During the previous funding periods of this grant, we learned fundamental aspects of the mechanism by which the protozoan parasite Trypanosoma cruzi gains access to the intracellular environment. Host cell lysosomes play a key role in this process. Trypomastigotes actively invade non-phagocytic cells by one of two mechanisms: 1) triggering Ca2+ signaling events at the surface of host cells that lead to lysosomal recruitment and exocytosis, a process that delivers intracellular membrane for formation of the parasitophorous vacuole;2) by invaginating the plasma membrane, a process that is rapidly followed by lysosomal fusion. Our studies revealed that in the absence of lysosomal fusion the T. cruzi invasion process is reversible, with infective trypomastigotes being released back into the extracellular medium. Thus, regardless of whether the initial cell entry event involves lysosomal fusion with the plasma membrane ornot, lysosomal fusion is essential to retain the parasites inside host cells, allowing completion of the life cycle. In the next funding period, we plan to test the hypothesis that lysosomal fusion is critical for T. cruzi invasion in two ways: 1) by delivering a high affinity trypomastigote receptor to the host cell surface, and 2) by acting as an intracellular "anchor" for trypomastigotes by promoting strong association to host cell microtubules.
In AIM 1 we will investigate whether the T. cruzi transialidase binds sialic acid moieties on the luminal domain of lysosomal glycoproteins, ensuring the close apposition of parasite and host cell membranes during invasion. To this end,in addition to biochemical interaction assays we will examine parasites expressingdifferent levels of transialidase, and host cell fibroblasts from mice deficient in Lampl and Lamp2, the two major sialic acid-containing glycoproteins of mammalian cell lysosomes.
In AIM 2 we will examine the mechanisms by which lysosomal fusion and host cell microtubules retain T. cruzi trypomastigotes inside host cells. Our hypothesis is that this process is mediated by specific molecular motors that link lysosomes to microtubules.
In AIM 3, we will investigate whether lysosomal proteases play an important role in the escape of T. cruzi from the vacuole where it resides shortly after infection. As in the past, we are confident that the new knowledge that we will gain in this process will advance our understanding of this important human parasite, and also uncover novel aspects of the biology of mammalian cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AI034867-19
Application #
8204804
Study Section
Special Emphasis Panel (NSS)
Program Officer
Mcgugan, Glen C
Project Start
1994-01-01
Project End
2014-12-31
Budget Start
2012-01-01
Budget End
2014-12-31
Support Year
19
Fiscal Year
2012
Total Cost
$471,608
Indirect Cost
$157,203
Name
University of Maryland College Park
Department
Anatomy/Cell Biology
Type
Schools of Earth Sciences/Natur
DUNS #
790934285
City
College Park
State
MD
Country
United States
Zip Code
20742
Tam, Christina; Flannery, Andrew R; Andrews, Norma (2013) Live imaging assay for assessing the roles of Ca2+ and sphingomyelinase in the repair of pore-forming toxin wounds. J Vis Exp :e50531
Flannery, Andrew R; Renberg, Rebecca L; Andrews, Norma W (2013) Pathways of iron acquisition and utilization in Leishmania. Curr Opin Microbiol 16:716-21
Fernandes, Maria Cecilia; Flannery, Andrew R; Andrews, Norma et al. (2013) Extracellular amastigotes of Trypanosoma cruzi are potent inducers of phagocytosis in mammalian cells. Cell Microbiol 15:977-91
Fernandes, Maria Cecilia; Andrews, Norma W (2012) Host cell invasion by Trypanosoma cruzi: a unique strategy that promotes persistence. FEMS Microbiol Rev 36:734-47
Cortez, Mauro; Huynh, Chau; Fernandes, Maria Cecilia et al. (2011) Leishmania promotes its own virulence by inducing expression of the host immune inhibitory ligand CD200. Cell Host Microbe 9:463-71
Fernandes, Maria Cecilia; Cortez, Mauro; Flannery, Andrew R et al. (2011) Trypanosoma cruzi subverts the sphingomyelinase-mediated plasma membrane repair pathway for cell invasion. J Exp Med 208:909-21
Jacques, Ismaele; Andrews, Norma W; Huynh, Chau (2010) Functional characterization of LIT1, the Leishmania amazonensis ferrous iron transporter. Mol Biochem Parasitol 170:28-36
Albertti, L A G; Macedo, A M; Chiari, E et al. (2010) Role of host lysosomal associated membrane protein (LAMP) in Trypanosoma cruzi invasion and intracellular development. Microbes Infect 12:784-9
Idone, Vincent; Tam, Christina; Andrews, Norma W (2008) Two-way traffic on the road to plasma membrane repair. Trends Cell Biol 18:552-9
Wilson, Jude; Huynh, Chau; Kennedy, Kathleen A et al. (2008) Control of parasitophorous vacuole expansion by LYST/Beige restricts the intracellular growth of Leishmania amazonensis. PLoS Pathog 4:e1000179

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