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Irritable bowel syndrome (IBS) is a functional gastrointestinal disorder characterized by recurrent abdominal pain or discomfort accompanied by altered bowel habits, often alongside psychological symptoms. Increasing evidence suggests that exercise interventions not only alleviate clinical symptoms but may also exert effects through modulation of the gut-immune axis. This study aims to systematically compare the effects of different exercise modalities on symptoms, quality of life, and psychological status in IBS patients, whilst exploring potential immunological mechanisms. The PubMed, Cochrane Library, EMBASE, and Web of Science databases were systematically searched for literature from inception to June 2025, and conventional Meta-analysis and Web Meta-analysis were performed using RevMan 5.4 and R 4.3.3 software. Sixteen studies were included, covering interventions such as running, moderate-intensity aerobic exercise, Pilates, yoga, and Baguazhang. Moderate-intensity aerobic exercise and Pilates demonstrated significant effects (P < 0.05) in improving depression and anxiety scores, as well as IBS-SSS and IBS-QOL scores. Running and aerobic exercise showed the best overall efficacy. Mechanistically, exercise interventions may have a synergistic effect on the brain-gut-immune axis by enhancing parasympathetic activity, modulating the HPA axis, improving gut microbiota, strengthening intestinal barrier function, and reducing systemic inflammation. This approach alleviates gastrointestinal symptoms while enhancing mental wellbeing. Various exercise interventions may improve clinical symptoms and quality of life in patients with irritable bowel syndrome to a certain extent, and may possess potential immunomodulatory effects. As a relatively safe and cost-effective non-pharmacological treatment, exercise holds considerable clinical application potential in the comprehensive management of irritable bowel syndrome. https://www.crd.york.ac.uk/PROSPERO/, identifier CRD420251132835.

Algicidal bacteria are important in the control of toxic dinoflagellate blooms, but studies on the environmental behavior of related algal toxins are still lacking. In this study, Bacillus subtilis S3 (S3) showed the highest algicidal activity against Alexandrium pacificum (Group IV) out of six Bacillus strains. When treated with 0.5% (v/v) S3 bacterial culture and sterile supernatant, the algicidal rates were 69.74% and 70.22% at 12 h, respectively, and algicidal substances secreted by S3 were considered the mechanism of algicidal effect. During the algicidal process, the rapid proliferation of Alteromonas sp. in the phycosphere of A. pacificum may have accelerated the algal death. Moreover, the algicidal development of S3 released large amounts of intracellular paralytic shellfish toxins (PSTs) into the water, as the extracellular PSTs increased by 187.88% and 231.47% at 12 h, compared with the treatment of bacterial culture and sterile supernatant at 0 h, respectively. Although the total amount of PSTs increased slightly, the total toxicity of the algal sample decreased as GTX1/4 was transformed by S3 into GTX2/3 and GTX5. These results more comprehensively reveal the complex relationship between algicidal bacteria and microalgae, providing a potential source of biological control for harmful algal blooms and toxins.

In this study, Karenia brevis 165 (K. brevis 165), a Chinese strain, was used to research brevetoxin (BTX) metabolites. The sample pretreatment method for the enrichment of BTX metabolites in an algal culture medium was improved here. The method for screening and identifying intracellular and extracellular BTX metabolites was established based on liquid chromatography-time-of-flight mass spectrometry (LC-ToF-MS) and liquid chromatography triple quadrupole tandem mass spectrometry (LC-QqQ-MS/MS). The results show that the recovery rates for BTX toxins enriched by a hydrophilic–lipophilic balance (HLB) extraction column were higher than those with a C18 extraction column. This method was used to analyze the profiles of extracellular and intracellular BTX metabolites at different growth stages of K. brevis 165. This is the first time a Chinese strain of K. brevis has been reported that can produce toxic BTX metabolites. Five and eight kinds of BTX toxin metabolites were detected in the cell and culture media of K. brevis 165, respectively. Brevenal, a toxic BTX metabolite antagonist, was found for the first time in the culture media. The toxic BTX metabolites and brevenal in the K. brevis 165 cell and culture media were found to be fully proven in terms of the necessity of establishing a method for screening and identifying toxic BTX metabolites. The results found by qualitatively and quantitatively analyzing BTX metabolites produced by K. brevis 165 at different growth stages show that the total toxic BTX metabolite contents in single cells ranged between 6.78 and 21.53 pg/cell, and the total toxin concentration in culture media ranged between 10.27 and 449.11 μg/L. There were significant differences in the types and contents of toxic BTX metabolites with varying growth stages. Therefore, when harmful algal blooms occur, the accurate determination of BTX metabolite types and concentrations will be helpful to assess the ecological disaster risk in order to avoid hazards and provide appropriate disaster warnings.

