TY - JOUR
T1 - Fecal microbiota transplantation as tool to study the interrelation between microbiota composition and miRNA expression
AU - Wortelboer, Koen
AU - Bakker, Guido J.
AU - Winkelmeijer, Maaike
AU - van Riel, Natal
AU - Levin, Evgeni
AU - Nieuwdorp, Max
AU - Herrema, Hilde
AU - Davids, Mark
N1 - Funding Information:
KW is supported by a Novo Nordisk Foundation CAMIT grant 2018 ( 28232 ). MN is supported by a DFN-DON grant 2020 ( 2020.10.002 ) and a ZONMW VICI grant 2020 ( 09150182010020 ). NvR is supported by a ZONMW Metabolic Adaptation , Transitions and Resilience in Overweight individualS (MATRyOSka) grant ( 645.001.003 ). HH is supported by a Senior Fellowship of the Dutch Diabetes Research Foundation ( 2019.82.004 ). The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/4/1
Y1 - 2022/4/1
N2 - The intestinal gut microbiota is important for human metabolism and immunity and can be influenced by many host factors. A recently emerged host factor is secreted microRNA (miRNA). Previously, it has been shown that secreted miRNAs can influence the growth of certain bacteria and conversely, that shifts in the microbiota can alter the composition of secreted miRNAs. Here, we sought to further investigate the interaction between the gut microbiota and secreted miRNAs by the use of fecal microbiota transplantation (FMT). Subjects with the metabolic syndrome received either an autologous (n = 4) or allogenic (n = 14) FMT. Fecal samples were collected at baseline and 6 weeks after FMT, from which the microbiome and miRNA composition were determined via 16S rRNA sequencing and miRNA sequencing, respectively. We observed a significant correlation between the fecal miRNA expression and microbiota composition, both before and after FMT. Our results suggest that the FMT-induced shift in microbiota altered the fecal miRNA profile, indicated by correlations between differentially abundant microbes and miRNAs. This idea of a shift in miRNA composition driven by changes in the microbiota was further strengthened by the absence of a direct effect of specific miRNAs on the growth of specific bacterial strains.
AB - The intestinal gut microbiota is important for human metabolism and immunity and can be influenced by many host factors. A recently emerged host factor is secreted microRNA (miRNA). Previously, it has been shown that secreted miRNAs can influence the growth of certain bacteria and conversely, that shifts in the microbiota can alter the composition of secreted miRNAs. Here, we sought to further investigate the interaction between the gut microbiota and secreted miRNAs by the use of fecal microbiota transplantation (FMT). Subjects with the metabolic syndrome received either an autologous (n = 4) or allogenic (n = 14) FMT. Fecal samples were collected at baseline and 6 weeks after FMT, from which the microbiome and miRNA composition were determined via 16S rRNA sequencing and miRNA sequencing, respectively. We observed a significant correlation between the fecal miRNA expression and microbiota composition, both before and after FMT. Our results suggest that the FMT-induced shift in microbiota altered the fecal miRNA profile, indicated by correlations between differentially abundant microbes and miRNAs. This idea of a shift in miRNA composition driven by changes in the microbiota was further strengthened by the absence of a direct effect of specific miRNAs on the growth of specific bacterial strains.
KW - Fecal microbiota transplantation
KW - Intestinal microbiome
KW - Metabolic syndrome
KW - Microbiota
KW - microRNA
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123701181&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/35091345
U2 - 10.1016/j.micres.2022.126972
DO - 10.1016/j.micres.2022.126972
M3 - Article
C2 - 35091345
SN - 0944-5013
VL - 257
JO - Microbiological Research
JF - Microbiological Research
M1 - 126972
ER -