Osteoarthritis induced by destabilization of the medial meniscus is reduced in germ-free mice

被引:100
作者
Ulici, V. [1 ]
Kelley, K. L. [1 ]
Azcarate-Peril, M. A. [2 ,3 ]
Cleveland, R. J. [1 ]
Sartor, R. B. [4 ,5 ]
Schwartz, T. A. [1 ,6 ]
Loeser, R. F. [1 ]
机构
[1] Univ North Carolina Chapel Hill, Thurston Arthrit Res Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, Div Gastroenterol & Hepatol, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, Microbiome Core Facil, Ctr Gastrointestinal Biol & Dis, Sch Med, Chapel Hill, NC 27515 USA
[4] Univ North Carolina Chapel Hill, Div Gastroenterol & Hepatol, Dept Med, Chapel Hill, NC USA
[5] Univ North Carolina Chapel Hill, Gnotobiot Core Facil, Ctr Gastrointestinal Biol & Dis, Sch Med, Chapel Hill, NC USA
[6] Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Biostat, Chapel Hill, NC 27515 USA
关键词
Osteoarthritis; Cartilage; Microbiome; Germ-free; DMM; LBP; GUT MICROBIOTA; RHEUMATOID-ARTHRITIS; IMMUNE-SYSTEM; MURINE MODEL; INFLAMMATION; EXPRESSION; RESISTANCE; DYSBIOSIS; SEVERITY; DELETION;
D O I
10.1016/j.joca.2018.05.016
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Objective: To determine the contribution of the gut microbiota to the development of injury-induced osteoarthritis (OA). Design: OA was induced using the destabilized medial meniscus (DMM) model in 20 germ-free (GF) C57BL/ 6J male mice housed in a gnotobiotic facility and 23 strain-matched specific pathogen free (SPF) mice in 2 age groups -13.5 weeks avg age at DMM (17 SPF and 15 GF) and 43 weeks avg age at DMM (6 SPF and 5 GF). OA severity was measured using scores for articular cartilage structure (ACS), loss of safranin O (SafO) staining, osteophyte size, and synovial hyperplasia. Microbiome analysis by 16S rRNA amplicon sequencing was performed on stool samples and LPS and LPS binding protein (LBP) were measured in plasma. Results: Compared to the SPF DMM mice, the maximum (MAX) ACS score per joint was 28% lower (p = 0.036) in GF DMM mice while the SafO sum score of all sections evaluated per joint was decreased by 31% (p = 0.009). The differences between SPF and GF mice in these scores were greater when only the younger mice were included in the analysis. The younger GF DMM mice also had significant reductions in osteophyte size (36%, P = 0.0119) and LBP (27%, P = 0.007) but not synovial scores or LPS. Differences in relative abundance of a number of Operational Taxonomic Units (OTUs) were noted between SPF mice with high vs low maximum ACS scores. Conclusions: These results suggest factors related to the gut microbiota promote the development of OA after joint injury. (c) 2018 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1098 / 1109
页数:12
相关论文
共 34 条
[1]
A comparison of sequencing platforms and bioinformatics pipelines for compositional analysis of the gut microbiome [J].
Allali, Imane ;
Arnold, Jason W. ;
Roach, Jeffrey ;
Cadenas, Maria Belen ;
Butz, Natasha ;
Hassan, Hosni M. ;
Koci, Matthew ;
Ballou, Anne ;
Mendoza, Mary ;
Ali, Rizwana ;
Azcarate-Peril, M. Andrea .
BMC MICROBIOLOGY, 2017, 17
[2]
[Anonymous], SCI REP UK
[3]
Pre-rheumatoid arthritis: predisposition and transition to clinical synovitis [J].
Arend, William P. ;
Firestein, Gary S. .
NATURE REVIEWS RHEUMATOLOGY, 2012, 8 (10) :573-586
[4]
Mechanisms underlying the resistance to diet-induced obesity in germ-free mice [J].
Backhed, Fredrik ;
Manchester, Jill K. ;
Semenkovich, Clay F. ;
Gordon, Jeffrey I. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (03) :979-984
[5]
Regulation of inflammation by microbiota interactions with the host [J].
Blander, J. Magarian ;
Longman, Randy S. ;
Iliev, Iliyan D. ;
Sonnenberg, Gregory F. ;
Artis, David .
NATURE IMMUNOLOGY, 2017, 18 (08) :851-860
[6]
Gut-derived lipopolysaccharide augments adipose macrophage accumulation but is not essential for impaired glucose or insulin tolerance in mice [J].
Caesar, Robert ;
Reigstad, Christopher S. ;
Backhed, Helene Kling ;
Reinhardt, Christoph ;
Ketonen, Maria ;
Lunden, Gunnel Ostergren ;
Cani, Patrice D. ;
Backhed, Fredrik .
GUT, 2012, 61 (12) :1701-1707
[7]
Relationship between inflammation, the gut microbiota, and metabolic osteoarthritis development: studies in a rat model [J].
Collins, K. H. ;
Paul, H. A. ;
Reimer, R. A. ;
Seerattan, R. A. ;
Hart, D. A. ;
Herzog, W. .
OSTEOARTHRITIS AND CARTILAGE, 2015, 23 (11) :1989-1998
[8]
Intestinal Dysbiosis in Ankylosing Spondylitis [J].
Costello, Mary-Ellen ;
Ciccia, Francesco ;
Willner, Dana ;
Warrington, Nicole ;
Robinson, Philip C. ;
Gardiner, Brooke ;
Marshall, Mhairi ;
Kenna, Tony J. ;
Triolo, Giovanni ;
Brown, Matthew A. .
ARTHRITIS & RHEUMATOLOGY, 2015, 67 (03) :686-691
[9]
Microbes, the gut and ankylosing spondylitis [J].
Costello, Mary-Ellen ;
Elewaut, Dirk ;
Kenna, Tony J. ;
Brown, Matthew A. .
ARTHRITIS RESEARCH & THERAPY, 2013, 15 (03)
[10]
Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes [J].
Creely, S. J. ;
McTernan, P. G. ;
Kusminski, C. M. ;
Fisher, Ff. M. ;
Da Silva, N. F. ;
Khanolkar, M. ;
Evans, M. ;
Harte, A. L. ;
Kumar, S. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2007, 292 (03) :E740-E747