Standardized white spot syndrome virus (WSSV) inoculation procedures for intramuscular or oral routes

被引:38
作者
Escobedo-Bonilla, CM
Audoorn, L
Wille, M
Alday-Sanz, V
Sorgeloos, P
Pensaert, MB
Nauwynck, HJ
机构
[1] Univ Ghent, Fac Vet Med, Virol Lab, B-9820 Merelbeke, Belgium
[2] Univ Ghent, Lab Aquaculture & Artemia Reference Ctr, Fac Biosci Engn, B-9000 Ghent, Belgium
[3] Univ Ghent, Dept Appl Math Biometr & Proc Control, B-9000 Ghent, Belgium
[4] INVE Technol, B-9200 Dendermonde, Belgium
关键词
Litopenaeus vannamei; WSSV; experimental inoculation; intramuscular route; oral route LT50; probit analysis;
D O I
10.3354/dao068181
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
In the past, strategies to control white spot syndrome virus (WSSV) were mostly tested by infectivity trials in vivo using immersion or per os inoculation of undefined WSSV infectious doses, which complicated comparisons between experiments. In this study, the reproducibility of 3 defined doses (10, 30 and 90 shrimp infectious doses 50% endpoint [SID50]) of WSSV was determined in 3 experiments using intramuscular (i.m.) or oral inoculation in specific pathogen-free (SPF) Litopenaeus vannamei. Reproducibility was determined by the time of onset of disease, cumulative mortality, and median lethal time (LT50). By i.m. route, the 3 doses induced disease between 24 and 36 h post inoculation (hpi). Cumulative mortality was 100% at 84 hpi with doses of 30 and 90 SID50 and 108 hpi with a dose of 10 SID50. The LT50 of the doses 10, 30 and 90 SID50 were 52, 51 and 49 hpi and were not significantly different (p > 0.05). Shrimp orally inoculated with 10, 30 or 90 SID50 developed disease between 24 and 36 hpi. Cumulative mortality was 100% at 108 hpi with doses of 30 and 90 SID50 and 120 hpi with a dose of 10 SID50. The LT50 of 10, 30 and 90 SID50 were 65, 57 and 50 hpi; these were significantly different from each other (p < 0.05). A dose of 30 SID50 was selected as the standard for further WSSV challenges by i.m. or oral routes. These standardized inoculation procedures may be applied to other crustacea and WSSV strains in order to achieve comparable results among experiments.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 62 条
[1]  
AGRESTI A., 2019, INTRO CATEGORICAL DA
[2]  
Ceccaldi HJ., 1997, CRUSTACEAN NUTR, P261
[3]   Effect of dietary β-1,3-glucan on resistance to white spot syndrome virus (WSSV) in postlarval and juvenile Penaeus monodon [J].
Chang, CF ;
Su, MS ;
Chen, HY ;
Lo, CF ;
Kou, GH ;
Liao, IC .
DISEASES OF AQUATIC ORGANISMS, 1999, 36 (03) :163-168
[4]   Detection of white spot syndrome associated baculovirus in experimentally infected wild shrimp, crab and lobsters by in situ hybridization [J].
Chang, PS ;
Chen, HC ;
Wang, YC .
AQUACULTURE, 1998, 164 (1-4) :233-242
[5]   An integrated optical oxygen sensor fabricated using rapid-prototyping techniques [J].
Chang-Yen, DA ;
Gale, BK .
LAB ON A CHIP, 2003, 3 (04) :297-301
[6]   Identification of a nucleocapsid protein (VP35) gene of shrimp white spot syndrome virus and characterization of the motif important for targeting VP35 to the nuclei of transfected insect cells [J].
Chen, LL ;
Leu, JH ;
Huang, CJ ;
Chou, CM ;
Chen, SM ;
Wang, CH ;
Lo, CF ;
Kou, GH .
VIROLOGY, 2002, 293 (01) :44-53
[7]   Effect of fucoidan on disease resistance of black tiger shrimp [J].
Chotigeat, W ;
Tongsupa, S ;
Supamataya, K ;
Phongdara, A .
AQUACULTURE, 2004, 233 (1-4) :23-30
[8]   Pathogenicity of a baculovirus infection causing white spot syndrome in cultured penaeid shrimp in Taiwan [J].
Chou, HY ;
Huang, CY ;
Wang, CH ;
Chiang, HC ;
Lo, CF .
DISEASES OF AQUATIC ORGANISMS, 1995, 23 (03) :165-173
[9]   Experimental infection of European crustaceans with white spot syndrome virus (WSSV) [J].
Corbel, V ;
Zuprizal ;
Shi, Z ;
Huang, C ;
Sumartono ;
Arcier, JM ;
Bonami, JR .
JOURNAL OF FISH DISEASES, 2001, 24 (07) :377-382
[10]   A synthetic antibacterial peptide from Mytilus galloprovincialis reduces mortality due to white spot syndrome virus in palaemonid shrimp [J].
Dupuy, JW ;
Bonami, JR ;
Roch, P .
JOURNAL OF FISH DISEASES, 2004, 27 (01) :57-64