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Msg  32027 of 34492  at  3/1/2010 6:16:13 PM  by

chernobyltermite

Strong Buy

using ZFNs to study host-pathogen interactions

Current Opinion in Immunology
Article in Press, Corrected Proof - Note to users

doi:10.1016/j.coi.2010.01.006 | How to Cite or Link Using DOI
Copyright © 2010 Published by Elsevier Ltd.



Host–microbe interactions in the developing zebrafish




References and further reading may be available for this article. To view references and further reading you must purchase this article.

Michelle Kanther1, 2 and John F Rawls2, 3, E-mail The Corresponding Author

1 Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

2 Department of Cell and Molecular Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

3 Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA


Available online 12 February 2010.

The amenability of the zebrafish to in vivo imaging and genetic analysis has fueled expanded use of this vertebrate model to investigate the molecular and cellular foundations of host–microbe relationships. Study of microbial encounters in zebrafish hosts has concentrated on developing embryonic and larval stages, when the advantages of the zebrafish model are maximized. A comprehensive understanding of these host–microbe interactions requires appreciation of the developmental context into which a microbe is introduced, as well as the effects of that microbial challenge on host ontogeny. In this review, we discuss how in vivo imaging and genetic analysis in zebrafish has advanced our knowledge of host–microbe interactions in the context of a developing vertebrate host. We focus on recent insights into immune cell ontogeny and function, commensal microbial relationships in the intestine, and microbial pathogenesis in zebrafish hosts.



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Figure 1. Developmental milestones in zebrafish host–microbe interactions. Schematic depiction of anatomical sites (a) and approximate durations (b) of hematopoietic activity in developing zebrafish. The eye (e), yolk (y) and gastrointestinal tract (gray) are indicated in a. Relocation of definitive hematopoietic stem cells (HSCs) between sites is represented by arrows in b. Primitive erythropoiesis occurs in the intermediate cell mass (ICM, blue) which is active not,  vert, similar11–30 hpf [59], whereas primitive myelopoiesis begins in the rostral blood island (RBI) and later the yolk (pink) from not,  vert, similar12 to 40 hpf [11]. HSCs appear in the aorta-gonad-mesonephros region (AGM, red) not,  vert, similar26 hpf until not,  vert, similar3 dpf [[15] and [16]]. These HSCs are mobilized to seed the caudal hematopoietic tissue (PBI/CHT; green) and pronephros (brown) as early as 32 hpf, and the thymus (purple) as early as 48 hpf [[14], [15], [16] and [17]]. Definitive hematopoiesis in the CHT begins de novo not,  vert, similar24 hpf [13] and continues until at least 14 dpf [14]. Cells from the CHT contribute to the pronephros and thymus as early as 48 hpf [[14] and [15]]. B cell development initates in the pancreas (orange) starting 4 dpf [21], although the hematopoietic origins of these cells remain unknown. The thymus, pancreas, and pronephros/kidney subsequently serve as sites of definitive hematopoiesis into adult stages [[9] and [10]]. (c) Within this dynamic developmental context, important milestones relevant to zebrafish immunity and microbial interactions are indicated and referenced.



 
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