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唾液蛋白酶抑制剂作为潜在的抗蜱疫苗。

Salivary Protease Inhibitors as Potential Anti-Tick Vaccines.

机构信息

Laboratory of Physiology of Hematophagous Insects, Department of Parasitology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Laboratory of Cell-Cell Interactions, Department of Morphology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

出版信息

Front Immunol. 2021 Feb 4;11:611104. doi: 10.3389/fimmu.2020.611104. eCollection 2020.

DOI:10.3389/fimmu.2020.611104
PMID:33633731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7901972/
Abstract

is the main tick associated with human bites in Brazil and the main vector of , the causative agent of the most severe form of Brazilian spotted fever. Molecules produced in the salivary glands are directly related to feeding success and vector competence. In the present study, we identified sequences of salivary proteins that may be involved in hematophagy and selected three proteins that underwent functional characterization and evaluation as vaccine antigens. Among the three proteins selected, one contained a Kunitz_bovine pancreatic trypsin inhibitor domain (named AsKunitz) and the other two belonged to the 8.9 kDa and basic tail families of tick salivary proteins (named As8.9kDa and AsBasicTail). Expression of the messenger RNA (mRNA) encoding all three proteins was detected in the larvae, nymphs, and females at basal levels in unfed ticks and the expression levels increased after the start of feeding. Recombinant proteins rAs8.9kDa and rAsBasicTail inhibited the enzymatic activity of factor Xa, thrombin, and trypsin, whereas rAsKunitz inhibited only thrombin activity. All three recombinant proteins inhibited the hemolysis of both the classical and alternative pathways; this is the first description of tick members of the Kunitz and 8.9kDa families being inhibitors of the classical complement pathway. Mice immunization with recombinant proteins caused efficacies against A. females from 59.4% with rAsBasicTail immunization to more than 85% by immunization with rAsKunitz and rAs8.9kDa. The mortality of nymphs fed on immunized mice reached 70-100%. Therefore, all three proteins are potential antigens with the possibility of becoming a new tool in the control of .

摘要

是与巴西人类咬伤相关的主要蜱虫,也是 的主要载体, 是巴西斑点热最严重形式的病原体。唾液腺中产生的分子与摄食成功和媒介能力直接相关。在本研究中,我们鉴定了 唾液蛋白的序列,这些序列可能与吸血有关,并选择了三种蛋白质进行功能表征和作为疫苗抗原的评估。在选择的三种蛋白质中,一种含有 Kunitz_bovine 胰腺蛋白酶抑制剂结构域(命名为 AsKunitz),另外两种属于蜱唾液蛋白的 8.9 kDa 和碱性尾部家族(命名为 As8.9kDa 和 AsBasicTail)。在未进食的幼蜱、若蜱和雌蜱中,编码所有三种蛋白质的信使 RNA(mRNA)在基础水平上表达,在开始进食后表达水平增加。重组蛋白 rAs8.9kDa 和 rAsBasicTail 抑制了因子 Xa、凝血酶和胰蛋白酶的酶活性,而 rAsKunitz 仅抑制了凝血酶的活性。所有三种重组蛋白均抑制了经典和替代途径的溶血;这是首次描述蜱的 Kunitz 和 8.9 kDa 家族成员是经典补体途径的抑制剂。用重组蛋白免疫小鼠引起的功效为 59.4%,用 rAsBasicTail 免疫为 85%以上,用 rAsKunitz 和 rAs8.9kDa 免疫为 85%以上。免疫小鼠上的若蜱死亡率达到 70-100%。因此,所有三种蛋白质都是潜在的抗原,有可能成为控制 的新工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/6e0dc442766f/fimmu-11-611104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/9df426e76922/fimmu-11-611104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/602f35299c49/fimmu-11-611104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/19154e4ad723/fimmu-11-611104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/ffc85f7e321a/fimmu-11-611104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/49119196d7cf/fimmu-11-611104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/f3618bbd66c1/fimmu-11-611104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/6e0dc442766f/fimmu-11-611104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/9df426e76922/fimmu-11-611104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/602f35299c49/fimmu-11-611104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/19154e4ad723/fimmu-11-611104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/ffc85f7e321a/fimmu-11-611104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/49119196d7cf/fimmu-11-611104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/f3618bbd66c1/fimmu-11-611104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/7901972/6e0dc442766f/fimmu-11-611104-g007.jpg

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