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My research is mainly focused on identification and characterization of virulence factors involved in the intracellular survival of Mycobacterium tuberculosis (the etiological agent of Tuberculosis) and Mycobacterium avium (prevalent pathogen in HIV-patients). I identify M. tuberculosis effector proteins secreted within the human macrophages and dissecting cellular processes, targeted by these effectors, through genetic, bioinformatics and proteomic approaches to gain insights and establish the mechanism of mycobacterium pathogenesis. I also study the bacterial response to anti-tuberculosis compounds (new and in use ones) to understand fundamental aspects of M. tuberculosis response to therapy. The multidisciplinary approaches employing bacterial genetics, high throughput screening libraries, gene knockout systems, cell biology, high-resolution microscopy and mass-spectrometric techniques are used in the laboratory.
Danelishvili L, Wu M, Stang BV, Harriff M, Cirillo SLG, Cirillo S, Cirillo JD, Cirillo J, Bildfell RJ, Arbogast B et al.. 2007. Identification of Mycobacterium avium pathogenicity island important for macrophage and amoeba infection.. Proceedings of the National Academy of Sciences of the United States of America. 104(26):11038-43.
Patel D, Danelishvili L, Yamazaki Y, Alonso M, Paustian ML, Bannantine JP, Meunier-Goddik L, Bermudez LE. 2006. The ability of Mycobacterium avium subsp. paratuberculosis to enter bovine epithelial cells is influenced by preexposure to a hyperosmolar environment and intracellular passage in bovine mammary epithelial cells.. Infection and immunity. 74(5):2849-55.
Yamazaki Y, Danelishvili L, Wu M, Hidaka E, Katsuyama T, Stang BV, Petrofsky M, Bildfell RJ, Bermudez LE. 2006. The ability to form biofilm influences Mycobacterium avium invasion and translocation of bronchial epithelial cells.. Cellular microbiology. 8(5):806-14.