Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống
1
/ 179 trang
THÔNG TIN TÀI LIỆU
Thông tin cơ bản
Định dạng
Số trang
179
Dung lượng
2,42 MB
Nội dung
FUNCTION STUDIES ON RING PROTEINS IN WHITE SPOT SYNDROME VIRUS FANG HE NATIONAL UNIVERSITY OF SINGAPORE 2009 FUNCTION STUDIES ON RING PROTEINS IN WHITE SPOT SYNDROME VIRUS FANG HE (B.Sc. Shanghai Jiao Tong University) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY TEMASEK LIFE SCIENCES LABORATORY AND DEPARTMENT OF BIOLOGICAL SCIENCES NATIONAL UNIVERSITY OF SINGAPORE 2009 Abstract White Spot Syndrome Virus, Nimaviridiae Whispovirus, is one of the major viral pathogens in the aquaculture industry responsible for high mortality in cultured shrimp. The infection mechanisms of WSSV have not been fully characterized at the molecular level due to the large size and uniqueness of its genome. This study was undertaken to advance our understanding of the specific function of RING-containing proteins in viral pathogenesis. A preliminary search for regulatory protein candidates in WSSV using functional domain determination identified four predicted viral proteins containing a RING-H2 domain. Among them, the three proteins WSSV222, WSSV249 and WSSV403 can be expressed in both E.coli and insect cells, suggesting their potential expression in shrimp. In this study, emphasis has been placed on the characterization of WSSV222 and WSSV403. WSSV222 exhibits RING-H2-dependent E3 ligase activity in vitro in the presence of the conjugating enzyme UbcH6. Mutations in the RING-H2 domain abolished WSSV222-dependent ubiquitination, displaying the importance of this domain. Yeast two-hybrid and pull-down analyses revealed that WSSV222 interacts with a shrimp tumor suppressor-like protein (TSL) sharing 60% identity with human OVCA1. A stable TSL-expressing cell line derived from the human ovarian cancer cell line A2780 was established, where a TSL-dependent prolonged G1 phase was observed. Based on this, WSSV222-mediated ubiquitination and MG132-sensitive degradation of TSL were detected both in the TSL-expressing cell line and in shrimp primary cell culture. Transient expression of TSL in BHK cells leads to apoptosis, which was rescued by the coexpression of WSSV222. Taken together, I these data suggest that WSSV222 acts as an anti-apoptosis protein by ubiquitinmediated proteolysis of TSL to ensure successful WSSV replication in shrimp. Overexpression of WSSV222 in SF9 and BHK cells could be silenced by specific anti-WSSV222 siRNA. Further, WSSV-challenged shrimp were treated with the anti-222 siRNA to knockdown WSSV222. The survival rate and the efficiency of WSSV replication were assessed to evaluate the efficacy of anti-222 siRNA to inhibit WSSV infection in shrimp. The anti-222 siRNA reduced the cumulative mortality in shrimp challenged with 103 copies of WSSV and delayed the mean time to death in shrimp challenged with the higher dosage of 106 copies. The results of real time quantitative PCR showed that virus replication was delayed and reduced in the WSSV-challenged shrimp treated with anti-222 siRNA in comparison to the challenged shrimp treated with random siRNA. Coimmunoprecipitation assays revealed that WSSV222 silencing inhibited the degradation of TSL in WSSV-challenged shrimp. These results indicate that WSSV222 is required for efficient replication of WSSV in shrimp. WSSV403 acts as a viral E3 ligase which can ubiquitinate itself in vitro in the presence of an E2 conjugating enzyme from shrimp. WSSV403 can be activated by a series of E2 variants. In RT-PCR and real time PCR, the transcription of WSSV403 was detected in specific-pathogen-free shrimp, suggesting its role as a latency-associated gene. Identified in yeast two-hybrid and verified by pull-down assays, WSSV403 is able to bind to a shrimp protein phosphatase, an interaction partner for another latent protein WSSV427. This study suggests that WSSV403 could be a regulator of latency state of WSSV by virtue of its E3 ligase function. II In summary, the studies presented here indicate that viral RING proteins are involved in ubiquitination events and interactions with a diverse range of shrimp proteins and play important roles as regulators of virus replication. In order to establish an effcient viral protein expression system, efforts have been made in the studies on WSSV immediate-early promoter one (IE1). The production of H5 HA of influenza virus by baculovirus was enhanced with WSSV IE1 promoter, especially compared with CMV promoter. This contributed to effective elicitation of HA-specific antibody in vaccinated chickens. This study provides an alternative choice for baculovirus based vaccine production. III Table of Contents List of Figures List of Table Acknowledgements VII VIII IX Chapter Introduction 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 1.10 WSSV AND ITS HOST RANGE…………………………………………………………………. PATHOLOGY AND TISSUE TROPISM OF WSSV…………………………………………… WSSV GENOME AND CLASSIFICATION…………………………………………………… MORPHOLOGY AND STRUCTURAL PROTEINS OF WSSV……………………… … . 