1. Babesia bovis dihydroorotate dehydrogenase (BboDHODH) is a novel molecular target of drug for bovine babesiosis.
- Author
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Kamyingkird K, Cao S, Masatani T, Moumouni PF, Vudriko P, Mousa AA, Terkawi MA, Nishikawa Y, Igarashi I, and Xuan X
- Subjects
- Amino Acid Sequence, Animals, Babesiosis metabolism, Blotting, Western, Cattle, Cloning, Molecular, Computational Biology, DNA Primers genetics, Dihydroorotate Dehydrogenase, Drug Delivery Systems, Drug Discovery, Escherichia coli, Microscopy, Confocal, Molecular Sequence Data, Oxidoreductases Acting on CH-CH Group Donors genetics, Phylogeny, Recombinant Fusion Proteins genetics, Recombinant Fusion Proteins metabolism, Babesia bovis enzymology, Babesiosis drug therapy, Cattle Diseases drug therapy, Cattle Diseases parasitology, Enzyme Inhibitors metabolism, Oxidoreductases Acting on CH-CH Group Donors metabolism
- Abstract
The emergence of drug resistance and adverse side effects of current bovine babesiosis treatment suggest that the search of new drug targets and development of safer and effective compounds are required. This study focuses on dihydroorotate dehydrogenase (DHODH), the fourth enzyme of pyrimidine biosynthesis pathway as a potential drug target for bovine babesiosis. Recombinant Babesia bovis DHODH protein (rBboDHODH) was produced in Escherichia coli and used for characterization and measurement of enzymatic activity. Furthermore, the effects of DHODH inhibitors were evaluated in vitro. The recombinant B. bovis DHODH histidine fusion protein (rBboDHODH) had 42.4-kDa molecular weight and exhibited a specific activity of 475.7 ± 245 Unit/mg, a Km = 276.2 µM for L-dihydroorotate and a Km= 94.41 µM for decylubiquinone. A 44-kDa band of native BboDHODH was detected by Western blot analysis and found in parasites mitochondria using a confocal microscope. Among DHODH inhibitors, atovaquone (ATV) and leflunomide (LFN) significantly inhibited the activity of rBboDHODH as well as the growth of B. bovis in vitro. The half maximal inhibitory concentration (IC50) of ATV and LFN was 2.38 ± 0.53 nM and 52.41 ± 11.47 µM, respectively. These results suggest that BboDHODH might be a novel target for development of new drug for treatment of B. bovis infection.
- Published
- 2014
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