Deng Mingqi, Templeton Thomas J, London Nicole R, Bauer Carrey, Schroeder Alison A, Abrahamsen Mitchell S
Department of Veterinary PathoBiology, University of Minnesota, St. Paul 55108, USA.
Infect Immun. 2002 Dec;70(12):6987-95. doi: 10.1128/IAI.70.12.6987-6995.2002.
Cryptosporidium parvum is recognized as an enteropathogen of great worldwide medical and veterinary importance, yet understanding of its pathogenesis has been hampered in part by limited knowledge of the invasion machinery of this parasite. Recently, genes containing thrombospondin type 1 (TSP1) domains have been identified in several genera of apicomplexans, including thrombospondin-related adhesive proteins (TRAPs) that have been implicated as key molecules for parasite motility and adhesion onto host cell surfaces. Previously, a large-scale random survey of the C. parvum genome conducted in our laboratory revealed the presence of multiple genomic DNA sequences with a high degree of similarity to known apicomplexan TRAP genes. In the present study, TBLASTN screening of available C. parvum genomic sequences by using TSP1 domains as queries identified a total of 12 genes possessing TSP1-like domains. All genes have putative signal peptide sequences, one or more TSP1-like domains, plus additional extracellular protein modules such as Kringle, epidermal growth factor, and Apple domains. Two genes, putative paralogs CpTSP8 and CpTSP9, contain predicted introns near their amino termini, which were verified by comparing PCR products from cDNA versus genomic DNA templates. Reverse transcription-PCR analysis of transcript levels reveals that C. parvum TSP genes were developmentally regulated with distinct patterns of expression during in vitro infection. TRAPC1, CpTSP3, and CpTSP11 were expressed at high levels during both early and late stages of infection, whereas CpTSP2, CpTSP5, CpTSP6, CpTSP8, and CpTSP9 were maximally expressed during the late stages of infection. Only CpTSP4 was highly expressed solely at an early stage of infection.
微小隐孢子虫被公认为是一种在全球范围内具有重大医学和兽医意义的肠道病原体,但对其发病机制的理解在一定程度上受到了对该寄生虫入侵机制了解有限的阻碍。最近,在几个顶复门属中发现了含有1型血小板反应蛋白(TSP1)结构域的基因,包括血小板反应蛋白相关黏附蛋白(TRAPs),这些蛋白被认为是寄生虫运动和黏附于宿主细胞表面的关键分子。此前,我们实验室对微小隐孢子虫基因组进行的大规模随机调查显示,存在多个与已知顶复门TRAP基因高度相似的基因组DNA序列。在本研究中,以TSP1结构域为查询序列对可用的微小隐孢子虫基因组序列进行TBLASTN筛选,共鉴定出12个具有TSP1样结构域的基因。所有基因都有推定的信号肽序列、一个或多个TSP1样结构域,以及其他细胞外蛋白模块,如kringle结构域、表皮生长因子结构域和苹果结构域。两个基因,推定的旁系同源物CpTSP8和CpTSP9,在其氨基末端附近含有预测的内含子,通过比较来自cDNA与基因组DNA模板的PCR产物得以验证。转录水平的逆转录PCR分析表明,微小隐孢子虫TSP基因在体外感染期间受到发育调控,具有不同的表达模式。TRAPC1、CpTSP3和CpTSP11在感染的早期和晚期均高水平表达,而CpTSP2、CpTSP5、CpTSP6、CpTSP8和CpTSP9在感染晚期表达量最高。只有CpTSP4仅在感染早期高度表达。