10 NON-STRUCTURAL PROTEINS IN WSSV…………………………………………………. 12 VACCINE STRATEGIES FOR CONTROL OF WSSV INFECTION .…………………… 15 UBIQUITINATION IN VIRUS INFECTION…………………………………………………… 20 VIRUS-RELATED APOPTOSIS IN HOST CELLS…………………………………………. 21 RING-CONTAINING PROTEINS IN WSSV…………………………………………………… 22 RESEARCH OUTLINE AND OBJECTIVES………………………………………………… .23 Chapter WSSV222 encodes a viral E3 ligase and mediates degradation of a host tumor suppressor via ubiquitination 2.1 2.2 2.2.1 2.2.2 2.2.2 2.2.3 2.2.4 2.2.5 2.2.6 2.2.7 2.2.8 2.3 2.3.1 2.3.2 2.3.3 2.3.4 2.3.5 2.3.6 2.4 26 INTRODUCTION………………………………………………………………………………… 27 MATERIALS AND METHODS…………………………………………………………… … 29 RACE PCR, wild type and mutants cloning…………………………………………………….29 Construction of shrimp cDNA library…………………………………………………………….30 Yeast two-hybrid assays………………………………………………………………………….31 Expression, purification of proteins and antibody preparation………………………………. 32 Pull-down assays…………………………………………………………………………………. 33 Cell culture, immunofluorescence and confocal microscopy………………………………… 33 Ubiquitination assays in vitro and in vivo………………………………………………………. 35 DNA Fragmentation Assays…………………………………………………………………… 36 FACS Analysis……………………………………………………………………………………. 36 RESULTS…………………………………………………………………………………………. 37 WSSV222 is a RING-H2 E3 ligase…………………………………………………………… 37 TSL, a shrimp orthologue for OVCA1, is a WSSV222 target……………………………… . 40 WSSV222 interacts with and ubiquitinates TSL in vitro……………………………………… 43 TSL is ubiquitinated for degradation by WSSV222 in vivo………………………………… . 46 TSL is subjected to ubiquitination and degradation in WSSV-infected shrimp cells……… 49 WSSV222 rescues apoptosis induced by transient expression of TSL in BHK cells…… . 51 DISCUSSION………………………………………………………………………………………53 Chapter Viral ubiquitin ligase WSSV222 is required for efficient WSSV replication in shrimp 58 IV 3.1 3.2 3.2.1 3.2.2 3.2.3 3.2.4 3.2.5 3.2.6 3.2.7 3.3 3.3.1 3.3.2 3.3.3 3.3.4 3.3.5 3.4 INTRODUCTION…………………………………………………………………………………. 59 MATERIALS AND METHODS………………………………………………………………… 61 Synthesis of siRNAs……………………………………………………………………………… 61 Shrimp culture, WSSV infection and siRNA injection………………………………………… 61 In vitro silencing of WSSV222………………………………………………………………… . 62 Reverse transcription PCR and Real time quantitative PCR………………………………… 62 Co-immunoprecipitation and western blot analysis…………………………………………… 63 Fluorimetric assay of caspase activity…………………………………………………………. 64 Statistical analysis……………………………………………………………………………… . 65 RESULTS……………………………………………………………………………………… 66 WSSV222 silencing in cultured cells and WSSV infected shrimps…………………………. 66 WSSV222 silencing delayed death time in WSSV infected shrimp………………………… 70 Delayed and reduced WSSV replication in shrimp with WSSV222 silencing……………… 72 WSSV222 is required for TSL degradation in WSSV infected shrimp……………………… 74 WSSV222 contributes to the regulation on WSSV associated apoptosis in shrimp……….76 DISCUSSION………………………………………………………………………………………78 Chapter Identification and characterization of WSSV403 as a viral E3 ligase involved in virus latency 4.1 4.2 4.2.1 4.2.2 4.2.3 4.2.4 4.2.5 4.3 4.3.1 4.3.2 4.3.3 4.4 83 INTRODUCTION…………………………………………………………………………………. 84 MATERIALS AND METHODS………………………………………………………………… 86 Reverse transcription PCR and real time PCR……………………………………………… .86 Expression, purification of proteins and antibody preparation………………………………. 86 Pull-down assays…………………………………………………………………………………. 87 Ubiquitination assays in vitro……………………………………………………………………. 87 Yeast two-hybrid assays………………………………………………………………………… 88 RESULTS…………………………………………………………………………………………. 89 WSSV403 is a RING-H2 E3 ligase…………………………………………………………… . 89 WSSV403 is a latency-associated gene……………………………………………………… 91 WSSV403 interacts with shrimp phosphatase………………………………………………… 93 DISCUSSION………………………………………………………………………………………95 Chapter WSSV ie1 promoter is more efficient than CMV promoter to express H5 from influenza virus in baculovirus as a chicken vaccine 98 5.1 5.2 5.3 5.3.1 5.3.2 5.3.3 5.3.4 5.3.5 5.3.6 5.3.7 5.3.7 5.3.8 5.4 5.4.1 5.4.2 5.4.3 ABSTRACT………………………………………………………………………………………. 99 INTRODUCTION………………………………………………………………………………. 