» Articles » PMID: 37699894

Phage-microbe Dynamics After Sterile Faecal Filtrate Transplantation in Individuals with Metabolic Syndrome: a Double-blind, Randomised, Placebo-controlled Clinical Trial Assessing Efficacy and Safety

Overview
Journal Nat Commun
Specialty Biology
Date 2023 Sep 12
PMID 37699894
Authors
Affiliations
Soon will be listed here.
Abstract

Bacteriophages (phages) are bacterial viruses that have been shown to shape microbial communities. Previous studies have shown that faecal virome transplantation can decrease weight gain and normalize blood glucose tolerance in diet-induced obese mice. Therefore, we performed a double-blind, randomised, placebo-controlled pilot study in which 24 individuals with metabolic syndrome were randomised to a faecal filtrate transplantation (FFT) from a lean healthy donor (n = 12) or placebo (n = 12). The primary outcome, change in glucose metabolism, and secondary outcomes, safety and longitudinal changes within the intestinal bacteriome and phageome, were assessed from baseline up to 28 days. All 24 included subjects completed the study and are included in the analyses. While the overall changes in glucose metabolism are not significantly different between both groups, the FFT is well-tolerated and without any serious adverse events. The phage virion composition is significantly altered two days after FFT as compared to placebo, which coincides with more virulent phage-microbe interactions. In conclusion, we provide evidence that gut phages can be safely administered to transiently alter the gut microbiota of recipients.

Citing Articles

Causal role of the gut microbiome in certain human diseases: a narrative review.

Prosty C, Katergi K, Papenburg J, Lawandi A, Lee T, Shi H eGastroenterology. 2025; 2(3):e100086.

PMID: 39944364 PMC: 11770457. DOI: 10.1136/egastro-2024-100086.


The role of the early-life gut microbiome in childhood asthma.

Boulund U, Thorsen J, Trivedi U, Tranaes K, Jiang J, Shah S Gut Microbes. 2025; 17(1):2457489.

PMID: 39882630 PMC: 11784655. DOI: 10.1080/19490976.2025.2457489.


Bacterial and viral assemblages in ulcerative colitis patients following fecal microbiota and fecal filtrate transfer.

Junca H, Steube A, Mrowietz S, Stallhofer J, Vital M, Dos Anjos Borges L ISME Commun. 2025; 5(1):ycae167.

PMID: 39830095 PMC: 11740987. DOI: 10.1093/ismeco/ycae167.


The role of fecal microbiota transplantation in type 2 diabetes mellitus treatment.

Wang H, Li S, Zhang L, Zhang N Front Endocrinol (Lausanne). 2024; 15:1469165.

PMID: 39735647 PMC: 11671274. DOI: 10.3389/fendo.2024.1469165.


Impact of Gut Microbiome Interventions on Glucose and Lipid Metabolism in Metabolic Diseases: A Systematic Review and Meta-Analysis.

Mederle A, Dima M, Stoicescu E, Capastraru B, Levai C, Hategan O Life (Basel). 2024; 14(11).

PMID: 39598283 PMC: 11595434. DOI: 10.3390/life14111485.


References
1.
Cammarota G, Ianiro G, Tilg H, Rajilic-Stojanovic M, Kump P, Satokari R . European consensus conference on faecal microbiota transplantation in clinical practice. Gut. 2017; 66(4):569-580. PMC: 5529972. DOI: 10.1136/gutjnl-2016-313017. View

2.
Hoyles L, McCartney A, Neve H, Gibson G, Sanderson J, Heller K . Characterization of virus-like particles associated with the human faecal and caecal microbiota. Res Microbiol. 2014; 165(10):803-12. DOI: 10.1016/j.resmic.2014.10.006. View

3.
Patel A, Noble R, Steele J, Schwalbach M, Hewson I, Fuhrman J . Virus and prokaryote enumeration from planktonic aquatic environments by epifluorescence microscopy with SYBR Green I. Nat Protoc. 2007; 2(2):269-76. DOI: 10.1038/nprot.2007.6. View

4.
Dabke K, Hendrick G, Devkota S . The gut microbiome and metabolic syndrome. J Clin Invest. 2019; 129(10):4050-4057. PMC: 6763239. DOI: 10.1172/JCI129194. View

5.
Nurk S, Meleshko D, Korobeynikov A, Pevzner P . metaSPAdes: a new versatile metagenomic assembler. Genome Res. 2017; 27(5):824-834. PMC: 5411777. DOI: 10.1101/gr.213959.116. View