Parasites of the trypanosomatid protozoan genus Leishmania are responsible for a spectrum of tropical diseases that affect more than 10 million people worldwide, and depending on the specific species and immune status of the infected person, can be severe or fatal. In Brasil, Africa and the Mediterranean basin, leishmaniasis is a common opportunistic infection in AIDS patients. The goal of this proposal is to develop methods for the genetic identification of genes and proteins likely to play important roles in the infectious cycle of the protozoan parasite Leishmania. The premise is that the availability of powerful molecular genetic tools, and identification of genes important to parasite virulence, will radically advance our ability to develop improved control strategies. In previous studies methods were developed for manipulating the parasite genome in a variety of ways, and performing functional genetic rescue. These led to the identification of several candidate virulence genes. The role of genes such as UBF], implicated in parasite DNA repair pathways essential for survival, will be pursued. With rapid progress in the Leishmania genome project, and recent breakthroughs in the development of new methods suitable for genome-wide surveys of parasite gene expression, the time is appropriate to initiate a series of 'functional genomic' studies oriented towards characterizing expression from the complete parasite genome. The goal is to identify genes showing patterns of expression suggestive of functional roles in the infectious cycle, for example stage-specific expression or alterations in response to relevant stimuli. We will use mariner-based transpositional systems to systematically generate GFP gene fusions in defined segments of the parasite genome in vitro or the entire genome in vivo. These methods have the advantage of studying expression at the protein level, allowing the cumulative effect of regulation at both nucleic acid and protein levels to be evaluated. Promising preliminary data with DNA microarrays have been gathered, and a series of investigations of Leishmania gene expression under a variety of relevant developmental stages and environmental treatments will be carried out.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI029646-13
Application #
6488926
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Program Officer
Gottlieb, Michael
Project Start
1990-03-01
Project End
2005-12-31
Budget Start
2002-01-01
Budget End
2002-12-31
Support Year
13
Fiscal Year
2002
Total Cost
$487,027
Indirect Cost
Name
Washington University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Grybchuk, Danyil; Akopyants, Natalia S; Kostygov, Alexei Y et al. (2018) Viral discovery and diversity in trypanosomatid protozoa with a focus on relatives of the human parasite Leishmania. Proc Natl Acad Sci U S A 115:E506-E515
Kohl, Kid; Zangger, Haroun; Rossi, Matteo et al. (2018) Importance of polyphosphate in the Leishmania life cycle. Microb Cell 5:371-384
Hartley, Mary-Anne; Eren, Remzi O; Rossi, Matteo et al. (2018) Leishmania guyanensis parasites block the activation of the inflammasome by inhibiting maturation of IL-1?. Microb Cell 5:137-149
Robinson, John I; Beverley, Stephen M (2018) Concentration of 2'C-methyladenosine triphosphate by Leishmania guyanensis enables specific inhibition of Leishmania RNA virus 1 via its RNA polymerase. J Biol Chem 293:6460-6469
Brettmann, Erin A; Lye, Lon-Fye; Beverley, Stephen M (2018) Spontaneous excision and facilitated recovery as a control for phenotypes arising from RNA interference and other dominant transgenes. Mol Biochem Parasitol 220:42-45
Eren, Remzi Onur; Kopelyanskiy, Dmitry; Moreau, Dimitri et al. (2018) Development of a semi-automated image-based high-throughput drug screening system. Front Biosci (Elite Ed) 10:242-253
Davenport, Bennett J; Martin, Casey G; Beverley, Stephen M et al. (2018) SODB1 is essential for Leishmania major infection of macrophages and pathogenesis in mice. PLoS Negl Trop Dis 12:e0006921
Matveyev, Andrey V; Alves, João M P; Serrano, Myrna G et al. (2017) The Evolutionary Loss of RNAi Key Determinants in Kinetoplastids as a Multiple Sporadic Phenomenon. J Mol Evol 84:104-115
Mandell, Michael A; Beverley, Stephen M (2017) Continual renewal and replication of persistent Leishmania major parasites in concomitantly immune hosts. Proc Natl Acad Sci U S A 114:E801-E810
Rossi, Matteo; Castiglioni, Patrik; Hartley, Mary-Anne et al. (2017) Type I interferons induced by endogenous or exogenous viral infections promote metastasis and relapse of leishmaniasis. Proc Natl Acad Sci U S A 114:4987-4992

Showing the most recent 10 out of 104 publications