Correlative light-electron microscopy methods to characterize the ultrastructural features of the replicative and dormant liver stages of Plasmodium parasites

被引:1
|
作者
Mitchell, Gabriel [1 ]
Torres, Laura [1 ]
Fishbaugher, Matthew E. [2 ]
Lam, Melanie [1 ]
Chuenchob, Vorada [2 ]
Zalpuri, Reena [3 ]
Ramasubban, Shreya [3 ]
Baxter, Caitlin N. [3 ]
Flannery, Erika L. [2 ]
Harupa, Anke [2 ]
Mikolajczak, Sebastian A. [2 ]
Jorgens, Danielle M. [3 ]
机构
[1] Novartis, Open Innovat Global Hlth Dis Area, Biomed Res, Emeryville, CA 02139 USA
[2] Novartis, Global Hlth Dis Area, Biomed Res, Emeryville, CA USA
[3] Univ Calif Berkeley, Electron Microscope Lab, Berkeley, CA USA
关键词
Plasmodium berghei; Plasmodium cynomolgi; CLEM; TEM; Schizonts; Hypnozoites; Relapsing malaria; Transmission electron microscopy; Hepatocytes; Mitochondria; MITOCHONDRIA;
D O I
10.1186/s12936-024-04862-w
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundThe infection of the liver by Plasmodium parasites is an obligatory step leading to malaria disease. Following hepatocyte invasion, parasites differentiate into replicative liver stage schizonts and, in the case of Plasmodium species causing relapsing malaria, into hypnozoites that can lie dormant for extended periods of time before activating. The liver stages of Plasmodium remain elusive because of technical challenges, including low infection rate. This has been hindering experimentations with well-established technologies, such as electron microscopy. A deeper understanding of hypnozoite biology could prove essential in the development of radical cure therapeutics against malaria. ResultsThe liver stages of the rodent parasite Plasmodium berghei, causing non-relapsing malaria, and the simian parasite Plasmodium cynomolgi, causing relapsing malaria, were characterized in human Huh7 cells or primary non-human primate hepatocytes using Correlative Light-Electron Microscopy (CLEM). Specifically, CLEM approaches that rely on GFP-expressing parasites (GFP-CLEM) or on an immunofluorescence assay (IFA-CLEM) were used for imaging liver stages. The results from P. berghei showed that host and parasite organelles can be identified and imaged at high resolution using both CLEM approaches. While IFA-CLEM was associated with more pronounced extraction of cellular content, samples' features were generally well preserved. Using IFA-CLEM, a collection of micrographs was acquired for P. cynomolgi liver stage schizonts and hypnozoites, demonstrating the potential of this approach for characterizing the liver stages of Plasmodium species causing relapsing malaria. ConclusionsA CLEM approach that does not rely on parasites expressing genetically encoded tags was developed, therefore suitable for imaging the liver stages of Plasmodium species that lack established protocols to perform genetic engineering. This study also provides a dataset that characterizes the ultrastructural features of liver stage schizonts and hypnozoites from the simian parasite species P. cynomolgi.
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页数:13
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