Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy

Author:

Liffner Benjamin1ORCID,Cepeda Diaz Ana Karla23ORCID,Blauwkamp James1ORCID,Anaguano David45,Frolich Sonja67ORCID,Muralidharan Vasant45ORCID,Wilson Danny W678ORCID,Dvorin Jeffrey D39ORCID,Absalon Sabrina1ORCID

Affiliation:

1. Department of Pharmacology and Toxicology, Indiana University School of Medicine

2. Biological and Biomedical Sciences, Harvard Medical School

3. Division of Infectious Diseases, Boston Children’s Hospital

4. Center for Tropical and Emerging Global Diseases, University of Georgia

5. Department of Cellular Biology, Franklin College of Arts and Sciences, University of Georgia

6. Research Centre for Infectious Diseases, School of Biological Sciences, University of Adelaide

7. Institute for Photonics and Advanced Sensing, University of Adelaide

8. Burnet Institute, 85 Commercial Road

9. Department of Pediatrics, Harvard Medical School

Abstract

Apicomplexan parasites exhibit tremendous diversity in much of their fundamental cell biology, but study of these organisms using light microscopy is often hindered by their small size. Ultrastructural expansion microscopy (U-ExM) is a microscopy preparation method that physically expands the sample by ~4.5×. Here, we apply U-ExM to the human malaria parasite Plasmodium falciparum during the asexual blood stage of its lifecycle to understand how this parasite is organized in three dimensions. Using a combination of dye-conjugated reagents and immunostaining, we have cataloged 13 different P. falciparum structures or organelles across the intraerythrocytic development of this parasite and made multiple observations about fundamental parasite cell biology. We describe that the outer centriolar plaque and its associated proteins anchor the nucleus to the parasite plasma membrane during mitosis. Furthermore, the rhoptries, Golgi, basal complex, and inner membrane complex, which form around this anchoring site while nuclei are still dividing, are concurrently segregated and maintain an association to the outer centriolar plaque until the start of segmentation. We also show that the mitochondrion and apicoplast undergo sequential fission events while maintaining an association with the outer centriolar plaque during cytokinesis. Collectively, this study represents the most detailed ultrastructural analysis of P. falciparum during its intraerythrocytic development to date and sheds light on multiple poorly understood aspects of its organelle biogenesis and fundamental cell biology.

Funder

American Heart Association

National Institutes of Health

NHMRC

Hospital Research Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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