Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.

Malaria parasites reside inside erythrocytes and the disease manifestations are linked to the growth inside infected erythrocytes (IE). The growth of the parasite is mostly confined to the trophozoite stage during which nuclear division occurs followed by the formation of cell bodies (schizogony). T...

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Main Authors: Sudipta Das, Himanish Basu, Reshma Korde, Rita Tewari, Shobhona Sharma
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3415463?pdf=render
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spelling doaj-6d8aaf7b8f59478f9225277e17e7cb3b2020-11-25T00:57:28ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742012-01-0188e100285810.1371/journal.ppat.1002858Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.Sudipta DasHimanish BasuReshma KordeRita TewariShobhona SharmaMalaria parasites reside inside erythrocytes and the disease manifestations are linked to the growth inside infected erythrocytes (IE). The growth of the parasite is mostly confined to the trophozoite stage during which nuclear division occurs followed by the formation of cell bodies (schizogony). The mechanism and regulation of schizogony are poorly understood. Here we show a novel role for a Plasmodium falciparum 60S stalk ribosomal acidic protein P2 (PfP2) (PFC0400w), which gets exported to the IE surface for 6-8 hrs during early schizogony, starting around 26-28 hrs post-merozoite invasion. The surface exposure is demonstrated using multiple PfP2-specific monoclonal antibodies, and is confirmed through transfection using PfP2-GFP. The IE surface-exposed PfP2-protein occurs mainly as SDS-resistant P2-homo-tetramers. Treatment with anti-PfP2 monoclonals causes arrest of IEs at the first nuclear division. Upon removal of the antibodies, about 80-85% of synchronized parasites can be released even after 24 hrs of antibody treatment. It has been reported that a tubovesicular network (TVN) is set up in early trophozoites which is used for nutrient import. Anti-P2 monoclonal antibodies cause a complete fragmentation of TVN by 36 hrs, and impairs lipid import in IEs. These may be downstream causes for the cell-cycle arrest. Upon antibody removal, the TVN is reconstituted, and the cell division progresses. Each of the above properties is observed in the rodent malaria parasite species P. yoelii and P. berghei. The translocation of the P2 protein to the IE surface is therefore likely to be of fundamental importance in Plasmodium cell division.http://europepmc.org/articles/PMC3415463?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sudipta Das
Himanish Basu
Reshma Korde
Rita Tewari
Shobhona Sharma
spellingShingle Sudipta Das
Himanish Basu
Reshma Korde
Rita Tewari
Shobhona Sharma
Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
PLoS Pathogens
author_facet Sudipta Das
Himanish Basu
Reshma Korde
Rita Tewari
Shobhona Sharma
author_sort Sudipta Das
title Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
title_short Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
title_full Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
title_fullStr Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
title_full_unstemmed Arrest of nuclear division in Plasmodium through blockage of erythrocyte surface exposed ribosomal protein P2.
title_sort arrest of nuclear division in plasmodium through blockage of erythrocyte surface exposed ribosomal protein p2.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2012-01-01
description Malaria parasites reside inside erythrocytes and the disease manifestations are linked to the growth inside infected erythrocytes (IE). The growth of the parasite is mostly confined to the trophozoite stage during which nuclear division occurs followed by the formation of cell bodies (schizogony). The mechanism and regulation of schizogony are poorly understood. Here we show a novel role for a Plasmodium falciparum 60S stalk ribosomal acidic protein P2 (PfP2) (PFC0400w), which gets exported to the IE surface for 6-8 hrs during early schizogony, starting around 26-28 hrs post-merozoite invasion. The surface exposure is demonstrated using multiple PfP2-specific monoclonal antibodies, and is confirmed through transfection using PfP2-GFP. The IE surface-exposed PfP2-protein occurs mainly as SDS-resistant P2-homo-tetramers. Treatment with anti-PfP2 monoclonals causes arrest of IEs at the first nuclear division. Upon removal of the antibodies, about 80-85% of synchronized parasites can be released even after 24 hrs of antibody treatment. It has been reported that a tubovesicular network (TVN) is set up in early trophozoites which is used for nutrient import. Anti-P2 monoclonal antibodies cause a complete fragmentation of TVN by 36 hrs, and impairs lipid import in IEs. These may be downstream causes for the cell-cycle arrest. Upon antibody removal, the TVN is reconstituted, and the cell division progresses. Each of the above properties is observed in the rodent malaria parasite species P. yoelii and P. berghei. The translocation of the P2 protein to the IE surface is therefore likely to be of fundamental importance in Plasmodium cell division.
url http://europepmc.org/articles/PMC3415463?pdf=render
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