Distinct signals from the microbiota promote different aspects of zebrafish gut differentiation

被引:473
作者
Bates, Jennifer M.
Mittge, Erika
Kuhlman, Julie
Baden, Katrina N.
Cheesman, Sarah E.
Guillemin, Karen [1 ]
机构
[1] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
[2] Univ Oregon, Inst Neurosci, Eugene, OR 97403 USA
关键词
zebrafish; intestine; gut; epithelial maturation; microbiota; microflora; bacteria; lipopolysaccharide; intestinal alkaline phosphatase; Gal alpha 1,3Gal glycan;
D O I
10.1016/j.ydbio.2006.05.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
All animals exist in intimate associations with microorganisms that play important roles in the hosts' normal development and tissue physiology. In vertebrates, the most populous and complex community of microbes resides in the digestive tract. Here, we describe the establishment of the gut microbiota and its role in digestive tract differentiation in the zebrafish model vertebrate, Danio rerio. We find that in the absence of the microbiota, the gut epithelium is arrested in aspects of its differentiation, as revealed by the lack of brush border intestinal alkaline phosphatase activity, the maintenance of immature patterns of glycan expression and a paucity of goblet and enteroendocrine cells. In addition, germ-free intestines fail to take up protein macromolecules in the distal intestine and exhibit faster motility. Reintroduction of a complex microbiota at later stages of development or mono-association of germ-free larvae with individual constituents of the microbiota reverses all of these germ-free phenotypes. Exposure of germ-free zebrafish to heat-killed preparations of the microbiota or bacterial lipopolysaccharide is sufficient to restore alkaline phosphatase activity but not mature patterns of Gal alpha 1,3Gal containing glycans, indicating that the host perceives and responds to its associated microbiota. by at least two distinct pathways. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:374 / 386
页数:13
相关论文
共 66 条
[11]   LECTINS ARE SENSITIVE TOOLS FOR DEFINING THE DIFFERENTIATION PROGRAMS OF MOUSE GUT EPITHELIAL-CELL LINEAGES [J].
FALK, P ;
ROTH, KA ;
GORDON, JI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :G987-G1003
[12]   Creating and maintaining the gastrointestinal ecosystem: What we know and need to know from gnotobiology [J].
Falk, PG ;
Hooper, LV ;
Midtvedt, T ;
Gordon, JI .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (04) :1157-+
[13]   Is persistent bacterial infection good for your health? [J].
Falkow, S .
CELL, 2006, 124 (04) :699-702
[14]   Genetic analysis of digestive physiology using fluorescent phospholipid reporters [J].
Farber, SA ;
Pack, M ;
Ho, SY ;
Johnson, LD ;
Wagner, DS ;
Dosch, R ;
Mullins, MC ;
Hendrickson, HS ;
Hendrickson, EK ;
Halpern, ME .
SCIENCE, 2001, 292 (5520) :1385-1388
[15]   Notch signals control the fate of immature progenitor cells in the intestine [J].
Fre, S ;
Huyghe, M ;
Mourikis, P ;
Robine, S ;
Louvard, D ;
Artavanis-Tsakonas, S .
NATURE, 2005, 435 (7044) :964-968
[16]   Non-pathogenic bacteria modulate colonic epithelial gene expression in germ-free mice [J].
Fukushima, K ;
Ogawa, H ;
Takahashi, K ;
Naito, H ;
Funayama, Y ;
Kitayama, T ;
Yonezawa, H ;
Sasaki, I .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2003, 38 (06) :626-634
[17]  
Galili U, 1999, Subcell Biochem, V32, P1
[18]   Nerves, reflexes, and the enteric nervous system - Pathogenesis of the irritable bowel syndrome [J].
Gershon, MD .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2005, 39 (04) :S184-S193
[19]   Diverse restriction fragment length polymorphism patterns of the PCR-amplified 16S rRNA genes in Aeromonas veronii strains and possible misidentification of Aeromonas species [J].
Graf, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (10) :3194-3197
[20]   Wnt signaling in the intestinal epithelium: from endoderm to cancer [J].
Gregorieff, A ;
Clevers, H .
GENES & DEVELOPMENT, 2005, 19 (08) :877-890