Christie K E, Graham D A, McLoughlin M F, Villoing S, Todd D, Knappskog D
Intervet Norbio, Thormohlensgt. 55, 5008, Bergen, Norway.
Dis Aquat Organ. 2007 Mar 29;75(1):13-22. doi: 10.3354/dao075013.
Atlantic salmon Salmo salar L. pre-smolts were experimentally infected with 2 different isolates of salmonid alphavirus (SAV): a Subtype 1 isolate from Ireland and a Subtype 3 isolate from Norway. Sequential samples of tissue and blood were collected during a period of 20 wk post injection and subjected to virus isolation from kidney tissue and serum, detection of viral nucleic acid in heart tissue and serum by real-time RT-PCR, detection of specific antibodies by virus neutralisation assay, and histopathological examination. Successful reproduction of pancreas disease (PD) was obtained by intraperitoneal (i.p.) injection of both isolates. No mortality was observed post infection in either group, but typical PD histopathological lesions in heart and pancreas tissue were observed with both isolates. The prevalence and severity of lesions in the pancreas, heart, skeletal muscle and brain were similar in both groups with only subtle differences recorded. Re-isolation of virus from kidney tissue was performed at 7 and 14 d post infection (d p.i.) only and was positive for both test groups at both sampling points. Isolation of virus from sera from both groups was positive at 4 to 14 d p.i., but was negative at later sampling points when antibody production had begun. Virus may be detected only during the acute phase using both methods. Specific neutralising antibodies could be detected for both test groups from Day 21 p.i. until the end of the experiment at 140 d p.i. Peak antibody titres were seen 70 d p.i. Using real-time RT-PCR, pancreas disease virus (PDV)-specific RNA was detected frequently in serum samples up to 14 d p.i. and occasionally thereafter. In contrast, viral RNA could still be detected in the heart tissue of fish from both groups for at least 140 d p.i.
大西洋鲑(Salmo salar L.)的前洄游幼鱼被实验性感染了两种不同的鲑鱼α病毒(SAV)分离株:一种来自爱尔兰的1型分离株和一种来自挪威的3型分离株。在注射后20周内采集组织和血液的连续样本,并对肾脏组织和血清进行病毒分离,通过实时逆转录聚合酶链反应检测心脏组织和血清中的病毒核酸,通过病毒中和试验检测特异性抗体,并进行组织病理学检查。通过腹腔注射这两种分离株均成功引发了胰腺疾病(PD)。两组感染后均未观察到死亡,但两种分离株均在心脏和胰腺组织中观察到典型的PD组织病理学病变。两组胰腺、心脏、骨骼肌和大脑中病变的发生率和严重程度相似,仅记录到细微差异。仅在感染后7天和14天(dpi)从肾脏组织中再次分离病毒,两个测试组在两个采样点均呈阳性。两组血清在感染后4至14天病毒分离呈阳性,但在抗体产生开始后的后期采样点呈阴性。使用这两种方法仅在急性期可检测到病毒。从感染后第21天直至实验结束(140 dpi),两个测试组均可检测到特异性中和抗体。抗体滴度峰值出现在70 dpi。使用实时逆转录聚合酶链反应,在感染后14天内血清样本中经常检测到胰腺疾病病毒(PDV)特异性RNA,此后偶尔也能检测到。相比之下,两组鱼的心脏组织中至少在140 dpi仍可检测到病毒RNA。