100 MATERIALS AND METHODS……………………………………………………………… 102 Viruses and cells. … ………………………………………………………………………… 102 Luciferase activity assay………………………………………………………………………. 102 Construction of recombinant baculoviruses…………………………………………………. 103 Recombinant baculovirus purification………………………………………….……………. 104 Animal experiments…………………………………………………………………………… 104 Serological assays…………………………………………….……………………………… 105 Immunofluorescence assays……………………………….………………………………… 106 Immunohistochemistry……………………………….…………… .………………………… 106 Statistical analysis……………………………….……………………………… …………… 107 RESULTS………………………………………………………………………………………. 108 WSSV ie1 promoter mediates efficient protein expression in SF9 cells……………… . 108 WSSV ie1 promoter stimulates strong H5 hemagglutinin expression in baculovirus… . 110 Immunogenicity of H5 hemagglutinin expressed by WSSV ie1 promoter in chickens… 115 V 5.4.4 5.5 Significant antigen expression in chicken tissue by HA-VSVG coexpression constructs 119 DISCUSSION…………………………………………………………………………………… 120 Chapter General Discussion 6.1 6.2 6.2 123 ON THE ROLE OF RING PROTEINS IN WSSV………………………………………… 124 IN THE LIGHT OF NEW FINDINGS…………………………………………………………. 126 THAT WHICH REMAINS……………………………………………………………………… 128 Chapter Bibliography 131 VI List of Figures Figure 1. WSSV222, 249 and 403 contain RING-H2 domains…………………………………… 25 Figure 2. WSSV222 is a RING-containing E3 ligase………………………………………………… .39 Figure 3. Shrimp tumor suppressor-like (TSL) protein is functionally similar to human OVCA1… 42 Figure 4. WSSV222 interacts with & ubiquitinates shrimp tumor-suppressor–like protein in vitro .45 Figure 5. WSSV222 ubiquitinates and mediates degradation on shrimp TSL in vivo…………….…48 Figure 6. TSL is degraded and ubiquitinated in WSSV-infected shrimp cells…………………….… 50 Figure 7. WSSV222 antagonizes TSL-induced apoptosis in BHK cells………………………….… .52 Figure 8. Specific WSSV222 siRNA induces WSSV222 silencing in cultured cells……………… 68 Figure 9. Specific WSSV222 siRNA induces WSSV222 silencing in WSSV challenged shrimp… 69 Figure 10. Efficacy of 222 siRNA in WSSV-challenged shrimp……………………………………… 71 Figure 11. WSSV222 silencing results in the delay and reduction of WSSV gene expression in shrimp challenged with WSSV 73 Figure 12. Co-immunoprecipitation and western blot showed TSL degradation in normal and WSSV-challenged shrimp treated with 20 uM MG132……………………………………………… .75 Figure 13. WSSV222 silencing has effects on cell apoptosis in shrimp during WSSV infection… .77 Figure 14. WSSV403 is a viral E3 ubiquitin ligase 90 Figure 15. Detection of WSSV403 transcript in shrimp……………………………………………… 92 Figure 16. WSSV403 can interact with a shrimp protein phosphatase……………………………… 94 Figure 17. Comparison of promoter activity of WSSV ie1 and CMV promoter in luciferase assays in different cell lines……………………………………………………………………………………… .109 Figure 18. Schematic representation of the construction of variant baculoviruses in the study 113 Figure 19. Efficient production of activated HA protein of influenza virus by WSSV ie1 promoter in baculovirus …………………………………………………………………………………………… .114 Figure 20. Immunogenicity of HA-expressing baculoviruses………………………………… ………118 VII List of Table Table 1. Elicitation of influenza A virus HA specific antibody in chickens immunized with HA expressing recombinant baculovirus.……………………………………………………………… 117 VIII Rijiravanich, A., Browdy, C. L., and Withyachumnarnkul, B. (2008). Knocking down caspase-3 by RNAi reduces mortality in Pacific white shrimp Penaeus (Litopenaeus) vannamei challenged with a low dose of white-spot syndrome virus. Fish Shellfish Immunol 24(3), 308-13. Robalino, J., Bartlett, T., Shepard, E., Prior, S., Jaramillo, G., Scura, E., Chapman, R. W., Gross, P. S., Browdy, C. L., and Warr, G. W. (2005). Double-stranded RNA induces sequence-specific antiviral silencing in addition to nonspecific immunity in a marine shrimp: convergence of RNA interference and innate immunity in the invertebrate antiviral response? J Virol 79(21), 13561-71. Robalino, J., Browdy, C. L., Prior, S., Metz, A., Parnell, P., Gross, P., and Warr, G. (2004). Induction of antiviral immunity by double-stranded RNA in a marine invertebrate. J Virol 78(19), 10442-8. Rost, M., Mann, S., Lambert, C., Doring, T., Thome, N., and Prange, R. (2006). Gamma-adaptin, a novel ubiquitin-interacting adaptor, and Nedd4 ubiquitin ligase control hepatitis B virus maturation. J Biol Chem 281(39), 29297-308. Rout, N., Kumar, S., Jaganmohan, S., and Murugan, V. (2007). DNA vaccines encoding viral envelope proteins confer protective immunity against WSSV in black tiger shrimp. Vaccine 25(15), 2778-86. 