4.6 Article

Differentiating Trypanosoma cruzi in a Host Mammalian Cell Imaged in Aqueous Liquid by Atmospheric Scanning Electron Microscopy

期刊

MICROBIOLOGY SPECTRUM
卷 10, 期 1, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.01413-21

关键词

kinetoplastida; electron microscopy; fluorescent image analysis; infectious disease; intracellular parasites; protozoa

资金

  1. Japan Society for the Promotion of Science KAKENHI [18K15141, 19K10091, 19H04209]
  2. CANON
  3. Grants-in-Aid for Scientific Research [18K15141, 19K10091, 19H04209] Funding Source: KAKEN

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Atmospheric Scanning Electron Microscopy (ASEM) is a powerful tool for high-resolution observation of wet specimens under atmospheric pressure. In this study, researchers successfully visualized the infection cycle of Trypanosoma cruzi in host mammalian cells using ASEM, which provided important insights into the internal structures of the parasite and the dynamic changes of host cellular structures.
Atmospheric Scanning Electron Microscopy (ASEM) is a powerful tool to observe a wet specimen at high resolution under atmospheric pressure. Here, we visualized a protozoan parasite Trypanosoma cruzi over the course of its infection cycle in the host mammalian cell. This is the first observation of intracellular parasite using a liquid-phase EM. Unlike regular SEM, aldehyde-fixed cell body of T. cruzi appears translucent, allowing the visualization of internal structures such as kinetoplast of trypomastigote and nucleus of amastigote. Plasma membrane of the host mammalian cell also appears translucent, which enabled direct observation of differentiating intracellular parasites and dynamic change of host cellular structures in their near-natural states. Various water-rich structures including micro- and macro- vesicles were visualized around T. cruzi. In addition, Correlative Light and Electron Microscopy exploiting open sample dish of ASEM allowed identification of parasite nucleus and transfected fluorescence-labeled parasites soon after internalization, while location of this morphological intermediate was otherwise obscure. Successful visualization of the differentiation of T. cruzi within the host cell demonstrated here opens up the possibility of using ASEM for observation of variety of intracellular parasites. IMPORTANCE Using Atmospheric Scanning Electron Microscopy (ASEM), we visualized interaction between infectious stage of Trypanosoma cruzi and completely intact host mammalian cell. Plasma membrane appears translucent under ASEM, which not only enables direct observation of T. cruzi within its host cell, but also reveals internal structures of the parasite itself. Sample deformation is minimal, since the specimen remains hydrated under atmospheric pressure at all times. This nature of ASEM, along with the open structure of ASEM sample dish, is suited for correlative light-electron microscopy, which can further be exploited in identification of fluorescent protein in the intracellular parasites.

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