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棘球蚴细粒棘球绦虫和多房棘球绦虫中 Kunitz 蛋白酶抑制剂的生物信息学比较及其在棘球蚴细粒棘球绦虫不同发育阶段表达的基因

Bioinformatic comparison of Kunitz protease inhibitors in Echinococcus granulosus sensu stricto and E. multilocularis and the genes expressed in different developmental stages of E. granulosus s.s.

机构信息

Basic Medicine College, Xinjiang Medical University, 830011, Urumqi, Xinjiang, China.

State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, WHO-Collaborating Centre for Prevention and Care Management of Echinococcosis, Xinjiang Medical University, The First Affiliated Hospital of Xinjiang Medical University, 830054, Urumqi, Xinjiang, China.

出版信息

BMC Genomics. 2021 Dec 18;22(1):907. doi: 10.1186/s12864-021-08219-4.

Abstract

BACKGROUND

Cystic and alveolar echinococcosis caused by the tapeworms Echinococcus granulosus sensu stricto (s.s.) and E. multilocularis, respectively, are important zoonotic diseases. Protease inhibitors are crucial for the survival of both Echinococcus spp. Kunitz-type inhibitors play a regulatory role in the control of protease activity. In this study,we identified Kunitz-type domain protease inhibitors(KDPIs) present in the genomes of these two tapeworms and analyzed the gene sequences using computational, structural bioinformatics and phylogenetic approaches to evaluate the evolutionary relationships of these genes. Hi-seq transcriptome analysis showed that E. granulosus s.s. KDPIs were differentially expressed in the different developmental stages. We validated some of the genes expressed in adult worm, protoscolex and cyst germinal membrane of E. granulosus s.s. and E. multilocularis by quantitative PCR.

RESULTS

A total of 19 genes from E. multilocularis and 23 genes from E. granulosus s.s. were predicted to be KDPIs with the most containing a single Kunitz-domain. A maximum likelihood method phylogenetic tree indicated that the E. granulosus s.s. and E. multilocularis Kunitz domain peptides were divided into three branches containing 9 clusters. The ratio of positively charged residues and neutral residues are different between E. multilocularis and E. granulosus s.s. KDPIs. We also found that E. multilocularis had higher percentage of sequences containing signal peptides (17/19, 89.47%) than that of E. granulosus s.s. (14/23, 60.87%). Transcript analysis showed all the E. granulosus s.s. KDPI genes were expressed differentially in four developmental stages of the worm. Transcription analysis showed that 9 KDPIs (including EG_07244,EGR_08716 and EGR_10096) were highly upregulated in adult worm, and 2 KDPIs (EG_09268 and EG_09490) were highly expressed in the cyst germinal membrane. Quantitative gene expression analysis(qPCR) of four genes confirmed the expression of these genes. EGR_08716 and its homologous gene (EmuJ_001137000) were highly and specifically expressed in adult worms of the two worms.

CONCLUSIONS

A total 19 and 23 KDPIs were identified in the genomes of E. multilocularis and E. granulosus s.s. , respectively. The differential expression of these KDPIs in different stages may indicate their different roles in the different hosts. The difference in characterization of KDPIs may be associated with the different pathology of metacestode stage of these two parasites.

摘要

背景

由细粒棘球绦虫严格种(s.s.)和多房棘球绦虫引起的包虫病和泡球蚴病分别是重要的人畜共患疾病。蛋白酶抑制剂对两种棘球绦虫的生存至关重要。Kunitz 型抑制剂在控制蛋白酶活性中发挥调节作用。在这项研究中,我们鉴定了这两种绦虫基因组中的 Kunitz 型结构域蛋白酶抑制剂(KDPIs),并通过计算、结构生物信息学和系统发育分析方法分析了基因序列,以评估这些基因的进化关系。Hi-seq 转录组分析显示,细粒棘球绦虫 s.s. 的 KDPIs 在不同发育阶段存在差异表达。我们通过定量 PCR 验证了细粒棘球绦虫 s.s. 和多房棘球绦虫成虫、原头蚴和包虫生发膜中表达的一些基因。

结果

从多房棘球绦虫中预测到 19 个基因,从细粒棘球绦虫 s.s. 中预测到 23 个基因,其中大多数包含单个 Kunitz 结构域。最大似然法系统发育树表明,细粒棘球绦虫 s.s. 和多房棘球绦虫的 Kunitz 结构域肽分为包含 9 个簇的三个分支。多房棘球绦虫和细粒棘球绦虫 s.s. KDPIs 中带正电荷和中性残基的比例不同。我们还发现,多房棘球绦虫比细粒棘球绦虫 s.s. 具有更高比例的含信号肽序列(17/19,89.47%)。转录分析表明,细粒棘球绦虫 s.s. 的所有 KDPI 基因在虫体的四个发育阶段均有差异表达。转录分析表明,9 个 KDPIs(包括 EG_07244、EGR_08716 和 EGR_10096)在成虫中高度上调,2 个 KDPIs(EG_09268 和 EG_09490)在生发膜中高度表达。四个基因的定量基因表达分析(qPCR)证实了这些基因的表达。EGR_08716 及其同源基因(EmuJ_001137000)在两种蠕虫的成虫中高度且特异性表达。

结论

在多房棘球绦虫和细粒棘球绦虫 s.s. 的基因组中分别鉴定到 19 个和 23 个 KDPIs。这些 KDPIs 在不同阶段的差异表达可能表明它们在不同宿主中的不同作用。KDPIs 特征的差异可能与这两种寄生虫的中绦期不同的病理学有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1a/8684654/6bec138f8e1c/12864_2021_8219_Fig1_HTML.jpg

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