4.6 Article

Characterization of two novel ADP ribosylation factors from giant freshwater prawn Macrobrachium rosenbergii and their responses to WSSV challenge

Journal

DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Volume 48, Issue 1, Pages 204-209

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dci.2014.10.006

Keywords

Macrobrachium rosenbergii; ADP ribosylation factor; WSSV; RNAi

Funding

  1. National Natural Science Foundation of China [31101926, 31170120, 31402332]
  2. National Natural Science Foundation of Jiangsu Province [BK20131401, BK20131453]
  3. Natural Science Fund of Colleges and Universities in Jiangsu Province [13KJB240002]
  4. High level talents in Nanjing Normal University Foundation [2012104XGQ0101]
  5. NSFC for Talents Training in Basic Science [J1103507]
  6. Jiangsu Agriculture Science and Technology Innovation Fund (JASTIF) [CX (12)3066]
  7. Project for Aquaculture in Jiangsu Province [PJ2011-65, Y2013-45, D2013-5-3, D2013-5-4]

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ADP-ribosylation factors (Arfs) are small GTP-binding proteins that have an essential function in intracellular trafficking and organelle structure. To date, little information is available on the Arfs in the economically important giant freshwater prawn Macrobrachium rosenbergii and their relationship to viral infection. Here we identified two Arf genes from M. rosenbergii (MrArf1 and MrArf2) for the first time. Phylogenetic analysis showed that MrArf1, together with MjArf1 from shrimp Marsupenaeus japonicus belonged to Class I Arfs. By contrast, MrArf2 didn't not match any of the Arfs classes of I/II/III, although it could be clustered with an Arf protein from M. japonicas called MjArfn, which may represent an analog of the Arf. MrArf1 was ubiquitously expressed in all the examined tissues, with the highest transcription level in the hepatopancreas, whereas MrArf2 was only highly expressed in the hepatopancreas and exhibited very low levels in the heart, stomach, gills and intestine. The expression level of MrArf1 in the gills was down-regulated post 24 h WSSV challenge, and reached the maximal level at 48 h. MrArf1 in the hepatopancreas went up from 24 to 48 h WSSV challenge. MrArf1 transcript in the gill also went down at 24 h and then was upregulated at 48 h WSSV challenge. MrArf2 increased significantly in the hepatopancreas 24 h after infection and then went down at 48 h WSSV challenge. RNAi results showed that knockdown of MrArf1 or MrArf2 could inhibit the expression of the envelope protein gene vp28 of the WSSV. So, it could be speculated that MrArfl and MrArf2 might play important roles in the innate immune system against WSSV infection. (C) 2014 Elsevier Ltd. All rights reserved.

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