alexa Targeting Ether Lipid Metabolism For Anti-leishmanial Chemotherapy
ISSN: 2155-9597

Journal of Bacteriology & Parasitology
Open Access

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3rd World Conference on Parasitology & Pathogenesis
July 12-13, 2017 Chicago, USA

Rachel Zufferey
St. John’s University, USA
ScientificTracks Abstracts: J Bacteriol Parasitol
DOI: 10.4172/2155-9597-C1-031
Statement of the Problem: Leishmaniasis is a parasitic disease transmitted by female sandflies. This disease is endemic in the tropical and subtropical areas of the world, and affects at least 12 million people worldwide. Every year, at least 2 million new cases are reported and 350 million humans are at risk of contracting this disease in more than 88 countries. The treatment of leishmaniasis relies primarily on expensive, poorly effective chemotherapeutic drugs that exhibit several undesirable side effects and can be sometimes difficult to administer. In addition, the rising occurrence of leishmaniasis and appearance of drug resistant parasites make the development of more effective drugs a necessity for the prevention and treatment of leishmaniasis. The purpose of this study is to characterize enzymes involved in the biosynthesis of the virulence factor lipophosphoglycan in order to identify suitable targets for chemotherapy. Methodology: Genes or enzymes of the ether lipid biosynthetic pathway were assessed, especially their involvement in lipophosphoglycan biosynthesis and in virulence. Findings: The dihydroxyacetonephosphate acyltransferase enzyme LmDAT localizes in the peroxisomes and is specific for palmitoyl- CoA as substrate. Furthermore, LmDAT is essential for lipophosphogycan biosynthesis, growth of the parasite, survival during the stationary phase of growth, ether lipid generation and for causing disease in mice. Lastly, a null mutant of LmDAT was found to mediate some protection in mice against an ulterior challenge of wild-type parasites. Conclusion & Significance: LmDAT may be a good target for chemotherapeutic intervention and the null mutant lacking LmDAT may serve as a potential live vaccine candidate.

Rachel Zufferey is a Parasitologist, studying lipid metabolism in Leishmania and Trypanosoma brucei. She is an Associate Professor in the Department of Biological Sciences at St. John’s University, Queens, NY, USA.

Email: [email protected]

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