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DOI 10.1645/ge-633r.1

Медицинская библиотека · The Journal of parasitology · 2006

Effects of polyamines on two strains of Trypanosoma brucei in infected rats and in vitro culture.

Nishimura Kazuhiko, Yanase Takako, Araki Noriko, Ohnishi Yoshihiro, Kozaki Shunji, Shima Kensuke, Asakura Masahiro, Samosomsuk Worada, Yamasaki Shinji

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Аннотация

We studied the effects of polyamines, which are necessary for proliferation and antioxidation in Trypanosoma brucei gambiense Wellcome strain (WS) and Trypanosoma brucei brucei ILtat 1.4 strain (IL). No difference was found in activity of ornithine decarboxylase (ODC), a key enzyme in polyamine synthesis in trypanosomes, in both strains maintained in vitro; higher (P < 0.05) ODC values were found in IL in vivo. However, WS in vivo exhibited higher proliferation rates with higher spermidine content and decreased host survival times than IL. The in vitro proliferation and polyamine contents of WS increased with the addition of polyamine to the 1-difluoromethylornithine culture medium, but not IL. These results suggested that WS uses extracellular polyamine for proliferation. In the in vitro culture, WS was less tolerant of hydrogen peroxide (oxidative stress) than IL, and malondialdehyde levels in WS were higher than in IL. The expression of trypanothione synthetase mRNA in WS in vitro was higher than in IL. These results suggest that IL is dependent on the synthesis of polyamines for proliferation and reduction of oxidative stress, whereas WS is dependent on the uptake of extracellular polyamines. A thorough understanding of the differences in the metabolic capabilities of various trypanosomes is important for the design of more effective medical treatments.

Для цитирования: Nishimura Kazuhiko, Yanase Takako, Araki Noriko, Ohnishi Yoshihiro, Kozaki Shunji, Shima Kensuke, Asakura Masahiro, Samosomsuk Worada, Yamasaki Shinji. Effects of polyamines on two strains of Trypanosoma brucei in infected rats and in vitro culture.. The Journal of parasitology. 2006. DOI: 10.1645/ge-633r.1.

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