基于聚合酶链反应的挤压饲料白斑病生物安全风险评估方法的建立。

IF 2.2 3区 农林科学 Q2 FISHERIES
Hung Nam Mai, Paul J Schofield, Wendy M Sealey, Tressa M Baker, Arun K Dhar
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引用次数: 0

摘要

配方饲料一直是全球水产养殖业增长的主要推动力。然而,如果配方饲料没有被证明不含传染性病原体,则可能构成生物安全风险。不幸的是,最近的PCR方法不能区分传染性病原体和相应病原体的灭活基因组片段。考虑到甲壳类动物缺乏不朽的细胞系,我们开发了一种传统的一步PCR检测方法,可用于筛选配方水产饲料。作为原理验证,制备了含有(w/w) 0.0%、0.2%和2% WSSV感染虾粕的挤压饲料,并采用一步常规PCR和针对WSSV DNA聚合酶基因的实时PCR进行筛选。将结果与woah推荐的WSSV巢式PCR和实时PCR进行比较。新开发的实时PCR方法和waah推荐的实时PCR方法检测挤压饲料中的WSSV DNA。在常规一步PCR中使用的3组引物中,有2组引物扩增成功,扩增子大小分别为334和341 bp。产生980 bp扩增子的引物集以及woah推荐的巢式PCR在挤压饲料中没有扩增WSSV。一步扩增980 bp扩增子的传统PCR检测WSSV特异性高,检测限为100拷贝。将添加了wssv的膨化饲料喂给无特定病原体(Specific Pathogen Free, SPF)的凡纳美对虾,经组织病理学和PCR检测,均未引起疾病,说明添加了wssv的膨化饲料不含感染性病毒。我们建议,实时PCR具有高通量,可用于初始筛选,任何WSSV检测阳性的样品都应使用扩增980 bp扩增子的一步常规PCR进一步检测。这将为WSSV配方饲料的生物安全性评估提供急需的实用解决方案,直到甲壳类细胞系可用于筛选感染性WSSV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a PCR-Based Assay for Assessing Biosecurity Risk of Extruded Feed for White Spot Disease.

Formulated aquafeed has been a primary driver for the growth of the aquaculture industry worldwide. However, formulated feed may pose a biosecurity risk if they are not proven to be free of infectious pathogens. Unforetunately, recent PCR methods cannot differentiate an infectious pathogen from an inactivated genomic fragment of the corresponding pathogen. Considering the lack of an immortal cell line in crustaceans, we developed a conventional one-step PCR assay that can be used to screen formulated aquafeed. As a proof-of-principle, extruded feed containing (w/w) 0.0%, 0.2% and 2% WSSV-infected shrimp meals were prepared and screened using a one-step conventional PCR and a real-time PCR targeting the WSSV DNA polymerase gene. The results were compared to the WOAH-recommended nested- and real-time PCR for WSSV. The newly developed and the WOAH-recommended real-time PCR methods detected WSSV DNA in the extruded feed. Among three primer sets used in one-step conventional PCR, two provided successful WSSV amplification with amplicon size of 334 and 341 bp, respectively. The primer set that generated an amplicon of 980 bp, as well as the WOAH-recommended nested PCR, did not amplify WSSV in the extruded feed. The one-step conventional PCR generating a 980 bp amplicon is highly specific in detecting WSSV, and the limit of detection is 100 copies. When WSSV-spiked extruded feed was fed to Specific Pathogen Free (SPF) Penaeus vannamei shrimp, it did not cause disease, as determined by histopathology and PCR assays, indicating that the WSSV-spiked extruded feed does not contain infectious virus. We propose that real-time PCR, for its high throughput ability, could be used for initial screening, and any samples that test positive for WSSV should be further tested using a one-step conventional PCR that amplifies a 980 bp amplicon. This will provide a much-needed practical solution for biosecurity assessment of formulated aquafeed for WSD until a crustacean cell line is available for screening infectious WSSV.

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来源期刊
Journal of fish diseases
Journal of fish diseases 农林科学-海洋与淡水生物学
CiteScore
4.60
自引率
12.00%
发文量
170
审稿时长
6 months
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
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