TY - JOUR
T1 - Moderate Traumatic Brain Injury Alters the Gastrointestinal Microbiome in a Time-Dependent Manner
AU - Nicholson, Susannah E.
AU - Watts, Lora T.
AU - Burmeister, David M.
AU - Merrill, Daniel
AU - Scroggins, Shannon
AU - Zou, Yi
AU - Lai, Zhao
AU - Grandhi, Ramesh
AU - Lewis, Aaron M.
AU - Newton, Larry M.
AU - Eastridge, Brian J.
AU - Schwacha, Martin G.
N1 - Funding Information:
Address reprint requests to Susannah E. Nicholson, MD, Department of Surgery, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78229. E-mail: Nicholson@uthscsa.edu The project described was supported by the National Center for Advancing Translational Sciences, National Institutes of Health, through Grant KL2 TR001118. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH or the Department of the Army and the Department of Defense. Support was also received by the University of Texas Health Science Center at San Antonio Military Health Institute, the Bob Kelso Endowment awarded to the UTHSCSA Department of Surgery and The Greehey Children’s Cancer Research Institute Genome Sequencing Facility’s Illumina MiSeq Pilot Grant. The authors report no conflicts of interest. DOI: 10.1097/SHK.0000000000001211 Copyright © 2019 by the Shock Society
Publisher Copyright:
© 2019 by the Shock Society.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - The microbiome is defined as the collective genomes of the microbes (composed of bacteria, bacteriophage, fungi, protozoa, and viruses) that colonize the human body, and alterations have been associated with a number of disease states. Changes in gut commensals can influence the neurologic system via the brain-gut axis, and systemic insults such as trauma or traumatic brain injury (TBI) may alter the gut microbiome. The objective of this study was to evaluate the gut microbiome in a preclinical TBI cortical impact model. Male rats underwent craniotomy and randomized to a sham group (n=4), or a moderate TBI (n=10) using a pneumatic impactor. MRI and behavioral assessments were performed pre-TBI and on days 2, 7, and 14 days thereafter. Microbiome composition was determined with 16s rRNA sequencing from fecal sample DNA pre-TBI and 2 hrs, 1, 3, and 7 days afterward. Alpha- and β-bacterial diversity, as well as organizational taxonomic units (OTUs), were determined. Significant changes in the gut microbiome were evident as early as 2 h after TBI as compared with pre-injured samples and sham rats. While there were varying trends among the phylogenetic families across time, some changes persisted through 7 days in the absence of therapeutic intervention. While large structural lesions and behavioral deficits were apparent post-TBI, there were modest but significant decreases in α-diversity. Moreover, both changes in representative phyla and α-diversity measures were significantly correlated with MRI-determined lesion volume. These results suggest that changes in the microbiome may represent a novel biomarker to stage TBI severity and predict functional outcome.
AB - The microbiome is defined as the collective genomes of the microbes (composed of bacteria, bacteriophage, fungi, protozoa, and viruses) that colonize the human body, and alterations have been associated with a number of disease states. Changes in gut commensals can influence the neurologic system via the brain-gut axis, and systemic insults such as trauma or traumatic brain injury (TBI) may alter the gut microbiome. The objective of this study was to evaluate the gut microbiome in a preclinical TBI cortical impact model. Male rats underwent craniotomy and randomized to a sham group (n=4), or a moderate TBI (n=10) using a pneumatic impactor. MRI and behavioral assessments were performed pre-TBI and on days 2, 7, and 14 days thereafter. Microbiome composition was determined with 16s rRNA sequencing from fecal sample DNA pre-TBI and 2 hrs, 1, 3, and 7 days afterward. Alpha- and β-bacterial diversity, as well as organizational taxonomic units (OTUs), were determined. Significant changes in the gut microbiome were evident as early as 2 h after TBI as compared with pre-injured samples and sham rats. While there were varying trends among the phylogenetic families across time, some changes persisted through 7 days in the absence of therapeutic intervention. While large structural lesions and behavioral deficits were apparent post-TBI, there were modest but significant decreases in α-diversity. Moreover, both changes in representative phyla and α-diversity measures were significantly correlated with MRI-determined lesion volume. These results suggest that changes in the microbiome may represent a novel biomarker to stage TBI severity and predict functional outcome.
KW - Brain-gut axis
KW - commensals
KW - gastrointestinal (GI)
KW - gut
KW - microbiome
KW - traumatic brain injury (TBI)
UR - http://www.scopus.com/inward/record.url?scp=85069901874&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85069901874&partnerID=8YFLogxK
U2 - 10.1097/SHK.0000000000001211
DO - 10.1097/SHK.0000000000001211
M3 - Article
C2 - 29953417
AN - SCOPUS:85069901874
SN - 1073-2322
VL - 52
SP - 240
EP - 248
JO - Shock
JF - Shock
IS - 2
ER -