Interactions between Roseburia intestinalis and diet modulate atherogenesis in a murine model
Kazuyuki Kasahara,Kimberly A. Krautkramer,Elin Org,Kymberleigh A. Romano,Robert L. Kerby,Eugenio I. Vivas,Margarete Mehrabian,John M. Denu,Fredrik Bäckhed,Aldons J. Lusis,Federico E. Rey +10 more
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TL;DR: Roseburia intestinalis is a butyrate-producing member of the gut microbiome that can use dietary plant polysaccharides to alter host metabolism, transcription and epigenetics, and lower inflammation and endotoxaemia, resulting in reduced atherosclerosis.
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Abstract: Humans with metabolic and inflammatory diseases frequently harbour lower levels of butyrate-producing bacteria in their gut. However, it is not known whether variation in the levels of these organisms is causally linked with disease development and whether diet modifies the impact of these bacteria on health. Here we show that a prominent gut-associated butyrate-producing bacterial genus (Roseburia) is inversely correlated with atherosclerotic lesion development in a genetically diverse mouse population. We use germ-free apolipoprotein E-deficient mice colonized with synthetic microbial communities that differ in their capacity to generate butyrate to demonstrate that Roseburia intestinalis interacts with dietary plant polysaccharides to: impact gene expression in the intestine, directing metabolism away from glycolysis and toward fatty acid utilization; lower systemic inflammation; and ameliorate atherosclerosis. Furthermore, intestinal administration of butyrate reduces endotoxaemia and atherosclerosis development. Together, our results illustrate how modifiable diet-by-microbiota interactions impact cardiovascular disease, and suggest that interventions aimed at increasing the representation of butyrate-producing bacteria may provide protection against atherosclerosis.
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Additional file 8 of Gut microbes exacerbate systemic inflammation and behavior disorders in neurologic disease CADASIL
Liu Sheng,Men Xuejiao,Guo Yang,Cai Wei,Gao Rongsui,Zhong Wei-cong,Guo Hua-ting,Ruan Hengfang,Chou Shuli,Jiang Chao,Zhou Hongwei,Zhao Wen-Jing,Lu Zhengqi +12 more
- 09 Sep 2023
Abstract: Additional file 8: Fig. S8. The comparison of VFs in two groups of metagenomic samples. (A) The CPM of total VFs in fecal samples from CADASIL patients and controls. (B) Significantly enriched VFs in the case group that belong to the T6SS category were shown. Case, n=24; Control, n=28.
Additional file 5 of Gut microbes exacerbate systemic inflammation and behavior disorders in neurologic disease CADASIL
Liu Sheng,Men Xuejiao,Guo Yang,Cai Wei,Gao Rongsui,Zhong Wei-cong,Guo Hua-ting,Ruan Hengfang,Chou Shuli,Jiang Chao,Zhou Hongwei,Zhao Wen-Jing,Lu Zhengqi +12 more
- 09 Sep 2023
TL;DR: This study examines the gut microbiome's impact on systemic inflammation and behavior disorders in CADASIL patients, finding significant differences in the relative abundance of top contributing species between control and case groups in four metabolic pathways.
