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Assessing various administration strategies for dsRNA vaccine delivery: a concise review of VP15-WSSV research progress in tiger shrimp Penaeus monodon
Corresponding Author(s) : Andi Parenrengi
Jurnal Ilmiah Perikanan dan Kelautan, 2025: IN PRESS ISSUE (JUST ACCEPTED MANUSCRIPT, 2025)
Abstract
Graphical Abstract
Highlight Research
1. The dsRNA application should correspond to the developmental stages of shrimp
2. Immersion method was commonly used for larvae for handling many individuals
3. Injection technique effectively delivered dsRNA to cells but was unsuitable for large-scale
4. Oral administration of pellet-enriched dsRNA was applicable to apply on shrimp larvae, juveniles, and broodstocks
Abstract
RNAi technology offers a novel powerful approach to silence gene expression by introducing double-stranded RNA (dsRNA) into the cell to degrade the mRNA at the post-transcriptional stage. An administration method of dsRNA delivery is one of the main considerations in applying the dsRNA vaccine for controlling pathogen infections. This mini-review was focused on the evaluation of three different methods (immersion, injection, and oral administration) of VP15-dsRNA vaccine delivery to the tiger shrimp post-WSSV challenge test. The immersion method was generally applied for the larval stage of tiger shrimp and seemed to be a simple technique for a large number of individuals in a small tank. The VP15-dsRNA application by immersion improved the survival of tiger shrimp larvae by 3.9% compared to the control groups. The injection technique was an effective way to deliver dsRNA to the cell, but it is difficult to apply in a large number of individuals or populations. The injection of VP15-dsRNA increased significantly the survival rate, proPO, and THC of tiger shrimp. A higher survival rate (75%) was exhibited in tiger shrimp injected with in vivo and in vitro VP15-dsRNA than in the control. Oral administration by pellet-enriched VP15-dsRNA was a useful way for larvae, juveniles, and broodstocks, but it has limitations since the pellet leaches into the water. The application of the VP15-dsRNA vaccine on the feed significantly enhanced the 26.7% higher survival rate compared to the control. The higher survival was also supported by a higher number of THC. The three VP15-dsRNA delivery methods provide potential approaches to increase tiger shrimp resistance to control pathogen infection
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- Asche, F., Anderson, J.L., Botta, R., Kumar, G., Abrahamsen, E.B., Nguyen, L.T., Valderrama, D. (2020). The economics of shrimp disease. J. Invertebr. Pathol,. 186:107397.
- Boonyakida, J., Nakanishi, T., Satoh, J., Shimahara, Y., Mekata, T., Park, E.Y. (2022). Immunostimulation of shrimp through oral administration of silkworm pupae expressing VP15 against WSSV. Fish Shellfish Immunol. 128:157–167.
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- Chaimongkon, D., Assavalapsakul, W., Panyim, S., Attasart, P., (2020). A multi-target dsRNA for simultaneous inhibition of yellow head virus and white spot syndrome virus in shrimp. J. Biotechnol, 321:48–56.
- Chakrobortty, D., Ali, M.R., Dey, B.K., Gupta, N., Islam, S.S., Sui, L. (2020). Viral contamination of tiger shrimp Penaeus monodon broodstock in Bangladesh. Aquac. Int. 28:2161–2172.
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- Cox, N., De Swaef, E., Corteel, M., Van Den Broeck, W., Bossier, P., Nauwynck, H.J., Dantas-Lima, J.J., (2024). Experimental infection models and their usefulness for white spot syndrome virus (WSSV) research in shrimp. Viruses,16:1–39.
- Escobedo-Bonilla, C.M. (2011). Application of RNA interference (RNAi) against viral infections in shrimp: A review. J. Antivirals Antiretrovir, S9:1–12.
- Fajardo, C., Mancera, J.M., Costas, B., De Donato, M., Martinez-Rodriguez, G. (2024). In vitro transcription of dsRNA-LjRab7-a tool for the development of interfering RNA as antiviral therapy in aquaculture of shrimp species. AACL Bioflux, 17:673–679.
- He, Y., Ju, C., Zhang, X. (2015). Roles of small RNAs in the immune defense mechanisms of crustaceans. Mol. Immunol. 68:399–403.
- Hsu, J.C.K., Huang, H.T., Lin, H.J., Chou, H.Y., Huang, P.Y., Prachumwat, A., Chen, L.L., (2022). Applying modified VP53A recombinant protein as an anti-white spot syndrome virus biological agent in Litopenaeus vannamei Farming. Viruses 14:1353.
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- Jariyapong, P., Chotwiwatthanakun, C., Direkbusarakom, S., Hirono, I., Wuthisuthimethavee, S., Weerachatyanukul, W. (2015). Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus. Aquaculture, 435:86–91.
