Mary E. Wilson, M.D.

M.D., University of Rochester School of Medicine & Dentistry, 1980

Professor of Internal Medicine and Microbiology

Campus address:

SW34Q GH

Mailing address:

200 Hawkins Drive

SW34Q General Hospital

Iowa City, IA 52242

Phone:

319-356-3169

Email:

mary-wilson@uiowa.edu

 

 

 

 

 

 

 

 

 

 

Molecular mechanisms of host-parasite interactions in leishmaniasis

Dr. Wilson's research focuses on the molecular and immunobiology of infection with the protozoan parasite, Leishmania chagasi, a cause of human visceral leishmaniasis. The lab examines interactions between the parasite and mammalian host that result in either survival or eradication of the parasite. Leishmania are obligate intracellular parasites of macrophages. Expression and localization of several important parasite virulence factors are studied, particularly parasite proteins involved in macrophage attachment and antioxidant defense. Phagocytosis induces dramatic changes in the host cell, leading to a unique pattern of gene activation characteristic of a non-inflammatory state that permits intracellular parasite survival. The lab has characterized changes in transcript expression, and changes in microRNAs underlying these gene expression patterns, using profiling approaches. Using confocal and electron microscopy the lab is investigating the bidirectional communication between the parasite and the host cell, including both host molecules recruited to the parasitophorous vacuole and parasite proteins released into the host cell. The ultimate changes in the systemic immune response induced by these changes in adaptive immune cells and their products (e.g., transforming growth factor-β, IL-10) are under investigation.

Field studies in both Brazil and Indian populations living in endemic regions are underway through collaborative projects with faculty in these countries. Humans develop widely divergent outcomes of Leishmania species infection, ranging from spontaneous cure to progressive, fatal visceral leishmaniasis. In collaboration with professors in northeast Brazil, India and Australia, Dr. Wilson’s group is examining allelic polymorphisms associated with different forms of disease, using both GWAS and candidate gene approaches. Other studies address new approaches to diagnosis, and vaccine development.

Recent publications

Ueno N., C.L. Bratt, N.E. Rodriguez, and M.E. Wilson. Differences in human macrophage receptor usage, lysosomal fusion kinetics and survival between logarithmic and metacyclic Leishmania infantum chagasi promastigotes. Cellular Microbiology 11(12):1827-1841, 2010. NIHMS 139267

Yao, C., Y. Li, J.E. Donelson, and M.E. Wilson. Proteomic examination of Leishmania chagasi plasma membrane proteins: contrast between avirulent and virulent (metacyclic) parasite forms. Proteomics Clin Appl 4:4–16, 2010.

Ettinger, N.A., P. Duggal, R.F.S. Braz, E.T. Nascimento, T.H. Beaty, S.M.B. Jeronimo, R.D. Pearson, J.M. Blackwell, L. Moreno, and M.E. Wilson. Genetic Admixture in Northeast Brazilians Exposed to Infection with the Protozoan Parasite Leishmania chagasi. Annals of Human Genetics 73:304–313, 2009.

Gaur U., M. Showalter, S. Hickerson, Rah Dalvi, S.J. Turco, M.E. Wilson, and S.M. Beverley. Leishmania donovani lacking the Golgi GDP-Man transporter LPG2 exhibit attenuated virulence in mammalian hosts. Exp Parasitol 122(3):182-91, 2009.


Ettinger, N.A. and M.E. Wilson. Macrophage and T-cell gene expression in a model of early infection with the protozoan, Leishmania chagasi. PLoS Negl Trop Dis 2(6): e252, 2008, and Featured Cover Illustration. PMCID: PMC2427198

Hsiao, C.-H.C., C. Yao, P.A. Storlie, J.E. Donelson, and M.E. Wilson. The major surface protease (MSP or GP63) in the intracellular amastigote life stage of Leishmania chagasi. Mol Biochem Parasitol 157(2): 148-159, 2008. PMID: 18067978; NIHMS 38613

Yao, C., Y. Chen, B. Sudan, J.E. Donelson, and M.E. Wilson. Leishmania chagasi: Homogenous metacyclic promastigotes isolated by buoyant density are highly virulent in a mouse model. Experimental Parasitology 118(1):129-133, 2008. PMID: 17706646

Jeronimo, S.M.B., P. Duggal, N.A. Ettinger, E.T. Nascimento, D.R.A. Martins, G. Monteiro, R.D. Pearson, J.M. Blackwell, T.H. Beaty, and M.E. Wilson. Genetic Predisposition to Self-Curing Infection with the Protozoan Leishmania chagasi: A Genome Wide Scan. J Infect Dis 196:1261-1269, 2007.

Jeronimo, S.M.B., A.K.B. Holst, S.E. Jamieson, R. Francis, D.R.A. Martins, N. Ettinger, E.T. Nascimento, E.N. Miller, H.J. Cordell, P. Duggal, T.H. Beaty, J.M. Blackwell, and M.E. Wilson. Genes at Human Chromosome 5q31.1 Regulate Delayed Type Hypersensitivity Responses Associated with Leishmania chagasi Infection. Genes and Immunity 8:539-551, 2007.

Yao, C., J.E. Donelson, and M.E. Wilson. Internal and surface-localized MSP of Leishmania and their differential release from promastigotes. Eukaryotic Cell 6(10):1905-1912, 2007.

See complete publication list at PubMed

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