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...
Autores principales: | , , , , |
---|---|
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 |