Comparative Colonisation Ability of Human Faecal Microbiome Transplantation Strategies in Murine Models DOI Creative Commons
Bon‐Hee Gu,

Ho Young Jung,

Chae‐Yun Rim

и другие.

Microbial Biotechnology, Год журнала: 2025, Номер 18(6)

Опубликована: Май 30, 2025

ABSTRACT The gut microbiome plays a crucial role in maintaining intestinal homeostasis and influencing immune‐mediated diseases. Human faecal microbiota transplantation (FMT) is often employed murine models to investigate the of human microbes disease regulation, but methods for effective colonisation require refinement. This study aimed assess efficiency model using FMT with faeces, focusing particularly on impact depletion via polyethylene glycol (PEG) comparing oral‐gastric gavage enema administration routes. Our findings revealed that PEG‐induced enhanced mice. Oral‐gastric prolonged colonisation, while facilitated quicker resolution dysbiosis, both inducing selective microbial time‐dependent manner. Notably, genera such as Bacteroides , Blautia Medicaternibacter Bifidobacteria were successfully colonised, whereas Roseburia Anaerostipes Anaerobutyricum Faecalibacterium failed establish post‐FMT. These highlight challenges replicating underscore importance selecting appropriate based desired outcomes. provides valuable insights into dynamics mice, contributing development more strategies treatment.

Язык: Английский

AGA Clinical Practice Guideline on Fecal Microbiota–Based Therapies for Select Gastrointestinal Diseases DOI Creative Commons
Anne F. Peery, Colleen Kelly, Dina Kao

и другие.

Gastroenterology, Год журнала: 2024, Номер 166(3), С. 409 - 434

Опубликована: Фев. 21, 2024

Fecal microbiota-based therapies include conventional fecal microbiota transplant and US Food Drug Administration-approved therapies, live-jslm spores live-brpk. The American Gastroenterological Association (AGA) developed this guideline to provide recommendations on the use of in adults with recurrent Clostridioides difficile infection; severe fulminant C inflammatory bowel diseases, including pouchitis; irritable syndrome.

Язык: Английский

Процитировано

68

Fecal microbiota transplantation: current challenges and future landscapes DOI
Abbas Yadegar, Haggai Bar‐Yoseph, Tanya Monaghan

и другие.

Clinical Microbiology Reviews, Год журнала: 2024, Номер 37(2)

Опубликована: Май 8, 2024

SUMMARYGiven the importance of gut microbial homeostasis in maintaining health, there has been considerable interest developing innovative therapeutic strategies for restoring microbiota. One such approach, fecal microbiota transplantation (FMT), is main "whole microbiome replacement" strategy and integrated into clinical practice guidelines treating recurrent

Язык: Английский

Процитировано

53

A systematic framework for understanding the microbiome in human health and disease: from basic principles to clinical translation DOI Creative Commons

Ziqi Ma,

Tao Zuo, Norbert Frey

и другие.

Signal Transduction and Targeted Therapy, Год журнала: 2024, Номер 9(1)

Опубликована: Сен. 23, 2024

Язык: Английский

Процитировано

28

Protective effects of fecal microbiota transplantation against ischemic stroke and other neurological disorders: an update DOI Creative Commons

Tousif Ahmed Hediyal,

Chandrasekaran Vichitra,

Nikhilesh Anand

и другие.

Frontiers in Immunology, Год журнала: 2024, Номер 15

Опубликована: Фев. 21, 2024

The bidirectional communication between the gut and brain or gut-brain axis is regulated by several microbes microbial derived metabolites, such as short-chain fatty acids, trimethylamine N-oxide, lipopolysaccharides. Gut microbiota (GM) produce neuroactives, specifically neurotransmitters that modulates local central neuronal functions. An imbalance intestinal commensals pathobionts leads to a disruption in dysbiosis, which affects barrier integrity gut-immune neuroimmune systems. Currently, fecal transplantation (FMT) recommended for treatment of recurrent

Язык: Английский

Процитировано

17

Probiotics and the microbiota-gut-brain axis in neurodegeneration: Beneficial effects and mechanistic insights DOI
Fatemeh Taghizadeh Ghassab,

Fatemeh Shamlou Mahmoudi,

Reyhaneh Taheri Tinjani

и другие.