Organic solvent nanofiltration (OSN), also known as solvent-resistant nanofiltration (SRNF), is an emerging membrane-based separation technique capable of efficiently separating molecules in the 200–1000 Da range within organic media. It holds considerable promise for applications in organic solvent systems, which are prevalent in the petrochemical, pharmaceutical and food processing industries. While OSN has been extensively studied in polar solvent systems, increasing attention is now being directed toward its performance in non-polar environments, driven by their substantial practical demand and application potential. Fluorinated and organosilicon-based materials have emerged as key components in the fabrication of high-performance OSN membranes for separation in non-polar solvent environments due to their exceptional chemical, thermal, and mechanical stability. This review systematically summarizes recent advances in the design and fabrication of fluorinated and organosilicon-based composite OSN membranes. Key separation mechanisms are discussed, with particular focus on their roles in the recovery and reuse of homogeneous catalysts in chemical and pharmaceutical processes. Finally, future research directions are proposed to guide the continued development and industrial deployment of the fluorine- and silicon-based OSN membranes in non-polar solvent applications.

Butuo Black sheep (BBS), an ancient indigenous Chinese breed, has co-evolved with the Yi people's semi-nomadic lifestyle and demonstrated exceptional adaptability to high-altitude migrations. However, a high-quality reference genome for BBS is still lacking. In this study, we established a high-quality chromosome-level genome assembly of BBS using PacBio HiFi sequencing. The final assembled genome size was approximately 2.95 Gb, with a contig N50 of 71.45 Mb and a scaffold N50 of 92.26 Mb. The genome assembly achieved a high Benchmarking Universal Single-Copy Orthologs (BUSCO) score of 95.9%, indicating its high completeness and quality. The de novo genome prediction revealed that repetitive sequences accounted for 47.74% of the genome, with long interspersed nuclear elements (LINEs) being the most abundant. Additionally, we present 50 BBS shotgun genomes sequenced using the Illumina HiSeq 2000 platform, with a mean coverage of 10.36×. The study generated approximately 1.2 terabytes of raw data, with 99.9% clean reads mapping successfully to the sheep reference genome at 99.6% coverage. This extensive dataset provides a valuable resource for studying genetic diversity and evolutionary patterns in BBS.

Toxic dinoflagellate blooms and microplastics are widespread coastal pollutants. In this study, the scallop, Argopecten irradians, was selected as an experimental organism to systematically investigate the single and combined toxic effects of polystyrene (PS) and the toxic dinoflagellate, Alexandrium pacificum. The results showed that both PS and algal cells could be ingested by A. irradians. The survival rate of A. irradians remained above 90% in both the single and combined treatment groups, indicating that 1 mg/L PS and 1500 cells/mL A. pacificum cells did not pose a serious threat to scallop survival in the short term. However, CAT, SOD, and GSH-ST activities, as well as MDA content, were all elevated in the combined treatment group. Transcriptomic analysis further revealed that A. pacificum primarily affected immune-related pathways, whereas PS might interfere with endocrine function through the release of additives. Combined exposure to PS and A. pacificum induced more complex synergistic effects, reflected in the metabolic stress of exogenous substances, and the disruption of developmental and homeostasis regulatory pathways. This study provides important theoretical support for assessing the threats posed by composite coastal pollution to aquaculture and marine ecological security.

Sharp declines in temperature pose a significant risk for mass mortality events in the Chinese soft-shelled turtle (Pelodiscus sinensis). To assess the effects of acute cold stress on intestinal health, turtles were exposed to temperatures of 28 °C (control), 14 °C, and 7 °C for 1, 2, 4, 8, and 16 days. The results showed that acute cold stress at 14 °C and 7 °C induced time-dependent alterations in intestinal morphology and histopathology. The damage was more severe at 7 °C, characterized by inflammatory cell infiltration, lymphoid hyperplasia, and extensive detachment and necrosis across the villi, muscle layer, and submucosa. 16S rDNA sequencing revealed significant shifts in intestinal microbiota composition in the 7 °C group, dominated by Helicobacter and Citrobacter. Transcriptomic analysis identified differentially expressed genes (DEGs) that respond to acute cold stress and are involved in the Toll-like receptor signaling pathway (Tlr2, Tlr4, Tlr5, Tlr7, and Tlr8), the NOD-like receptor signaling pathway (Traf6, Traf2, Casr, Rnasel, Pstpip1, Plcb2, Atg5, and Mfn2), apoptosis (Tuba1c, Ctsz, Ctsb, Kras, Hras, Pik3ca, Bcl2l11, Gadd45a, Pmaip1, Ddit3, and Fos), and the p53 signaling pathway (Serpine1, Sesn2, Ccng2, Igf1, Mdm2, Gadd45a, Pmaip1, and Cdkn1a). Metabolomic profiling highlighted differentially expressed metabolites (DEMs) that cope with acute cold stress, such as organic acids (oxoglutaric acid, L-aspartic acid, fumaric acid, DL-malic acid, and citric acid) and amino acids (including L-lysine, L-homoserine, and allysine). The integrated analysis of DEGs and DEMs underscored three key pathways modulated by acute cold stress: linoleic acid metabolism, neuroactive ligand–receptor interaction, and the FoxO signaling pathway. This study provides a comprehensive evaluation of intestinal health in Chinese soft-shelled turtles under acute cold stress and elucidates the underlying mechanisms.

