Cargando…

Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites

Merozoite invasion of host red blood cells (RBCs) is essential for survival of the human malaria parasite Plasmodium falciparum. Proteins involved with RBC binding and invasion are secreted from dual-club shaped organelles at the apical tip of the merozoite called the rhoptries. Here we characterise...

Descripción completa

Detalles Bibliográficos
Autores principales: Liffner, Benjamin, Balbin, Juan Miguel, Shami, Gerald J., Siddiqui, Ghizal, Strauss, Jan, Frölich, Sonja, Heinemann, Gary K., Edwards, Ella May, Alder, Arne, Wichers, Jan Stephan, Creek, Darren J., Tilley, Leann, Dixon, Matthew W. A., Gilberger, Tim-Wolf, Wilson, Danny W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828742/
https://www.ncbi.nlm.nih.gov/pubmed/35140336
http://dx.doi.org/10.1038/s42003-022-03020-9
_version_ 1784647908853809152
author Liffner, Benjamin
Balbin, Juan Miguel
Shami, Gerald J.
Siddiqui, Ghizal
Strauss, Jan
Frölich, Sonja
Heinemann, Gary K.
Edwards, Ella May
Alder, Arne
Wichers, Jan Stephan
Creek, Darren J.
Tilley, Leann
Dixon, Matthew W. A.
Gilberger, Tim-Wolf
Wilson, Danny W.
author_facet Liffner, Benjamin
Balbin, Juan Miguel
Shami, Gerald J.
Siddiqui, Ghizal
Strauss, Jan
Frölich, Sonja
Heinemann, Gary K.
Edwards, Ella May
Alder, Arne
Wichers, Jan Stephan
Creek, Darren J.
Tilley, Leann
Dixon, Matthew W. A.
Gilberger, Tim-Wolf
Wilson, Danny W.
author_sort Liffner, Benjamin
collection PubMed
description Merozoite invasion of host red blood cells (RBCs) is essential for survival of the human malaria parasite Plasmodium falciparum. Proteins involved with RBC binding and invasion are secreted from dual-club shaped organelles at the apical tip of the merozoite called the rhoptries. Here we characterise P. falciparum Cytosolically Exposed Rhoptry Leaflet Interacting protein 2 (PfCERLI2), as a rhoptry bulb protein that is essential for merozoite invasion. Phylogenetic analyses show that cerli2 arose through an ancestral gene duplication of cerli1. We show that PfCERLI2 is essential for blood-stage growth and localises to the cytosolic face of the rhoptry bulb. Inducible knockdown of PfCERLI2 led to a proportion of merozoites failing to invade and was associated with elongation of the rhoptry organelle during merozoite development and inhibition of rhoptry antigen processing. These findings identify PfCERLI2 as a protein that has key roles in rhoptry biology during merozoite invasion.
format Online
Article
Text
id pubmed-8828742
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-88287422022-02-24 Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites Liffner, Benjamin Balbin, Juan Miguel Shami, Gerald J. Siddiqui, Ghizal Strauss, Jan Frölich, Sonja Heinemann, Gary K. Edwards, Ella May Alder, Arne Wichers, Jan Stephan Creek, Darren J. Tilley, Leann Dixon, Matthew W. A. Gilberger, Tim-Wolf Wilson, Danny W. Commun Biol Article Merozoite invasion of host red blood cells (RBCs) is essential for survival of the human malaria parasite Plasmodium falciparum. Proteins involved with RBC binding and invasion are secreted from dual-club shaped organelles at the apical tip of the merozoite called the rhoptries. Here we characterise P. falciparum Cytosolically Exposed Rhoptry Leaflet Interacting protein 2 (PfCERLI2), as a rhoptry bulb protein that is essential for merozoite invasion. Phylogenetic analyses show that cerli2 arose through an ancestral gene duplication of cerli1. We show that PfCERLI2 is essential for blood-stage growth and localises to the cytosolic face of the rhoptry bulb. Inducible knockdown of PfCERLI2 led to a proportion of merozoites failing to invade and was associated with elongation of the rhoptry organelle during merozoite development and inhibition of rhoptry antigen processing. These findings identify PfCERLI2 as a protein that has key roles in rhoptry biology during merozoite invasion. Nature Publishing Group UK 2022-02-09 /pmc/articles/PMC8828742/ /pubmed/35140336 http://dx.doi.org/10.1038/s42003-022-03020-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liffner, Benjamin
Balbin, Juan Miguel
Shami, Gerald J.
Siddiqui, Ghizal
Strauss, Jan
Frölich, Sonja
Heinemann, Gary K.
Edwards, Ella May
Alder, Arne
Wichers, Jan Stephan
Creek, Darren J.
Tilley, Leann
Dixon, Matthew W. A.
Gilberger, Tim-Wolf
Wilson, Danny W.
Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title_full Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title_fullStr Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title_full_unstemmed Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title_short Cell biological analysis reveals an essential role for Pfcerli2 in erythrocyte invasion by malaria parasites
title_sort cell biological analysis reveals an essential role for pfcerli2 in erythrocyte invasion by malaria parasites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828742/
https://www.ncbi.nlm.nih.gov/pubmed/35140336
http://dx.doi.org/10.1038/s42003-022-03020-9
work_keys_str_mv AT liffnerbenjamin cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT balbinjuanmiguel cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT shamigeraldj cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT siddiquighizal cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT straussjan cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT frolichsonja cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT heinemanngaryk cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT edwardsellamay cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT alderarne cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT wichersjanstephan cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT creekdarrenj cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT tilleyleann cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT dixonmatthewwa cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT gilbergertimwolf cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites
AT wilsondannyw cellbiologicalanalysisrevealsanessentialroleforpfcerli2inerythrocyteinvasionbymalariaparasites