogated how genetic and pharmacologic perturbations of actin structure and function influence lifespan and various hallmarks of aging in Caenorhabditis elegans. Whole-animal and tissue-specific knockdown of actin and key actin-binding proteins (ABPs) - arx-2 (Arp2/3), unc-60 (cofilin), and lev-11 (tropomyosin) - led to premature disruption of filament organization, reduced lifespan, and tissue-specific physiological defects. Bulk and single-nucleus RNA-sequencing revealed that ABP knockdowns elicited a strongly "aged" transcriptome. Actin dysfunction broadly exacerbated many age-associated phenotypes, including mitochondrial dysfunction, lipid dysregulation, loss of proteostasis, impaired autophagy, and intestinal barrier failure. Pharmacological destabilization with Latrunculin A mirrored genetic knockdowns, while mild stabilization with Jasplakinolide modestly extended lifespan, emphasizing that optimal and finely-tuned actin function is critical for healthy aging. Finally, analysis of human genome-wide association data revealed that common ACTB polymorphisms correlate with differences in age-related decline in gait speed, suggesting evolutionary conservation of actins role in healthy aging. Taken together, our results provide a comprehensive and publicly accessible resource that maps, for the first time, how actin integrity intersects with diverse aging pathways across tissues and scales. This descriptive framework is intended to enable future mechanistic discovery by offering a deep, unbiased dataset that can be integrated with emerging studies to define how actin dynamics contribute to aging.

cell biology↗

Decrypting cellular engagement and recruitment from spatially resolved transcriptomics

The recruitment of the various types of cells into the tissue microenvironment and how these cells engage with other cells in the tissue sites play critical biological roles. However, it is difficult to study these processes on a genome-wide scale using traditional low-throughput experiments. To address this gap, we developed a fully interpretable multi-instance deep learner, coined "spacer". Spacer digests the transcriptomics and spatial modalities of spatially resolved transcriptomics (SRT) data in alignment with the biological principles of the tissue spatial architecture. We deployed spacer to a panel of 17 high definition and 20 low definition SRT datasets, for studying how stromal and immune cells were recruited into tumors and heart during myocarditis. Spacer discovered novel biological insights not affordable by prior spatial data analysis tools, which were validated by orthogonal immuno-peptidomics, spatial T cell receptor (TCR) sequencing, and single cell sequencing experiments. We discovered genes that encode more immunogenic peptides and that are involved in developmental pathways are more potent in recruiting T cells to local tumor sites, while the recruitment of B cells and macrophages is stipulated by a different molecular program. On the other hand, expression of mucins in the tumor cells was found to repel T cell localization. For the engaging cell side, we also uncovered T cell-intrinsic features that determine their localization, validated by spatial-TCR-seq data. Spacer also unexpectedly revealed that CD4+ T cells, though fewer in numbers, are more responsive than CD8+ T cells in the heart during myocarditis. Collectively, this study establishes a new spatially resolved paradigm for studying cellular localization mechanisms in situ and shifts the paradigm from descriptive mapping to mechanistic discovery.

bioinformatics↗

A unique mechanism explaining the outstanding performance of a newly discovered doxycycline riboswitch

Synthetic riboswitches offer a versatile and protein-independent solution for conditional gene regulation. They consist of a regulatory domain and an aptamer domain that binds a specific ligand, with their performance largely depending on the ability of the aptamer to control the regulatory domain. Expanding the range of synthetic riboswitches therefore requires the discovery and characterization of new regulatory aptamers. In the present study, we identified a doxycycline-binding aptamer with outstanding regulatory properties in both yeast and human cells which are based on a unique structural dynamic upon ligand binding. Single-molecule force spectroscopy revealed that doxycycline binding strongly stabilizes an intermediate aptamer conformation offering mechanistic insights into its function. The identification of the aptamer through a combination of parallel SELEX and subsequent in vivo screening in yeast, also provided valuable insights into selection dynamics and the first proof for the effectiveness of RNA Capture-SELEX in aptamer selection. Together, the presented data deepen our understanding of regulatory aptamer selection and functionality while adding a high-performing doxycycline-responsive aptamer to the synthetic biology toolbox.

