4.6 Article

Suppression of Shrimp Melanization during White Spot Syndrome Virus Infection

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JOURNAL OF BIOLOGICAL CHEMISTRY
卷 290, 期 10, 页码 6470-6481

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M114.605568

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资金

  1. Thailand Research Fund Senior Scholar [RTA5580008]
  2. Thailand Research Fund
  3. National Center for Genetic Engineering and Biotechnology
  4. National Science and Technology Development Agency [RSA5580046]
  5. Higher Education Research Promotion and National Research University Project of Thailand
  6. Office of the Higher Education Commission Grant [WCU-017-FW-57]
  7. Japan Science and Technology Agency (JST)/the Japan International Cooperation Agency (JICA)
  8. Science and Technology Research Partnership for Sustainable Development (SATREPS)
  9. Japan Society for the Promotion of Science (JSPS) core University Program
  10. Royal Golden Jubilee Ph.D. Program
  11. Chulalongkorn University
  12. 90th Anniversary of Chulalongkorn University Fund (Ratchadaphiseksomphot Endowment Fund)

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The melanization cascade, activated by the prophenoloxidase (proP0) system, plays a key role in the production of cytotoxic intermediates, as well as melanin products for microbial sequestration in invertebrates. Here, we show that the proPO system is an important component of the Penaeus inonodon shrimp immune defense toward a major viral pathogen, white spot syndrome virus (WSSV). Gene silencing of PmproP0(s) resulted in increased cumulative shrimp mortality after WSSV infection, whereas incubation of WSSV with an in vitro melanization reaction prior to injection into shrimp significantly increased the shrimp survival rate. The hemolymph phenoloxidase (PO) activity of WSSV-infected shrimp was extremely reduced at days 2 and 3 post-injection compared with uninftcted shrimp but was fully restored after the addition of exogenous trypsin, suggesting that WSSV probably inhibits the activity of some proteinases in the proPO cascade. Using yeast two-hybrid screening and co-immunoprecipitation assays, the viral protein WSSV453 was found to interact with the proP0-activating enzyme 2 (Pm1PAE2) of P. nionodon. Gene silencing of WSSV453 showed a significant increase of PO activity in WSSV-infected shrimp, whereas co-silencing of WSSV453 and PmPPAE2 did not, sug- gesting that silencing of WSSV453 partially restored the PO activity via PmPPAE2 in WSSV-infected shrimp. Moreover, the activation of PO activity in shrimp plasma by PmPPAE2 was significantly decreased by preincubation with recombinant WSSV453. These results suggest that the inhibition of the shrimp proPO system by WSSV partly occurs via the PmPPAE2-inhibiting activity of WSSV453.

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