Literature DB >> 16492710

The pH of the digestive vacuole of Plasmodium falciparum is not associated with chloroquine resistance.

Rhys Hayward1, Kevin J Saliba, Kiaran Kirk.   

Abstract

Chloroquine resistance in the human malaria parasite, Plasmodium falciparum, arises from decreased accumulation of the drug in the ;digestive vacuole' of the parasite, an acidic compartment in which chloroquine exerts its primary toxic effect. It has been proposed that changes in the pH of the digestive vacuole might underlie the decreased accumulation of chloroquine by chloroquine-resistant parasites. In this study we have investigated the digestive vacuole pH of a chloroquine-sensitive and a chloroquine-resistant strain of P. falciparum, using a range of dextran-linked pH-sensitive fluorescent dyes. The estimated digestive vacuole pH varied with the concentration and pK(a) of the dye, ranging from approximately 3.7-6.5. However, at low dye concentrations the estimated digestive vacuole pH of both the chloroquine-resistant and chloroquine-sensitive strains converged in the range 4.5-4.9. The results suggest that there is no significant difference in digestive vacuole pH of chloroquine-sensitive and chloroquine-resistant parasites, and that digestive vacuole pH does not play a primary role in chloroquine resistance.

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Year:  2006        PMID: 16492710     DOI: 10.1242/jcs.02795

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  53 in total

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Review 2.  Know your enemy: understanding the role of PfCRT in drug resistance could lead to new antimalarial tactics.

Authors:  Robert L Summers; Megan N Nash; Rowena E Martin
Journal:  Cell Mol Life Sci       Date:  2012-06       Impact factor: 9.261

3.  Genetic linkage of pfmdr1 with food vacuolar solute import in Plasmodium falciparum.

Authors:  Petra Rohrbach; Cecilia P Sanchez; Karen Hayton; Oliver Friedrich; Jigar Patel; Amar Bir Singh Sidhu; Michael T Ferdig; David A Fidock; Michael Lanzer
Journal:  EMBO J       Date:  2006-06-22       Impact factor: 11.598

Review 4.  Transporters involved in resistance to antimalarial drugs.

Authors:  Stephanie G Valderramos; David A Fidock
Journal:  Trends Pharmacol Sci       Date:  2006-09-25       Impact factor: 14.819

5.  The neutral lipid composition present in the digestive vacuole of Plasmodium falciparum concentrates heme and mediates β-hematin formation with an unusually low activation energy.

Authors:  Anh N Hoang; Rebecca D Sandlin; Aneesa Omar; Timothy J Egan; David W Wright
Journal:  Biochemistry       Date:  2010-11-08       Impact factor: 3.162

6.  Differences in trans-stimulated chloroquine efflux kinetics are linked to PfCRT in Plasmodium falciparum.

Authors:  Cecilia P Sanchez; Petra Rohrbach; Jeremy E McLean; David A Fidock; Wilfred D Stein; Michael Lanzer
Journal:  Mol Microbiol       Date:  2007-04       Impact factor: 3.501

7.  Colorimetric high-throughput screen for detection of heme crystallization inhibitors.

Authors:  Margaret A Rush; Mary Lynn Baniecki; Ralph Mazitschek; Joseph F Cortese; Roger Wiegand; Jon Clardy; Dyann F Wirth
Journal:  Antimicrob Agents Chemother       Date:  2009-03-23       Impact factor: 5.191

8.  Endocytic Profiling of Cancer Cell Models Reveals Critical Factors Influencing LNP-Mediated mRNA Delivery and Protein Expression.

Authors:  Edward J Sayers; Samantha E Peel; Anna Schantz; Richard M England; Maya Beano; Stephanie M Bates; Arpan S Desai; Sanyogitta Puri; Marianne B Ashford; Arwyn T Jones
Journal:  Mol Ther       Date:  2019-08-05       Impact factor: 11.454

9.  Chloroquine resistance-conferring mutations in pfcrt give rise to a chloroquine-associated H+ leak from the malaria parasite's digestive vacuole.

Authors:  Adele M Lehane; Kiaran Kirk
Journal:  Antimicrob Agents Chemother       Date:  2008-10-13       Impact factor: 5.191

Review 10.  Drug-resistant malaria - an insight.

Authors:  John E Hyde
Journal:  FEBS J       Date:  2007-09       Impact factor: 5.542

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