La Fauce Kathy A, Owens Leigh
School of Veterinary and Biomedical Sciences, Solander Drive, James Cook University, Townsville, Qld 4811, Australia.
J Invertebr Pathol. 2008 May;98(1):1-6. doi: 10.1016/j.jip.2007.11.006. Epub 2007 Dec 3.
The lack of available cell lines has hampered the study of viral diseases in crustaceans. This is particularly important for aquaculture which has been plagued by viral diseases since its rapid expansion to meet with the growing demand for seafood products. This study was designed to find an alternative bioassay to cell lines by investigating the use of insects as potential animal models for Penaeus merguiensis densovirus (PmergDNV). Acheta domesticus (house cricket) and Tenebrio molitor (mealworms) were challenged with approximately 1x10(6) virions of PmergDNV by inoculation. PmergDNV was detected in 20% of Tenebrio molitor and 86.6% of Acheta domesticus challenged with PmergDNV. During a subsequent time course experiment, there was a non significant increase in PmergDNV titres (10(4-5) virions), reaching a maximum peak at day 5 (10(6) copies). A threshold of PmergDNV DNA level equal to or greater than 10(3) virions was necessary for mortality in Acheta domesticus. As the inoculum increased from 10(3) DNA copies to 10(4), 10(5), 10(6), mortality increased from 20% to 60%, 80% and 100%, respectively. This is the first evidence that insects may be directly used to study viruses from crustaceans and concludes Acheta domesticus may be used as a potential model to study Penaeus merguiensis densovirus.
可用细胞系的缺乏阻碍了甲壳类动物病毒性疾病的研究。这对于水产养殖尤为重要,因为自水产养殖为满足对海产品不断增长的需求而迅速扩张以来,一直受到病毒性疾病的困扰。本研究旨在通过研究将昆虫用作墨吉对虾浓核病毒(PmergDNV)潜在动物模型的用途,找到一种替代细胞系的生物测定方法。通过接种用约1x10(6)个PmergDNV病毒粒子对家蟋蟀(Acheta domesticus)和黄粉虫(Tenebrio molitor)进行攻毒。在用PmergDNV攻毒的黄粉虫中,20%检测到PmergDNV,在家蟋蟀中则为86.6%。在随后的时间进程实验中,PmergDNV滴度(10(4 - 5)个病毒粒子)无显著增加,在第5天达到最高峰值(10(6)个拷贝)。家蟋蟀死亡需要PmergDNV DNA水平阈值等于或大于10(3)个病毒粒子。随着接种物从10(3)个DNA拷贝增加到10(4)、10(5)、10(6),死亡率分别从20%增加到60%、80%和100%。这是昆虫可直接用于研究甲壳类动物病毒的首个证据,并得出家蟋蟀可作为研究墨吉对虾浓核病毒潜在模型的结论。