首页> 外文期刊>Diseases of Aquatic Organisms >Experimental infection of Atlantic salmon Salmo salar pre-smolts by i.p. injection with new Irish and Norwegian salmonid alphavirus (SAV) isolates: a comparative study
【24h】

Experimental infection of Atlantic salmon Salmo salar pre-smolts by i.p. injection with new Irish and Norwegian salmonid alphavirus (SAV) isolates: a comparative study

机译:i.p.感染大西洋鲑Salmo salar pre-smolts的实验。注射新的爱尔兰和挪威鲑鱼甲病毒(SAV)分离株:一项比较研究

获取原文
           

摘要

ABSTRACT: 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.
机译:摘要:大西洋鲑鱼 Salmo salar L。用两种不同的鲑鱼甲病毒(SAV)分离株对前大-进行实验感染:来自爱尔兰的亚型1分离株和来自挪威的亚型3分离株。在注射后20周内收集组织和血液的顺序样品,并从肾脏组织和血清中分离病毒,通过实时RT-PCR检测心脏组织和血清中的病毒核酸,通过病毒中和测定和组织病理学检查。通过腹膜内(i.p.)注射两种分离物获得成功的胰腺疾病(PD)繁殖。两组在感染后均未观察到死亡率,但是两种分离物均在心脏和胰腺组织中观察到典型的PD组织病理学损害。两组胰腺,心脏,骨骼肌和脑中病变的发生率和严重程度相似,仅记录了细微的差异。仅在感染后第7天和第14天(d p.i.)从肾脏组织中重新分离病毒,并且在两个采样点上两个测试组均呈阳性。两组从血清中分离出的病毒在p.i. 4到14 d呈阳性,但在抗体开始生产后的后期采样点呈阴性。两种方法都只能在急性期检测到病毒。从第21天开始,两个测试组均可检测到特异性中和抗体。直到实验结束(每天140天)。每天70 d出现峰值抗体滴度。使用实时RT-PCR,在长达14 d p.i的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。相反,在至少140 d p.i时,两组鱼类的心脏组织中仍可检测到病毒RNA。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号