The core–shell junctionless MOSFET (CS-JL FET) meets the process requirements of FD-SOI technology. The transistor body comprises a heavily doped ultrathin layer (core linking the source and the drain), located underneath an undoped layer (shell). Drain current, transconductance, and capacitance characteristics demonstrate striking performance improvement compared with conventional junctionless MOSFETs. The addition of the shell results in one order of magnitude higher mobility (peak value), transconductance, and drive current. The doping and thickness of the core can be engineered to achieve a positive threshold voltage for normally-off operation. The CS-JL FET is compatible with back-biasing and downscaling schemes. The physical mechanisms are revealed by emphasizing the roles of the main device parameters.

Preimplantation embryos undergo a series of important biological events, including epigenetic reprogramming and lineage differentiation, and the key genes and specific mechanisms that regulate these events are critical to reproductive success. Ubiquitin-specific protease 7 (USP7) is a deubiquitinase involved in the regulation of a variety of cellular functions, yet its precise function and mechanism in preimplantation embryonic development remain unknown. Our results showed that RNAi-mediated silencing of USP7 in mouse embryos or treatment with P5091, a small molecule inhibitor of USP7, significantly reduced blastocyst rate and blastocyst quality, and decreased total and trophectoderm cell numbers per blastocyst, as well as destroyed normal lineage differentiation. The results of single-cell RNA-seq, reverse transcription-quantitative polymerase chain reaction, western blot, and immunofluorescence staining indicated that interference with USP7 caused failure of the morula-to-blastocyst transition and was accompanied by abnormal expression of key genes (Cdx2, Oct4, Nanog, Sox2) for lineage differentiation, decreased transcript levels, increased global DNA methylation, elevated repressive histone marks (H3K27me3), and decreased active histone marks (H3K4me3 and H3K27ac). Notably, USP7 may regulate the transition from the morula to blastocyst by stabilizing the target protein YAP through the ubiquitin-proteasome pathway. In conclusion, our results suggest that USP7 may play a crucial role in preimplantation embryonic development by regulating lineage differentiation and key epigenetic modifications. Summary Sentence By knocking down USP7 or treating with an inhibitor, the blastocyst rate was significantly reduced. Knockdown of USP7 may cause lineage differentiation failure through deubiquitinating YAP. Furthermore, developmental failure was accompanied by severe disruptions in transcriptional activation and epigenetic modifications. Graphical Abstract

Preimplantation embryos undergo a series of important biological events, including epigenetic reprogramming and lineage differentiation, and the key genes and specific mechanisms that regulate these events are critical to reproductive success. USP7 is a deubiquitinase involved in the regulation of a variety of cellular functions, yet its precise function and mechanism in preimplantation embryonic development remain unknown. Our results showed that RNAi-mediated silencing of USP7 in mouse embryos or treatment with P5091, a small molecule inhibitor of USP7, significantly reduced blastocyst rate and blastocyst quality, and decreased total and TE cell numbers per blastocyst, as well as destroying normal lineage differentiation. The results of single-cell RNA-seq, RT-qPCR, western blot, and immunofluorescence staining indicated that interference with USP7 caused failure of the morula-to-blastocyst transition and was accompanied by abnormal expression of key genes (Cdx2, Oct4, Nanog, Sox2) for lineage differentiation, decreased transcript levels, increased global DNA methylation, elevated repressive histone marks (H3K27me3), and decreased active histone marks (H3K4me3 and H3K27ac). Notably, USP7 may regulate the transition from the morula to blastocyst by stabilizing the target protein YAP through the ubiquitin-proteasome pathway. In conclusion, our results suggest that USP7 may play a crucial role in preimplantation embryonic development by regulating lineage differentiation and key epigenetic modifications.