The objective of this research is to gain an understanding of the mechanism(s) underlying drug resistance in the human parasite, Trichomonas vaginalis. Strains of T. vaginalis that are resistant to metronidazole, the only drug available in the U.S. for treatment, arise at a low frequency. Our preliminary studies show that four clinical isolates, refractory to treatment with metronidazole, have decreased intracellular levels of ferredoxin and its mRNA. Ferredoxin is a hydrogenosomal protein which is required to reduce metronidazole to its cytotoxic form. To our knowledge, this is the first demonstration of drug resistance arising due to the inability of the cell to chemically modify a drug to its active form. Additionally, we have shown that ferredoxin gene transcription is reduced in two of these resistant isolates. This indicates that regulation of gene expression is the basis of resistance.
The specific aims of the proposed studies are: 1) to examine the levels of ferredoxin, as well as other hydrogenosomal proteins which are involved in drug activation, in additional sensitive and resistant lines. Resistant cell lines which have decreased intracellular levels of ferredoxin will be examined to determine if ferredoxin mRNA and/or gene transcription is altered. 2)to examine the 5' and 3' sequences flanking the ferredoxin gene in resistant and sensitive strains for differences which might account for altered transcription of the gene in resistant lines. DNA sequence motifs, and the proteins which bind to such putative transcriptional regulatory elements, will be studied. In addition to examining the mechanism of drug resistance, these studies provide a framework for exploring gene expression in this primitive eukaryote. Thus, the proposed investigation addresses both medically and fundamentally important aspects of the biology of this human pathogen. A better knowledge of the mechanisms underlying resistance will be critical for designing effective treatment regimens for cases refractory to treatment. In addition to treating trichomoniasis, metronidazole is commonly used in treatment of infections caused by other anaerobic organisms, such as Entamoeba, Giardia, Bacteroides, and Clostridium. Isolates of these organisms which are relatively resistant to the drug have been reported, but virtually nothing is known regarding the mechanism of resistance. Thus our studies on metronidazole resistance in T. vaginalis may possibly shed light on the basis of resistance in a number of pathogenic bacteria and protozoa.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI030537-01A1
Application #
3145556
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1991-09-01
Project End
1994-08-31
Budget Start
1991-09-01
Budget End
1992-08-31
Support Year
1
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Simoes-Barbosa, Augusto; Chakrabarti, Kausik; Pearson, Michael et al. (2012) Box H/ACA snoRNAs are preferred substrates for the trimethylguanosine synthase in the divergent unicellular eukaryote Trichomonas vaginalis. RNA 18:1656-65
Smith, Alias J; Chudnovsky, Lorissa; Simoes-Barbosa, Augusto et al. (2011) Novel core promoter elements and a cognate transcription factor in the divergent unicellular eukaryote Trichomonas vaginalis. Mol Cell Biol 31:1444-58
Smith, Alias; Johnson, Patricia (2011) Gene expression in the unicellular eukaryote Trichomonas vaginalis. Res Microbiol 162:646-54
Simoes-Barbosa, Augusto; Hirt, Robert P; Johnson, Patricia J (2010) A metazoan/plant-like capping enzyme and cap modified nucleotides in the unicellular eukaryote Trichomonas vaginalis. PLoS Pathog 6:e1000999
Simoes-Barbosa, Augusto; Louly, Camila; Franco, Octavio L et al. (2008) The divergent eukaryote Trichomonas vaginalis has an m7G cap methyltransferase capable of a single N2 methylation. Nucleic Acids Res 36:6848-58
Simoes-Barbosa, Augusto; Meloni, Dionigia; Wohlschlegel, James A et al. (2008) Spliceosomal snRNAs in the unicellular eukaryote Trichomonas vaginalis are structurally conserved but lack a 5'-cap structure. RNA 14:1617-31
Lau, Audrey O T; Smith, Alias J; Brown, Mark T et al. (2006) Trichomonas vaginalis initiator binding protein (IBP39) and RNA polymerase II large subunit carboxy terminal domain interaction. Mol Biochem Parasitol 150:56-62
Vanacova, Stepanka; Yan, Weihong; Carlton, Jane M et al. (2005) Spliceosomal introns in the deep-branching eukaryote Trichomonas vaginalis. Proc Natl Acad Sci U S A 102:4430-5
Land, Kirkwood M; Delgadillo-Correa, Maria G; Tachezy, Jan et al. (2004) Targeted gene replacement of a ferredoxin gene in Trichomonas vaginalis does not lead to metronidazole resistance. Mol Microbiol 51:115-22
Schumacher, Maria A; Lau, Audrey O T; Johnson, Patricia J (2003) Structural basis of core promoter recognition in a primitive eukaryote. Cell 115:413-24

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