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Mud crab susceptibility to disease from white spot syndrome virus is species-dependent
BACKGROUND: Based on a report for one species (Scylla serrata), it is widely believed that mud crabs are relatively resistant to disease caused by white spot syndrome virus (WSSV). We tested this hypothesis by determining the degree of susceptibility in two species of mud crabs, Scylla olivacea and...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001434/ https://www.ncbi.nlm.nih.gov/pubmed/21092125 http://dx.doi.org/10.1186/1756-0500-3-315 |
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author | Somboonna, Naraporn Mangkalanan, Seksan Udompetcharaporn, Attasit Krittanai, Chartchai Sritunyalucksana, Kallaya Flegel, TW |
author_facet | Somboonna, Naraporn Mangkalanan, Seksan Udompetcharaporn, Attasit Krittanai, Chartchai Sritunyalucksana, Kallaya Flegel, TW |
author_sort | Somboonna, Naraporn |
collection | PubMed |
description | BACKGROUND: Based on a report for one species (Scylla serrata), it is widely believed that mud crabs are relatively resistant to disease caused by white spot syndrome virus (WSSV). We tested this hypothesis by determining the degree of susceptibility in two species of mud crabs, Scylla olivacea and Scylla paramamosain, both of which were identified by mitochondrial 16 S ribosomal gene analysis. We compared single-dose and serial-dose WSSV challenges on S. olivacea and S. paramamosain. FINDINGS: In a preliminary test using S. olivacea alone, a dose of 1 × 10(6 )WSSV copies/g gave 100% mortality within 7 days. In a subsequent test, 17 S. olivacea and 13 S. paramamosain were divided into test and control groups for challenge with WSSV at 5 incremental, biweekly doses starting from 1 × 10(4 )and ending at 5 × 10(6 )copies/g. For 11 S. olivacea challenged, 3 specimens died at doses between 1 × 10(5 )and 5 × 10(5 )copies/g and none died for 2 weeks after the subsequent dose (1 × 10(6 )copies/g) that was lethal within 7 days in the preliminary test. However, after the final challenge on day 56 (5 × 10(6 )copies/g), the remaining 7 of 11 S. olivacea (63.64%) died within 2 weeks. There was no mortality in the buffer-injected control crabs. For 9 S. paramamosain challenged in the same way, 5 (55.56%) died after challenge doses between 1 × 10(4 )and 5 × 10(5 )copies/g, and none died for 2 weeks after the challenge dose of 1 × 10(6 )copies/g. After the final challenge (5 × 10(6 )copies/g) on day 56, no S. paramamosain died during 2 weeks after the challenge, and 2 of 9 WSSV-infected S. paramamosain (22.22%) remained alive together with the control crabs until the end of the test on day 106. Viral loads in these survivors were low when compared to those in the moribund crabs. CONCLUSIONS: S. olivacea and S. paramamosain show wide variation in response to challenge with WSSV. S. olivacea and S. paramamosain are susceptible to white spot disease, and S. olivacea is more susceptible than S. paramamosain. Based on our single-challenge and serial challenge results, and on previous published work showing that S. serrata is relatively unaffected by WSSV infection, we propose that susceptibility to white spot disease in the genus Scylla is species-dependent and may also be dose-history dependent. In practical terms for shrimp farmers, it means that S. olivacea and S. paramamosain may pose less threat as WSSV carriers than S. serrata. For crab farmers, our results suggest that rearing of S. serrata would be a better choice than S. paramamosain or S. olivacea in terms of avoiding losses from seasonal outbreaks of white spot disease. |
format | Text |
id | pubmed-3001434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30014342010-12-15 Mud crab susceptibility to disease from white spot syndrome virus is species-dependent Somboonna, Naraporn Mangkalanan, Seksan Udompetcharaporn, Attasit Krittanai, Chartchai Sritunyalucksana, Kallaya Flegel, TW BMC Res Notes Short Report BACKGROUND: Based on a report for one species (Scylla serrata), it is widely believed that mud crabs are relatively resistant to disease caused by white spot syndrome virus (WSSV). We tested this hypothesis by determining the degree of susceptibility in two species of mud crabs, Scylla olivacea and Scylla paramamosain, both of which were identified by mitochondrial 16 S ribosomal gene analysis. We compared single-dose and serial-dose WSSV challenges on S. olivacea and S. paramamosain. FINDINGS: In a preliminary test using S. olivacea alone, a dose of 1 × 10(6 )WSSV copies/g gave 100% mortality within 7 days. In a subsequent test, 17 S. olivacea and 13 S. paramamosain were divided into test and control groups for challenge with WSSV at 5 incremental, biweekly doses starting from 1 × 10(4 )and ending at 5 × 10(6 )copies/g. For 11 S. olivacea challenged, 3 specimens died at doses between 1 × 10(5 )and 5 × 10(5 )copies/g and none died for 2 weeks after the subsequent dose (1 × 10(6 )copies/g) that was lethal within 7 days in the preliminary test. However, after the final challenge on day 56 (5 × 10(6 )copies/g), the remaining 7 of 11 S. olivacea (63.64%) died within 2 weeks. There was no mortality in the buffer-injected control crabs. For 9 S. paramamosain challenged in the same way, 5 (55.56%) died after challenge doses between 1 × 10(4 )and 5 × 10(5 )copies/g, and none died for 2 weeks after the challenge dose of 1 × 10(6 )copies/g. After the final challenge (5 × 10(6 )copies/g) on day 56, no S. paramamosain died during 2 weeks after the challenge, and 2 of 9 WSSV-infected S. paramamosain (22.22%) remained alive together with the control crabs until the end of the test on day 106. Viral loads in these survivors were low when compared to those in the moribund crabs. CONCLUSIONS: S. olivacea and S. paramamosain show wide variation in response to challenge with WSSV. S. olivacea and S. paramamosain are susceptible to white spot disease, and S. olivacea is more susceptible than S. paramamosain. Based on our single-challenge and serial challenge results, and on previous published work showing that S. serrata is relatively unaffected by WSSV infection, we propose that susceptibility to white spot disease in the genus Scylla is species-dependent and may also be dose-history dependent. In practical terms for shrimp farmers, it means that S. olivacea and S. paramamosain may pose less threat as WSSV carriers than S. serrata. For crab farmers, our results suggest that rearing of S. serrata would be a better choice than S. paramamosain or S. olivacea in terms of avoiding losses from seasonal outbreaks of white spot disease. BioMed Central 2010-11-20 /pmc/articles/PMC3001434/ /pubmed/21092125 http://dx.doi.org/10.1186/1756-0500-3-315 Text en Copyright ©2010 Somboonna et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Somboonna, Naraporn Mangkalanan, Seksan Udompetcharaporn, Attasit Krittanai, Chartchai Sritunyalucksana, Kallaya Flegel, TW Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title | Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title_full | Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title_fullStr | Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title_full_unstemmed | Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title_short | Mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
title_sort | mud crab susceptibility to disease from white spot syndrome virus is species-dependent |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001434/ https://www.ncbi.nlm.nih.gov/pubmed/21092125 http://dx.doi.org/10.1186/1756-0500-3-315 |
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