Rodriguez-Valle Manuel, Xu Tao, Kurscheid Sebastian, Lew-Tabor Ala E
The University of Queensland, Queensland Alliance for Agriculture & Food Innovation, Queensland Biosciences Precinct, 306 Carmody Rd, St. Lucia Qld, 4072, Australia.
University Hospital Lausanne, Lausanne, VD, Switzerland.
Parasit Vectors. 2015 Jan 7;8:7. doi: 10.1186/s13071-014-0605-4.
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.
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.
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).
This study constitutes an important contribution and improvement to the knowledge about the physiologic role of R. microplus serpins during the host-tick interaction.
微小牛蜱通过分泌到蜱唾液中的复杂蛋白质阵列来逃避宿主的止血系统。丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制因子)是唾液的重要组成部分,在硬蜱科中由一个大型蛋白酶抑制剂家族所代表。这些分泌型和非分泌型抑制剂可调节参与不同生理过程的多种重要蛋白酶。
通过一个名为Yabi的基于网络的生物信息学环境对微小牛蜱丝氨酸蛋白酶抑制因子序列进行鉴定。使用生物信息学方法在BmiGi V1、BmiGi V2.1、五个抑制性消减杂交文库、澳大利亚蜱转录组文库和RmiTR V1上进行数据库搜索。使用不同的成虫组织和蜱发育阶段进行半定量PCR。克隆四个已鉴定的微小牛蜱丝氨酸蛋白酶抑制因子的cDNA并在毕赤酵母中表达,以便利用蛋白酶抑制试验确定这些丝氨酸蛋白酶抑制因子的生物学靶点。
在我们的分析中鉴定出的22个丝氨酸蛋白酶抑制因子中,共有4个是新的微小牛蜱丝氨酸蛋白酶抑制因子,分别命名为RmS - 19至RmS - 22。DNA和预测的氨基酸序列分析表明微小牛蜱丝氨酸蛋白酶抑制因子序列具有高度保守性。表达数据表明,除了RmS - 6仅在若虫中表达以及RmS - 14仅在成年雌性卵巢中表达外,RmS在其他组织中普遍表达。RmS - 19和RmS - 20在所有分析的组织样本中均有表达,表明它们在微小牛蜱发育的寄生和非寄生阶段均发挥重要作用。在卵巢中未检测到RmS - 21,在卵巢和若虫样本中未鉴定出RmS - 22,但在其他分析样本中均有表达。总共4种表达的重组丝氨酸蛋白酶抑制因子对胰凝乳蛋白酶(RmS - 1和RmS - 6)、胰凝乳蛋白酶/弹性蛋白酶(RmS - 3)和凝血酶(RmS - 15)表现出蛋白酶特异性抑制作用。
本研究对微小牛蜱丝氨酸蛋白酶抑制因子在宿主 - 蜱相互作用过程中的生理作用的认识做出了重要贡献并有所改进。