Elucidating Host Cell Uptake by Malaria Parasites

2019 ◽  
Vol 35 (5) ◽  
pp. 333-335 ◽  
Author(s):  
Brendan Elsworth ◽  
Caroline D. Keroack ◽  
Manoj T. Duraisingh
2006 ◽  
Vol 59 (3) ◽  
pp. 779-794 ◽  
Author(s):  
Tobias Spielmann ◽  
Donald L. Gardiner ◽  
Hans-Peter Beck ◽  
Katharine R. Trenholme ◽  
David J. Kemp

2004 ◽  
Vol 32 (3) ◽  
pp. 353-359 ◽  
Author(s):  
Virgilio L Lew ◽  
Lynn Macdonald ◽  
Hagai Ginsburg ◽  
Miriam Krugliak ◽  
Teresa Tiffert

2017 ◽  
Vol 47 (2-3) ◽  
pp. 119-127 ◽  
Author(s):  
Paul R. Gilson ◽  
Scott A. Chisholm ◽  
Brendan S. Crabb ◽  
Tania F. de Koning-Ward

2021 ◽  
Author(s):  
Jan Stephan Wichers ◽  
Carolina van Gelder ◽  
Gwendolin Fuchs ◽  
Julia Mareike Ruge ◽  
Emma Pietsch ◽  
...  

ABSTRACTDuring the symptomatic human blood phase, malaria parasites replicate within red blood cells. Parasite proliferation relies on the uptake of nutrients, such as amino acids, from the host cell and the blood plasma, requiring transport across multiple membranes. Amino acids are delivered to the parasite through the parasite surrounding vacuolar compartment by specialized nutrient-permeable channels of the erythrocyte membrane and the parasitophorous vacuole membrane (PVM). However, further transport of amino acid across the parasite plasma membrane (PPM) is currently not well characterized. In this study, we focused on a family of Apicomplexan amino acid transporters (ApiATs) that comprises five members in Plasmodium falciparum. First, we localized four of the PfApiATs at the PPM using endogenous GFP-tagging. Next, we applied reverse genetic approaches to probe into their essentiality during asexual replication and gametocytogenesis. Upon inducible knockdown and targeted gene disruption a reduced asexual parasite proliferation was detected for PfApiAT2 and PfApiAT4. Functional inactivation of individual PfApiATs targeted in this study had no effect on gametocyte development. Our data suggest that individual PfApiATs are partially redundant during asexual in vitro proliferation and fully redundant during gametocytogenesis of P. falciparum parasites.IMPORTANCEMalaria parasites live and multiply inside cells. To facilitate their extremely fast intracellular proliferation they hijack and transform their host cells. This also requires the active uptake of nutrients, such as amino acids, from the host cell and the surrounding environment through various membranes that are the consequence of the parasite’s intracellular lifestyle. In this manuscript we focus on a family of putative amino acid transporters termed ApiAT. We show expression and localization of four transporters in the parasite plasma membrane of Plasmodium falciparum-infected erythrocytes that represent one interface of the pathogen to its host cell. We probed into the impact of functional inactivation of individual transporters on parasite growth in asexual and sexual blood stages of P. falciparum and reveal that only two of them show a modest but significant reduction in parasite proliferation but no impact on gametocytogenesis pointing towards redundancy within this transporter family.


Science ◽  
1983 ◽  
Vol 221 (4612) ◽  
pp. 764-766 ◽  
Author(s):  
A. Fairfield ◽  
Meshnick ◽  
J. Eaton

1986 ◽  
Vol 72 (3) ◽  
pp. 323-329 ◽  
Author(s):  
Tania C. Araujo-Jorge ◽  
Elizabeth P. Sampaio ◽  
Wanderley Souza

2008 ◽  
Vol 24 (12) ◽  
pp. 557-563 ◽  
Author(s):  
Jake Baum ◽  
Tim-Wolf Gilberger ◽  
Freddy Frischknecht ◽  
Markus Meissner

ACS Nano ◽  
2014 ◽  
Vol 8 (12) ◽  
pp. 12560-12571 ◽  
Author(s):  
Adrian Najer ◽  
Dalin Wu ◽  
Andrej Bieri ◽  
Françoise Brand ◽  
Cornelia G. Palivan ◽  
...  

2000 ◽  
Vol 16 (10) ◽  
pp. 411-415 ◽  
Author(s):  
Chetan E Chitnis ◽  
M.J Blackman

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