Russo-Abrahão Thais, Koeller Carolina Macedo, Steinmann Michael E, Silva-Rito Stephanie, Marins-Lucena Thaissa, Alves-Bezerra Michele, Lima-Giarola Naira Ligia, de-Paula Iron Francisco, Gonzalez-Salgado Amaia, Sigel Erwin, Bütikofer Peter, Gondim Katia Calp, Heise Norton, Meyer-Fernandes José Roberto
Instituto de Microbiologia Professor Paulo de Góes, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Instituto de Bioquímica Médica Leopoldo de Meis, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, 21941-590, Brazil.
J Bioenerg Biomembr. 2017 Apr;49(2):183-194. doi: 10.1007/s10863-017-9695-y. Epub 2017 Feb 9.
Trypanosoma brucei is an extracellular protozoan parasite that causes human African trypanosomiasis or "sleeping sickness". During the different phases of its life cycle, T. brucei depends on exogenous inorganic phosphate (P), but little is known about the transport of P in this organism. In the present study, we showed that the transport of P across the plasma membrane follows Michaelis-Menten kinetics and is modulated by pH variation, with higher activity at acidic pH. Bloodstream forms presented lower P transport in comparison to procyclic forms, that displayed an apparent K = 0.093 ± 0.008 mM. Additionally, FCCP (H-ionophore), valinomycin (K-ionophore) and SCH28080 (H, K-ATPase inhibitor) inhibited the P transport. Gene Tb11.02.3020, previously described to encode the parasite H:myo-inositol transporter (TbHMIT), was hypothesized to be potentially involved in the H:P cotransport because of its similarity with the Pho84 transporter described in S. cerevisiae and other trypanosomatids. Indeed, the RNAi mediated knockdown remarkably reduced TbHMIT gene expression, compromised cell growth and decreased P transport by half. In addition, P transport was inhibited when parasites were incubated in the presence of concentrations of myo-inositol that are above 300 μM. However, when expressed in Xenopus laevis oocytes, two-electrode voltage clamp experiments provided direct electrophysiological evidence that the protein encoded by TbHMIT is definitely a myo-inositol transporter that may be only marginally affected by the presence of P. These results confirmed the presence of a P carrier in T. brucei, similar to the H-dependent inorganic phosphate system described in S. cerevisiae and other trypanosomatids. This transport system contributes to the acquisition of P and may be involved in the growth and survival of procyclic forms. In summary, this work presents the first description of a P transport system in T. brucei.
布氏锥虫是一种细胞外原生动物寄生虫,可导致人类非洲锥虫病或“昏睡病”。在其生命周期的不同阶段,布氏锥虫依赖外源无机磷酸盐(P),但关于该生物体中P的转运情况知之甚少。在本研究中,我们表明P跨质膜的转运遵循米氏动力学,并受pH变化调节,在酸性pH下活性更高。与前循环型相比,血流型的P转运较低,前循环型的表观K = 0.093±0.008 mM。此外,FCCP(H离子载体)、缬氨霉素(K离子载体)和SCH28080(H,K-ATP酶抑制剂)抑制P转运。基因Tb11.02.3020,先前描述为编码寄生虫H:肌醇转运体(TbHMIT),由于其与酿酒酵母和其他锥虫中描述的Pho84转运体相似,被推测可能参与H:P共转运。实际上,RNA干扰介导的敲低显著降低了TbHMIT基因表达,损害了细胞生长,并使P转运减少了一半。此外,当寄生虫在高于300μM的肌醇浓度下孵育时,P转运受到抑制。然而,当在非洲爪蟾卵母细胞中表达时,双电极电压钳实验提供了直接的电生理证据,表明TbHMIT编码的蛋白质绝对是一种肌醇转运体,可能仅受到P存在的轻微影响。这些结果证实了布氏锥虫中存在P载体,类似于酿酒酵母和其他锥虫中描述的H依赖性无机磷酸盐系统。这种转运系统有助于P的获取,并可能参与前循环型的生长和存活。总之,这项工作首次描述了布氏锥虫中的P转运系统。