CSIRO, Livestock Industries, Australian Animal Health Laboratory, 5 Portarlington Road, Geelong East, Victoria 3220, Australia.
Virus Res. 2012 May;165(2):207-13. doi: 10.1016/j.virusres.2012.02.017. Epub 2012 Feb 25.
In late 2005, acute mortalities occurred in abalone on farms located in Victoria, Australia. Disease was associated with infection by an abalone herpes virus (AbHV). Subsequently, starting in 2006, the disease (abalone viral ganglioneuritis; AVG) was discovered in wild abalone in Victorian open waters. Currently, it continues to spread, albeit at a slow rate, along the Victorian coast-line. Here, we report on experimental transmission trials that were carried out by immersion using water into which diseased abalone had shed infectious viral particles. At various time points following exposure, naïve abalone were assessed by an AbHV-specific real-time PCR and histological analyses including in situ hybridization (ISH). Results demonstrated that while exposed abalone began displaying clinical signs of the disease from 60 hours post exposure (hpe), they tested positive for the presence of viral DNA at 36 hpe. Of further interest, the AbHV DNA probe used in the ISH assay detected the virus as early as 48 hpe.
2005 年末,澳大利亚维多利亚州养殖场的鲍鱼出现急性死亡。疾病与鲍鱼疱疹病毒(AbHV)感染有关。随后,从 2006 年开始,在维多利亚州开放水域的野生鲍鱼中发现了这种疾病(鲍鱼病毒性神经节炎;AVG)。目前,它仍在沿着维多利亚州海岸线缓慢传播。在这里,我们报告了通过将患病鲍鱼释放传染性病毒颗粒的水浸泡进行的实验性传播试验。在暴露后的不同时间点,通过 AbHV 特异性实时 PCR 和包括原位杂交(ISH)在内的组织学分析来评估幼稚鲍鱼。结果表明,虽然暴露的鲍鱼在暴露后 60 小时(hpe)开始出现疾病的临床症状,但它们在 36 hpe 时检测到病毒 DNA 呈阳性。更有趣的是,ISH 检测中使用的 AbHV DNA 探针早在 48 hpe 时就检测到了病毒。