Burn injury alters the intestinal microbiome's taxonomic composition and functional gene expression

被引:32
作者
Beckmann, Nadine [1 ]
Pugh, Amanda M. [1 ]
Caldwell, Charles C. [1 ,2 ]
机构
[1] Univ Cincinnati, Dept Surg, 231 Bethesda Ave, Cincinnati, OH 45267 USA
[2] Shriners Hosp Children, Div Res, Cincinnati, OH 45229 USA
关键词
BACTERIAL TRANSLOCATION; GUT; MICROFLORA; INFECTION; ALIGNMENT; SCALD; ACID;
D O I
10.1371/journal.pone.0205307
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Burn patients have a high risk of sepsis-related mortality even after surviving the initial injury. Immunosuppression increases the risk of sepsis after burn injury, as does the disruption of the intestinal epithelial barrier, which allows the translocation of bacteria and bacterial products into the circulation. The integrity of the intestinal epithelial barrier is largely maintained by the intestinal microbiota. Burn injury has been reported to result in significant changes in the intestinal microbiome composition. In this mouse study, we confirm these taxonomic differences in a full-thickness scald injury model using CF-1 mice. For the first time, we also address alterations in functional gene expression of the intestinal microbiota after burn injury to assess the microbiome's physiological capabilities for overgrowth and pathogenic invasion: 38 pathways were differentially abundant between the sham and burn injury mice, including bacterial invasion of epithelial cells and gap- and adherens junction pathways.
引用
收藏
页数:12
相关论文
共 36 条
[1]   First report of Parabacteroides goldsteinii bacteraemia in a patient with complicated intra-abdominal infection [J].
Awadel-Kariem, F. Mustafa ;
Patel, P. ;
Kapoor, J. ;
Brazier, Jon S. ;
Goldstein, Ellie J. C. .
ANAEROBE, 2010, 16 (03) :223-225
[2]   Systemic inflammatory response syndrome in adult patients with nosocomial bloodstream infections due to enterococci [J].
Bar, Katharine ;
Wisplinghoff, Hilmar ;
Wenzel, Richard P. ;
Bearman, Gonzalo M. L. ;
Edmond, Michael B. .
BMC INFECTIOUS DISEASES, 2006, 6 (1)
[3]   Phylogenetic relationships of butyrate-producing bacteria from the human gut [J].
Barcenilla, A ;
Pryde, SE ;
Martin, JC ;
Duncan, SH ;
Stewart, CS ;
Henderson, C ;
Flint, HJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (04) :1654-1661
[4]   The intestinal microbiota dysbiosis and Clostridium difficile infection: is there a relationship with inflammatory bowel disease? [J].
Bien, Justyna ;
Palagani, Vindhya ;
Bozko, Przemyslaw .
THERAPEUTIC ADVANCES IN GASTROENTEROLOGY, 2013, 6 (01) :53-68
[5]   Trimmomatic: a flexible trimmer for Illumina sequence data [J].
Bolger, Anthony M. ;
Lohse, Marc ;
Usadel, Bjoern .
BIOINFORMATICS, 2014, 30 (15) :2114-2120
[6]   AN ORDINATION OF THE UPLAND FOREST COMMUNITIES OF SOUTHERN WISCONSIN [J].
BRAY, JR ;
CURTIS, JT .
ECOLOGICAL MONOGRAPHS, 1957, 27 (04) :326-349
[7]   Fast and sensitive protein alignment using DIAMOND [J].
Buchfink, Benjamin ;
Xie, Chao ;
Huson, Daniel H. .
NATURE METHODS, 2015, 12 (01) :59-60
[8]   Colonic microflora: Nutrition and health [J].
Cummings, JH ;
MacFarlane, GT .
NUTRITION, 1997, 13 (05) :476-478
[9]   Total Lipopolysaccharide from the Human Gut Microbiome Silences Toll-Like Receptor Signaling [J].
d'Hennezel, Eva ;
Abubucker, Sahar ;
Murphy, Leon O. ;
Cullen, Thomas W. .
MSYSTEMS, 2017, 2 (06)
[10]   Burn Injury Alters the Intestinal Microbiome and Increases Gut Permeability and Bacterial Translocation [J].
Earley, Zachary M. ;
Akhtar, Suhail ;
Green, Stefan J. ;
Naqib, Ankur ;
Khan, Omair ;
Cannon, Abigail R. ;
Hammer, Adam M. ;
Morris, Niya L. ;
Li, Xiaoling ;
Eberhardt, Joshua M. ;
Gamelli, Richard L. ;
Kennedy, Richard H. ;
Choudhry, Mashkoor A. .
PLOS ONE, 2015, 10 (07)