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东帝汶暴发非洲猪瘟期间的病毒环介导等温扩增(LAMP)检测野外验证。

Field Verification of an African Swine Fever Virus Loop-Mediated Isothermal Amplification (LAMP) Assay During an Outbreak in Timor-Leste.

机构信息

Agriculture Victoria Research, AgriBio Centre for AgriBioscience, Bundoora, VIC 3083, Australia.

Ministry of Agriculture and Fisheries, Government of Timor-Leste, Av. Nicolao Lobato, Comoro, Dili 0332, Timor-Leste.

出版信息

Viruses. 2020 Dec 15;12(12):1444. doi: 10.3390/v12121444.

Abstract

Recent outbreaks of African swine fever virus (ASFV) have seen the movement of this virus into multiple new regions with devastating impact. Many of these outbreaks are occurring in remote, or resource-limited areas, that do not have access to molecular laboratories. Loop-mediated isothermal amplification (LAMP) is a rapid point of care test that can overcome a range of inhibitors. We outline further development of a real-time ASFV LAMP, including field verification during an outbreak in Timor-Leste. To increase field applicability, the extraction step was removed and an internal amplification control (IAC) was implemented. Assay performance was assessed in six different sample matrices and verified for a range of clinical samples. A LAMP detection limit of 400 copies/rxn was determined based on synthetic positive control spikes. A colourmetric LAMP assay was also assessed on serum samples. Comparison of the LAMP assay to a quantitative polymerase chain reaction (qPCR) was performed on clinical ASFV samples, using both serum and oral/rectal swabs, with a substantial level of agreement observed. The further verification of the ASFV LAMP assay, removal of extraction step, implementation of an IAC and the assessment of a range of sample matrix, further support the use of this assay for rapid in-field detection of ASFV.

摘要

最近暴发的非洲猪瘟病毒(ASFV)已进入多个新的地区,造成了毁灭性的影响。其中许多疫情发生在偏远或资源有限的地区,这些地区无法获得分子实验室的支持。环介导等温扩增(LAMP)是一种快速的即时检测技术,可以克服多种抑制剂的影响。我们概述了实时 ASFV LAMP 的进一步开发,包括在东帝汶疫情期间的实地验证。为了提高现场适用性,我们去除了提取步骤并实施了内部扩增对照(IAC)。在六种不同的样本基质中评估了检测方法的性能,并对一系列临床样本进行了验证。基于合成阳性对照物的检测,确定了 LAMP 检测限为 400 拷贝/反应。还对血清样本进行了比色 LAMP 检测。对使用血清和口腔/直肠拭子的临床 ASFV 样本进行了 LAMP 检测与定量聚合酶链反应(qPCR)的比较,观察到相当大的一致性。对 ASFV LAMP 检测的进一步验证、提取步骤的去除、IAC 的实施以及对一系列样本基质的评估,进一步支持了该检测方法在现场快速检测 ASFV 的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b96a/7765541/99aaecd031fc/viruses-12-01444-g001.jpg

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