molecular biology↗

Impact of vitamin D deficiency on defective endometrial decidualization and the repressive role of vitamin D receptor (VDR) in the epigenomic network

Identifying the factors that regulate female reproduction is crucial to understanding how the environment affects female reproductive health. The vitamin D receptor (VDR) and its ligands (primarily 1,25(OH)2D3) have a recognized role in calcium homeostasis; however, their broader impact on female reproduction remains underexplored. We demonstrate that the VDR and its ligands are involved in the hormonal induction of uterine decidualization. Mice fed a vitamin D-deficient diet displayed an impaired hormonally induced decidual response. In a human telomerase reverse transcriptase-immortalized human endometrial stromal cell line (T-HESC), VDR decreased during in vitro decidualization. Small interfering RNA (siRNA) knockdown of VDR in T-HESC enhanced in vitro decidualization, while overexpression of VDR inhibited it. Chromatin accessibility and histone modification analyses revealed that VDR functions as a chromatin regulator, restricting accessibility and repressing transcription in specific genomic regions. Transcriptomic analyses confirmed that VDR broadly modulates gene expression, with most ligand-mediated effects occurring through the VDR. These findings identify VDR as a key regulator of transcriptional and chromatin landscapes in human endometrial stromal cells, offering novel insights into vitamin D signaling in reproduction. This study highlights the potential of targeting vitamin D pathways to treat uterine disorders associated with impaired decidualization and reduced fertility. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=80 SRC="FIGDIR/small/688535v2_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@6b048org.highwire.dtl.DTLVardef@11f7b4corg.highwire.dtl.DTLVardef@1d7dbfaorg.highwire.dtl.DTLVardef@ab3894_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗

Streptavidins play a multifunctional role within a biotin-pathway antibiotic network encoded in a biosynthetic supercluster

Streptavidin, the well-known biotin-binding protein extensively used in biotechnology, is naturally co-produced in Streptomyces avidinii alongside stravidins--inhibitors of biotin biosynthesis. Here, we uncover and activate a conserved genomic region flanked by two streptavidin genes, revealing multiple biosynthetic gene clusters that produce diverse biotin-related metabolites, including stravidins, acidomycin, -methyl-KAPA, -methyldesthiobiotin, and the novel non-proteinogenic amino acid ANDA. We show -methyldesthiobiotin arises from -methyl-KAPA, illustrating how methylated analogues interfere with distinct steps of biotin biosynthesis. Contrary to the view that streptavidin functions solely by sequestering biotin, our biochemical, structural, and bioactivity analyses demonstrate that it also binds acidomycin, neutralizing its antibacterial activity to protect the producer while likely facilitating compound secretion. The crystal structure of the streptavidin-acidomycin complex reveals the molecular basis for this dual functionality. Our findings establish a multifunctional streptavidin that integrates biotin sequestration and self-resistance to balance an antibiotic network targeting the biotin pathway in microbial competition.

microbiology↗

Assessment of Visual Function in Mice Using Light/Dark Box and Multi-Feature Machine Learning

The light/dark box test can be used to assess visual function in rodents based on their spontaneous behavior in response to light. Commonly used assay relies on a single behavioral metric, dwell time in the light or dark compartment, which may be influenced by factors other than vision, leading to unreliable assessment results. To overcome this, we developed a multi-feature machine learning paradigm by extracting multiple mouse behavioral metrics, standardizing them as features to train machine learning models, thereby achieving reliable and automated vision assessment. We systematically compared the classification performance of single-metric versus multi-feature machine learning approaches in sighted and blind mice, using wild-type and rhodopsin-deficient mice, with a subset further subjected to double optic nerve crush. We found that the multi-feature method can improve classification performance and exhibit great robustness to different experimental settings. Additionally, we further improved model performance by applying feature importance analysis and constructing an optimized feature subset. These findings suggest that the reliability of commonly used single dwell time measure for vision assessment could become unreliable, as shown in our experiment, probably because in addition to vision other factors also impact dwell time. Our study demonstrated an improved assessment method based on a combination of multiple behavior features through machine learning. Author SummaryAssessing visual function in mice is essential for studying eye diseases and drug development. The light/dark box test evaluates visual function by measuring the spontaneous behavioral response of mice to light, providing a training-free behavioral approach that helps simplify the assessment process and improve research efficiency. However, traditional light/dark box tests rely on a single behavioral metric, dwell time in the light or dark compartment, to assess visual function, which may be influenced by factors other than vision, such as anxiety and exploratory behavior, leading to limited reliability of assessment results. Here, we demonstrate that integrating multiple behavioral features through machine learning can improve the reliability and stability of vision assessment. By automatically tracking and analyzing various behavioral metrics of mice, such as movement patterns, speed, and spatial preferences, the proposed method can more reliably distinguish between sighted and blind mice. Furthermore, the method demonstrates stable performance across different experimental settings, showing good applicability. This automated, reliable, and easily generalizable method can provide a convenient and efficient means for visual assessment in preclinical research, facilitating vision disease research and drug development.