Additional file 1 of Gut microbiota, circulating inflammatory markers and metabolites, and carotid artery atherosclerosis in HIV infection
Wang Zheng,Hanna, David B.,Schwartz Tara,Wang Tao,Post, Wendy S,Landay, Alan L.,Hodis, Howard N.,Weber, Kathleen M.,French, Audrey,Golub, Elizabeth T.,Lazar, Jason,Gustafson, Deborah,Sharma, Anjali,Anastos, Kathryn,Clish, Clary B.,Burk, Robert D.,Kaplan, Robert C.,Knight Rob,Qi, Qibin +18 more
- 13 Aug 2024
Abstract: Additional file 1: Supplementary methods. Supplementary results. Figure S1. Number of participants for omics measurements. Figure S2. Microbial community level assessment. (A) α-diversity analyses by carotid artery plaque status. (B) Principal coordinates analysis (PCoA) of β-diversity using weighted UniFrac distances. Figure S3. Comparison of Amplicon 16S rRNA Sequencing and Shotgun Metagenomics Sequencing: plaque-associated bacterial genera. Figure S4. Spearman correlations between plaque-associated bacterial species and traditional CVD risk factors. Figure S5. Average relative abundance of plaque-associated species by viral suppression, among women on ART. Figure S6. Differentially abundant species according to Carotid Artery Plaque status, stratified by HIV infection. Figure S7. Correlations between plaque-associated bacterial species and plasma metabolites (A) polar metabolites (B) lipids. Figure S8. Associations between microbial species and plaque status, adjusted for metabolomic profiles. Table S1. Characteristics of study participants. Table S2. Characteristics of women on ART, by viral load. Table S3. Associations of gut microbial species with HIV status. Table S4. Associations of gut microbial species with HIV-specific variables, among women with HIV. Table S5. Associations of gut microbial species with Viral load, among women on ART. Table S6. Associations of bacterial species with Plaque status, stratified by HIV status. Table S7. GMB functional enzymes and carotid artery plaque: enrichment test. Table S8. Associations of proteomic inflammatory markers PLSDA PCs with plaque status, stratified by HIV status. Table S9. Associations of GMB-associated metabolites with Plaque status, stratified by HIV status. Table S10. Correlations between bacterial species and Imidazole propionate. Table S11. Conditional analysis (mutual adjustment) highlight key ImP-associated GMB species out of ImP-correlated species. Table S12. Correlations between ImP associate bacterial species and hutH. Table S13. The presence of hutH in specific species: Sequence Alignment analyses.
The amelioration of purified Pleurotus abieticola polysaccharide on atherosclerosis in ApoE−/− mice
Lei Xing,Fange Kong,Chunxia Wang,Lanzhou Li,Shichao Peng,Di Wang,Changtian Li +6 more
TL;DR: This study provides experimental evidence of the auxiliary applicability of PAPS2 in atherosclerosis treatment and shows anti-inflammatory effects partially related to the inhibition of toll-like receptor 4 (TLR4)/nuclear factor kappa-B (NF-κB) signaling induced by lipopolysaccharide (LPS) in RAW 264.7 cells.
Act Locally, Act Globally-Microbiota, Barriers, and Cytokines in Atherosclerosis.
TL;DR: In this article, the authors summarize the knowledge about the function of cytokines at mucosal barriers and the interplay between cytokines, barriers, and microbiota and discuss their known and potential implications for atherosclerosis development.
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Yukihiro Furusawa,Yuuki Obata,Shinji Fukuda,Takaho A. Endo,Gaku Nakato,Daisuke Takahashi,Yumiko Nakanishi,Chikako Uetake,Keiko Kato,Tamotsu Kato,Masumi Takahashi,Noriko N. Fukuda,Shinnosuke Murakami,Eiji Miyauchi,Shingo Hino,Koji Atarashi,Satoshi Onawa,Yumiko Fujimura,Trevor Lockett,Julie M. Clarke,David L. Topping,Masaru Tomita,Shohei Hori,Osamu Ohara,Tatsuya Morita,Haruhiko Koseki,Jun Kikuchi,Kenya Honda,Koji Hase,Hiroshi Ohno +29 more
TL;DR: It is shown that a large bowel microbial fermentation product, butyrate, induces the differentiation of colonic Treg cells in mice and ameliorated the development of colitis induced by adoptive transfer of CD4+ CD45RBhi T cells in Rag1−/− mice.
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Human nutrition, the gut microbiome and the immune system.
Andrew L. Kau,Philip P. Ahern,Nicholas W. Griffin,Andrew L. Goodman,Andrew L. Goodman,Jeffrey I. Gordon +5 more
TL;DR: Understanding how the diet and nutritional status influence the composition and dynamic operations of the authors' gut microbial communities, and the innate and adaptive arms of the immune system, should help to address several pressing global health problems.
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