Department of Molecular Parasitology, Sungkyunkwan University School of Medicine and Center for Molecular Medicine, Samsung Biomedical Research Institute, Suwon 446-740, Republic of Korea.
Parasitology. 2012 Sep;139(10):1361-74. doi: 10.1017/S0031182012000613. Epub 2012 Jun 1.
Taenia solium, a causative agent of taeniasis and cysticercosis, has evolved a repertoire of lipid uptake mechanisms. Proteome analysis of T. solium excretory-secretory products (TsESP) identified 10 kDa proteins displaying significant sequence identity with cestode hydrophobic-ligand-binding-proteins (HLBPs). Two distinct 362- and 352-bp-long cDNAs encoding 264- and 258-bp-long open reading frames (87 and 85 amino acid polypeptides) were isolated by mining the T. solium expressed sequence tags and a cDNA library screening (TsHLBP1 and TsHLBP2; 94% sequence identity). They clustered into the same clade with those found in Moniezia expansa and Hymenolepis diminuta. Genomic structure analysis revealed that these genes might have originated from a common ancestor. Both the crude TsESP and bacterially expressed recombinant proteins exhibited binding activity toward 1-anilinonaphthalene-8-sulfonic acid (1,8-ANS), which was competitively inhibited by oleic acid. The proteins also bound to cis-parinaric acid (cPnA) and 16-(9-anthroyloxy) palmitic acid (16-AP), but showed no binding activity against 11-[(5-dimethylaminonaphthalene-1-sulfonyl) amino] undecanoic acid (DAUDA) and dansyl-DL-α-aminocaprylic acid (DACA). Unsaturated fatty acids (FAs) showed greater affinity than saturated FAs. The proteins were specifically expressed in adult worms throughout the strobila. The TsHLBPs might be involved in uptake and/or sequestration of hydrophobic molecules provided by their hosts, thus contributing to host-parasite interface interrelationships.
猪带绦虫是带绦虫病和囊尾蚴病的病原体,它进化出了一系列脂质摄取机制。对猪带绦虫排泄分泌产物(TsESP)的蛋白质组分析鉴定出 10 kDa 蛋白,这些蛋白与绦虫疏水性配体结合蛋白(HLBPs)具有显著的序列同一性。通过挖掘猪带绦虫表达序列标签和 cDNA 文库筛选,分离出两个不同的 362 和 352 bp 长的 cDNA,分别编码 264 和 258 bp 长的开放阅读框(87 和 85 个氨基酸多肽)。这些 cDNA 被命名为 TsHLBP1 和 TsHLBP2,它们与 Moniezia expansa 和 Hymenolepis diminuta 中的同源物聚类在一起。基因组结构分析表明,这些基因可能起源于一个共同的祖先。粗提的 TsESP 和细菌表达的重组蛋白都表现出与 1-苯胺基萘-8-磺酸(1,8-ANS)的结合活性,该活性可被油酸竞争性抑制。这些蛋白还与顺式-壬烯酸(cPnA)和 16-(9-蒽酰氧基)棕榈酸(16-AP)结合,但对 11-[(5-二甲基氨基萘-1-磺酰基)氨基]十一烷酸(DAUDA)和丹磺酰基-DL-α-氨基己酸(DACA)没有结合活性。不饱和脂肪酸(FAs)的亲和力大于饱和 FAs。这些蛋白在整个虫体的成虫中特异性表达。TsHLBPs 可能参与宿主提供的疏水分子的摄取和/或隔离,从而有助于宿主-寄生虫界面的相互关系。