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从阳性侧向流动装置中回收病毒RNA和传染性口蹄疫病毒。

Recovery of viral RNA and infectious foot-and-mouth disease virus from positive lateral-flow devices.

作者信息

Fowler Veronica L, Bankowski Bartlomiej M, Armson Bryony, Di Nardo Antonello, Valdazo-Gonzalez Begoña, Reid Scott M, Barnett Paul V, Wadsworth Jemma, Ferris Nigel P, Mioulet Valérie, King Donald P

机构信息

Vesicular Disease Reference Laboratory, The Pirbright Institute, Pirbright, Surrey, United Kingdom.

Vesicular Disease Reference Laboratory, The Pirbright Institute, Pirbright, Surrey, United Kingdom; Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Science, University of Glasgow, Glasgow, United Kingdom.

出版信息

PLoS One. 2014 Oct 14;9(10):e109322. doi: 10.1371/journal.pone.0109322. eCollection 2014.

Abstract

Foot-and-mouth disease Virus (FMDV) is an economically important, highly contagious picornavirus that affects both wild and domesticated cloven hooved animals. In developing countries, the effective laboratory diagnosis of foot-and-mouth disease (FMD) is often hindered by inadequate sample preservation due to difficulties in the transportation and storage of clinical material. These factors can compromise the ability to detect and characterise FMD virus in countries where the disease is endemic. Furthermore, the high cost of sending infectious virus material and the biosecurity risk it presents emphasises the need for a thermo-stable, non-infectious mode of transporting diagnostic samples. This paper investigates the potential of using FMDV lateral-flow devices (LFDs) for dry transportation of clinical samples for subsequent nucleic acid amplification, sequencing and recovery of infectious virus by electroporation. FMDV positive samples (epithelial suspensions and cell culture isolates) representing four FMDV serotypes were applied to antigen LFDs: after which it was possible to recover viral RNA that could be detected using real-time RT-PCR. Using this nucleic acid, it was also possible to recover VP1 sequences and also successfully utilise protocols for amplification of complete FMD virus genomes. It was not possible to recover infectious FMDV directly from the LFDs, however following electroporation into BHK-21 cells and subsequent cell passage, infectious virus could be recovered. Therefore, these results support the use of the antigen LFD for the dry, non-hazardous transportation of samples from FMD endemic countries to international reference laboratories.

摘要

口蹄疫病毒(FMDV)是一种具有重要经济意义、高度传染性的小核糖核酸病毒,可感染野生和家养偶蹄动物。在发展中国家,由于临床样本运输和储存困难导致样本保存不当,常常阻碍口蹄疫(FMD)的有效实验室诊断。在该病流行的国家,这些因素会影响检测和鉴定口蹄疫病毒的能力。此外,运送传染性病毒材料成本高昂且存在生物安全风险,这凸显了对一种热稳定、无传染性的诊断样本运输方式的需求。本文研究了使用口蹄疫病毒侧向流动装置(LFD)对临床样本进行干式运输,以便后续进行核酸扩增、测序以及通过电穿孔法回收传染性病毒的潜力。将代表四种口蹄疫病毒血清型的口蹄疫病毒阳性样本(上皮细胞悬液和细胞培养分离株)应用于抗原LFD:之后能够回收可用实时逆转录聚合酶链反应(RT-PCR)检测的病毒RNA。利用这种核酸,还能够回收VP1序列,并且成功采用了扩增完整口蹄疫病毒基因组的方案。无法直接从LFD中回收传染性口蹄疫病毒,然而,将其电穿孔导入幼仓鼠肾细胞(BHK-21)并随后进行细胞传代后,能够回收传染性病毒。因此,这些结果支持使用抗原LFD对来自口蹄疫流行国家的样本进行干式、无危害运输,以便送往国际参考实验室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2f0/4196899/70f51adff07c/pone.0109322.g001.jpg

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