Life Sciences, Год журнала: 2024, Номер 350, С. 122748 - 122748

Опубликована: Июнь 5, 2024

Язык: Английский

Процитировано

10

Editorial: Gut microbiota and gastrointestinal disorders, volume II DOI Creative Commons
Abbas Yadegar, Aryan Salahi‐Niri, Yan‐Dong Wang

и другие.

Frontiers in Medicine, Год журнала: 2025, Номер 12

Опубликована: Март 17, 2025

The human gut microbiota, an intricate ecosystem of bacteria, viruses, fungi, and archaea, plays a pivotal role in maintaining gastrointestinal (GI) homeostasis (1). Recent advancements microbiome research have unveiled its profound influence on various GI disorders, including gastric cancer, inflammatory bowel disease (IBD), irritable syndrome (IBS), acute pancreatitis, Clostridioides difficile infection (CDI) (2). Understanding the interplay between microbiota these disorders offers promising avenues for novel therapeutic interventions, next-generation probiotics, fecal transplantation (FMT), targeted microbiome-oriented modulation (3,4).Gastric cancer remains significant global health burden, ranking as fourth leading cause cancer-related mortality. Dysbiosis, characterized by altered microbial diversity composition, is hallmark carcinogenesis (Marashi et al.). Helicobacter pylori wellestablished risk factor, yet eradication alone does not fully restore equilibrium. Studies suggest that certain bacterial species, such Lactobacillus, enhance immunotherapy responses, whereas antibiotic-induced dysbiosis can reduce efficacy chemotherapy al.) (5,6). Probiotic supplementation post-gastrectomy has demonstrated potential mitigating inflammation fostering healthier milieu (7). IBD, encompassing Crohn's ulcerative colitis, immune-mediated disorder driven complex genetic, environmental, factors (Ning (8). Dysbiosis relationship metabolic functions extends beyond tract. Emerging explored bidirectional connection insulin-like growth factor 1 (IGF-1), key regulator growth-related pathways (Zheng been implicated modulating IGF-1 levels, suggesting consequences imbalances. This insight broadens scope microbiome-targeted therapies to include alongside diseases.The expanding knowledge underscores need precision medicine approaches. Personalized profiling could guide tailored optimizing outcomes. Probiotics, prebiotics, synbiotics, nextgeneration microbiome-based therapies, engineered consortia postbiotics, offer exciting prospects. Moreover, metagenomics metabolomics will further elucidate host-microbe interactions, paving way strategies (13).In conclusion, published studies this Research Topic highlight integral determinant disease. From IBS multifaceted (Stange Harnessing interventions holds immense revolutionizing management, shifting from symptomatic treatment root-cause (14). As continues unravel complexities future gastroenterology lies leveraging microscopic powerhouse transformative healthcare solutions.

Язык: Английский

Процитировано

1

Deciphering the Structural and Functional Paradigms of Clostridioides difficile Toxins TcdA and TcdB DOI Creative Commons

Mohammad Qutub,

Amol Tatode, Ujban Hussain

и другие.

