» Articles » PMID: 24069359

Role of Efflux Pumps and Intracellular Thiols in Natural Antimony Resistant Isolates of Leishmania Donovani

Overview
Journal PLoS One
Date 2013 Sep 27
PMID 24069359
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In view of the recent upsurge in the phenomenon of therapeutic failure, drug resistance in Leishmania, developed under natural field conditions, has become a great concern yet little understood. Accordingly, the study of determinants of antimony resistance is urgently warranted. Efflux transporters have been reported in Leishmania but their role in clinical resistance is still unknown. The present study was designed to elucidate the mechanism of natural antimony resistance in L. donovani field isolates by analyzing the functionality of efflux pump(s) and expression profiles of known genes involved in transport and thiol based redox metabolism.

Methodology/principal Findings: We selected 7 clinical isolates (2 sensitive and 5 resistant) in addition to laboratory sensitive reference and SbIII resistant mutant strains for the present study. Functional characterization using flow cytometry identified efflux pumps that transported substrates of both P-gp and MRPA and were inhibited by the calmodulin antagonist trifluoperazine. For the first time, verapamil sensitive efflux pumps for rhodamine 123 were observed in L. donovani that were differentially active in resistant isolates. RT-PCR confirmed the over-expression of MRPA in isolates with high resistance index only. Resistant isolates also exhibited consistent down regulation of AQP1 and elevated intracellular thiol levels which were accompanied with increased expression of ODC and TR genes. Interestingly, γ-GCS is not implicated in clinical resistance in L. donovani isolates.

Conclusions/significance: Here we demonstrate for the first time, the role of P-gp type plasma membrane efflux transporter(s) in antimony resistance in L. donovani field isolates. Further, decreased levels of AQP1 and elevated thiols levels have emerged as biomarkers for clinical resistance.

Citing Articles

Identification of CβS and ODC antimony resistance markers in anthroponotic cutaneous leishmaniasis field isolates by gene expression profiling.

Zarrinkar F, Sharifi I, Oliaee R, Afgar A, Molaakbari E, Bamorovat M Parasite Epidemiol Control. 2025; 28:e00413.

PMID: 39959455 PMC: 11830360. DOI: 10.1016/j.parepi.2025.e00413.


Possibility of re-purposing antifungal drugs posaconazole & isavuconazole against promastigote form of Leishmania major.

Bhusal C, Beniwal P, Singh S, Kaur D, Kaur U, Kaur S Indian J Med Res. 2024; 160(5):466-478.

PMID: 39737513 PMC: 11683497. DOI: 10.25259/IJMR_569_2024.


Antimony resistance and gene expression in : spotlight on molecular and proteomic aspects.

Madusanka R, Karunaweera N, Silva H, Selvapandiyan A Parasitology. 2023; 151(1):1-14.

PMID: 38012864 PMC: 10941051. DOI: 10.1017/S0031182023001129.


Recent Advances in Chemotherapeutics for Leishmaniasis: Importance of the Cellular Biochemistry of the Parasite and Its Molecular Interaction with the Host.

Singh R, Kashif M, Srivastava P, Manna P Pathogens. 2023; 12(5).

PMID: 37242374 PMC: 10222285. DOI: 10.3390/pathogens12050706.


Knockout of Tyrosine Aminotransferase Gene by Homologous Recombination Arrests Growth and Disrupts Redox Homeostasis in Leishmania Parasite.

Sasidharan S, Saudagar P Parasitol Res. 2022; 121(11):3229-3241.

PMID: 36056961 DOI: 10.1007/s00436-022-07642-0.


References
1.
Livak K, Schmittgen T . Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 2002; 25(4):402-8. DOI: 10.1006/meth.2001.1262. View

2.
Sinha S, Sundaram S, Kumar V, Tripathi A . Antimony resistance during Visceral Leishmaniasis: A possible consequence of serial mutations in ABC transporters of Leishmania species. Bioinformation. 2011; 6(3):107-10. PMC: 3089883. DOI: 10.6026/97320630006107. View

3.
Kaatz G, Moudgal V, Seo S, Kristiansen J . Phenothiazines and thioxanthenes inhibit multidrug efflux pump activity in Staphylococcus aureus. Antimicrob Agents Chemother. 2003; 47(2):719-26. PMC: 151737. DOI: 10.1128/AAC.47.2.719-726.2003. View

4.
Legare D, Papadopoulou B, Roy G, Mukhopadhyay R, Haimeur A, Dey S . Efflux systems and increased trypanothione levels in arsenite-resistant Leishmania. Exp Parasitol. 1997; 87(3):275-82. DOI: 10.1006/expr.1997.4222. View

5.
Shapiro A, Ling V . The mechanism of ATP-dependent multidrug transport by P-glycoprotein. Acta Physiol Scand Suppl. 1998; 643:227-34. View