Yoanna Eissler, David Tapia, Cristian B Canales-Aguirre, José Manuel Yáñez
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引用次数: 0
Abstract
This study presents a comprehensive molecular and epidemiological characterisation of infectious pancreatic necrosis virus (IPNV) in Chilean salmon aquaculture. Between 2015 and 2016, 26 sampling events were conducted in freshwater and seawater farms spanning a broad latitudinal gradient (30.3° S to 52.6° S). Three diagnostic methods were used: Quantitative real-time Polymerase Chain Reaction (PCR) (qRT-PCR) (targeting VP1 and VP2 protein coding genes), nested PCR and virus isolation in CHSE-214 cells. In addition, a 523-bp VP2 gene fragment was sequenced directly from samples. These approaches were employed to assess detection sensitivity and to explore IPNV genogroup distribution and persistence. Nested PCR and viral isolation detected IPNV in 50 of 53 samples, outperforming qRT-PCR, which detected only 39. Phylogenetic analysis of the 523-bp VP2 gene fragment classified the isolates into two genogroups-5 (Salmo salar) and 1 (Oncorhynchus spp.), confirming host-specific associations. Identical or near-identical sequences were identified in geographically distant farms and temporally spaced samples, suggesting persistent isolates and potential long-distance spread, likely via egg transfers or fish movement. The most severe mortality event (> 125,000 fish) occurred during a genogroup 1 outbreak (Isla del Rey, GMTS, O. kisutch), followed by genogroup 5 outbreaks documented in Molco Alto (PMLC, S. salar) and Chayahue (S. salar). Although less frequently detected, genogroup 1 was associated with higher virulence, particularly in coho salmon. These findings highlight the need of integrated diagnostic strategies, genogroup-specific monitoring and strengthened biosecurity to mitigate the impact of IPNV in Chilean salmon farming.
本研究提出了智利鲑鱼养殖中感染性胰腺坏死病毒(IPNV)的综合分子和流行病学特征。2015年至2016年期间,在宽纬度梯度(30.3°S至52.6°S)的淡水和海水养殖场进行了26次采样。采用实时荧光定量聚合酶链反应(qRT-PCR)(针对VP1和VP2蛋白编码基因)、巢式PCR和病毒分离三种诊断方法对CHSE-214细胞进行检测。此外,直接从样本中测序了一个523 bp的VP2基因片段。这些方法用于评估检测灵敏度和探索IPNV基因群分布和持久性。巢式PCR和病毒分离在53份样本中检测到50份IPNV,优于qRT-PCR,后者仅检测到39份。523 bp VP2基因片段的系统发育分析将分离物分为两个基因群-5 (Salmo salar)和1 (Oncorhynchus spp.),证实了宿主特异性关联。在地理位置遥远的农场和时间间隔的样本中发现了相同或接近相同的序列,表明持续分离和潜在的长距离传播,可能通过卵子转移或鱼类运动。最严重的死亡事件(125,000条鱼)发生在基因1组暴发期间(Isla del Rey, GMTS, O. kisutch),其次是Molco Alto (PMLC, S. salar)和Chayahue (S. salar)记录的基因5组暴发。虽然不常被发现,但基因组1与较高的毒力有关,特别是在银鲑中。这些发现突出表明,需要采取综合诊断策略、针对基因组的监测和加强生物安全,以减轻IPNV对智利鲑鱼养殖的影响。
期刊介绍:
Journal of Fish Diseases enjoys an international reputation as the medium for the exchange of information on original research into all aspects of disease in both wild and cultured fish and shellfish. Areas of interest regularly covered by the journal include:
-host-pathogen relationships-
studies of fish pathogens-
pathophysiology-
diagnostic methods-
therapy-
epidemiology-
descriptions of new diseases