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Essentiality of Plasmodium falciparum plasmepsin V

The malaria parasite replicates within erythrocytes. The pathogenesis of clinical malaria is in large part due to the capacity of the parasite to remodel its host cell. To do this, intraerythrocytic stages of Plasmodium falciparum export more than 300 proteins that dramatically alter the morphology...

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Autores principales: Boonyalai, Nonlawat, Collins, Christine R., Hackett, Fiona, Withers-Martinez, Chrislaine, Blackman, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281190/
https://www.ncbi.nlm.nih.gov/pubmed/30517136
http://dx.doi.org/10.1371/journal.pone.0207621
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author Boonyalai, Nonlawat
Collins, Christine R.
Hackett, Fiona
Withers-Martinez, Chrislaine
Blackman, Michael J.
author_facet Boonyalai, Nonlawat
Collins, Christine R.
Hackett, Fiona
Withers-Martinez, Chrislaine
Blackman, Michael J.
author_sort Boonyalai, Nonlawat
collection PubMed
description The malaria parasite replicates within erythrocytes. The pathogenesis of clinical malaria is in large part due to the capacity of the parasite to remodel its host cell. To do this, intraerythrocytic stages of Plasmodium falciparum export more than 300 proteins that dramatically alter the morphology of the infected erythrocyte as well as its mechanical and adhesive properties. P. falciparum plasmepsin V (PfPMV) is an aspartic protease that processes proteins for export into the host erythrocyte and is thought to play a key role in parasite virulence and survival. However, although standard techniques for gene disruption as well as conditional protein knockdown have been previously attempted with the pfpmv gene, complete gene removal or knockdown was not achieved so direct genetic proof that PMV is an essential protein has not been established. Here we have used a conditional gene excision approach combining CRISPR-Cas9 gene editing and DiCre-mediated recombination to functionally inactivate the pfpmv gene. The resulting mutant parasites displayed a severe growth defect. Detailed phenotypic analysis showed that development of the mutant parasites was arrested early in the ring-to-trophozoite transition in the erythrocytic cycle following gene excision. Our findings are the first to elucidate the effects of PMV gene disruption, showing that it is essential for parasite viability in asexual blood stages. The mutant parasites can now be used as a platform to further dissect the Plasmodium protein export pathway.
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spelling pubmed-62811902018-12-20 Essentiality of Plasmodium falciparum plasmepsin V Boonyalai, Nonlawat Collins, Christine R. Hackett, Fiona Withers-Martinez, Chrislaine Blackman, Michael J. PLoS One Research Article The malaria parasite replicates within erythrocytes. The pathogenesis of clinical malaria is in large part due to the capacity of the parasite to remodel its host cell. To do this, intraerythrocytic stages of Plasmodium falciparum export more than 300 proteins that dramatically alter the morphology of the infected erythrocyte as well as its mechanical and adhesive properties. P. falciparum plasmepsin V (PfPMV) is an aspartic protease that processes proteins for export into the host erythrocyte and is thought to play a key role in parasite virulence and survival. However, although standard techniques for gene disruption as well as conditional protein knockdown have been previously attempted with the pfpmv gene, complete gene removal or knockdown was not achieved so direct genetic proof that PMV is an essential protein has not been established. Here we have used a conditional gene excision approach combining CRISPR-Cas9 gene editing and DiCre-mediated recombination to functionally inactivate the pfpmv gene. The resulting mutant parasites displayed a severe growth defect. Detailed phenotypic analysis showed that development of the mutant parasites was arrested early in the ring-to-trophozoite transition in the erythrocytic cycle following gene excision. Our findings are the first to elucidate the effects of PMV gene disruption, showing that it is essential for parasite viability in asexual blood stages. The mutant parasites can now be used as a platform to further dissect the Plasmodium protein export pathway. Public Library of Science 2018-12-05 /pmc/articles/PMC6281190/ /pubmed/30517136 http://dx.doi.org/10.1371/journal.pone.0207621 Text en © 2018 Boonyalai et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Boonyalai, Nonlawat
Collins, Christine R.
Hackett, Fiona
Withers-Martinez, Chrislaine
Blackman, Michael J.
Essentiality of Plasmodium falciparum plasmepsin V
title Essentiality of Plasmodium falciparum plasmepsin V
title_full Essentiality of Plasmodium falciparum plasmepsin V
title_fullStr Essentiality of Plasmodium falciparum plasmepsin V
title_full_unstemmed Essentiality of Plasmodium falciparum plasmepsin V
title_short Essentiality of Plasmodium falciparum plasmepsin V
title_sort essentiality of plasmodium falciparum plasmepsin v
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281190/
https://www.ncbi.nlm.nih.gov/pubmed/30517136
http://dx.doi.org/10.1371/journal.pone.0207621
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