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Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment

机译:Rhipicephalus microplus丝氨酸蛋白酶抑制剂家族:注释,表达和功能鉴定

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Background Rhipicephalus (Boophilus) microplus evades the host’s haemostatic system through a complex protein array secreted into tick saliva. Serine protease inhibitors (serpins) conform an important component of saliva which are represented by a large protease inhibitor family in Ixodidae. These secreted and non-secreted inhibitors modulate diverse and essential proteases involved in different physiological processes. Methods The identification of R. microplus serpin sequences was performed through a web-based bioinformatics environment called Yabi. The database search was conducted on BmiGi V1, BmiGi V2.1, five SSH libraries, Australian tick transcriptome libraries and RmiTR V1 using bioinformatics methods. Semi quantitative PCR was carried out using different adult tissues and tick development stages. The cDNA of four identified R. microplus serpins were cloned and expressed in Pichia pastoris in order to determine biological targets of these serpins utilising protease inhibition assays. Results A total of four out of twenty-two serpins identified in our analysis are new R. microplus serpins which were named as RmS-19 to RmS-22. The analyses of DNA and predicted amino acid sequences showed high conservation of the R. microplus serpin sequences. The expression data suggested ubiquitous expression of RmS except for RmS-6 and RmS-14 that were expressed only in nymphs and adult female ovaries, respectively. RmS-19, and -20 were expressed in all tissues samples analysed showing their important role in both parasitic and non-parasitic stages of R. microplus development. RmS-21 was not detected in ovaries and RmS-22 was not identified in ovary and nymph samples but were expressed in the rest of the samples analysed. A total of four expressed recombinant serpins showed protease specific inhibition for Chymotrypsin (RmS-1 and RmS-6), Chymotrypsin / Elastase (RmS-3) and Thrombin (RmS-15). Conclusion This study constitutes an important contribution and improvement to the knowledge about the physiologic role of R. microplus serpins during the host-tick interaction.
机译:背景Rhipicephalus(Boophilus)microplus通过分泌到壁虱唾液中的复杂蛋白质阵列逃避宿主的止血系统。丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)符合唾液的重要组成部分,由唾液x科中的大型蛋白酶抑制剂家族代表。这些分泌的和非分泌的抑制剂调节参与不同生理过程的多种必需蛋白酶。方法通过称为Yabi的基于Web的生物信息学环境,进行了R. microplus serpin序列的鉴定。使用生物信息学方法对BmiGi V1,BmiGi V2.1,五个SSH库,澳大利亚壁虱转录组文库和RmiTR V1进行了数据库搜索。使用不同的成人组织和壁虱发育阶段进行半定量PCR。为了鉴定这些丝氨酸蛋白酶抑制蛋白的生物学靶标,克隆了四种已鉴定的微小螺旋体丝氨酸蛋白酶抑制蛋白的cDNA,并在毕赤酵母中表达。结果我们分析中确定的22个丝氨酸蛋白酶抑制剂中共有4个是新的R. microplus丝氨酸蛋白酶抑制剂,其命名为RmS-19至RmS-22。 DNA和预测的氨基酸序列分析表明,R。microplus丝氨酸蛋白酶抑制剂丝氨酸蛋白酶抑制剂序列高度保守。表达数据表明,除了仅在若虫和成年雌性卵巢中表达的RmS-6和RmS-14之外,RmS普遍存在。 RmS-19和-20在所有分析的组织样品中均有表达,显示了它们在R. microplus发育的寄生阶段和非寄生阶段均具有重要作用。在卵巢中未检测到RmS-21,在卵巢和若虫样品中未鉴定到RmS-22,但在分析的其余样品中均表达了RmS-22。总共四个表达的重组丝氨酸蛋白酶抑制剂显示出对胰凝乳蛋白酶(RmS-1和RmS-6),胰凝乳蛋白酶/弹性蛋白酶(RmS-3)和凝血酶(RmS-15)的蛋白酶特异性抑制。结论这项研究为了解细小R. micropin丝氨酸蛋白酶抑制剂在宿主-滴答相互作用中的生理作用提供了重要的贡献和改进。

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