153 Rowe, T., Abernathy, R. A., Hu-Primmer, J., Thompson, W. W., Lu, X., Lim, W., Fukuda, K., Cox, N. J., and Katz, J. M. (1999). Detection of antibody to avian influenza A (H5N1) virus in human serum by using a combination of serologic assays. J Clin Microbiol 37(4), 937-43. Safdar, A., and Cox, M. M. (2007). Baculovirus-expressed influenza vaccine. A novel technology for safe and expeditious vaccine production for human use. Expert Opin Investig Drugs 16(7), 927-34. Sahtout, A. H., Hassan, M. D., and Shariff, M. (2001). DNA fragmentation, an indicator of apoptosis, in cultured black tiger shrimp Penaeus monodon infected with white spot syndrome virus (WSSV). Dis Aquat Organ 44(2), 155-9. Sahul-Hameed A.S., S. M., Sudhakaran R., Balasubramanian G., Syed-Musthaq S., (2006). Quantitative assessment of apoptotic hemocytes in white spot syndrome virus (WSSV)-infected penaeid shrimp, Penaeus monodon and Penaeus indicus, by flow cytometric analysis. . Aquaculture 201, 179-186. Sambrook, J., Russell, D. W., and Sambrook, J. (2001). "Molecular Cloning: A Laboratory Manual." Cold Spring Harbor Laboratory, NY. Sarathi, M., Simon, M. C., Ahmed, V. P., Kumar, S. R., and Hameed, A. S. (2008a). Silencing VP28 gene of white spot syndrome virus of shrimp by bacterially expressed dsRNA. Mar Biotechnol (NY) 10(2), 198-206. 154 Sarathi, M., Simon, M. C., Venkatesan, C., and Hameed, A. S. (2008b). Oral administration of bacterially expressed VP28dsRNA to protect Penaeus monodon from white spot syndrome virus. Mar Biotechnol (NY) 10(3), 242-9. Scheffner, M., Huibregtse, J. M., Vierstra, R. D., and Howley, P. M. (1993). The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53. Cell 75(3), 495-505. Schultz, D. C., Vanderveer, L., Berman, D. B., Hamilton, T. C., Wong, A. J., and Godwin, A. K. (1996). Identification of two candidate tumor suppressor genes on chromosome 17p13.3. Cancer Res 56(9), 1997-2002. Schwartz, A. L., and Ciechanover, A. (1999). The ubiquitin-proteasome pathway and pathogenesis of human diseases. Annu Rev Med 50, 57-74. Segura-Morales, C., Pescia, C., Chatellard-Causse, C., Sadoul, R., Bertrand, E., and Basyuk, E. (2005). Tsg101 and Alix interact with murine leukemia virus Gag and cooperate with Nedd4 ubiquitin ligases during budding. J Biol Chem 280(29), 27004-12. Shackelford, J., and Pagano, J. S. (2005). Targeting of host-cell ubiquitin pathways by viruses. Essays Biochem 41, 139-56. Sharma, J. M. (1999). Introduction to poultry vaccines and immunity. Adv Vet Med 41, 481-94. 155 Shi, Z., Wang, H., Zhang, J., Xie, Y., Li, L., Chen, X., Edgerton, B. F., and Bonami, J. R. (2005). Response of crayfish, Procambarus clarkii, haemocytes infected by white spot syndrome virus. J Fish Dis 28(3), 151-6. Shih, W. L., Hsu, H. W., Liao, M. H., Lee, L. H., and Liu, H. J. (2004). Avian reovirus sigmaC protein induces apoptosis in cultured cells. Virology 321(1), 65-74. Sinclair, J., and Sissons, P. (2006). Latency and reactivation of human cytomegalovirus. J Gen Virol 87(Pt 7), 1763-79. Sloane, B. F., Yan, S., Podgorski, I., Linebaugh, B. E., Cher, M. L., Mai, J., Cavallo-Medved, D., Sameni, M., Dosescu, J., and Moin, K. (2005). Cathepsin B and tumor proteolysis: contribution of the tumor microenvironment. Semin Cancer Biol 15(2), 149-57. Sritunyalucksana, K., Wannapapho, W., Lo, C. F., and Flegel, T. W. (2006). PmRab7 is a VP28-binding protein involved in white spot syndrome virus infection in shrimp. J Virol 80(21), 10734-42. Stewart, D., Ghosh, A., and Matlashewski, G. (2005). Involvement of nuclear export in human papillomavirus type 18 E6-mediated ubiquitination and degradation of p53. J Virol 79(14), 8773-83. Sun, W., Khoo, H. E., and Tan, C. H. (2005). Adenosine induced apoptosis in BHK cells via P1 receptors and equilibrative nucleoside transporters. J Biochem Mol Biol 38(3), 314-9. 156 Swayne, D. E., Perdue, M. L., Beck, J. R., Garcia, M., and Suarez, D. L. (2000). Vaccines protect chickens against H5 highly pathogenic avian influenza in the face of genetic changes in field viruses over multiple years. Vet Microbiol 74(1-2), 165-72. Syed Musthaq, S., Madhan, S., Sahul Hameed, A. S., and Kwang, J. (2009). Localization of VP28 on the baculovirus envelope and its immunogenicity against white spot syndrome virus in Penaeus monodon. Virology. Syed Musthaq, S., Sudhakaran, R., Balasubramanian, G., and Sahul Hameed, A. S. (2006). Experimental transmission and tissue tropism of white spot syndrome virus (WSSV) in two species of lobsters, Panulirus homarus and Panulirus ornatus. J Invertebr Pathol 93(2), 75-80. Takada, A., Kuboki, N., Okazaki, K., Ninomiya, A., Tanaka, H., Ozaki, H., Itamura, S., Nishimura, H., Enami, M., Tashiro, M., Shortridge, K. F., and Kida, H. (1999). Avirulent Avian influenza virus as a vaccine strain against a potential human pandemic. J Virol 73(10), 8303-7. Tanaka, H., Park, C. H., Ninomiya, A., Ozaki, H., Takada, A., Umemura, T., and Kida, H. (2003). Neurotropism of the 1997 Hong Kong H5N1 influenza virus in mice. Vet Microbiol 95(1-2), 1-13. Tang, X., Wu, J., Sivaraman, J., and Hew, C. L. (2007). Crystal structures of major envelope proteins VP26 and VP28 from white spot syndrome virus shed light on their evolutionary relationship. J Virol 81(12), 6709-17. 