Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.

Live cell imaging of recombinant malarial parasites encoding fluorescent probes provides critical insights into parasite-host interactions and life cycle progression. In this study, we generated a red fluorescent line of the murine malarial parasite Plasmodium berghei. To allow constitutive and abun...

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Main Authors: Marion Hliscs, Carolin Nahar, Friedrich Frischknecht, Kai Matuschewski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3754930?pdf=render
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spelling doaj-10c5db2458fc4feebe7439775d4cd6aa2020-11-25T01:22:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7277110.1371/journal.pone.0072771Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.Marion HliscsCarolin NaharFriedrich FrischknechtKai MatuschewskiLive cell imaging of recombinant malarial parasites encoding fluorescent probes provides critical insights into parasite-host interactions and life cycle progression. In this study, we generated a red fluorescent line of the murine malarial parasite Plasmodium berghei. To allow constitutive and abundant expression of the mCherry protein we profiled expression of all members of the P. berghei heat shock protein 70 (HSP70) family. We identified PbHSP70/1, an invariant ortholog of Plasmodium falciparum HSP70-1, as the protein with the highest expression levels during Plasmodium blood, mosquito, and liver infection. Stable allelic insertion of a mCherry expression cassette into the PbHsp70/1 locus created constitutive red fluorescent P. berghei lines, termed Pbred. We show that these parasites can be used for live imaging of infected host cells and organs, including hepatocytes, erythrocytes, and whole Anopheles mosquitoes. Quantification of the fluorescence intensity of several Pbred parasite stages revealed significantly enhanced signal intensities in comparison to GFP expressed under the control of the constitutive EF1alpha promoter. We propose that systematic transcript profiling permits generation of reporter parasites, such as the Pbred lines described herein.http://europepmc.org/articles/PMC3754930?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marion Hliscs
Carolin Nahar
Friedrich Frischknecht
Kai Matuschewski
spellingShingle Marion Hliscs
Carolin Nahar
Friedrich Frischknecht
Kai Matuschewski
Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
PLoS ONE
author_facet Marion Hliscs
Carolin Nahar
Friedrich Frischknecht
Kai Matuschewski
author_sort Marion Hliscs
title Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
title_short Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
title_full Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
title_fullStr Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
title_full_unstemmed Expression profiling of Plasmodium berghei HSP70 genes for generation of bright red fluorescent parasites.
title_sort expression profiling of plasmodium berghei hsp70 genes for generation of bright red fluorescent parasites.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Live cell imaging of recombinant malarial parasites encoding fluorescent probes provides critical insights into parasite-host interactions and life cycle progression. In this study, we generated a red fluorescent line of the murine malarial parasite Plasmodium berghei. To allow constitutive and abundant expression of the mCherry protein we profiled expression of all members of the P. berghei heat shock protein 70 (HSP70) family. We identified PbHSP70/1, an invariant ortholog of Plasmodium falciparum HSP70-1, as the protein with the highest expression levels during Plasmodium blood, mosquito, and liver infection. Stable allelic insertion of a mCherry expression cassette into the PbHsp70/1 locus created constitutive red fluorescent P. berghei lines, termed Pbred. We show that these parasites can be used for live imaging of infected host cells and organs, including hepatocytes, erythrocytes, and whole Anopheles mosquitoes. Quantification of the fluorescence intensity of several Pbred parasite stages revealed significantly enhanced signal intensities in comparison to GFP expressed under the control of the constitutive EF1alpha promoter. We propose that systematic transcript profiling permits generation of reporter parasites, such as the Pbred lines described herein.
url http://europepmc.org/articles/PMC3754930?pdf=render
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