Nyame A Kwame, Yoshino Timothy P, Cummings Richard D
Department of Biochemistry and Molecular Biology, The Oklahoma Center for Medical Glycobiology, University of Oklahoma Health Sciences Center, Oklahoma City 73104, USA.
J Parasitol. 2002 Oct;88(5):890-7. doi: 10.1645/0022-3395(2002)088[0890:DEOLFL]2.0.CO;2.
We report the expression of 3 well-characterized adult Schistosoma mansoni glycan antigens among molluscan stages of the parasite. These antigens are LacdiNAc (LDN; GalNAcbeta1-4GlcNAc-R), fucosylated LacdiNAc (LDNF; GalNAc[Fucal-3]beta1-4GlcNAc-R), and Lewis x (Le(x); Gal[Fucalpha1-3]beta1-4GlcNAc-R). The presence of the glycans was determined by both immunoblot and immunohistological methods using monoclonal antibodies that specifically recognize each glycan epitope. Immunoblot analyses reveal that LDN and LDNF epitopes are expressed on many different glycoproteins, including eggs, mother sporocysts, daughter sporocysts, and cercariae, although LDN expression among daughter sporocysts is greatly reduced. LDN and LDNF epitopes are localized on the tegument and in the intrasporocyst cell masses of both in vitro-derived and in vivo-derived mother sporocysts and in the daughter sporocysts derived on day 16 after infection. Unexpectedly, high levels of LDN and LDNF glycans were detected in the infected, but not in the uninfected, snail hemolymph, suggesting that the infecting larvae secrete LDN and LDNF glycoconjugates into the snail hosts. In contrast, the expression of Le(x) antigen among the molluscan stages is highly restricted. Le(x) is present on a few high-molecular weight glycoproteins in eggs and cercariae but is undetectable in mother and daughter sporocysts. Taken together with our earlier studies on vertebrate stages of S. mansoni, these results show that LDN and LDNF glycans are conserved during schistosome development. The study further extends the evidence that Le(x) is a developmentally regulated antigen in schistosomes.
我们报道了3种特征明确的曼氏血吸虫成年期聚糖抗原在该寄生虫软体动物阶段的表达情况。这些抗原分别是乳糖-N-新四糖(LDN;GalNAcbeta1-4GlcNAc-R)、岩藻糖基化乳糖-N-新四糖(LDNF;GalNAc[Fucalpha1-3]beta1-4GlcNAc-R)和Lewis x(Le(x);Gal[Fucalpha1-3]beta1-4GlcNAc-R)。通过使用特异性识别每种聚糖表位的单克隆抗体,采用免疫印迹和免疫组织学方法确定了聚糖的存在。免疫印迹分析表明,LDN和LDNF表位在许多不同的糖蛋白上表达,包括虫卵、母胞蚴、子胞蚴和尾蚴,尽管子胞蚴中LDN表达大幅降低。LDN和LDNF表位定位于体外培养和体内获取的母胞蚴以及感染后第16天产生的子胞蚴的体表和胞蚴内细胞团中。出乎意料的是,在感染的而非未感染的钉螺血淋巴中检测到高水平的LDN和LDNF聚糖,这表明感染性幼虫向钉螺宿主分泌LDN和LDNF糖缀合物。相比之下,Le(x)抗原在软体动物阶段的表达受到高度限制。Le(x)存在于虫卵和尾蚴中的一些高分子量糖蛋白上,但在母胞蚴和子胞蚴中未检测到。结合我们早期对曼氏血吸虫脊椎动物阶段的研究,这些结果表明LDN和LDNF聚糖在血吸虫发育过程中是保守的。该研究进一步扩展了证据,表明Le(x)是血吸虫中一种受发育调控的抗原。