4.6 Article

Function of Litopenaeus vannamei RPL4A-L and RPS16 in WSSV infection

期刊

AQUACULTURE REPORTS
卷 21, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.aqrep.2021.100803

关键词

Litopenaeus vannamei; LvRPL4-L; LvRPS16; WSSV; Immune response

资金

  1. National Key Research and Development Program of China [2018YFD0900501]
  2. National Science Foundation of China [31672679]
  3. Central Public-interest Scientific Institution Basal Research Fund [2020TD39]
  4. Central Public-interest Scientific Institution Basal Research Fund, YSFRI, CAFS [20603022020016]

向作者/读者索取更多资源

Ribosomes are crucial in the antiviral immune response of Litopenaeus vannamei, with LvRPL4-L and LvRPS16 showing increased expression after WSSV infection. Silencing of LvRPL4-L or LvRPS16 led to significantly higher viral copy numbers and mortality rates. This study provides insight into the role of LvRPL4-L and LvRPS16 in the immune response of L. vannamei against WSSV.
Ribosome, as basic components of the protein synthesis machinery, plays an important role in normal cellular physiology, cellular responses and pathogenesis. Ribosome consists of a large subunit (60S) and a small subunit (40S). In Litopenaeus vannamei (L. vannamei), the function of the 60S ribosome protein L4A-Like (LvRPL4A-L) and the 40S ribosome protein S16 (LvRPS16) in white spot syndrome virus (WSSV) infection was unclear. In the present study, the tissue distribution assay showed that LvRPL4-L and LvRPS16 were expressed in all selected tissues. The expressions of LvRPL4-L and LvRPS16 at the mRNA level were mainly distributed in the muscle, stomach, and hepatopancreas. Besides, the relative expressions of LvRPL4-L and LvRPS16 were up-regulated in the hepatopancreas and stomach of WSSV-challenged shrimp. In addition, after LvRPL4-L or LvRPS16 silencing and WSSV infection, the relative expressions of immediate early gene IE1 and late gene VP28 were significantly up-regulated. Meanwhile, compared with the control group, the viral copy number and cumulative mortality rate of the LvRPL4-L- or LvRPS16-silenced group were also significantly increased. We, for the first time, reported the function of LvRPL4-L and LvRPS16 in the antiviral immune response of L. vannamei.

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