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改进对所列鱼类疾病 IHNV 和 VHS 的监测中的诊断程序。

Improvement of a diagnostic procedure in surveillance of the listed fish diseases IHN and VHS.

机构信息

Chemisches und Veterinäruntersuchungsamt Stuttgart (Chemical and Veterinary Investigations Office Stuttgart), Fellbach, Germany.

Federal Research Institute for Animal Health, Institute of Infectology, Friedrich Loeffler Institute, Greifswald-Insel Riems, Germany.

出版信息

J Fish Dis. 2019 Apr;42(4):559-572. doi: 10.1111/jfd.12968. Epub 2019 Feb 19.

Abstract

Infectious haematopoietic necrosis (IHN) and viral haemorrhagic septicaemia (VHS) are OIE-listed and notifiable viral fish diseases which are controlled by eradication and surveillance programmes globally. The present study provides improved RT-qPCR procedures based on recently described OIE protocols. Improvements comprise the design of a new TaqMan® probe, replacing a TaqMan® MGB probe that turned out to show impaired binding. Reason for this is SNPs detected in the nucleoprotein N gene sequences of IHNV strains targeted by the RT-qPCR. Furthermore, the IHNV and VHSV RT-qPCR assays were realized as one-step and one-run procedures supplemented by an endogenous control system. The IHNV and VHSV RT-qPCR assays are characterized by a technical sensitivity of 19 and 190 gene equivalents (cRNA) and an analytical sensitivity of 2-7 and 13 TCID /ml, respectively. For verification purposes, 105 IHNV and 165 VHSV isolates and several non-targeted viral and bacterial pathogens were included and returned adequate results. However, in field samples divergent results left 14 samples of 154 undetected for IHNV and one sample of 127 for VHSV using cell culture. The study shows that RT-qPCR assays ensure facilitated and reliable testing on IHNV and VHSV in eradication and surveillance programmes.

摘要

传染性造血器官坏死病(IHN)和病毒性出血性败血症(VHS)是被世界动物卫生组织(OIE)列为应通报的病毒性鱼类疾病,通过在全球范围内实施根除和监测计划进行控制。本研究基于 OIE 最近描述的协议,提供了改进的 RT-qPCR 程序。改进包括设计一种新的 TaqMan®探针,取代结合性能受损的 TaqMan® MGB 探针。造成这种情况的原因是 IHNV 株的核蛋白 N 基因序列中检测到的 SNP,这些 SNP 是 RT-qPCR 靶向的。此外,IHNV 和 VHSV RT-qPCR 检测方法实现了一步法和单运行程序,并辅以内源性控制系统。IHNV 和 VHSV RT-qPCR 检测方法的技术灵敏度分别为 19 和 190 个基因当量(cRNA),分析灵敏度分别为 2-7 和 13 TCID /ml。为了验证目的,包括了 105 个 IHNV 株和 165 个 VHSV 株,以及一些非靶向的病毒和细菌病原体,结果均令人满意。然而,在田间样本中,154 个样本中有 14 个样本和 127 个样本中的 1 个样本经细胞培养检测不到 IHNV 和 VHSV,结果出现分歧。该研究表明,RT-qPCR 检测方法可确保在根除和监测计划中方便、可靠地检测 IHNV 和 VHSV。

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