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动质体循环利用葡萄糖分解产物和三羧酸循环中间产物,以刺激在生理浓度脯氨酸存在下的生长。

Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline.

机构信息

Univ. Bordeaux, CNRS, Microbiologie Fondamentale et Pathogénicité (MFP), UMR 5234, Bordeaux, France.

Univ. Bordeaux, CNRS, Centre de Résonance Magnétique des Systèmes Biologiques (CRMSB), UMR 5536, Bordeaux, France.

出版信息

PLoS Pathog. 2021 Mar 1;17(3):e1009204. doi: 10.1371/journal.ppat.1009204. eCollection 2021 Mar.

Abstract

Trypanosoma brucei, a protist responsible for human African trypanosomiasis (sleeping sickness), is transmitted by the tsetse fly where the procyclic forms of the parasite develop in the proline-rich (1-2 mM) and glucose-depleted digestive tract. Proline is essential for the midgut colonization of the parasite in the insect vector, however other carbon sources could be available and used to feed its central metabolism. Here we show that procyclic trypanosomes can consume and metabolize metabolic intermediates, including those excreted from glucose catabolism (succinate, alanine and pyruvate), with the exception of acetate, which is the ultimate end-product excreted by the parasite. Among the tested metabolites, tricarboxylic acid (TCA) cycle intermediates (succinate, malate and α-ketoglutarate) stimulated growth of the parasite in the presence of 2 mM proline. The pathways used for their metabolism were mapped by proton-NMR metabolic profiling and phenotypic analyses of thirteen RNAi and/or null mutants affecting central carbon metabolism. We showed that (i) malate is converted to succinate by both the reducing and oxidative branches of the TCA cycle, which demonstrates that procyclic trypanosomes can use the full TCA cycle, (ii) the enormous rate of α-ketoglutarate consumption (15-times higher than glucose) is possible thanks to the balanced production and consumption of NADH at the substrate level and (iii) α-ketoglutarate is toxic for trypanosomes if not appropriately metabolized as observed for an α-ketoglutarate dehydrogenase null mutant. In addition, epimastigotes produced from procyclics upon overexpression of RBP6 showed a growth defect in the presence of 2 mM proline, which is rescued by α-ketoglutarate, suggesting that physiological amounts of proline are not sufficient per se for the development of trypanosomes in the fly. In conclusion, these data show that trypanosomes can metabolize multiple metabolites, in addition to proline, which allows them to confront challenging environments in the fly.

摘要

布氏锥虫,一种引起人类非洲锥虫病(昏睡病)的原生动物,由采采蝇传播,寄生虫的前循环形式在前肠中发育,前肠中富含脯氨酸(1-2mM)且葡萄糖耗竭。脯氨酸对寄生虫在昆虫媒介中的中肠定殖至关重要,但其他碳源可能可用并用于支持其中心代谢。在这里,我们表明前环锥虫可以消耗和代谢代谢中间产物,包括从葡萄糖分解代谢中排泄的那些(琥珀酸、丙氨酸和丙酮酸),但醋酸盐除外,醋酸盐是寄生虫排泄的最终终产物。在测试的代谢物中,三羧酸 (TCA) 循环中间产物(琥珀酸、苹果酸和α-酮戊二酸)在 2mM 脯氨酸存在的情况下刺激寄生虫的生长。通过质子-NMR 代谢谱分析和影响中央碳代谢的 13 个 RNAi 和/或缺失突变体的表型分析,绘制了它们的代谢途径。我们表明:(i) 苹果酸通过 TCA 循环的还原和氧化分支转化为琥珀酸,这表明前环锥虫可以使用完整的 TCA 循环;(ii) α-酮戊二酸的消耗率极高(比葡萄糖高 15 倍),这是由于在底物水平上 NADH 的产生和消耗平衡;(iii) 如果不能适当代谢,如α-酮戊二酸脱氢酶缺失突变体,α-酮戊二酸对锥虫是有毒的。此外,前环虫在 RBP6 过表达后产生的epimastigotes 在 2mM 脯氨酸存在下表现出生长缺陷,但可通过α-酮戊二酸挽救,这表明生理量的脯氨酸本身不足以支持锥虫在蝇中的发育。总之,这些数据表明,锥虫除了脯氨酸外,还可以代谢多种代谢物,这使它们能够在蝇中面对具有挑战性的环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e8c/7951978/1c2b84e7b2fa/ppat.1009204.g001.jpg

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