157 Tani, H., Limn, C. K., Yap, C. C., Onishi, M., Nozaki, M., Nishimune, Y., Okahashi, N., Kitagawa, Y., Watanabe, R., Mochizuki, R., Moriishi, K., and Matsuura, Y. (2003). In vitro and in vivo gene delivery by recombinant baculoviruses. J Virol 77(18), 9799-808. Tapay, L. M., Lu, Y., Gose, R. B., Nadala, E. C., Jr., Brock, J. A., and Loh, P. C. (1997). Development of an in vitro quantal assay in primary cell cultures for a non-occluded baculo-like virus of penaeid shrimp. J Virol Methods 64(1), 37-41. Thomas, M., Pim, D., and Banks, L. (1999). The role of the E6-p53 interaction in the molecular pathogenesis of HPV. Oncogene 18(53), 7690-700. Tincu, J. A., and Taylor, S. W. (2004). Antimicrobial peptides from marine invertebrates. Antimicrob Agents Chemother 48(10), 3645-54. Treanor, J. J., Schiff, G. M., Couch, R. B., Cate, T. R., Brady, R. C., Hay, C. M., Wolff, M., She, D., and Cox, M. M. (2006). Dose-related safety and immunogenicity of a trivalent baculovirus-expressed influenza-virus hemagglutinin vaccine in elderly adults. J Infect Dis 193(9), 1223-8. Treanor, J. J., Schiff, G. M., Hayden, F. G., Brady, R. C., Hay, C. M., Meyer, A. L., Holden-Wiltse, J., Liang, H., Gilbert, A., and Cox, M. (2007). Safety and immunogenicity of a baculovirus-expressed hemagglutinin influenza vaccine: a randomized controlled trial. Jama 297(14), 1577-82. 158 Treanor, J. J., Wilkinson, B. E., Masseoud, F., Hu-Primmer, J., Battaglia, R., O'Brien, D., Wolff, M., Rabinovich, G., Blackwelder, W., and Katz, J. M. (2001). Safety and immunogenicity of a recombinant hemagglutinin vaccine for H5 influenza in humans. Vaccine 19(13-14), 1732-7. Triantafilou, K., Takada, Y., and Triantafilou, M. (2001). Mechanisms of integrin-mediated virus attachment and internalization process. Crit Rev Immunol 21(4), 311-22. Tsai, J. M., Wang, H. C., Leu, J. H., Hsiao, H. H., Wang, A. H., Kou, G. H., and Lo, C. F. (2004). Genomic and proteomic analysis of thirty-nine structural proteins of shrimp white spot syndrome virus. J Virol 78(20), 11360-70. Tsai, J. M., Wang, H. C., Leu, J. H., Wang, A. H., Zhuang, Y., Walker, P. J., Kou, G. H., and Lo, C. F. (2006). Identification of the nucleocapsid, tegument, and envelope proteins of the shrimp white spot syndrome virus virion. J Virol 80(6), 3021-9. Tsai, M. F., Lo, C. F., van Hulten, M. C., Tzeng, H. F., Chou, C. M., Huang, C. J., Wang, C. H., Lin, J. Y., Vlak, J. M., and Kou, G. H. (2000). Transcriptional analysis of the ribonucleotide reductase genes of shrimp white spot syndrome virus. Virology 277(1), 92-9. Tschopp, J., Thome, M., Hofmann, K., and Meinl, E. (1998). The fight of viruses against apoptosis. Curr Opin Genet Dev 8(1), 82-7. 159 Tzeng, H. F., Chang, Z. F., Peng, S. E., Wang, C. H., Lin, J. Y., Kou, G. H., and Lo, C. F. (2002). Chimeric polypeptide of thymidine kinase and thymidylate kinase of shrimp white spot syndrome virus: thymidine kinase activity of the recombinant protein expressed in a baculovirus/insect cell system. Virology 299(2), 248-55. Udawatte, C., and Ripps, H. (2005). The spread of apoptosis through gapjunctional channels in BHK cells transfected with Cx32. Apoptosis 10(5), 1019-29. van de Braak C.B.T., B. M. H. A., Huisman E.A., Rombout J.H.W.M., van der Knaap W.P.W., (2002). Preliminary study on haemocyte response to white spot syndrome virus infection in black tiger shrimp Penaeus monodon. . Dis Aquat Organ 51, 149-155. van Hulten, M. C., Goldbach, R. W., and Vlak, J. M. (2000). Three functionally diverged major structural proteins of white spot syndrome virus evolved by gene duplication. J Gen Virol 81(Pt 10), 2525-9. van Hulten, M. C., Tsai, M. F., Schipper, C. A., Lo, C. F., Kou, G. H., and Vlak, J. M. (2000a). Analysis of a genomic segment of white spot syndrome virus of shrimp containing ribonucleotide reductase genes and repeat regions. J Gen Virol 81(Pt 2), 307-16. 