Stable engraftment of human microbiota into mice with a single oral gavage following antibiotic conditioning

被引:131
作者
Staley, Christopher [1 ]
Kaiser, Thomas [1 ]
Beura, Lalit K. [2 ,3 ]
Hamilton, Matthew J. [1 ]
Weingarden, Alexa R. [1 ]
Bobr, Aleh [2 ,4 ]
Kang, Johnthomas [2 ,4 ]
Masopust, David [2 ,3 ]
Sadowsky, Michael J. [1 ,5 ]
Khoruts, Alexander [1 ,2 ,4 ]
机构
[1] Univ Minnesota, BioTechnol Inst, St Paul, MN 55108 USA
[2] Univ Minnesota, Ctr Immunol, 2101 6th St SE,Room 3-184,Wallin Med Biosci Bldg, Minneapolis, MN 55414 USA
[3] Univ Minnesota, Dept Microbiol & Immunol, Minneapolis, MN 55414 USA
[4] Univ Minnesota, Dept Med, Div Gastroenterol, Minneapolis, MN 55414 USA
[5] Univ Minnesota, Dept Soil Water & Climate, St Paul, MN 55108 USA
来源
MICROBIOME | 2017年 / 5卷
关键词
Antibiotics; Fecal microbiota transplantation; Germ-free; Humanization; Mouse model; FECAL MICROBIOTA; IMMUNE-SYSTEM; COMMENSAL BACTERIA; GUT MICROBIOTA; HOST; TRANSPLANTATION; ECOLOGY; MODEL; IMPROVEMENT; METABOLISM;
D O I
10.1186/s40168-017-0306-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Human microbiota-associated (HMA) animal models relying on germ-free recipient mice are being used to study the relationship between intestinal microbiota and human disease. However, transfer of microbiota into germ-free animals also triggers global developmental changes in the recipient intestine, which can mask disease-specific attributes of the donor material. Therefore, a simple model of replacing microbiota into a developmentally mature intestinal environment remains highly desirable. Results: Here we report on the development of a sequential, three-course antibiotic conditioning regimen that allows sustained engraftment of intestinal microorganisms following a single oral gavage with human donor microbiota. SourceTracker, a Bayesian, OTU-based algorithm, indicated that 59.3 +/- 3.0% of the fecal bacterial communities in treated mice were attributable to the donor source. This overall degree of microbiota engraftment was similar in mice conditioned with antibiotics and germ-free mice. Limited surveys of systemic and mucosal immune sites did not show evidence of immune activation following introduction of human microbiota. Conclusions: The antibiotic treatment protocol described here followed by a single gavage of human microbiota may provide a useful, complimentary HMA model to that established in germ-free facilities. The model has the potential for further in-depth translational investigations of microbiota in a variety of human disease states.
引用
收藏
页数:13
相关论文
共 61 条
  • [11] AN ORDINATION OF THE UPLAND FOREST COMMUNITIES OF SOUTHERN WISCONSIN
    BRAY, JR
    CURTIS, JT
    [J]. ECOLOGICAL MONOGRAPHS, 1957, 27 (04) : 326 - 349
  • [12] Commensal bacteria at the interface of host metabolism and the immune system
    Brestoff, Jonathan R.
    Artis, David
    [J]. NATURE IMMUNOLOGY, 2013, 14 (07) : 676 - 684
  • [13] Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
    Caporaso, J. Gregory
    Lauber, Christian L.
    Walters, William A.
    Berg-Lyons, Donna
    Huntley, James
    Fierer, Noah
    Owens, Sarah M.
    Betley, Jason
    Fraser, Louise
    Bauer, Markus
    Gormley, Niall
    Gilbert, Jack A.
    Smith, Geoff
    Knight, Rob
    [J]. ISME JOURNAL, 2012, 6 (08) : 1621 - 1624
  • [14] Gut Immune Maturation Depends on Colonization with a Host-Specific Microbiota
    Chung, Hachung
    Pamp, Suenje J.
    Hill, Jonathan A.
    Surana, Neeraj K.
    Edelman, Sanna M.
    Troy, Erin B.
    Reading, Nicola C.
    Villablanca, Eduardo J.
    Wang, Sen
    Mora, Jorge R.
    Umesaki, Yoshinori
    Mathis, Diane
    Benoist, Christophe
    Relman, David A.
    Kasper, Dennis L.
    [J]. CELL, 2012, 149 (07) : 1578 - 1593
  • [15] Comparison of two next-generation sequencing technologies for resolving highly complex microbiota composition using tandem variable 16S rRNA gene regions
    Claesson, Marcus J.
    Wang, Qiong
    O'Sullivan, Orla
    Greene-Diniz, Rachel
    Cole, James R.
    Ross, R. Paul
    O'Toole, Paul W.
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 (22) : e200
  • [16] NONPARAMETRIC MULTIVARIATE ANALYSES OF CHANGES IN COMMUNITY STRUCTURE
    CLARKE, KR
    [J]. AUSTRALIAN JOURNAL OF ECOLOGY, 1993, 18 (01): : 117 - 143
  • [17] The Ribosomal Database Project: improved alignments and new tools for rRNA analysis
    Cole, J. R.
    Wang, Q.
    Cardenas, E.
    Fish, J.
    Chai, B.
    Farris, R. J.
    Kulam-Syed-Mohideen, A. S.
    McGarrell, D. M.
    Marsh, T.
    Garrity, G. M.
    Tiedje, J. M.
    [J]. NUCLEIC ACIDS RESEARCH, 2009, 37 : D141 - D145
  • [18] Altering the Intestinal Microbiota during a Critical Developmental Window Has Lasting Metabolic Consequences
    Cox, Laura M.
    Yamanishi, Shingo
    Sohn, Jiho
    Alekseyenko, Alexander V.
    Leung, Jacqueline M.
    Cho, Ilseung
    Kim, Sungheon G.
    Li, Huilin
    Gao, Zhan
    Mahana, Douglas
    Rodriguez, Jorge G. Zarate
    Rogers, Arlin B.
    Robine, Nicolas
    Loke, P'ng
    Blaser, Martin J.
    [J]. CELL, 2014, 158 (04) : 705 - 721
  • [19] The Microbiome and Inflammatory Bowel Disease: Is There a Therapeutic Role for Fecal Microbiota Transplantation?
    Damman, Christopher J.
    Miller, Samuel I.
    Surawicz, Christina M.
    Zisman, Timothy L.
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2012, 107 (10) : 1452 - 1459
  • [20] Functional Profiling of Unfamiliar Microbial Communities Using a Validated De Novo Assembly Metatranscriptome Pipeline
    Davids, Mark
    Hugenholtz, Floor
    dos Santos, Vitor Martins
    Smidt, Hauke
    Kleerebezem, Michiel
    Schaap, Peter J.
    [J]. PLOS ONE, 2016, 11 (01):