Inhibition of white spot syndrome virus replication in Penaeus monodon by combined silencing of viral rr2 and shrimp PmRab7

被引:67
作者
Attasart, Pongsopee [1 ]
Kaewkhaw, Rossukon [1 ]
Chimwai, Chaweewan [1 ]
Kongphom, Ukrit [1 ]
Namramoon, Orathai [1 ]
Panyim, Sakol [1 ,2 ]
机构
[1] Mahidol Univ, Inst Mol Biol & Genet, Salaya 73170, Nakhon Pathom, Thailand
[2] Mahidol Univ, Fac Sci, Dept Biochem, Bangkok 10400, Thailand
关键词
Penaeus monodon; White spot syndrome virus; RNAi; rr2; PmRab7; DOUBLE-STRANDED-RNA; RIBONUCLEOTIDE REDUCTASE; WSSV INFECTION; IMMUNITY; DSRNA; GENE; EXPRESSION; INDUCTION; SEQUENCE; CELLS;
D O I
10.1016/j.virusres.2009.06.018
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Although a significant progress has been achieved on dsRNA mediated anti-virus strategy development, there is still no effective means to control the virulent white spot syndrome virus (WSSV). Six double-stranded RNAs specific to different essential genes of WSSV (ie1, ie3, pol (DNA polymerase), rr2 (ribonucleotide reductase small subunit), vp26, and vp28) were employed to suppress viral replication in shrimp. At the condition that non-specific inhibitory effect was overwhelmed, the relative protective degree of these dsRNAs against WSSV infection (rr2 > ie3 > vp26, vp28 > iel > pol) was observed by semiquantitative PCR. Besides, more than one injection of dsRNA was needed for an efficient viral inhibition. To improve viral protection in Penaeus monodon, synchronized blocking of viral cellular transport (by dsRNA-PmRab7) and viral essential gene synthesis (by dsRNA-rr2) was first performed in this study. The suppression effects of shrimp mortality by either combined dsRNAs of rr2 and PmRab7 or dsRNA-rr2 alone was monitored for 8 days after viral challenge. Approximately 95% of shrimp survivals were detected from both combined dsRNAs and dsRNA-rr2 alone whereas all shrimp without dsRNA were dead. It revealed that there was no additive inhibitory effect of the combined dsRNAs over dsRNA-rr2 alone. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 133
页数:7
相关论文
共 31 条
[1]
Studies on the immunomodulatory effect of extract of Cyanodon dactylon in shrimp, Penaeus monodon, and its efficacy to protect the shrimp from white spot syndrome virus (WSSV) [J].
Balasubramanian, G. ;
Sarathi, M. ;
Venkatesan, C. ;
Thomas, John ;
Hameed, A. S. Sahul .
FISH & SHELLFISH IMMUNOLOGY, 2008, 25 (06) :820-828
[2]
Chalermporn Ongvarrasopone, 2007, ScienceAsia, V33, P35, DOI 10.2306/scienceasia1513-1874.2007.33.035
[3]
Transcriptional analysis of the DNA polymerase gene of shrimp white spot syndrome virus [J].
Chen, LL ;
Wang, HC ;
Huang, CJ ;
Peng, SE ;
Chen, YG ;
Lin, SJ ;
Chen, WY ;
Dai, CF ;
Yu, HT ;
Wang, CH ;
Lo, CF ;
Kou, GH .
VIROLOGY, 2002, 301 (01) :136-147
[4]
Influence of selected Indian immunostimulant herbs against white spot syndrome virus (WSSV) infection in black tiger shrimp, Penaeus monodon with reference to haematological, biochemical and immunological changes [J].
Citarasu, Thavasimuthu ;
Sivaram, Veeramani ;
Immanuel, Grasian ;
Rout, Namita ;
Murugan, Vadivel .
FISH & SHELLFISH IMMUNOLOGY, 2006, 21 (04) :372-384
[5]
RNA-triggered gene silencing [J].
Fire, A .
TRENDS IN GENETICS, 1999, 15 (09) :358-363
[6]
Ha YM, 2008, J MICROBIOL BIOTECHN, V18, P964
[7]
RNA interference [J].
Hannon, GJ .
NATURE, 2002, 418 (6894) :244-251
[8]
Inhibition of hepatitis B virus replication by shRNAs in stably HBV expressed HEPG2 2.2.15 cell lines [J].
Kayhan, H. ;
Karatayli, E. ;
Turkyilmaz, A. R. ;
Sahin, F. ;
Yurdaydin, C. ;
Bozdayi, A. M. .
ARCHIVES OF VIROLOGY, 2007, 152 (05) :871-879
[9]
Protection of shrimp (Penaeus chinensis) against white spot syndrome virus (WSSV) challenge by double-stranded RNA [J].
Kim, Chun Soo ;
Kosuke, Zenke ;
Nam, Yoon Kwon ;
Kim, Sung Koo ;
Kim, Ki Hong .
FISH & SHELLFISH IMMUNOLOGY, 2007, 23 (01) :242-246
[10]
FUNCTIONAL DISSECTION OF THE AUTOGRAPHA-CALIFORNICA NUCLEAR POLYHEDROSIS-VIRUS IMMEDIATE-EARLY-1 TRANSCRIPTIONAL REGULATORY PROTEIN [J].
KOVACS, GR ;
CHOI, J ;
GUARINO, LA ;
SUMMERS, MD .
JOURNAL OF VIROLOGY, 1992, 66 (12) :7429-7437