160 Van Hulten, M. C., and Vlak, J. M. (2001). Identification and phylogeny of a protein kinase gene of white spot syndrome virus. Virus Genes 22(2), 2017. van Hulten, M. C., Westenberg, M., Goodall, S. D., and Vlak, J. M. (2000b). Identification of two major virion protein genes of white spot syndrome virus of shrimp. Virology 266(2), 227-36. van Hulten, M. C., Witteveldt, J., Peters, S., Kloosterboer, N., Tarchini, R., Fiers, M., Sandbrink, H., Lankhorst, R. K., and Vlak, J. M. (2001a). The white spot syndrome virus DNA genome sequence. Virology 286(1), 7-22. van Hulten, M. C., Witteveldt, J., Snippe, M., and Vlak, J. M. (2001b). White spot syndrome virus envelope protein VP28 is involved in the systemic infection of shrimp. Virology 285(2), 228-33. van Regenmortel, M. H., Mayo, M. A., Fauquet, C. M., and Maniloff, J. (2000). Virus nomenclature: consensus versus chaos. Arch Virol 145(10), 2227-32. Vaseeharan, B., Prem Anand, T., Murugan, T., and Chen, J. C. (2006). Shrimp vaccination trials with the VP292 protein of white spot syndrome virus. Lett Appl Microbiol 43(2), 137-42. Vaux, D. L., and Silke, J. (2005). IAPs, RINGs and ubiquitylation. Nat Rev Mol Cell Biol 6(4), 287-97. 161 Velilla, P. A., Hoyos, A., Rojas, M., Patino, P. J., Velez, L. A., and Rugeles, M. T. (2005). Apoptosis as a mechanism of natural resistance to HIV-1 infection in an exposed but uninfected population. J Clin Virol 32(4), 329-35. Venegas, C. A., Nonaka, L., Mushiake, K., Nishizawa, T., and Murog, K. (2000). Quasi-immune response of Penaeus japonicus to penaeid rod-shaped DNA virus (PRDV). Dis Aquat Organ 42(2), 83-9. Villarreal, L. P., Defilippis, V. R., and Gottlieb, K. A. (2000). Acute and persistent viral life strategies and their relationship to emerging diseases. Virology 272(1), 1-6. Wan, Q., Xu, L., and Yang, F. (2008). VP26 of white spot syndrome virus functions as a linker protein between the envelope and nucleocapsid of virions by binding with VP51. J Virol 82(24), 12598-601. Wang, C. H., H. N. Yang, C. Y. Tang, C. H. Lu, G. H. Kou, and C. F. Lo. (2000). Ultrastructure of white spot syndrome virus development in primary lymphoid organ cell cultures. . Dis Aquat Organ 41, 91-104. Wang, C. H., and Yang, H. N., Tang, C. Y., Lu, C. H., Kou, G. H. and Lo, C. F. (2000). Ultrastructure of white spot syndrome virus development in primary lymphoid organ cell cultures. Dis Aquat Organ 41, 91-104. 162 Wang H.C., L. A. T., Yii D.M., Chang Y.S., Kou G.H., Lo C.F. (2003). DNA microarrays of the white spot syndrome virus genome: genes expressed in the gills of infected shrimp. . Mar Biotechnol (NY) 6, S106-S111. Wang H.C., W. H. C., Kou G.H., Lo C.F., Huang W.P., (2007). Identification of icp11, the most highly expressed gene of shrimp white spot syndrome virus (WSSV). . Dis Aquat Organ 74, 179-189. Wang, H. C., Wang, H. C., Ko, T. P., Lee, Y. M., Leu, J. H., Ho, C. H., Huang, W. P., Lo, C. F., and Wang, A. H. (2008a). White spot syndrome virus protein ICP11: A histone-binding DNA mimic that disrupts nucleosome assembly. Proc Natl Acad Sci U S A. Wang, L., Zhi, B., Wu, W., and Zhang, X. (2008b). Requirement for shrimp caspase in apoptosis against virus infection. Dev Comp Immunol 32(6), 706-15. Wang Q., W. B. L., Redman R.M., Lightner D.V., (1999). Per os challenge of Litopenaeus vannamei postlarvae and Farfantepenaeus duorarum juveniles with six geographic isolates of white spot syndrome virus. Aquaculture 170, 179-184. Wang, S., Fang, L., Fan, H., Jiang, Y., Pan, Y., Luo, R., Zhao, Q., Chen, H., and Xiao, S. (2007). Construction and immunogenicity of pseudotype baculovirus expressing GP5 and M protein of porcine reproductive and respiratory syndrome virus. Vaccine. 163 Wang, S., Nath, N., Fusaro, G., and Chellappan, S. (1999a). Rb and prohibitin target distinct regions of E2F1 for repression and respond to different upstream signals. Mol Cell Biol 19(11), 7447-60. Wang, Y., Liu, W, Seah, JN, Lam, CS, Xiang, JH, Korzh, V, Kwang, J (2002). White spot syndrome virus (WSSV) infects specific hemocytes of the shrimp Penaeus merguiensis. Dis Aquat Organ 52(3), 249-259. Wang, Y. G., Hassan, M. D., Shariff, M., Zamri, S. M., and Chen, X. (1999b). Histopathology and cytopathology of white spot syndrome virus (WSSV) in cultured Penaeus monodon from peninsular Malaysia with emphasis on pathogenesis and the mechanism of white spot formation. Dis Aquat Organ 39(1), 1-11. Wang, Y. T., Liu, W., Seah, J. N., Lam, C. S., Xiang, J. H., Korzh, V., and Kwang, J. (2002). White spot syndrome virus (WSSV) infects specific hemocytes of the shrimp Penaeus merguiensis. Dis Aquat Organ 52(3), 249-59. Wang, Z., Chua, H. K., Gusti, A. A., He, F., Fenner, B., Manopo, I., Wang, H., and Kwang, J. (2005). RING-H2 protein WSSV249 from white spot syndrome virus sequesters a shrimp ubiquitin-conjugating enzyme, PvUbc, for viral pathogenesis. J Virol 79(14), 8764-72. 