H2O2 dynamics in the malaria parasite Plasmodium falciparum

2017 | journal article. A publication with affiliation to the University of Göttingen.

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​H2O2 dynamics in the malaria parasite Plasmodium falciparum​
Rahbari, M.; Rahlfs, S.; Jortzik, E.; Bogeski, I.   & Becker, K.​ (2017) 
PLoS ONE12(4) art. e0174837​.​ DOI: https://doi.org/10.1371/journal.pone.0174837 

Documents & Media

journal.pone.0174837.pdf1.85 MBAdobe PDF

License

Published Version

Special user license Goescholar License

Details

Authors
Rahbari, Mahsa; Rahlfs, Stefan; Jortzik, Esther; Bogeski, Ivan ; Becker, Katja
Abstract
Hydrogen peroxide is an important antimicrobial agent but is also crucially involved in redox signaling and pathogen-host cell interactions. As a basis for systematically investigating intracellular H2O2 dynamics and regulation in living malaria parasites, we established the genetically encoded fluorescent H2O2 sensors roGFP2-Orp1 and HyPer-3 in Plasmodium falciparum. Both ratiometric redox probes as well as the pH control SypHer were expressed in the cytosol of blood-stage parasites. Both redox sensors showed reproducible sensitivity towards H2O2 in the lower micromolar range in vitro and in the parasites. Due to the pH sensitivity of HyPer-3, we used parasites expressing roGFP2-Orp1 for evaluation of short-, medium-, and long-term effects of antimalarial drugs on H2O2 levels and detoxification in Plasmodium. None of the quinolines or artemisinins tested had detectable direct effects on the H2O2 homeostasis at pharmacologically relevant concentrations. However, pre-treat-ment of the cells with antimalarial drugs or heat shock led to a higher tolerance towards exogenous H2O2. The systematic evaluation and comparison of the two genetically encoded cytosolic H2O2 probes in malaria parasites provides a basis for studying parasite-host cell interactions or drug effects with spatio-temporal resolution while preserving cell integrity.
Issue Date
2017
Status
published
Publisher
Public Library Science
Journal
PLoS ONE 
ISSN
1932-6203

Reference

Citations


Social Media