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- Namikoshi, A., Wu, J.L., Yamashita, T., Nishizawa, T., Nishioka, T., Arimoto, M., Muroga, K. (2004). Vaccination trials with Penaeus japonicus to induce resistance to white spot syndrome virus. Aquaculture, 229:25–35.
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References
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Asche, F., Anderson, J.L., Botta, R., Kumar, G., Abrahamsen, E.B., Nguyen, L.T., Valderrama, D. (2020). The economics of shrimp disease. J. Invertebr. Pathol,. 186:107397.
Boonyakida, J., Nakanishi, T., Satoh, J., Shimahara, Y., Mekata, T., Park, E.Y. (2022). Immunostimulation of shrimp through oral administration of silkworm pupae expressing VP15 against WSSV. Fish Shellfish Immunol. 128:157–167.
Boonyakida, J., Xu, J., Satoh, J., Nakanishi, T., Mekata, T., Kato, T., Park, E.Y. (2020). Antigenic properties of VP15 from white spot syndrome virus in kuruma shrimp Marsupenaeus japonicus. Fish Shellfish Immunol. 101:152–158.
Chaimongkon, D., Assavalapsakul, W., Panyim, S., Attasart, P., (2020). A multi-target dsRNA for simultaneous inhibition of yellow head virus and white spot syndrome virus in shrimp. J. Biotechnol, 321:48–56.
Chakrobortty, D., Ali, M.R., Dey, B.K., Gupta, N., Islam, S.S., Sui, L. (2020). Viral contamination of tiger shrimp Penaeus monodon broodstock in Bangladesh. Aquac. Int. 28:2161–2172.
Chen, S., Zhong, Q., Liao, X., Wang, H., Xiao, B., He, J., Li, C., (2024). Modulation of the unfolded protein response by white spot syndrome virus via wsv406 targeting BiP to facilitate viral replication. Virol. Sin., 39:938–950.
Cox, N., De Swaef, E., Corteel, M., Van Den Broeck, W., Bossier, P., Nauwynck, H.J., Dantas-Lima, J.J., (2024). Experimental infection models and their usefulness for white spot syndrome virus (WSSV) research in shrimp. Viruses,16:1–39.
Escobedo-Bonilla, C.M. (2011). Application of RNA interference (RNAi) against viral infections in shrimp: A review. J. Antivirals Antiretrovir, S9:1–12.
Fajardo, C., Mancera, J.M., Costas, B., De Donato, M., Martinez-Rodriguez, G. (2024). In vitro transcription of dsRNA-LjRab7-a tool for the development of interfering RNA as antiviral therapy in aquaculture of shrimp species. AACL Bioflux, 17:673–679.
He, Y., Ju, C., Zhang, X. (2015). Roles of small RNAs in the immune defense mechanisms of crustaceans. Mol. Immunol. 68:399–403.
Hsu, J.C.K., Huang, H.T., Lin, H.J., Chou, H.Y., Huang, P.Y., Prachumwat, A., Chen, L.L., (2022). Applying modified VP53A recombinant protein as an anti-white spot syndrome virus biological agent in Litopenaeus vannamei Farming. Viruses 14:1353.
Islam, S.M.R., Ahmed, R., Sharmen, F., Hossain, M., Chakma, K., Tanni, A.A., Akash, A.A., Hossain, M.E., Chowdhury, M.S.N., Siddiki, A.Z., Hossain, A., Mandal, S.C., Crandall, K.A., Rahnavard, A., Sharifuzzaman, S.M., Mannan, A., (2024). infecting cultured black tiger shrimp (Penaeus monodon) in Bangladesh. Microbiol. Resour. Announc, 13:11–15.
Jariyapong, P., Chotwiwatthanakun, C., Direkbusarakom, S., Hirono, I., Wuthisuthimethavee, S., Weerachatyanukul, W. (2015). Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus. Aquaculture, 435:86–91.
Jonjaroen, V., Jitrakorn, S., Charoonnart, P., Kaewsaengon, P., Thinkohkaew, K., Payongsri, P., Surarit, R., Saksmerprome, V., Niamsiri, N., (2025). Optimizing chitosan nanoparticles for oral delivery of double-stranded RNA in treating white spot disease in shrimp: Key insights and practical implications. Int. J. Biol. Macromol, 290:138970.
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Kiataramgul, A., Maneenin, S., Purton, S., Areechon, N., Hirono, I., Brocklehurst, T.W., Unajak, S., 2020. An oral delivery system for controlling white spot syndrome virus infection in shrimp using transgenic microalgae. Aquaculture, 521:735022.
