Parasitology Research

, Volume 110, Issue 5, pp 1911–1917

Leishmania major protein disulfide isomerase as a drug target

Enzymatic and functional characterization
  • Noureddine Ben Khalaf
  • Géraldine De Muylder
  • Hechmi Louzir
  • James McKerrow
  • Mehdi Chenik
Original Paper

DOI: 10.1007/s00436-011-2717-5

Cite this article as:
Ben Khalaf, N., De Muylder, G., Louzir, H. et al. Parasitol Res (2012) 110: 1911. doi:10.1007/s00436-011-2717-5

Abstract

Leishmaniasis is a major health problem worldwide and tools available for their control are limited. Effective vaccines are still lacking, drugs are toxic and expensive, and parasites develop resistance to chemotherapy. In this context, new antimicrobials are urgently needed to control the disease in both human and animal. Here, we report the enzymatic and functional characterization of a Leishmania virulence factor, Leishmania major Protein disulfide isomerase (LmPDI) that could constitute a potential drug target. LmPDI possesses domain structure organization similar to other PDI family members (a, a′, b, b′ and c domains), and it displays the three enzymatic and functional activities specific of PDI family members: isomerase, reductase and chaperone. These results suggest that LmPDI plays a key role in assisting Leishmania protein folding via its capacity to catalyze formation, breakage, and rearrangement of disulfide bonds in nascent polypeptides. Moreover, Bacitracin, a reductase activity inhibitor, and Ribostamycin, a chaperone activity inhibitor, were tested in LmPDI enzymatic assays and versus Leishmania promastigote in vitro cultures and Leishmania amastigote multiplication inside infected THP-1-derived macrophages. Bacitracin inhibited both isomerase and reductase activities, while Ribostamycin had no effect on the chaperone activity. Interestingly, Bacitracin blocked in vitro promastigote growth as well as amastigote multiplication inside macrophages with EC50 values of 39 μM. These results suggest that LmPDI may constitute an interesting target for the development of new anti-Leishmania drugs.

Abbreviations

LmPDI

Leishmania major protein disulfide isomerase

PDI

Protein disulfide isomerase

Supplementary material

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Supplemental data 1(PPT 112 kb)
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Supplemental data 2(PPT 227 kb)
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Supplemental data 3(PPT 131 kb)
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Supplemental data 4(PPT 127 kb)

Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Noureddine Ben Khalaf
    • 1
    • 3
  • Géraldine De Muylder
    • 2
  • Hechmi Louzir
    • 1
  • James McKerrow
    • 2
  • Mehdi Chenik
    • 1
    • 3
  1. 1.Laboratory of Immunopathology Vaccinology and Molecular Genetics (LIVGM)Institut Pasteur de TunisTunis-BelvédèreTunisia
  2. 2.Sandler Center for Drug DiscoveryUniversity of CaliforniaSan FranciscoUSA
  3. 3.Laboratory of Medical Parasitology, Biotechnology and BiomoleculesInstitut Pasteur de TunisTunis-BelvédèreTunisia