animal behavior and cognition↗

FAM19A4 Enhances Neutrophil Respiratory Burst via p38 MAPK in Lethal Sepsis

Sepsis causes high mortality and resource strain, with neutrophil-derived reactive oxygen species (ROS) contributing to excessive inflammation. The secretory protein FAM19A4 modulates ROS release, but its role in sepsis was unclear. We measured elevated FAM19A4 levels in septic patients and cecal ligation and puncture (CLP) mice, correlating with increased mortality. Fam19a4-/- mice subjected to CLP showed significantly improved survival and attenuated multiorgan injury without impaired peritoneal bacterial clearance or altered circulating neutrophil counts. Deficiency reduced the cell counts of neutrophil (Ly6G+) and macrophage (F4/80+) in lungs and liver, diminished systemic ROS production tracked by bioluminescence, and decreased neutrophil extracellular trap (NET) formation in serum and lung tissue. In vitro, FAM19A4 enhanced neutrophil phagocytosis and ROS generation but did not affect lipopolysaccharide-induced chemotaxis. Mechanistically, bulk RNA sequencing, western blotting, and the p38 inhibitor SB203580 demonstrated that FAM19A4 drives neutrophil ROS release specifically through p38 MAPK signaling activation. These results indicate that FAM19A4 is upregulated during sepsis and exacerbates outcomes by enhancing neutrophil ROS production via p38 MAPK, representing a promising therapeutic target for this condition.

molecular biology↗

Integrated Proteomic and Epigenomic Analysis Reveals IGF2 as a Vulnerability in PRC2-Deficient Malignant Peripheral Nerve Sheath Tumors

Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive sarcomas with limited therapeutic options. Loss of the Polycomb repressive complex 2 (PRC2), via inactivating mutations in SUZ12 or EED, occurs frequently in MPNSTs and is associated with poor prognosis. However, the downstream chromatin and signaling consequences of these mutations remain incompletely understood. Here, we show that PRC2 deficiency in MPNST cells induces coordinated chromatin remodeling, characterized by loss of repressive H3K27me3 and gain of activating marks, including H3K27ac and H3K36me2. Integrative epigenomic, transcriptomic, and proteomic profiling revealed that this chromatin reprogramming activates a fetal-like growth signature centered on insulin-like growth factor 2 (IGF2) and its post-transcriptional regulators, Insulin-like Growth Factor 2 mRNA-Binding Protein (IGF2BP1-3). Functional studies demonstrate that PRC2-deficient cells are selectively dependent on IGF2 for proliferation, and that restoration of SUZ12 suppresses IGF2 expression and reduces growth. Analysis of human MPNST tumors confirms upregulation of the IGF2-IGF2BP axis in PRC2-deficient tumors, highlighting its clinical relevance. Together, these findings link PRC2 loss to activation of fetal growth factor-driven oncogenic signaling and identify IGF2 and its regulatory network as potential vulnerabilities in this aggressive tumor subtype.

cancer biology↗

Humanized APOE mouse brain volume increases over age irrespective of sex and APOE genotype: Implications for translational validity to the human

