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用于快速检测的粗提物定量聚合酶链反应的验证

Validation of qPCR from a crude extract for the rapid detection of .

作者信息

Ma Chao, Tian Zhuo, Yang Lili, Cao Jijuan

机构信息

Key Laboratory of Biotechnology and Bioresources Utilization of Ministry of Education, Dalian Minzu University, Dalian, China.

Dalian Customs Technology Center, Dalian, China.

出版信息

Aquac Int. 2022;30(5):2679-2690. doi: 10.1007/s10499-022-00920-9. Epub 2022 Jul 25.

Abstract

UNLABELLED

White spot disease (WSD) has posed a serious threat to the China and the global shrimp aquaculture. In order to diagnose (WSSV) early and prevent the spread and outbreak of WSD, it is necessary to establish a highly sensitive WSSV diagnosis method suitable for shrimp farming sites. In this study, a pre-amplification qPCR assay from the crude extract of samples heated lysis was established, which was further compared with the universal qPCR assay to verify the shrimp samples. The limit of detection (LOD) of pre-amplification qPCR assay and universal qPCR assay was 2.80 copies and 20.57 copies per reaction at 95% CI, respectively. It had good WSSV specificity and did not show cross-detection of (IHHNV), (HPV), (EHP), (AHPND), (NHPB), and (DIV1). A total of 36 shrimp samples were detected as WSSV DNA positive by pre-amplification qPCR with crude extract from samples heated lysis and universal qPCR with DNA extraction. The diagnostic sensitivity and specificity were 97.22% (85.5 ~ 99.9%, 95% CI) and 100% (81.5 ~ 100%, 95% CI), respectively. The agreement Kappa value was 0.959 (0.879 ~ 1, 95% CI), and the analysis results were basically consistent. Eliminating the tedious steps of extracting DNA and using pre-amplified qPCR to detect WSSV in shrimp, it is a good choice for aquaculture farms.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s10499-022-00920-9.

摘要

未标记

白斑病(WSD)对中国乃至全球的对虾养殖业构成了严重威胁。为了早期诊断白斑综合征病毒(WSSV)并防止WSD的传播和爆发,有必要建立一种适用于对虾养殖场所的高度灵敏的WSSV诊断方法。在本研究中,建立了一种基于加热裂解样品粗提物的预扩增定量PCR检测方法,并将其与通用定量PCR检测方法进行进一步比较以验证对虾样品。预扩增定量PCR检测方法和通用定量PCR检测方法在95%置信区间下的检测限分别为每个反应2.80拷贝和20.57拷贝。该方法具有良好的WSSV特异性,未显示对传染性皮下和造血组织坏死病毒(IHHNV)、肝胰腺细小病毒(HPV)、对虾肝肠胞虫(EHP)、急性肝胰腺坏死病(AHPND)、诺维氏弧菌(NHPB)和对虾虹彩病毒1型(DIV1)的交叉检测。用加热裂解样品的粗提物通过预扩增定量PCR和DNA提取后的通用定量PCR共检测了36份对虾样品为WSSV DNA阳性。诊断敏感性和特异性分别为97.22%(85.5 ~ 99.9%,95%置信区间)和100%(81.5 ~ 100%,95%置信区间)。一致性Kappa值为0.959(0.879 ~ 1,95%置信区间),分析结果基本一致。省去了提取DNA的繁琐步骤,使用预扩增定量PCR检测对虾中的WSSV,这对养殖场来说是个不错的选择。

补充信息

在线版本包含可在10.1007/s10499-022-00920-9获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a03/9309450/5eb11ae038c1/10499_2022_920_Fig1_HTML.jpg

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