TY - JOUR
T1 - A multi-factorial observational study on sequential fecal microbiota transplant in patients with medically refractory clostridioides difficile infection
AU - Monaghan, Tanya M.
AU - Duggal, Niharika A.
AU - Rosati, Elisa
AU - Griffin, Ruth
AU - Hughes, Jamie
AU - Roach, Brandi
AU - Yang, David Y.
AU - Wang, Christopher
AU - Wong, Karen
AU - Saxinger, Lynora
AU - Pučić-Baković, Maja
AU - Vučković, Frano
AU - Klicek, Filip
AU - Lauc, Gordan
AU - Tighe, Paddy
AU - Mullish, Benjamin H.
AU - Blanco, Jesus Miguens
AU - McDonald, Julie A.K.
AU - Marchesi, Julian R.
AU - Xue, Ning
AU - Dottorini, Tania
AU - Acharjee, Animesh
AU - Franke, Andre
AU - Li, Yingrui
AU - Wong, Gane Ka Shu
AU - Polytarchou, Christos
AU - Yau, Tung On
AU - Christodoulou, Niki
AU - Hatziapostolou, Maria
AU - Wang, Minkun
AU - Russell, Lindsey A.
AU - Kao, Dina H.
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/11
Y1 - 2021/11
N2 - Fecal microbiota transplantation (FMT) is highly effective in recurrent Clostridioides difficile infection (CDI); increasing evidence supports FMT in severe or fulminant Clostridioides difficile infection (SFCDI). However, the multifactorial mechanisms that underpin the efficacy of FMT are not fully understood. Systems biology approaches using high-throughput technologies may help with mechanistic dissection of host-microbial interactions. Here, we have undertaken a deep phenomics study on four adults receiving sequential FMT for SFCDI, in which we performed a longitudinal, integrative analysis of multiple host factors and intestinal microbiome changes. Stool samples were profiled for changes in gut microbiota and metabolites and blood samples for alterations in targeted epigenomic, metabonomic, glycomic, immune proteomic, immunophenotyping, immune functional assays, and T-cell receptor (TCR) repertoires, respectively. We characterised temporal trajectories in gut microbial and host immunometabolic data sets in three responders and one non-responder to sequential FMT. A total of 562 features were used for analysis, of which 78 features were identified, which differed between the responders and the non-responder. The observed dynamic phenotypic changes may potentially suggest immunosenescent signals in the non-responder and may help to underpin the mechanisms accompanying successful FMT, although our study is limited by a small sample size and significant heterogeneity in patient baseline characteristics. Our multi-omics integrative longitudinal analytical approach extends the knowledge regarding mechanisms of efficacy of FMT and highlights preliminary novel signatures, which should be validated in larger studies.
AB - Fecal microbiota transplantation (FMT) is highly effective in recurrent Clostridioides difficile infection (CDI); increasing evidence supports FMT in severe or fulminant Clostridioides difficile infection (SFCDI). However, the multifactorial mechanisms that underpin the efficacy of FMT are not fully understood. Systems biology approaches using high-throughput technologies may help with mechanistic dissection of host-microbial interactions. Here, we have undertaken a deep phenomics study on four adults receiving sequential FMT for SFCDI, in which we performed a longitudinal, integrative analysis of multiple host factors and intestinal microbiome changes. Stool samples were profiled for changes in gut microbiota and metabolites and blood samples for alterations in targeted epigenomic, metabonomic, glycomic, immune proteomic, immunophenotyping, immune functional assays, and T-cell receptor (TCR) repertoires, respectively. We characterised temporal trajectories in gut microbial and host immunometabolic data sets in three responders and one non-responder to sequential FMT. A total of 562 features were used for analysis, of which 78 features were identified, which differed between the responders and the non-responder. The observed dynamic phenotypic changes may potentially suggest immunosenescent signals in the non-responder and may help to underpin the mechanisms accompanying successful FMT, although our study is limited by a small sample size and significant heterogeneity in patient baseline characteristics. Our multi-omics integrative longitudinal analytical approach extends the knowledge regarding mechanisms of efficacy of FMT and highlights preliminary novel signatures, which should be validated in larger studies.
KW - Clostridioides difficile
KW - Fecal microbiota transplantation
KW - Host-microbial interactions
KW - Immunosenescence
KW - Systems biology
UR - http://www.scopus.com/inward/record.url?scp=85119293584&partnerID=8YFLogxK
U2 - 10.3390/cells10113234
DO - 10.3390/cells10113234
M3 - Article
C2 - 34831456
AN - SCOPUS:85119293584
SN - 2073-4409
VL - 10
JO - Cells
JF - Cells
IS - 11
M1 - 3234
ER -