164 Wang, Z., Hu, L., Yi, G., Xu, H., Qi, Y., and Yao, L. (2004). ORF390 of white spot syndrome virus genome is identified as a novel anti-apoptosis gene. Biochem Biophys Res Commun 325(3), 899-907. Westenberg, M., Heinhuis, B., Zuidema, D., and Vlak, J. M. (2005). siRNA injection induces sequence-independent protection in Penaeus monodon against white spot syndrome virus. Virus Res 114(1-2), 133-9. Witteveldt, J., Van Hulten, M. C., and Vlak, J. M. (2001). Identification and phylogeny of a non-specific endonuclease gene of white spot syndrome virus of shrimp. Virus Genes 23(3), 331-7. Wongprasert, K., Khanobdee, K., Glunukarn, S. S., Meeratana, P., and Withyachumnarnkul, B. (2003). Time-course and levels of apoptosis in various tissues of black tiger shrimp Penaeus monodon infected with white-spot syndrome virus. Dis Aquat Organ 55(1), 3-10. Wongprasert, K., Sangsuriya, P., Phongdara, A., and Senapin, S. (2007). Cloning and characterization of a caspase gene from black tiger shrimp (Penaeus monodon)-infected with white spot syndrome virus (WSSV). J Biotechnol 131(1), 9-19. 165 Wongteerasupaya C., V. J. E., Sriurairatana S., Nash G.L., Alarajamorn A., Boonsaeng V., Panyim S., Tassanakajon A., Withyachumnarkul B., Flegel T.W. (1995a). A non-occluded, systemic baculovirus that occurs in cells of ectodermal and mesodermal origin and causes high mortality in the black tiger prawn Penaeus monodon. Dis Aquat Organ 21, 69-77. Wongteerasupaya C., V. J. E., Sriurairatana S., Nash G.L., Alarajamorn A., Boonsaeng V., Panyim S., Tassanakajon A., Withyachumnarkul B., Flegel T.W. (1995b). A non-occluded, systemic baculovirus that occurs in cells of ectodermal and mesodermal origin and causes high mortality in the black tiger prawn Penaeus monodon. . Dis Aquat Organ 21, 69-77. Wu, J. L., Nishioka, T., Mori, K., Nishizawa, T., and Muroga, K. (2002). A timecourse study on the resistance of Penaeus japonicus induced by artificial infection with white spot syndrome virus. Fish Shellfish Immunol 13(5), 391-403. Xie, X., Xu, L., and Yang, F. (2006). Proteomic analysis of the major envelope and nucleocapsid proteins of white spot syndrome virus. J Virol 80(21), 10615-23. Xu, J., Han, F., and Zhang, X. (2007). Silencing shrimp white spot syndrome virus (WSSV) genes by siRNA. Antiviral Res 73(2), 126-31. 166 Yang, D. G., Chung, Y. C., Lai, Y. K., Lai, C. W., Liu, H. J., and Hu, Y. C. (2007). Avian influenza virus hemagglutinin display on baculovirus envelope: cytoplasmic domain affects virus properties and vaccine potential. Mol Ther 15(5), 989-96. Yang, F., He, J., Lin, X., Li, Q., Pan, D., Zhang, X., and Xu, X. (2001). Complete genome sequence of the shrimp white spot bacilliform virus. J Virol 75(23), 11811-20. Yang, Y., Li, C. C., and Weissman, A. M. (2004). Regulating the p53 system through ubiquitination. Oncogene 23(11), 2096-106. Yang, Y., and Yu, X. (2003). Regulation of apoptosis: the ubiquitous way. Faseb J 17(8), 790-9. Yang, Y. L., and Li, X. M. (2000). The IAP family: endogenous caspase inhibitors with multiple biological activities. Cell Res 10(3), 169-77. Yasuda, J., Hunter, E., Nakao, M., and Shida, H. (2002). Functional involvement of a novel Nedd4-like ubiquitin ligase on retrovirus budding. EMBO Rep 3(7), 636-40. Ye, F. C., Zhou, F. C., Xie, J. P., Kang, T., Greene, W., Kuhne, K., Lei, X. F., Li, Q. H., and Gao, S. J. (2008). Kaposi's Sarcoma-Associated Herpesvirus Latent Gene vFLIP Inhibits Viral Lytic Replication through NF{kappa}B-Mediated Suppression of the AP-1 Pathway: A Novel Mechanism of Virus Control of Latency. J Virol. 167 Yi, G., Wang, Z., Qi, Y., Yao, L., Qian, J., and Hu, L. (2004). Vp28 of shrimp white spot syndrome virus is involved in the attachment and penetration into shrimp cells. J Biochem Mol Biol 37(6), 726-34. Yoganandhan, K., Syed Musthaq, S., Narayanan, R. B., and Sahul Hameed, A. S. (2004). Production of polyclonal antiserum against recombinant VP28 protein and its application for the detection of white spot syndrome virus in crustaceans. J Fish Dis 27(9), 517-22. Zhao, Z. Y., Yin, Z. X., Xu, X. P., Weng, S. P., Rao, X. Y., Dai, Z. X., Luo, Y. W., Yang, G., Li, Z. S., Guan, H. J., Li, S. D., Chan, S. M., Yu, X. Q., and He, J. G. (2009). A novel C-type lectin from the shrimp Litopenaeus vannamei possesses anti-white spot syndrome virus activity. J Virol 83(1), 347-56. Zhou, Q., Xu, L., Li, H., Qi, Y. P., and Yang, F. (2009). Four Major Envelope Proteins of White Spot Syndrome Virus Bind to Form a Complex. J Virol. 168 [...]