Escobedo-Bonilla C M, Audoorn L, Wille M, Alday-Sanz V, Sorgeloos P, Pensaert M B, Nauwynck H J
Laboratory of Aquaculture & Artemia Reference Center, Faculty of Bioscience Engineering, Ghent University, Rozier 44, 9000 Ghent, Belgium.
Dis Aquat Organ. 2006 Mar 2;68(3):181-8. doi: 10.3354/dao068181.
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.
过去,控制白斑综合征病毒(WSSV)的策略大多通过体内感染试验进行测试,采用浸泡或口服接种未明确的WSSV感染剂量,这使得实验之间的比较变得复杂。在本研究中,使用特定病原体-free(SPF)凡纳滨对虾,通过肌肉注射(i.m.)或口服接种,在3个实验中确定了3种确定剂量(10、30和90个虾感染剂量50%终点[SID50])的WSSV的可重复性。通过疾病发病时间、累积死亡率和中位致死时间(LT50)来确定可重复性。通过肌肉注射途径,这3种剂量在接种后24至36小时(hpi)引发疾病。接种30和90 SID50剂量时,在84 hpi累积死亡率为100%,接种10 SID50剂量时在108 hpi累积死亡率为100%。10、30和90 SID50剂量的LT50分别为52、51和49 hpi,且差异不显著(p>0.05)。口服接种10、30或90 SID50的对虾在24至36 hpi发病。接种30和90 SID50剂量时,在108 hpi累积死亡率为100%,接种10 SID50剂量时在120 hpi累积死亡率为100%。10、30和90 SID50的LT50分别为65、57和50 hpi;这些彼此之间差异显著(p<0.05)。选择30 SID50剂量作为通过肌肉注射或口服途径进行进一步WSSV攻毒的标准。这些标准化的接种程序可应用于其他甲壳类动物和WSSV毒株,以便在实验之间获得可比结果。