4.7 Article

MicroRNAs profiles of Chinese Perch Brain (CPB) cells infected with Siniperca chuatsi rhabdovirus (SCRV)

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 84, 期 -, 页码 1075-1082

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2018.11.020

关键词

Siniperca chuatsi rhabdovirus; CPB cell; miRNA; Deep sequencing

资金

  1. Central Public-interest Scientific Institution Basal Research Fund, CAFS [2017HY-ZD0305]
  2. Pearl River Science & Technology Nova Program of Guangzhou City [201710010087]
  3. National Natural Science Foundation of China [31772889, 31572657]
  4. Special fund for Science and technology from Hubei Province [2015BBA228]
  5. Wuhan Science and Technology Bureau [2016020101010089]
  6. Department of Education of Guangdong Province [KA170500G]
  7. Chinese Postdoctoral Science Foundation [189103]

向作者/读者索取更多资源

MicroRNAs are non-coding RNAs, which widely participate in biological processes. In recent years, Siniperca chuatsi rhabdovirus (SCRV) has caused mass mortality in Chinese perch (Siniperca chuatsi). To identify specific miRNAs involved in SCRV infection, deep sequencing of microRNA on Chinese perch brain cell line (CPB) with or without SCRV infection were performed at 6 and 12 h post of infection (hpi). Totally 382 miRNAs were identified, including 217 known miRNA aligned with zebrafish miRNAs and 165 novel miRNAs by MiRDeep2 program. Of which 15 and 35 differentially-expressed miRNAs were determined respectively to 6 and 12 hpi. Nine miRNAs were selected randomly from the differentially-expressed miRNAs and validated by quantitative real-time PCR (qRT-PCR). These results were consistent with the microRNA sequencing results. Besides, target genes of 98 differentially-expressed miRNAs were predicted. Three of miRNAs (miR-122, miR-214, miR-135a) were selected, and its effects were analyzed in CPC cells transfected with appropriate miRNA mimics/inhibitors to evaluate its regulation effects by qRT-PCR and western blot. The results demonstrated that miR-214 inhibited the replication of SCRV, while miR-122 promoted the replication of SCRV and there was no correlation between the iniR-135a and SCRV replication. These results will pave a new way for the development of effective strategies against the SCRV infection.

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