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雷氏毛毕吸虫(裂体科)及其软体动物宿主静水椎实螺(椎实螺科)的肽酶:寄生虫在软体动物体内阶段cDNA文库的构建与筛选

Peptidases of Trichobilharzia regenti (Schistosomatidae) and its molluscan host Radix peregra S. Lat. (Lymnaeidae): construction and screening of cDNA library from intramolluscan stages of the parasite.

作者信息

Dolecková Katerina, Kasný Martin, Mikes Libor, Mutapi Francisca, Stack Colin, Mountford Adrian P, Horák Petr

机构信息

Department of Parasitology, Faculty of Science, Charles University in Prague, Vinicná 7, 128 44 Prague 2, Czech Republic.

出版信息

Folia Parasitol (Praha). 2007 Jun;54(2):94-8.

Abstract

Trichobilharzia regenti is a neurotropic bird schistosome,causing cercarial dermatitis in humans. In this study, ZAP cDNA expression library from Radix peregra s. lat. hepatopancreases containing intramolluscan stages of T. regenti was constructed and screened using PCR with specific and degenerate primers, designed according to previously described serine and cysteine peptidases of other parasite species. Full-length sequences of cathepsins B1 and L, and two serine peptidases, named RpSP1 and RpSP2, were obtained. The protein-protein BLAST analysis and parallel control reactions with template from hepatopancreases of T. regenti non-infected snails revealed that only cathepsin B1 was of parasite origin. The remaining sequences were derived from the snail intermediate host, which implies that the initial source of parasite mRNA was contaminated by snail tissue. Regardless of this contamination, the cDNA library remains an excellent molecular tool for detection and identification of bioactive molecules in T. regenti cercariae.

摘要

雷根氏毛毕吸虫是一种嗜神经性鸟类血吸虫,可导致人类尾蚴性皮炎。在本研究中,利用根据其他寄生虫物种先前描述的丝氨酸和半胱氨酸蛋白酶设计的特异性和简并引物,通过PCR构建并筛选了来自包含雷根氏毛毕吸虫螺内阶段的宽体扁卷螺肝胰腺的ZAP cDNA表达文库。获得了组织蛋白酶B1和L以及两种丝氨酸蛋白酶(命名为RpSP1和RpSP2)的全长序列。蛋白质-蛋白质BLAST分析以及与未感染雷根氏毛毕吸虫的蜗牛肝胰腺模板的平行对照反应表明,只有组织蛋白酶B1来源于寄生虫。其余序列来自蜗牛中间宿主,这意味着寄生虫mRNA的初始来源被蜗牛组织污染。尽管存在这种污染,该cDNA文库仍然是检测和鉴定雷根氏毛毕吸虫尾蚴中生物活性分子的优秀分子工具。

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