| Literature DB >> 32495834 |
Torben Sølbeck Rasmussen1, Anna Kirstine Koefoed1, Rasmus Riemer Jakobsen1, Ling Deng1, Josué L Castro-Mejía1, Anders Brunse2, Horst Neve3, Finn Kvist Vogensen1, Dennis Sandris Nielsen1.
Abstract
Gut microbiome (GM) composition and function are linked to human health and disease, and routes for manipulating the GM have become an area of intense research. Due to its high treatment efficacy, the use of fecal microbiota transplantation (FMT) is generally accepted as a promising experimental treatment for patients suffering from GM imbalances (dysbiosis), e.g. caused by recurrent Clostridioides difficile infections (rCDI). Mounting evidence suggests that bacteriophages (phages) play a key role in successful FMT treatment by restoring the dysbiotic bacterial GM. As a refinement to FMT, removing the bacterial component of donor feces by sterile filtration, also referred to as fecal virome transplantation (FVT), decreases the risk of invasive infections caused by bacteria. However, eukaryotic viruses and prophage-encoded virulence factors remain a safety issue. Recent in vivo studies show how cascading effects are initiated when phage communities are transferred to the gut by e.g. FVT, which leads to changes in the GM composition, host metabolome, and improve host health such as alleviating symptoms of obesity and type-2-diabetes (T2D). In this review, we discuss the promises and limitations of FVT along with the perspectives of using FVT to treat various diseases associated with GM dysbiosis. © FEMS 2020.Entities:
Keywords: bacteriophages; cascading effects; dysbiosis; fecal virome transplantation; gut microbiome; phage therapy
Year: 2020 PMID: 32495834 DOI: 10.1093/femsre/fuaa020
Source DB: PubMed Journal: FEMS Microbiol Rev ISSN: 0168-6445 Impact factor: 16.408