Translational validity of mouse models of human aging and late-onset Alzheimers disease (LOAD) risk are essential for both fundamental mechanistic science and therapeutic development. Given that the strongest risk factors for LOAD are age, female sex, and APOE-{varepsilon}4 carriership, models must reflect these biological variables and disease phenotypes. The use of mouse models with humanized APOE (hAPOE) is a key strategy to advance translational validity. To initially address translational validity of the hAPOE mouse model, we conducted ex-vivo magnetic resonance imaging analysis of brain volumes in male and female mice across APOE genotypes ({varepsilon}3/{varepsilon}3, {varepsilon}3/{varepsilon}4, {varepsilon}4/{varepsilon}4) and ages corresponding to a human lifespan of approximately 30-70 years (6-25 months in mice). The primary outcomes indicated that total MRI brain volume increased with age (an average of 2.12mm3 per month), irrespective of sex or APOE genotype. Additionally, APOE-{varepsilon}4 carriers had greater total brain volumes than non-carriers. No sex differences were observed in total brain volume. Voxelwise analyses revealed a pattern of localized morphometric changes independent of differences in total brain volume. Age-related volumetric increases were distributed across subcortical regions (e.g., thalami, hippocampi), while age-related decreases were evident across cortical regions, notably the bilateral parieto-temporal and frontal lobes. Additionally, sex differences were evident after controlling for total brain volume, with females showing greater cortex-dominant volumes while males showed a pattern of greater volumes in regions including cerebellar cortices, olfactory bulbs, and striata. No genotypic effects were observed in the voxelwise analysis after correcting for multiple comparisons, suggesting that APOE genotype does not drive localized volume differences independent of total brain volume. These findings indicate that, at the MRI level of analysis, this humanized APOE mouse model does not recapitulate the volumetric atrophy typically seen in human brain aging and Alzheimers disease. The results suggest that humanized APOE alone is insufficient to induce the LOAD atrophy phenotype. This model may better serve as a platform for studying vulnerable aging rather than a primary model for progressive neurodegenerative atrophy.

neuroscience↗

Integrating theory and machine learning to reveal determinants of plasmid copy number

Plasmids are extrachromosomal mobile genetic elements whose copy numbers (PCNs) critically influence microbial evolution, antibiotic resistance and pathogenicity. Despite their importance and immense diversity, the ecological, evolutionary and molecular factors determining PCN remain poorly understood. Here, we present a theoretical model to explain the empirical power-law relationship between plasmid size and copy number, one of the fundamental quantitative principles governing PCN control. However, this relationship alone has limited predictive power. To improve PCN prediction, we introduce a data-driven approach incorporating diverse features. Trained on >10,000 plasmids, our machine learning model achieves significantly enhanced accuracy, with plasmid-encoded protein domains emerging as key predictors. Applying this framework, we conduct the first comprehensive analysis of PCN distributions across hundreds of thousands of metagenomic plasmids (IMG/PR database) and tens of thousands of clinical isolates, uncovering niche specific taxonomic PCN hotspots and ecological adaptations. These results provide critical insights into plasmid ecology, ARG surveillance and shed lights on the gut plasmidome, a "dark matter" in human microbiome.

microbiology↗

RNA viruses in water shape the viromes of shrimp and fish in aquaculture systems

Aquatic environments host immense RNA viral diversity, yet the extent to which waterborne viruses influence the virome of aquatic animals remains unclear. Here, we conducted a comprehensive longitudinal metatranscriptomic analysis of water, shrimp, and fish across multiple culture stages in aquaculture systems. We identified 3,211 RNA viruses spanning 21 viral supergroups, with 97.4% representing novel species. Water exhibited the greatest viral diversity (3,093 species), followed by shrimp (1,280) and fish (398), with most viruses detected in shrimp and fish also detected in water. Diversity analyses revealed increasing richness and significant compositional shifts in 92 high-abundance viruses (>1,000 RPM) across culture stages. Viral abundance in aquatic animals was strongly correlated with that in water, and the temporal trajectories of the 16 most abundant viruses were closely synchronized between water and shrimp. Furthermore, 337 virus species were shared among shrimp and two fish species, of which 309 were present in water. These findings demonstrated that RNA viruses in water shape the composition and dynamics of aquatic animal viromes, underscoring the importance of water virome surveillance and management for disease prevention in shrimp aquaculture.

microbiology↗