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Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development

Despite the critical role of Plasmodium sporozoites in malaria transmission, we still know little about the mechanisms underlying their development in mosquitoes. Here, we use single-cell RNA sequencing to characterize the gene expression profiles of 16,038 Plasmodium berghei sporozoites isolated th...

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Autores principales: Bogale, Haikel N., Pascini, Tales V., Kanatani, Sachie, Sá, Juliana M., Wellems, Thomas E., Sinnis, Photini, Vega-Rodríguez, Joel, Serre, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958459/
https://www.ncbi.nlm.nih.gov/pubmed/33653959
http://dx.doi.org/10.1073/pnas.2023438118
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author Bogale, Haikel N.
Pascini, Tales V.
Kanatani, Sachie
Sá, Juliana M.
Wellems, Thomas E.
Sinnis, Photini
Vega-Rodríguez, Joel
Serre, David
author_facet Bogale, Haikel N.
Pascini, Tales V.
Kanatani, Sachie
Sá, Juliana M.
Wellems, Thomas E.
Sinnis, Photini
Vega-Rodríguez, Joel
Serre, David
author_sort Bogale, Haikel N.
collection PubMed
description Despite the critical role of Plasmodium sporozoites in malaria transmission, we still know little about the mechanisms underlying their development in mosquitoes. Here, we use single-cell RNA sequencing to characterize the gene expression profiles of 16,038 Plasmodium berghei sporozoites isolated throughout their development from midgut oocysts to salivary glands, and from forced salivation experiments. Our results reveal a succession of tightly regulated changes in gene expression occurring during the maturation of sporozoites and highlight candidate genes that could play important roles in oocyst egress, sporozoite motility, and the mechanisms underlying the invasion of mosquito salivary glands and mammalian hepatocytes. In addition, the single-cell data reveal extensive transcriptional heterogeneity among parasites isolated from the same anatomical site, suggesting that Plasmodium development in mosquitoes is asynchronous and regulated by intrinsic as well as environmental factors. Finally, our analyses show a decrease in transcriptional activity preceding the translational repression observed in mature sporozoites and associated with their quiescent state in salivary glands, followed by a rapid reactivation of the transcriptional machinery immediately upon salivation.
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spelling pubmed-79584592021-03-19 Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development Bogale, Haikel N. Pascini, Tales V. Kanatani, Sachie Sá, Juliana M. Wellems, Thomas E. Sinnis, Photini Vega-Rodríguez, Joel Serre, David Proc Natl Acad Sci U S A Biological Sciences Despite the critical role of Plasmodium sporozoites in malaria transmission, we still know little about the mechanisms underlying their development in mosquitoes. Here, we use single-cell RNA sequencing to characterize the gene expression profiles of 16,038 Plasmodium berghei sporozoites isolated throughout their development from midgut oocysts to salivary glands, and from forced salivation experiments. Our results reveal a succession of tightly regulated changes in gene expression occurring during the maturation of sporozoites and highlight candidate genes that could play important roles in oocyst egress, sporozoite motility, and the mechanisms underlying the invasion of mosquito salivary glands and mammalian hepatocytes. In addition, the single-cell data reveal extensive transcriptional heterogeneity among parasites isolated from the same anatomical site, suggesting that Plasmodium development in mosquitoes is asynchronous and regulated by intrinsic as well as environmental factors. Finally, our analyses show a decrease in transcriptional activity preceding the translational repression observed in mature sporozoites and associated with their quiescent state in salivary glands, followed by a rapid reactivation of the transcriptional machinery immediately upon salivation. National Academy of Sciences 2021-03-09 2021-03-02 /pmc/articles/PMC7958459/ /pubmed/33653959 http://dx.doi.org/10.1073/pnas.2023438118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Bogale, Haikel N.
Pascini, Tales V.
Kanatani, Sachie
Sá, Juliana M.
Wellems, Thomas E.
Sinnis, Photini
Vega-Rodríguez, Joel
Serre, David
Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title_full Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title_fullStr Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title_full_unstemmed Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title_short Transcriptional heterogeneity and tightly regulated changes in gene expression during Plasmodium berghei sporozoite development
title_sort transcriptional heterogeneity and tightly regulated changes in gene expression during plasmodium berghei sporozoite development
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958459/
https://www.ncbi.nlm.nih.gov/pubmed/33653959
http://dx.doi.org/10.1073/pnas.2023438118
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