4.5 Article

CLARITY and PACT-based imaging of adult zebrafish and mouse for whole-animal analysis of infections

Journal

DISEASE MODELS & MECHANISMS
Volume 8, Issue 12, Pages 1643-1650

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dmm.021394

Keywords

Zebrafish; Infection; PACT; CLARITY; Imaging; Mouse; Tuberculosis; Mycobacteria

Funding

  1. American Cancer Society Postdoctoral Fellowship [PF-13-223-01-MPC]
  2. Australian National Health and Medical Research Council CJ Martin Early Career Fellowship
  3. National Science Foundation Graduate Research Fellowship
  4. Duke University Center for AIDS Research, a National Institutes of Health (NIH) [5P30 AI064518]
  5. Mallinckrodt Scholar Award
  6. Searle Scholar Award
  7. Vallee Foundation Young Investigator Award
  8. Duke School of Medicine and Clinical and Translational Science Award Core Facility Voucher [UL1TR001117]
  9. NIH [1DP2-OD008614]
  10. NIH/NIAID [1R21AI111067]

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Visualization of infection and the associated host response has been challenging in adult vertebrates. Owing to their transparency, zebrafish larvae have been used to directly observe infection in vivo; however, such larvae have not yet developed a functional adaptive immune system. Cells involved in adaptive immunity mature later and have therefore been difficult to access optically in intact animals. Thus, the study of many aspects of vertebrate infection requires dissection of adult organs or ex vivo isolation of immune cells. Recently, CLARITY and PACT (passive clarity technique) methodologies have enabled clearing and direct visualization of dissected organs. Here, we show that these techniques can be applied to image host-pathogen interactions directly in whole animals. CLARITY and PACT-based clearing of whole adult zebrafish and Mycobacterium tuberculosis-infected mouse lungs enables imaging of mycobacterial granulomas deep within tissue to a depth of more than 1 mm. Using established transgenic lines, we were able to image normal and pathogenic structures and their surrounding host context at high resolution. We identified the three-dimensional organization of granuloma-associated angiogenesis, an important feature of mycobacterial infection, and characterized the induction of the cytokine tumor necrosis factor (TNF) within the granuloma using an established fluorescent reporter line. We observed heterogeneity in TNF induction within granuloma macrophages, consistent with an evolving view of the tuberculous granuloma as a non-uniform, heterogeneous structure. Broad application of this technique will enable new understanding of host-pathogen interactions in situ.

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