Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Faculty of Natural Sciences, Department of Life Sciences, Imperial College London, London, United Kingdom.
PLoS Pathog. 2024 Jun 27;20(6):e1012333. doi: 10.1371/journal.ppat.1012333. eCollection 2024 Jun.
The bloodstream form of Trypanosoma brucei expresses large poly-N-acetyllactosamine (pNAL) chains on complex N-glycans of a subset of glycoproteins. It has been hypothesised that pNAL may be required for receptor-mediated endocytosis. African trypanosomes contain a unique family of glycosyltransferases, the GT67 family. Two of these, TbGT10 and TbGT8, have been shown to be involved in pNAL biosynthesis in bloodstream form Trypanosoma brucei, raising the possibility that deleting both enzymes simultaneously might abolish pNAL biosynthesis and provide clues to pNAL function and/or essentiality. In this paper, we describe the creation of a TbGT10 null mutant containing a single TbGT8 allele that can be excised upon the addition of rapamycin and, from that, a TbGT10 and TbGT8 double null mutant. These mutants were analysed by lectin blotting, glycopeptide methylation linkage analysis and flow cytometry. The data show that the mutants are defective, but not abrogated, in pNAL synthesis, suggesting that other GT67 family members can compensate to some degree for loss of TbGT10 and TbGT8. Despite there being residual pNAL synthesis in these mutants, certain glycoproteins appear to be particularly affected. These include the lysosomal CBP1B serine carboxypeptidase, cell surface ESAG2 and the ESAG6 subunit of the essential parasite transferrin receptor (TfR). The pNAL deficient TfR in the mutants continued to function normally with respect to protein stability, transferrin binding, receptor mediated endocytosis of transferrin and subcellular localisation. Further the pNAL deficient mutants were as viable as wild type parasites in vitro and in in vivo mouse infection experiments. Although we were able to reproduce the inhibition of transferrin uptake with high concentrations of pNAL structural analogues (N-acetylchito-oligosaccharides), this effect disappeared at lower concentrations that still inhibited tomato lectin uptake, i.e., at concentrations able to outcompete lectin-pNAL binding. Based on these findings, we recommend revision of the pNAL-dependent receptor mediated endocytosis hypothesis.
布氏锥虫血腔变体在一组糖蛋白的复杂 N-糖链上表达大型多-N-乙酰乳糖胺 (pNAL) 链。据推测,pNAL 可能是受体介导的内吞作用所必需的。非洲锥虫含有一组独特的糖基转移酶,即 GT67 家族。其中两种,TbGT10 和 TbGT8,已被证明参与布氏锥虫血腔变体的 pNAL 生物合成,这增加了同时删除这两种酶可能会使 pNAL 生物合成完全终止的可能性,并为研究 pNAL 的功能和/或必要性提供线索。在本文中,我们描述了创建一个 TbGT10 缺失突变体的过程,该突变体含有一个可在添加雷帕霉素时切除的单 TbGT8 等位基因,从而构建了 TbGT10 和 TbGT8 双缺失突变体。通过凝集素印迹、糖肽甲基化连接分析和流式细胞术对这些突变体进行了分析。数据表明,这些突变体在 pNAL 合成中存在缺陷,但没有完全丧失,这表明其他 GT67 家族成员可以在一定程度上补偿 TbGT10 和 TbGT8 的缺失。尽管这些突变体中仍有残留的 pNAL 合成,但某些糖蛋白似乎受到特别影响。这些糖蛋白包括溶酶体 CBP1B 丝氨酸羧肽酶、细胞表面 ESAG2 和必需寄生虫转铁蛋白受体 (TfR) 的 ESAG6 亚基。突变体中缺乏 pNAL 的 TfR 在蛋白稳定性、转铁蛋白结合、转铁蛋白受体介导的内吞作用和亚细胞定位方面仍能正常发挥作用。此外,缺乏 pNAL 的突变体在体外和体内小鼠感染实验中与野生型寄生虫一样具有活力。尽管我们能够用高浓度的 pNAL 结构类似物(N-乙酰壳寡糖)重现转铁蛋白摄取的抑制作用,但这种作用在仍能抑制番茄凝集素摄取的较低浓度下消失,即在能够与凝集素-pNAL 结合竞争的浓度下。基于这些发现,我们建议修改 pNAL 依赖性受体介导的内吞作用假说。