4.4 Article

Establishment of Three Francisella Infections in Zebrafish Embryos at Different Temperatures

Journal

INFECTION AND IMMUNITY
Volume 82, Issue 6, Pages 2180-2194

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00077-14

Keywords

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Funding

  1. Norwegian School of Veterinary Sciences
  2. University of Oslo
  3. Research Council of Norway

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Francisella spp. are facultative intracellular pathogens identified in increasingly diverse hosts, including mammals. F. noatunensis subsp. orientalis and F. noatunensis subsp. noatunensis infect fish inhabiting warm and cold waters, respectively, while F. tularensis subsp. novicida is highly infectious for mice and has been widely used as a model for the human pathogen F. tularensis. Here, we established zebrafish embryo infection models of fluorescently labeled F. noatunensis subsp. noatunensis, F. noatunensis subsp. orientalis, and F. tularensis subsp. novicida at 22, 28, and 32 C, respectively. All infections led to significant bacterial growth, as shown by reverse transcription- quantitative PCR (RT-qPCR), and to a robust proinflammatory immune response, dominated by increased transcription of tumor necrosis factor alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta). F. noatunensis subsp. orientalis was the most virulent, F. noatunensis subsp. noatunensis caused chronic infection, and F. tularensis subsp. novicida showed moderate virulence and led to formation of relatively small granuloma-like structures. The use of transgenic zebrafish strains with enhanced green fluorescent protein (EGFP)-labeled immune cells revealed their detailed interactions with Francisella species. All three strains entered preferentially into macrophages, which eventually assembled into granulomalike structures. Entry into neutrophils was also observed, though the efficiency of this event depended on the route of infection. The results demonstrate the usefulness of the zebrafish embryo model for studying infections caused by different Francisella species at a wide range of temperatures and highlight their interactions with immune cells.

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