Cargando…

Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development

BACKGROUND: The phylum Apicomplexa includes intracellular parasites causing immense global disease burden, the deadliest of them being the human malaria parasite Plasmodium falciparum, which invades and replicates within erythrocytes. The cytoskeletal protein actin is well conserved within apicomple...

Descripción completa

Detalles Bibliográficos
Autores principales: Das, Sujaan, Lemgruber, Leandro, Tay, Chwen L., Baum, Jake, Meissner, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557482/
https://www.ncbi.nlm.nih.gov/pubmed/28810863
http://dx.doi.org/10.1186/s12915-017-0406-2
_version_ 1783257214439391232
author Das, Sujaan
Lemgruber, Leandro
Tay, Chwen L.
Baum, Jake
Meissner, Markus
author_facet Das, Sujaan
Lemgruber, Leandro
Tay, Chwen L.
Baum, Jake
Meissner, Markus
author_sort Das, Sujaan
collection PubMed
description BACKGROUND: The phylum Apicomplexa includes intracellular parasites causing immense global disease burden, the deadliest of them being the human malaria parasite Plasmodium falciparum, which invades and replicates within erythrocytes. The cytoskeletal protein actin is well conserved within apicomplexans but divergent from mammalian actins, and was primarily reported to function during host cell invasion. However, novel invasion mechanisms have been described for several apicomplexans, and specific functions of the acto-myosin system are being reinvestigated. Of the two actin genes in P. falciparum, actin-1 (pfact1) is ubiquitously expressed in all life-cycle stages and is thought to be required for erythrocyte invasion, although its functions during parasite development are unknown, and definitive in vivo characterisation during invasion is lacking. RESULTS: Here we have used a conditional Cre-lox system to investigate the functions of PfACT1 during P. falciparum blood-stage development and host cell invasion. We demonstrate that PfACT1 is crucially required for segregation of the plastid-like organelle, the apicoplast, and for efficient daughter cell separation during the final stages of cytokinesis. Surprisingly, we observe that egress from the host cell is not an actin-dependent process. Finally, we show that parasites lacking PfACT1 are capable of microneme secretion, attachment and formation of a junction with the erythrocyte, but are incapable of host cell invasion. CONCLUSIONS: This study provides important mechanistic insights into the definitive essential functions of PfACT1 in P. falciparum, which are not only of biological interest, but owing to functional divergence from mammalian actins, could also form the basis for the development of novel therapeutics against apicomplexans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0406-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5557482
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55574822017-08-16 Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development Das, Sujaan Lemgruber, Leandro Tay, Chwen L. Baum, Jake Meissner, Markus BMC Biol Research Article BACKGROUND: The phylum Apicomplexa includes intracellular parasites causing immense global disease burden, the deadliest of them being the human malaria parasite Plasmodium falciparum, which invades and replicates within erythrocytes. The cytoskeletal protein actin is well conserved within apicomplexans but divergent from mammalian actins, and was primarily reported to function during host cell invasion. However, novel invasion mechanisms have been described for several apicomplexans, and specific functions of the acto-myosin system are being reinvestigated. Of the two actin genes in P. falciparum, actin-1 (pfact1) is ubiquitously expressed in all life-cycle stages and is thought to be required for erythrocyte invasion, although its functions during parasite development are unknown, and definitive in vivo characterisation during invasion is lacking. RESULTS: Here we have used a conditional Cre-lox system to investigate the functions of PfACT1 during P. falciparum blood-stage development and host cell invasion. We demonstrate that PfACT1 is crucially required for segregation of the plastid-like organelle, the apicoplast, and for efficient daughter cell separation during the final stages of cytokinesis. Surprisingly, we observe that egress from the host cell is not an actin-dependent process. Finally, we show that parasites lacking PfACT1 are capable of microneme secretion, attachment and formation of a junction with the erythrocyte, but are incapable of host cell invasion. CONCLUSIONS: This study provides important mechanistic insights into the definitive essential functions of PfACT1 in P. falciparum, which are not only of biological interest, but owing to functional divergence from mammalian actins, could also form the basis for the development of novel therapeutics against apicomplexans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-017-0406-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-15 /pmc/articles/PMC5557482/ /pubmed/28810863 http://dx.doi.org/10.1186/s12915-017-0406-2 Text en © Meissner et al. 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Das, Sujaan
Lemgruber, Leandro
Tay, Chwen L.
Baum, Jake
Meissner, Markus
Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title_full Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title_fullStr Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title_full_unstemmed Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title_short Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development
title_sort multiple essential functions of plasmodium falciparum actin-1 during malaria blood-stage development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557482/
https://www.ncbi.nlm.nih.gov/pubmed/28810863
http://dx.doi.org/10.1186/s12915-017-0406-2
work_keys_str_mv AT dassujaan multipleessentialfunctionsofplasmodiumfalciparumactin1duringmalariabloodstagedevelopment
AT lemgruberleandro multipleessentialfunctionsofplasmodiumfalciparumactin1duringmalariabloodstagedevelopment
AT taychwenl multipleessentialfunctionsofplasmodiumfalciparumactin1duringmalariabloodstagedevelopment
AT baumjake multipleessentialfunctionsofplasmodiumfalciparumactin1duringmalariabloodstagedevelopment
AT meissnermarkus multipleessentialfunctionsofplasmodiumfalciparumactin1duringmalariabloodstagedevelopment