4.7 Article

Methods for generating and colonizing gnotobiotic zebrafish

Journal

NATURE PROTOCOLS
Volume 3, Issue 12, Pages 1862-1875

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2008.186

Keywords

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Funding

  1. National Institutes of Health [DK073695, DK34987, DK07737, RR018603]
  2. University of North Carolina
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [P40RR018603] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK034987, K01DK073695, T32DK007737] Funding Source: NIH RePORTER

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Vertebrates are colonized at birth by complex and dynamic communities of microorganisms that can contribute significantly to host health and disease. The ability to raise animals in the absence of microorganisms has been a powerful tool for elucidating the relationships between animal hosts and their microbial residents. The optical transparency of the developing zebrafish and relative ease of generating germ-free (GF) zebrafish make it an attractive model organism for gnotobiotic research. Here we provide a protocol for generating zebrafish embryos; deriving and rearing GF zebrafish; and colonizing zebrafish with microorganisms. Using these methods, we typically obtain 80-90% sterility rates in our GF derivations with 90% survival in GF animals and 50-90% survival in colonized animals through larval stages. Obtaining embryos for derivation requires approximately 1-2 h, with a 3- to 8-h incubation period before derivation. Derivation of GF animals takes 1-1.5 h, and daily maintenance requires 1-2 h.

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