Deep sequencing-based identification of pathogen-specific microRNAs in the plasma of rabbits infected with Schistosoma japonicum

被引:120
作者
Cheng, Guofeng [1 ]
Luo, Rong [1 ]
Hu, Chao [1 ]
Cao, Jie [1 ]
Jin, Youxin [2 ]
机构
[1] Chinese Acad Agr Sci, Shanghai Vet Res Inst, Key Lab Anim Parasitol, Minist Agr, Shanghai 200241, Peoples R China
[2] Shanghai Univ, Sch Life Sci, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNA; Schistosoma japonicum; deep sequencing; diagnosis; biomarkers; BIOMARKERS; MECHANISM; PROTEINS; TARGETS; SERUM;
D O I
10.1017/S0031182013000917
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程]; 100103 [病原生物学];
摘要
Circulating microRNAs (miRNAs) have received considerable attention as a novel class of biomarkers for the diagnosis of cancer and as signalling molecules in mediating intercellular communication. Schistosomes, the causative agents of schistosomiasis, live in the blood vessels of a mammalian host in the adult stage. In the present study, we characterized schistosome-specific small RNA populations in the plasma of rabbits infected with Schistosoma japonicum (S. japonicum) using a deep sequencing method and then identified five schistosome-specific miRNAs, including four known miRNAs (Bantam, miR-3479, miR-10 and miR-3096), and one novel miRNA (miR-0001, miRBase ID: sja-miR-8185). Four of the five schistosome-specific miRNAs were also detected by real-time RT-PCR in the plasma of S. japonicum-infected mice. In addition, our study indicated that schistosome Argonaute 2/3 may be an excretory-secretory (ES) protein. In summary, our findings are expected to provide useful information for further development of novel biomarkers for the diagnosis of schistosomiasis and also for deeper understanding of the mechanism of host-parasite interaction.
引用
收藏
页码:1751 / 1761
页数:11
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