Bacteria, Год журнала: 2025, Номер 4(2), С. 21 - 21

Опубликована: Апрель 3, 2025

Clostridioides difficile Infection (CDI) continues to be a major cause of antibiotic-associated diarrhea and pseudomembranous colitis, fueled in large measure by virulence factors TcdA TcdB. These giant glucosyltransferase toxins interfere with host cytoskeletal integrity inflammatory signaling inhibiting Rho GTPase; however, the detailed structural dynamics, receptor selectivity, subcellular trafficking mechanisms remain part unspecified. This review integrates recent insights from cryo-electron microscopy (cryo-EM) X-ray crystallography describe quaternary architecture TcdA/B, emphasizing conformational changes key pore formation endosomal escape. We also examine genomic heterogeneity hypervirulent C. strains (e.g., ribotype 027), correlating toxin gene polymorphisms tcdC mutations) increased production virulence. Mechanistic explanations toxin-driven inflammasome activation epithelial barrier dysfunction are situated within immune evasion mechanisms, including microbiota-derived bile acid regulation stability. Subsequent innovative therapeutic strategies, encompassing utilization engineered neutralizing antibodies that specifically target autoprocessing domain alongside structure-guided small-molecule inhibitors, subjected rigorous evaluation. By integrating biology, systems-level omics, clinical epidemiology, this establishes comprehensive framework for understanding pathogenesis guiding next-generation precision antimicrobials.

Язык: Английский

Процитировано

1

Gut Microbiota Dysbiosis: Pathogenesis, Diseases, Prevention, and Therapy DOI Creative Commons
Vicky Yao,

Nairui Fan,

Shuxia Ma

и другие.

MedComm, Год журнала: 2025, Номер 6(5)

Опубликована: Апрель 18, 2025

ABSTRACT Dysbiosis refers to the disruption of gut microbiota balance and is pathological basis various diseases. The main pathogenic mechanisms include impaired intestinal mucosal barrier function, inflammation activation, immune dysregulation, metabolic abnormalities. These involve dysfunctions in gut–brain axis, gut–liver others cause broader effects. Although association between diseases caused by dysbiosis has been extensively studied, many questions remain regarding specific treatment strategies. This review begins examining causes summarizes potential representative imbalance. It integrates clinical evidence explore preventive therapeutic strategies targeting emphasizing importance understanding dysbiosis. Finally, we summarized development artificial intelligence (AI) research suggested that it will play a critical role future studies on combining multiomics technologies AI further uncover complex drive personalized

Язык: Английский

Процитировано

1

Exploring the role of a novel postbiotic bile acid: Interplay with gut microbiota, modulation of the farnesoid X receptor, and prospects for clinical translation DOI
Beibei Wang, Dong Woo Han, Xin‐Yue Hu

и другие.

Microbiological Research, Год журнала: 2024, Номер 287, С. 127865 - 127865

Опубликована: Авг. 6, 2024

Язык: Английский

Процитировано

9

Fecal microbiota transplantation alters gut phage communities in a clinical trial for obesity DOI Creative Commons

Michele Zuppi,

Tommi Vatanen, Brooke C. Wilson

и другие.

Microbiome, Год журнала: 2024, Номер 12(1)

Опубликована: Июль 6, 2024

Abstract Background Fecal microbiota transplantation (FMT) is a therapeutic intervention used to treat diseases associated with the gut microbiome. In human microbiome, phages have been implicated in influencing health, successful engraftment of donor correlated FMT treatment efficacy. The impact that gastrointestinal exert on health has primarily connected their ability modulate bacterial communities gut. Nonetheless, how affects recipients’ phage populations, and turn, this influences environment, not yet fully understood. study, we investigated effects phageome composition participants within Gut Bugs Trial (GBT), double-blind, randomized, placebo-controlled trial efficacy treating obesity comorbidities adolescents. Stool samples collected from donors at time recipients four points (i.e., baseline 6 weeks, 12 26 weeks post-intervention), underwent shotgun metagenomic sequencing. Phage sequences were identified characterized silico examine evidence assess extent FMT-induced alterations composition. Results Donor engrafted stably following FMT, composing significant proportion for entire course study (33.8 ± 1.2% females 33.9 3.7% males). varied between was positively alpha diversity. caused shift toward donors’ increased diversity variability over time. Conclusions significantly altered recipients' and, overall, microbial populations. increase consistent population dynamics. This proposes play critical role modulating environment suggests novel approaches understanding altering recipient’s registration registered Australian New Zealand Clinical Trials Registry (ACTR N12615001351505). protocol: protocol available https://bmjopen.bmj.com/content/9/4/e026174 .

Язык: Английский

Процитировано

8