98%
921
2 minutes
20
Purpose: This study aimed to examine the linkage between gut microbiome taxa and exercise-induced inflammation.
Methods: Twenty-five cyclists provided 4 stool samples during a 10-week period and cycled vigorously for 2.25 h at 67% maximal oxygen uptake (VO) in a laboratory setting. Blood samples were collected pre- and post-exercise, with additional samples collected at 1.5-h, 3-h, and 24-h post exercise. Primary outcomes included stool microbiome composition and alpha diversity via whole genome shotgun (WGS) sequencing (averaged from 4 stool samples) and a targeted panel of 75 plasma oxylipins. A total of 5719 taxa were identified, and the 339 that were present in more than 20% of stool samples were used in the analysis. Alpha diversity was calculated by evenness, and the Analysis of Composition of Microbiomes (ANCOM) differential abundance analysis was performed using Quantitative Insights Into Microbial Ecology-2 (QIIME2). A composite variable was calculated from 8 pro-inflammatory oxylipins generated from arachidonic acid (ARA) and cytochrome P-450 (CYP).
Results: ARA-CYP oxylipins were significantly elevated for at least 3-h post-exercise (p < 0.001); they were strongly and positively related to Prevotella copri (P. copri) abundance (R = 0.676, p < 0.001) and negatively related to gut microbiome alpha diversity (R = 0.771, p < 0.001).
Conclusion: This analysis revealed for the first time a novel, positive relationship between gut microbiome P. copri abundance in cyclists and post-exercise pro-inflammatory oxylipins. These data demonstrate that about two-thirds of the wide variance in inflammation following prolonged and intensive exercise is largely explained by the abundance of a single gut bacterial species: P. copri.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12145743 | PMC |
http://dx.doi.org/10.1016/j.jshs.2025.101039 | DOI Listing |
Clin Rheumatol
August 2025
Department of Rheumatology, The Second Hospital & Clinical Medical School, Lanzhou University, LanzhouGansu, 730030, China.
Introduction: Accumulating evidence has implicated gut microbiota and their metabolites in primary Sjögren's syndrome (pSS) pathogenesis. However, no study simultaneously explores the gut microbiome, microbial, and plasma metabolome in pSS patients.
Method: Thirty pSS patients and 60 healthy controls (HCs) were recruited.
Antonie Van Leeuwenhoek
August 2025
Department of Biomedical Science, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Two bacterial strains, B2-R-102 and W1-Q-101, were isolated from the feces of a healthy Korean individual. These strains were Gram-stain negative, anaerobic, and non-motile, growing optimally between 20 and 40 °C and at pH 5.5-8.
View Article and Find Full Text PDFBMC Microbiol
August 2025
Faculty of Medicine, Department of Medical Microbiology, Dokuz Eylul University, Izmir, Türkiye.
Background: The human gut microbiota comprises approximately 100 trillion microbial cells and produces a wide range of metabolites. Its composition is shaped by factors such as geography, dietary habits, and genetic background. Dysbiosis-an imbalance in this microbial ecosystem-has been associated with the development of metabolic diseases.
View Article and Find Full Text PDFFront Cell Infect Microbiol
August 2025
Department of Breast Medicine 1, Cancer Hospital of China Medical University, Liaoning Cancer Hospital, Shenyang, China.
Background: Substantial interstudy heterogeneity in cancer immunotherapy-associated biomarkers has hindered their clinical applicability. To address this challenge, we performed a comprehensive integration of publicly available global metagenomic datasets. By leveraging metagenomic profiling and machine learning approaches, this study aimed to elucidate gut microbial signatures associated with immune response in lung cancer (LC) and to evaluate the modulatory effects of antibiotic exposure.
View Article and Find Full Text PDFTurk J Obstet Gynecol
September 2025
Yozgat Bozok University Faculty of Medicine, Department of Obstetrics and Gynecology, Yozgat, Türkiye.
Objective: This study aimed to investigate the relationship between cervical intraepithelial neoplasia associated with human papillomavirus (HPV) infection and the vaginal microbiome.
Materials And Methods: In this study, the vaginal microbiota profile was compared among three groups of women: those with HPV infection and no cervical intraepithelial neoplasia (NILM, n=35), those with low-grade squamous intraepithelial lesions (LSIL, n=28), and those with high-grade squamous intraepithelial lesions (HSIL, n=24). Vaginal bacterial diversity was analyzed by deep sequencing of the V3-4 region of the barcoded gene using the Illumina MiSeq platform, considering alpha diversity, beta diversity, and taxon classifications.