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Koesharyani, I., Sudaryatma, P.E., Gardenia, L., Aryati, Y., Mahardika, K., Mufidah, T. (2023). Simultaneous pathogen detection of shrimp viruses on cultured tiger shrimps (Penaeus monodon) in Indonesia. Indones. Aquac. J., 18:79–86.
Krishnan, P., Gireesh-Babu, P., Rajendran, K. V., Chaudhari, A. (2009). RNA interference-based therapeutics for shrimp viral diseases. Dis. Aquat. Organ., 86: 263–272.
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Li, X., Xue, Q., Luan, S., Luo, K., Kong, J., Meng, X., (2024). Comparative transcriptomic analysis of WSSV-challenged Penaeus vannamei with variable resistance levels. Int. J. Mol. Sci. 25:25094961.
Liu, T., Qiao, Y., Jiang, H., Cao, X., Cheng, J., Jiang, G., Sun, X., Shen, H. (2025). Silencing of EhAQP1, EhPTP2, and EhTK Genes in Ecytonucleospora Hepatopenaei Using RNA Interference: A Potential Strategy for Preventing and Treating EHP Infection in Shrimp. Aquac. Res. 2025:1-10.
Loy, J.D., Mogler, M.A., Loy, D.S., Janke, B., Kamrud, K., Scura, E.D., Hank Harris, D.L., Bartholomay, L.C. (2012). dsRNA provides sequence-dependent protection against infectious myonecrosis virus in Litopenaeus vannamei. J. Gen. Virol. 93:880–888.
Mulyaningrum, S.R.H., Parenrengi, A., Tampangallo, B.R., Trismawanti, I. (2018). Response immune of black tiger shrimp Penaeus monodon to dsRNA VP-24 vaccine on different doses. J. Ris. Akuakultur, 13:77–84.
Namikoshi, A., Wu, J.L., Yamashita, T., Nishizawa, T., Nishioka, T., Arimoto, M., Muroga, K. (2004). Vaccination trials with Penaeus japonicus to induce resistance to white spot syndrome virus. Aquaculture, 229:25–35.
Nie, W., Chen, X., Tang, Y., Xu, N., Zhang, H. (2022). Potential dsRNAs can be delivered to aquatic for defense pathogens. Front. Bioeng. Biotechnol. 10:1–12.
Ongvarrasopone, C., Roshorm, Y., Panyim, S. (2007). A simple and cost effective method to generate dsRNA for RNAi studies in invertebrates. ScienceAsia, 33:35–39.
Parenrengi, A., Alimuddin, A., Tenriulo, A. (2017). Characteristic of a viral protein (VP-15) of white spot syndrome virus (WSSV) isolated from infected tiger shrimp Penaeus monodon (Fabricius, 1798). Indones. Aquac. J., 12:1–9.
Parenrengi, A., Lante, S., Tenriulo, A., Suryati, E., Rosmiati, R. (2020a). Research on improving the larval production system and the quality of prospective tiger prawn broodstock Penaeus monodon, Technical Report, Research Institute for Brackishwater Aquaculture and Fisheries Extension. Ministry of Marine Affairs and Fisheries, Maros, Indonesia, 219 pp.
Parenrengi, A., Mulyaningrum, S.R.H., Tenriulo, A., Nawang, A. (2018). Gene encoding viral protein 15 (VP-15) of white spot syndrome virus and its application as a recombinant vaccine to tiger shrimp Penaeus monodon (Text in Indonesian). J. Ris. Akuakultur, 13(1):57-65.
Parenrengi, A., Tenriulo, A., Alimuddin, A., Sukenda, S. (2021). Enhancement of tiger shrimp Penaeus monodon resistance to white spot syndrome virus by overexpression of antiviral gene. Int. J. Agric. Biol. 25:277–284.
Parenrengi, A., Tenriulo, A., Mulyaningrum, S.R.H., Lante, S., Nawang, A. (2019). The effects of in-vitro and in-vivo dsRNA application to survival rate and immune response of tiger shrimp, Penaeus monodon (Text in Indonesian). J. Ris. Akuakultur, 14(4):213-223.
Parenrengi, A., Tenriulo, A., Mulyaningrum, S.R.H., Suryati, E., Rosmiati, R., Lante, S., Nawang, A. (2021b). Effect of different doses of dsRNA VP15 vaccine for controlling white spot syndrome virus infection in tiger shrimp Penaeus monodon. IOP Conf. Ser. Earth Environ. Sci. 860:012031.
Parenrengi, A., Tenriulo, A., Suryati, E., Rosmiati, R., Lante, S., Azis, A.A., Alimuddin, A. (2022). Application of dsRNA VP15-WSSV by oral vaccination to increase survival rate and response immunes of tiger shrimp Penaeus monodon. Indian J. Anim. Res. 56:893–898.
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