... RING containing proteins in WSSV 2 Determination of the transcription profile of the viral E3 ligases during WSSV infection 3 Identification and characterization of host/shrimp interaction partners of these viral E3 ligases 4 Functional studies on these viral E3 ligases and their interaction partners during WSSV infection in shrimp 5 Comparative studies on WSSV immediate early promoter 1 in recombinant... al., 2005) 1.9 RING- containing proteins in WSSV A previous study (Freemont, 2000) has revealed that the RING finger domains of E3 ubiquitin ligases are involved in specific ubiquination events It is now recognized that the RING finger domain is present in the largest known class of E3 ubiquitin ligases (Borden, 2000; Yang and Yu, 2003) It has functions involved in cell-cycle control, oncogenesis and... of RING proteins in viral regulation will certainly pave the way for an increased understanding of WSSV and other viral infection mechanisms Therefore, to fully determine the function of RING proteins in WSSV, emphasis in this study is placed on the WSSV222 and WSSV403 proteins and the following research objectives were established: 1 Identification of viral E3 ubiquitin ligase activity of these RING. .. other virus infection models For unique viruses with a large genome like WSSV, it is thus important to reveal its infection mechanism, which might throw a light on new regulatory pathways in virus- host interaction As suggested by previous findings on WSSV RING proteins (Wang et al., 2005), they might play key roles in WSSV pathogenicity and infection machinery Studies focusing on the potential function. .. domains (A) Schematic representation of WSSV222 and 403 proteins by SMART program WSSV222 RING domain is from 308aa to 358 aa , while WSSV403 from 329 aa to 370 aa Pink bars indicated segments of low compositional complexity on WSSV222 Green bars indicated coiled coil regions on WSSV 403 (B) Alignment of the RING portion from RING proteins identified in WSSV These WSSV RING domains are of the C3H2C3 type... pathogenicity by taking a principal role in limiting inflammatory reactions at the site of infection and by inducing specific immunity In contrast, apoptosis enhances HIV-1 pathogenicity by inducing massive cell death in indispensable organs, signaling the onset of disease (Cossarizza, 2008; Velilla et al., 2005) Although replication of most viruses is suppressed by apoptosis of infected cells, certain viruses... in natural populations, persistent viral life strategy has not received much attention Persistence has been defined as the state in which a virus maintains its capacity for either continued or episodic reproduction in an individual host, subsequent to an initial period of productive infection and occurrence of an antiviral host response This definition also includes the condition known as latency in. .. in China from 1993 to 1994 (Cai S., 1995) The virus from the People's Republic of China has also been called Chinese baculovirus (CBV) The virus has also been taxonomically affiliated as: China virus disease, red disease (Alapide-Tendencia E.V., 1997), white 7 spot disease, and white spot baculovirus However, presently the virus is referred to as white spot syndrome virus (WSSV) Virus classification... attenuation of viral pathogenicity in shrimp Despite these findings, there is still no clear conclusion as to 20 the relative contribution of apoptosis to viral pathogenicity and/or host defensive responses in shrimp 1.8 Ubiquitination in virus infection Ubiquitin-mediated proteolysis plays an important role in a variety of basic pathways and processes during cell life and death In the ubiquitin-dependent... protein mediates direct binding with the UEV (ubiquitin E2 variant ) domain in the N-terminus of Tsg101 (tumor susceptibility gene 101), and two E3 ligases have been identified as regulators of HIV budding (Klinger and Schubert, 2005; Li and Wild, 2005) In addition, ubiquitination of APOBEC3G by an HIV-1 Vif-Cullin5-Elongin B-Elongin C complex is essential for Vif (virion infectivity factor) function . understanding of the specific function of RING- containing proteins in viral pathogenesis. A preliminary search for regulatory protein candidates in WSSV using functional domain determination identified. OF WSSV INFECTION …………………… 15 1.7 UBIQUITINATION IN VIRUS INFECTION…………………………………………………… 20 1.8 VIRUS- RELATED APOPTOSIS IN HOST CELLS…………………………………………. 21 1.9 RING- CONTAINING PROTEINS IN WSSV……………………………………………………. ligase function. III In summary, the studies presented here indicate that viral RING proteins are involved in ubiquitination events and interactions with a diverse range of shrimp proteins