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Trypanosome

Noble M E M, R K Wierenga, A-M Lambeir, F R Opperdoes, W H Thunnissen, K H Kalk, H Groendijk and W G J Hoi 1991. The Adaptability of the Active Site of Trypanosomal Triosephosphate Isomerase as Observed in the Crystal Structures of Three Different Complexes. Proteins Structure, Function and Genetics 10 50-69. [Pg.576]

Eflornithine (difluoromethylornithine, DFMO) inhibits the ornithine decarboxylase of the polyamine pathway, in both the trypanosome and the mammalian cell, by acting as an irreversible competitor of the natural substrate ornithine. Inhibition of ornithine decarboxylase results in depletion of the polyamines, putrescine, spermidine and spermine, which are essential for cell proliferation. Eflornithine selectively harms the parasite and not the mammalian cells, despite acting as an ornithine decarboxylase inhibitor in both cell types. This selectivity is explained by the lower rate of ornithine decarboxylase production in the parasite, as compared to mammalian cells. Due to the high turnover rate, mammalian cells are capable of quickly replenishing inhibited ornithine decarboxylase by newly... [Pg.179]

Melarsoprol, a trivalent organic melaminophenyl arsenic compound, kills intracerebral parasites of both T. brucei gambiense and T. brucei rhodesiense. Melarsoprol accumulates via an adenosine/adenine transporter in trypanosomes and is believed to inhibit glycolytic enzymes. Melarsoprol leads to a rapid lysis of trypanosomes. Melarsoprol is highly toxic to humans. [Pg.179]

Suramin, a symmetrical, polysulfonated naphthyl-amine, inhibits a number of trypanosomal enzymes however, the importance of these effects on parasite killing is not clear. [Pg.179]

Muhich, M.L. Boothroyd, J.C. (1989). Synthesis of trypanosome hsp70 mRNA is resistant to disruption of trans-splicing by heat shock Mol. Cell. Biol. 8, 3837-3846. [Pg.458]

Vickerman, K. (1974). Antigenic variation in African trypanosomes. Ciba Found. Symp. 25, 53-80. [Pg.235]

Hoet S, Stevigny C, Block S, et al. Alkaloids from Cassytha filiformis and related apor-phines anti-trypanosomal activity, cytotoxicity, and interaction with DNA and topoisomerases. Planta Med 2004 70 407-413. [Pg.164]

Welburn, S.C., Arnold, K., Maudlin, I. and Gooday, G.W. (1993) Rickettsia-like organisms and chitinase production in relation to transmission of trypanosomes by tsetse flies. Parasitology 107,141-145. [Pg.218]

Quinoxaline bis-A-oxides have been investigated as potential anti-cancer agents 93 <06BMC6917> and anti-trypanosomal agents 94 <06BMC5503>. In the latter case, a vanadyl complex was prepared in order to increase bioavailability. [Pg.409]

Bangs, J.D., Andrews, N.W., Hart, G.W., and Englund, P.T. (1986) Post-translational modification and intracellular transport of a trypanosome variant surface glycoprotein./. Cell Biol. 103, 255-263. [Pg.1045]

The second parasitic disease we want to consider is sleeping sickness, or African trypanosomiasis, as it is also known. Sleeping sickness results from an infection by protozoa called trypanosomes that are closely related to Leishmania, and, like leishmaniasis, sleeping sickness is spread by flies. On a more general level, however, the two diseases seem quite distinct. Leishmaniasis takes several forms, only one of which is fatal, but untreated sleeping sickness invariably leads to death. Leishmaniasis is a menace in much of the... [Pg.79]

Both male and female tsetse live solely on vertebrate blood, and the various species that carry sleeping sickness typically feed not only on humans but also on both domestic and wild animals. Infected flies pass on trypanosomes whenever they take a blood meal, so that the parasites not only move between flies and humans, but also infect a number of other hosts. Infected domestic animals develop nagana, but wild animals may show no sign of illness. They serve instead as healthy animal reservoirs of trypanosomes, permitting tsetse flies to pick up the parasites at any time without necessarily feeding on infected humans or domestic animals. For this reason and also because available drug therapies have proved no more practical here than for leishmaniasis, control of trypanosomiasis has long emphasized eradication of tsetse flies. [Pg.82]


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African trypanosomes, metabolism

Anti-trypanosomal agents

Cell free systems trypanosomes

DNA, forms circular, in trypanosomes

Enzymes trypanosomes

Genome trypanosomes

Trans-sialidases, trypanosomal

Trypanosomal

Trypanosomal biological activity

Trypanosomal infection

Trypanosome DNA circles

Trypanosome brucia

Trypanosome mitochondria

Trypanosomes

Trypanosomes drug resistance

Trypanosomes gene expression

Trypanosomes kinetoplast

Trypanosomes mechanism

Trypanosomes metabolism

Trypanosomes mitochondria

Trypanosomes molecular biology

Trypanosomes protein coding genes

Trypanosomes transcription

Trypanosomes, application

Trypanosomes, trans- splicing

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