Literature DB >> 31805442

Three-dimensional electron microscopy analysis reveals endopolygeny-like nuclear architecture segregation in Plasmodium oocyst development.

Tamasa Araki1, Satoru Kawai2, Soichiro Kakuta3, Hirotaka Kobayashi4, Yuko Umeki5, Yumiko Saito-Nakano5, Toshinori Sasaki6, Kisaburo Nagamune7, Yasuhiro Yasutomi8, Tomoyoshi Nozaki9, Blandine Franke-Fayard10, Shahid M Khan10, Hajime Hisaeda5, Takeshi Annoura11.   

Abstract

The genus Plasmodium is a unicellular eukaryotic parasite that is the causative agent of malaria, which is transmitted by Anopheline mosquito. There are a total of three developmental stages in the production of haploid parasites in the Plasmodium life cycle: the oocyst stage in mosquitoes and the liver and blood stages in mammalian hosts. The Plasmodium oocyst stage plays an important role in the production of the first generation of haploid parasites. Nuclear division is the most important event that occurs during the proliferation of all eukaryotes. However, obtaining the details of nuclear division at the oocyst stage is challenging owing to difficulties in preparation. In this study, we used focused-ion-beam-milling combined with scanning-electron-microscopy to report the 3D architecture during nuclear segregations in oocyst stage. This advanced technology allowed us to analyse the 3D details of organelle segregation inside the oocyst during sporogony formation. It was revealed that multiple nuclei were involved with several centrosomes in one germ nucleus during sporozoite budding (endopolygeny). Our high-resolution 3D analysis uncovered the endopolygeny-like nuclear architecture of Plasmodium in the definitive host. This nuclear segregation was different from that in the blood stage, and its similarity to other apicomplexan parasite nuclear divisions such as Sarcocystis is discussed.
Copyright © 2019. Published by Elsevier B.V.

Entities:  

Keywords:  Cell division; Endopolygeny; FIB-SEM; Nuclear division; Oocyst stage development; Organelle; Plasmodium

Year:  2019        PMID: 31805442     DOI: 10.1016/j.parint.2019.102034

Source DB:  PubMed          Journal:  Parasitol Int        ISSN: 1383-5769            Impact factor:   2.230


  5 in total

1.  Fussing About Fission: Defining Variety Among Mainstream and Exotic Apicomplexan Cell Division Modes.

Authors:  Marc-Jan Gubbels; Caroline D Keroack; Sriveny Dangoudoubiyam; Hanna L Worliczek; Aditya S Paul; Ciara Bauwens; Brendan Elsworth; Klemens Engelberg; Daniel K Howe; Isabelle Coppens; Manoj T Duraisingh
Journal:  Front Cell Infect Microbiol       Date:  2020-06-05       Impact factor: 5.293

Review 2.  Plasmodium-a brief introduction to the parasites causing human malaria and their basic biology.

Authors:  Shigeharu Sato
Journal:  J Physiol Anthropol       Date:  2021-01-07       Impact factor: 2.867

3.  Plasmodium sporozoite disintegration during skin passage limits malaria parasite transmission.

Authors:  Jessica Kehrer; Pauline Formaglio; Julianne Mendi Muthinja; Sebastian Weber; Danny Baltissen; Christopher Lance; Johanna Ripp; Janessa Grech; Markus Meissner; Charlotta Funaya; Rogerio Amino; Friedrich Frischknecht
Journal:  EMBO Rep       Date:  2022-04-11       Impact factor: 9.071

4.  Budding pouches and associated bubbles: 3D visualization of exo-membrane structures in plasmodium falciparum gametocytes.

Authors:  Eri Saki H Hayakawa; Marina Wayama; Fuyuki Tokumasu; Nobuhiko Ohno; Mami Matsumoto; Jiro Usukura
Journal:  Front Cell Infect Microbiol       Date:  2022-08-22       Impact factor: 6.073

5.  Three-dimensional ultrastructure of Plasmodium falciparum throughout cytokinesis.

Authors:  Rachel M Rudlaff; Stephan Kraemer; Jeffrey Marshman; Jeffrey D Dvorin
Journal:  PLoS Pathog       Date:  2020-06-08       Impact factor: 6.823

  5 in total

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