Müller Joachim, Vermathen Martina, Leitsch David, Vermathen Peter, Müller Norbert
Institute of Parasitology, Vetsuisse Faculty, University of Bern, Länggass-Strasse 122, CH-3012 Bern, Switzerland.
Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
Metabolites. 2020 Jan 30;10(2):53. doi: 10.3390/metabo10020053.
, a causative agent of persistent diarrhea in humans, domestic animals, and cattle, is usually treated with nitro compounds. Consequently, enzymes involved in anaerobic nitro reduction have been investigated in detail as potential targets. Their role within the normal metabolic context is, however, not understood. Using H high-resolution magic angle spinning (HR-MAS) NMR spectroscopy, we analyzed the metabolomes of trophozoites overexpressing three nitroreductases (NR1-NR3) and thioredoxin reductase (TrxR), most likely a scavenger of reactive oxygen species, as suggested by the results published in this study. We compared the patterns to convenient controls and to the situation in the nitro drug resistant strain C4 where NR1 is downregulated. We identified 27 metabolites in trophozoites. Excluding metabolites of high variability among different wildtype populations, only trophozoites overexpressing NR1 presented a distinct pattern of nine metabolites, in particular arginine catabolites, differing from the respective controls. This pattern matched a differential pattern between wildtype and strain C4. This suggests that NR1 interferes with arginine and thus energy metabolism. The exact metabolic function of NR1 (and the other nitroreductases) remains to be elucidated.
作为人类、家畜和牛持续性腹泻的病原体,通常用硝基化合物进行治疗。因此,参与厌氧硝基还原的酶作为潜在靶点已被详细研究。然而,它们在正常代谢环境中的作用尚不清楚。本研究结果表明,硫氧还蛋白还原酶(TrxR)可能是一种活性氧清除剂,我们使用高分辨率魔角旋转(HR-MAS)核磁共振波谱分析了过表达三种硝基还原酶(NR1-NR3)和硫氧还蛋白还原酶(TrxR)的滋养体的代谢组。我们将这些模式与方便的对照以及硝基耐药菌株C4(其中NR1下调)的情况进行了比较。我们在滋养体中鉴定出27种代谢物。排除不同野生型群体中高变异性的代谢物,只有过表达NR1的滋养体呈现出9种代谢物的独特模式,特别是精氨酸分解代谢物,与各自的对照不同。这种模式与野生型和C4菌株之间的差异模式相匹配。这表明NR1干扰精氨酸,从而干扰能量代谢。NR1(和其他硝基还原酶)的确切代谢功能仍有待阐明。