Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus

© 2014 Elsevier B.V. We tested the use of Macrobrachium rosenbergii nodavirus-like particles (MrNv-VLPs) as a delivery mechanism to carry therapeutic agents against white spot syndrome in shrimp. We used constructed double-stranded RNA called VP28 (VP28 dsRNA) against WSSV envelope genes to confer p...

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Main Authors: Pitchanee Jariyapong, Charoonroj Chotwiwatthanakun, Sataporn Direkbusarakom, Ikuo Hirono, Suwit Wuthisuthimethavee, Wattana Weerachatyanukul
Other Authors: Walailak University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/35240
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spelling th-mahidol.352402018-11-23T16:33:24Z Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus Pitchanee Jariyapong Charoonroj Chotwiwatthanakun Sataporn Direkbusarakom Ikuo Hirono Suwit Wuthisuthimethavee Wattana Weerachatyanukul Walailak University Mahidol University National University Corporation Tokyo University of Marine Science and Technology Agricultural and Biological Sciences © 2014 Elsevier B.V. We tested the use of Macrobrachium rosenbergii nodavirus-like particles (MrNv-VLPs) as a delivery mechanism to carry therapeutic agents against white spot syndrome in shrimp. We used constructed double-stranded RNA called VP28 (VP28 dsRNA) against WSSV envelope genes to confer protection against the pathogen. Results showed that MrNv-VLP was able to encapsulate VP28 dsRNA. Using enhanced green fluorescent protein (EGFP) as a reporter, we found that VLP penetrated various shrimp tissues including the muscle, hepatopancreas, and gill. A statistically significant relative survival rate of 44.5% was obtained in the group of shrimp receiving encapsulated VP28 dsRNA-VLP after WSSV challenge as compared to 100% mortality in the control shrimp at 7. days post-infection. Shrimp treated with EGFP dsRNA loaded into MrNv-VLPs showed relatively similar motility rates as those of controls. Moreover, MrNv-VLP encapsulation improved VP28 dsRNA efficiency against WSSV. A higher survival rate of 16.7% was observed in the group of shrimp receiving encapsulated VP28 dsRNA-VLP when compared to those receiving naked VP28 dsRNA. These results indicate that MrNv-VLP is a good candidate for use as a therapeutic delivery system against shrimp diseases due to its self-reassembly property, broad target of various shrimp tissues and immune enhancement. 2018-11-23T09:33:24Z 2018-11-23T09:33:24Z 2015-01-01 Article Aquaculture. Vol.435, (2015), 86-91 10.1016/j.aquaculture.2014.09.034 00448486 2-s2.0-84908431508 https://repository.li.mahidol.ac.th/handle/123456789/35240 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84908431508&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Agricultural and Biological Sciences
spellingShingle Agricultural and Biological Sciences
Pitchanee Jariyapong
Charoonroj Chotwiwatthanakun
Sataporn Direkbusarakom
Ikuo Hirono
Suwit Wuthisuthimethavee
Wattana Weerachatyanukul
Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
description © 2014 Elsevier B.V. We tested the use of Macrobrachium rosenbergii nodavirus-like particles (MrNv-VLPs) as a delivery mechanism to carry therapeutic agents against white spot syndrome in shrimp. We used constructed double-stranded RNA called VP28 (VP28 dsRNA) against WSSV envelope genes to confer protection against the pathogen. Results showed that MrNv-VLP was able to encapsulate VP28 dsRNA. Using enhanced green fluorescent protein (EGFP) as a reporter, we found that VLP penetrated various shrimp tissues including the muscle, hepatopancreas, and gill. A statistically significant relative survival rate of 44.5% was obtained in the group of shrimp receiving encapsulated VP28 dsRNA-VLP after WSSV challenge as compared to 100% mortality in the control shrimp at 7. days post-infection. Shrimp treated with EGFP dsRNA loaded into MrNv-VLPs showed relatively similar motility rates as those of controls. Moreover, MrNv-VLP encapsulation improved VP28 dsRNA efficiency against WSSV. A higher survival rate of 16.7% was observed in the group of shrimp receiving encapsulated VP28 dsRNA-VLP when compared to those receiving naked VP28 dsRNA. These results indicate that MrNv-VLP is a good candidate for use as a therapeutic delivery system against shrimp diseases due to its self-reassembly property, broad target of various shrimp tissues and immune enhancement.
author2 Walailak University
author_facet Walailak University
Pitchanee Jariyapong
Charoonroj Chotwiwatthanakun
Sataporn Direkbusarakom
Ikuo Hirono
Suwit Wuthisuthimethavee
Wattana Weerachatyanukul
format Article
author Pitchanee Jariyapong
Charoonroj Chotwiwatthanakun
Sataporn Direkbusarakom
Ikuo Hirono
Suwit Wuthisuthimethavee
Wattana Weerachatyanukul
author_sort Pitchanee Jariyapong
title Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
title_short Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
title_full Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
title_fullStr Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
title_full_unstemmed Delivery of double stranded RNA by Macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
title_sort delivery of double stranded rna by macrobrachium rosenbergii nodavirus-like particles to protect shrimp from white spot syndrome virus
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/35240
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