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Variations in the Peritrophic Matrix Composition of Heparan Sulphate from the Tsetse Fly Glossina morsitans morsitans

机译:采采蝇Glossina morsitans morsitans硫酸乙酰肝素的周围营养基质组成的变化

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摘要

Tsetse flies are the principal insect vectors of African trypanosomes—sleeping sickness in humans and Nagana in cattle. One of the tsetse fly species, Glossina morsitans morsitans, is host to the parasite, Trypanosoma brucei, a major cause of African trypanosomiasis. Precise details of the life cycle have yet to be established, but the parasite life cycle involves crossing the insect peritrophic matrix (PM). The PM consists of the polysaccharide chitin, several hundred proteins, and both glycosamino- and galactosaminoglycan (GAG) polysaccharides. Owing to the technical challenges of detecting small amounts of GAG polysaccharides, their conclusive identification and composition have not been possible until now. Following removal of PMs from the insects and the application of heparinases (bacterial lyase enzymes that are specific for heparan sulphate (HS) GAG polysaccharides), dot blots with a HS-specific antibody showed heparan sulphate proteoglycans (HSPGs) to be present, consistent with Glossina morsitans morsitans genome analysis, as well as the likely expression of the HSPGs syndecan and perlecan. Exhaustive HS digestion with heparinases, fluorescent labeling of the resulting disaccharides with BODIPY fluorophore, and separation by strong anion exchange chromatography then demonstrated the presence of HS for the first time and provided the disaccharide composition. There were no significant differences in the type of disaccharide species present between genders or between ages (24 vs. 48 h post emergence), although the HS from female flies was more heavily sulphated overall. Significant differences, which may relate to differences in infection between genders or ages, were evident, however, in overall levels of 2-O-sulphation between sexes and, for females, between 24 and 48 h post-emergence, implying a change in expression or activity for the 2-O-sulphotransferase enzyme. The presence of significant quantities of disaccharides containing the monosaccharide GlcNAc6S contrasts with previous findings in Drosophila melanogaster and suggests subtle differences in HS fine structure between species of the Diptera.
机译:采采蝇是非洲锥虫的主要昆虫媒介,即人类的昏睡病和牛的长g。采采蝇中的一种,即Glossina morsitans morsitans,是该寄生虫布鲁氏锥虫的宿主,锥虫是非洲锥虫病的主要原因。生命周期的精确细节尚未确定,但寄生虫的生命周期涉及穿越昆虫的营养层(PM)。 PM由多糖几丁质,数百种蛋白质以及糖胺聚糖和半乳糖胺聚糖(GAG)多糖组成。由于检测少量GAG多糖的技术挑战,直到现在,它们的结论性鉴定和组成仍无法实现。从昆虫身上清除PM并应用肝素酶(硫酸乙酰肝素(HS)GAG多糖特有的细菌裂解酶)后,用HS特异性抗体的斑点印迹显示存在硫酸乙酰肝素蛋白聚糖(HSPG),与Glossina morsitans morsitans基因组分析以及HSPGs syndecan和perlecan的可能表达。用肝素酶进行详尽的HS消化,用BODIPY荧光团对所得二糖进行荧光标记,并通过强阴离子交换色谱分离,然后首次证明了HS的存在并提供了二糖的组成。尽管雌蝇的HS总体上被硫酸化程度更高,但性别之间或年龄之间(出苗后24 vs. 48 h)存在的二糖种类类型没有显着差异。但是,在性别之间以及在女性出苗后24至48小时之间的2-O硫酸盐总体水平上,存在明显的差异,这可能与性别或年龄之间的感染差异有关。或2-O-磺基转移酶的活性。含有单糖GlcNAc6S的大量二糖的存在与果蝇(Drosophila melanogaster)先前的发现形成了鲜明对比,并表明双翅目物种之间HS精细结构存在细微差异。

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