Huang Fuqiang, Dang Zhisheng, Zhang Haoji, Yagi Kinpei, Kim Kyeongsoon, Joseph Magona, Pu Wenjun, Oku Yuzaburo
Parasitology Laboratory, School of Veterinary Medicine, Faculty of Agriculture, Tottori University, 680-0945, Tottori, Japan; The United Graduate School of Veterinary Science, Yamaguchi University, Yamaguchi 753-8515, Japan; School of Life Science and Engineering, Foshan University, Foshan 528231, People's Republic of China.
National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Shanghai 200025, People's Republic of China; Key Laboratory of Parasite and Vector Biology, Ministry of Health, MOH, Shanghai 200025, People's Republic of China; National Center for International Research on Tropical Diseases, Shanghai 200025, People's Republic of China; WHO Collaborating Center for Tropical Diseases, Shanghai 200025, People's Republic of China.
Vet Parasitol. 2017 Oct 15;245:153-159. doi: 10.1016/j.vetpar.2017.05.006. Epub 2017 May 12.
Alveolar echinococcosis (AE) is a worldwide zoonosis caused by E. multilocularis. Humans become infected through oral ingestion of the eggs. Host of E. multilocularis produces immune responses that help to either reject and/or limit the growth of this parasite, and in response the parasite produces molecules against this immune attack. This study identifies candidate key molecules in the early infection phase and the chronic stage of the parasite infestation, through comparison of gene expression of 4- and 16-week metacestodes. First, RNA was isolated from 4- and 16-weeks metacestodes of E. multilocularis (Nemuro strain). Thereafter, clean reads with lengths of 50bp or longer were compared against a reference genome using TopHat. Functional annotation of transcripts of E. multilocularis were investigated using multi-step bioinformatics tools. At the gene ontology (GO) level, 356 and 1774 transmembrane (TM) predicted proteins of the E. multilocularis were mapped to an enhanced 'hydrolase activity' and increased 'transmembrane transporter activity', respectively. In addition, comparison of gene expression level between 4- and 16-week metacestode revealed 168 different expression (DE) genes. This study has demonstrated that, the expression levels of predicted ES and TM proteins in E. multilocularis change in the transformation from one stage to another. Genes that are highly expressed in immature or mature metacestode could be explored as novel candidates for diagnostic antigens and vaccine targets.
泡型包虫病(AE)是一种由多房棘球绦虫引起的全球性人畜共患病。人类通过经口摄入虫卵而感染。多房棘球绦虫的宿主会产生免疫反应,以帮助排斥和/或限制这种寄生虫的生长,而作为回应,寄生虫会产生对抗这种免疫攻击的分子。本研究通过比较4周龄和16周龄幼虫的基因表达,确定了寄生虫感染早期和慢性期的候选关键分子。首先,从多房棘球绦虫(根室株)的4周龄和16周龄幼虫中分离RNA。此后,使用TopHat将长度为50bp或更长的干净读段与参考基因组进行比较。使用多步生物信息学工具研究多房棘球绦虫转录本的功能注释。在基因本体(GO)水平上,多房棘球绦虫的356个和1774个预测跨膜(TM)蛋白分别被映射到增强的“水解酶活性”和增加的“跨膜转运蛋白活性”。此外,4周龄和16周龄幼虫之间基因表达水平的比较揭示了168个差异表达(DE)基因。本研究表明,多房棘球绦虫中预测的ES和TM蛋白的表达水平在从一个阶段转变到另一个阶段时会发生变化。在未成熟或成熟幼虫中高表达的基因可作为诊断抗原和疫苗靶点的新候选物进行探索。