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High-throughput identification of microRNAs in Taenia hydatigena, a cestode threatening livestock breeding industry
Jin'en Wu1, Jing Yang1, Guitian He1
1State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, CAAS, Lanzhou 730046, China.
Abstract:
Infection of Cysticercus tenuicollis, the larval stage of Taenia hydatigena, is extensively found in sheep and pigs and jeopardizes the breeding and meat industry. miRNAs are a subclass of small noncoding regulatory RNAs and closely associated with the pathogenesis and biology of parasites. Here, using HiSeq sequencing we identified 49 known and 2 potential novel miRNAs in C. tenuicollis, of which both thy-miR-71 and -87 were predominant. Using RT-qPCR, 6 selected miRNAs were validated, and thy-miR-71 and -miR-87 were confirmed to be highly expressed, with the copy number of approximately 82,340 ± 2079 and 19,580 ± 609 per 1 ng total RNA, respectively. Similar to other cestodes, T. hydatigena was predicted to have two conserved miRNA clusters thy-miR-71/2c/2b and thy-miR-4989/277, and three members of the former were confirmed to reside sequentially within the genomic region of 253 bp by PCR. The current data provide us a valuable resource for further studies of a role of miRNAs in T. hydatigena biology and infection.
Insights
Researchers identified 49 known and 2 novel microRNAs (miRNAs) in Cysticercus tenuicollis, a parasite affecting livestock. The study highlights the high expression of thy-miR-71 and thy-miR-87, offering insights into parasite biology.
Area of Science:
- Parasitology
- Molecular Biology
- Genomics
Background:
- Cysticercus tenuicollis, the larval stage of Taenia hydatigena, significantly impacts sheep and pig industries.
- MicroRNAs (miRNAs) are crucial regulatory RNAs involved in parasite pathogenesis and biology.
Purpose of the Study:
- To identify and characterize miRNAs in C. tenuicollis.
- To investigate the expression levels and genomic organization of key miRNAs.
Main Methods:
- HiSeq sequencing for miRNA identification.
- RT-qPCR for miRNA expression validation.
- PCR for confirming miRNA cluster organization.
Main Results:
- Identified 49 known and 2 potential novel miRNAs in C. tenuicollis.
- thy-miR-71 and thy-miR-87 were found to be highly expressed.
- Confirmed the sequential arrangement of three miRNAs within a conserved cluster.
Conclusions:
- The study provides a valuable resource for understanding miRNA roles in T. hydatigena biology and infection.
- Identified key miRNAs for potential future research into parasite control.
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