Studies are proposed to evaluate the hypothesis that marine bacteria produce compounds that can inhibit the growth of mycobacteria. The control of mycobacteria is of significant concern throughout the world as pathogenic species, such as Mycobacterium tuberculosis, show increasing rates of resistance to the antibiotics currently available. A second hypothesis, based on preliminary observations in our laboratory as well as related work described in the literature, proposes that antibiotic production can be induced in marine bacteria. This hypothesis will be tested through the challenge of pure cultures of marine bacteria with a mycobacterium. If results of these experiments are consistent with previous observations, induction could represent a significant new tool in the search for novel antibiotic compounds. The mycobacteria to be used in the work art CSU San Marcos will include M. marinum, a marine/aquatic bacterium known to cause a disease commonly referred to as swimming pool granuloma. This mycobacterial species can be handled safely in our laboratory, and it can serve as an indicator species for anti- mycobacterial activity in general. In addition, 3 non-pathogenic mycobacterial strains encompassing a wide range of physiological characteristics found in mycobacteria will be purchased from the ATCC and used as indicator strains. Any extracts or pure compounds exhibiting inhibitory activity against any of the 4 indicator strains will be submitted to th4e TAACF for anti-tuberculosis screening. This proposal focuses on the isolation and culture of genera of marine bacteria previously shown to include producers of novel antibiotics, such as Chromacterium and Alteromonas. Bacterial isolates will be grown in pure culture and their metabolic products extracted. Each extract will then be tested for the presence of anti-mycobacterial compounds using an agar disk elution assay and chemical evaluation (NMR, TLC). Promising bacterial strains will be cultured on a large scale, and their extracts will be subjected to in-depth chemical and biological analyses. Chemical separation methods will include various chromatographic methods. Structure elucidation will be performing using a variety of modern spectroscopic techniques in conjunction with standard degradation, derivation and synthetic methods as needed. Biological assays will be conducted with each separation step. Overall, the research will target anti- mycobacterial compounds, with particular focus on the discovery of potential therapies for tuberculosis and infections caused by M. marinum.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Minority Biomedical Research Support - MBRS (S06)
Project #
5S06GM059833-03
Application #
6504126
Study Section
Minority Programs Review Committee (MPRC)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
3
Fiscal Year
2001
Total Cost
$230,840
Indirect Cost
Name
California State University San Marcos
Department
Type
DUNS #
176262681
City
San Marcos
State
CA
Country
United States
Zip Code
92078
Melkani, Girish C; Sielaff, Robin; Zardeneta, Gustavo et al. (2012) Interaction of oxidized chaperonin GroEL with an unfolded protein at low temperatures. Biosci Rep 32:299-303
Pasquini, Sarah C; Vourlitis, George L (2010) Post-fire primary production and plant community dynamics in chaparral stands exposed to varying levels of nitrogen deposition. J Arid Environ 74:310-314
Vourlitis, George L; Pasquini, Sarah C (2009) Experimental dry-season N deposition alters species composition in southern Californian mediterranean-type shrublands. Ecology 90:2183-9
Hizer, S E; Tamulis, W G; Robertson, L M et al. (2008) Evidence of multiple retrotransposons in two litopenaeid species. Anim Genet 39:363-73
Melkani, Girish C; Sielaff, Robin L; Zardeneta, Gustavo et al. (2008) Divalent cations stabilize GroEL under conditions of oxidative stress. Biochem Biophys Res Commun 368:625-30
Trujillo, Keith A; Zamora, Juan J; Warmoth, Kathleen P (2008) Increased response to ketamine following treatment at long intervals: implications for intermittent use. Biol Psychiatry 63:178-83
Mendez, Ian A; Trujillo, Keith A (2008) NMDA receptor antagonists inhibit opiate antinociceptive tolerance and locomotor sensitization in rats. Psychopharmacology (Berl) 196:497-509
Mothe, Bianca R; Stewart, Barbara S; Oseroff, Carla et al. (2007) Chronic lymphocytic choriomeningitis virus infection actively down-regulates CD4+ T cell responses directed against a broad range of epitopes. J Immunol 179:1058-67
Trujillo, Keith A; Castaneda, Edward; Martinez, Diana et al. (2006) Biological research on drug abuse and addiction in Hispanics: current status and future directions. Drug Alcohol Depend 84 Suppl 1:S17-28
Melkani, Girish C; Zardeneta, Gustavo; Mendoza, Jose A (2005) On the chaperonin activity of GroEL at heat-shock temperature. Int J Biochem Cell Biol 37:1375-85

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