TY - JOUR
T1 - Personalized Gut Mucosal Colonization Resistance to Empiric Probiotics Is Associated with Unique Host and Microbiome Features
AU - Zmora, Niv
AU - Zilberman-Schapira, Gili
AU - Suez, Jotham
AU - Mor, Uria
AU - Dori-Bachash, Mally
AU - Bashiardes, Stavros
AU - Kotler, Eran
AU - Zur, Maya
AU - Regev-Lehavi, Dana
AU - Brik, Rotem Ben-Zeev
AU - Federici, Sara
AU - Cohen, Yotam
AU - Linevsky, Raquel
AU - Rothschild, Daphna
AU - Moor, Andreas E.
AU - Ben-Moshe, Shani
AU - Harmelin, Alon
AU - Itzkovitz, Shalev
AU - Maharshak, Nitsan
AU - Shibolet, Oren
AU - Shapiro, Hagit
AU - Pevsner-Fischer, Meirav
AU - Sharon, Itai
AU - Halpern, Zamir
AU - Segal, Eran
AU - Elinav, Eran
N1 - Publisher Copyright: © 2018 Elsevier Inc.
PY - 2018/9/6
Y1 - 2018/9/6
N2 - Empiric probiotics are commonly consumed by healthy individuals as means of life quality improvement and disease prevention. However, evidence of probiotic gut mucosal colonization efficacy remains sparse and controversial. We metagenomically characterized the murine and human mucosal-associated gastrointestinal microbiome and found it to only partially correlate with stool microbiome. A sequential invasive multi-omics measurement at baseline and during consumption of an 11-strain probiotic combination or placebo demonstrated that probiotics remain viable upon gastrointestinal passage. In colonized, but not germ-free mice, probiotics encountered a marked mucosal colonization resistance. In contrast, humans featured person-, region- and strain-specific mucosal colonization patterns, hallmarked by predictive baseline host and microbiome features, but indistinguishable by probiotics presence in stool. Consequently, probiotics induced a transient, individualized impact on mucosal community structure and gut transcriptome. Collectively, empiric probiotics supplementation may be limited in universally and persistently impacting the gut mucosa, meriting development of new personalized probiotic approaches.
AB - Empiric probiotics are commonly consumed by healthy individuals as means of life quality improvement and disease prevention. However, evidence of probiotic gut mucosal colonization efficacy remains sparse and controversial. We metagenomically characterized the murine and human mucosal-associated gastrointestinal microbiome and found it to only partially correlate with stool microbiome. A sequential invasive multi-omics measurement at baseline and during consumption of an 11-strain probiotic combination or placebo demonstrated that probiotics remain viable upon gastrointestinal passage. In colonized, but not germ-free mice, probiotics encountered a marked mucosal colonization resistance. In contrast, humans featured person-, region- and strain-specific mucosal colonization patterns, hallmarked by predictive baseline host and microbiome features, but indistinguishable by probiotics presence in stool. Consequently, probiotics induced a transient, individualized impact on mucosal community structure and gut transcriptome. Collectively, empiric probiotics supplementation may be limited in universally and persistently impacting the gut mucosa, meriting development of new personalized probiotic approaches.
UR - http://www.scopus.com/inward/record.url?scp=85052760428&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2018.08.041
DO - 10.1016/j.cell.2018.08.041
M3 - مقالة
C2 - 30193112
SN - 0092-8674
VL - 174
SP - 1388-1405.e21
JO - Cell
JF - Cell
IS - 6
ER -