@article{6dab8a01e4254a768ec016bfe0e179d5,
title = "Host–Microbiota Interactions in the Esophagus During Homeostasis and Allergic Inflammation",
abstract = "Background & Aims: Microbiota composition and mechanisms of host–microbiota interactions in the esophagus are unclear. We aimed to uncover fundamental information about the esophageal microbiome and its potential significance to eosinophilic esophagitis (EoE). Methods: Microbiota composition, transplantation potential, and antibiotic responsiveness in the esophagus were established via 16S ribosomal RNA sequencing. Functional outcomes of microbiota colonization were assessed by RNA sequencing analysis of mouse esophageal epithelium and compared with the human EoE transcriptome. The impact of dysbiosis was assessed using a preclinical model of EoE. Results: We found that the murine esophagus is colonized with diverse microbial communities within the first month of life. The esophageal microbiota is distinct, dominated by Lactobacillales, and demonstrates spatial heterogeneity as the proximal and distal esophagus are enriched in Bifidobacteriales and Lactobacillales, respectively. Fecal matter transplantation restores the esophageal microbiota, demonstrating that the local environment drives diversity. Microbiota colonization modifies esophageal tissue morphology and gene expression that is enriched in pathways associated with epithelial barrier function and overlapping with genes involved in EoE, including POSTN, KLK5, and HIF1A. Finally, neonatal antibiotic treatment reduces the abundance of Lactobacillales and exaggerates type 2 inflammation in the esophagus. Clinical data substantiated loss of esophageal Lactobacillales in EoE compared with controls. Conclusions: The esophagus has a unique microbiome with notable differences between its proximal and distal regions. Fecal matter transplantation restores the esophageal microbiome. Antibiotic-induced dysbiosis exacerbates disease in a murine model of EoE. Collectively, these data establish the composition, transplantation potential, antibiotic responsiveness, and host–microbiota interaction in the esophagus and have implications for gastrointestinal health and disease.",
keywords = "Bifidobacteria, Esophagus, Firmicutes, Lactobacillales, Lactobacillus",
author = "Michael Brusilovsky and Riyue Bao and Mark Rochman and Kemter, {Andrea M.} and Nagler, {Cathryn R.} and Rothenberg, {Marc E.}",
note = "Funding Information: The authors are grateful to Stephanie M. Greenwald and Sarah Owens for 16S ribosomal RNA amplicon library preparation and sequencing at Argonne National Laboratory. The authors would like to thank Shawna Hottinger for editorial support. Michael Brusilovsky, PhD (Conceptualization: Lead; Data curation: Lead; Formal analysis: Lead; Investigation: Lead; Methodology: Lead; Project administration: Lead; Supervision: Lead; Validation: Lead; Visualization: Lead; Writing – original draft: Lead; Writing – review & editing: Lead). Riyue Bao, PhD (Formal analysis: Supporting; Methodology: Equal; Software: Lead; Validation: Supporting; Visualization: Lead; Writing – original draft: Supporting; Writing – review & editing: Supporting). Mark Rochman, PhD (Formal analysis: Equal; Methodology: Equal; Software: Equal; Validation: Supporting; Visualization: Supporting; Writing – original draft: Supporting; Writing – review & editing: Supporting). Andrea M. Kemter, PhD (Investigation: Supporting; Methodology: Supporting; Validation: Supporting; Writing – original draft: Supporting; Writing – review & editing: Supporting). Cathryn R. Nagler, PhD (Conceptualization: Equal; Data curation: Equal; Funding acquisition: Equal; Investigation: Equal; Project administration: Equal; Resources: Equal; Supervision: Equal; Writing – original draft: Equal; Writing – review & editing: Equal). Marc E. Rothenberg, MD, PhD (Conceptualization: Lead; Data curation: Lead; Funding acquisition: Lead; Methodology: Lead; Project administration: Lead; Resources: Lead; Supervision: Lead; Writing – original draft: Lead; Writing – review & editing: Lead). Funding Marc E. Rothenberg was supported by NIH R01 A1045898, the CURED Foundation, and Dave and Denise Bunning Sunshine Foundation. Cathryn R. Nagler was supported by NIH R01 AI146099 and the Moss Family Foundation. The Center for Research Informatics is funded by the Biological Sciences Division at the University of Chicago, with additional support provided by The Institute for Translational Medicine, Clinical and Translational Award (NIH 5UL1 TR002389-02) and The University of Chicago Comprehensive Cancer Center Support Grant (NIH P30 CA014599). Funding Information: Funding Marc E. Rothenberg was supported by NIH R01 A1045898, the CURED Foundation, and Dave and Denise Bunning Sunshine Foundation. Cathryn R. Nagler was supported by NIH R01 AI146099 and the Moss Family Foundation. The Center for Research Informatics is funded by the Biological Sciences Division at the University of Chicago, with additional support provided by The Institute for Translational Medicine, Clinical and Translational Award (NIH 5UL1 TR002389-02) and The University of Chicago Comprehensive Cancer Center Support Grant (NIH P30 CA014599). Publisher Copyright: {\textcopyright} 2022 AGA Institute",
year = "2022",
month = feb,
day = "1",
doi = "10.1053/j.gastro.2021.10.002",
language = "English",
volume = "162",
pages = "521--534.e8",
journal = "Gastroenterology",
issn = "0016-5085",
publisher = "W.B. Saunders Ltd",
number = "2",
}