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澳大利亚内陆地区虫媒病毒的可部署分子检测

Deployable Molecular Detection of Arboviruses in the Australian Outback.

作者信息

Inglis Timothy J J, Bradbury Richard S, McInnes Russell L, Frances Stephen P, Merritt Adam J, Levy Avram, Nicholson Jay, Neville Peter J, Lindsay Michael, Smith David W

机构信息

Division of Microbiology and Infectious Diseases, PathWest Laboratory Medicine WA, Nedlands, Australia. School of Pathology and Laboratory Medicine, The University of Western Australia, Crawley, Australia. 3rd Health Support Battalion, Adelaide, Australia.

3rd Health Support Battalion, Adelaide, Australia. School of Medical and Applied Sciences, Central Queensland University, Rockhampton, Australia.

出版信息

Am J Trop Med Hyg. 2016 Sep 7;95(3):633-8. doi: 10.4269/ajtmh.15-0878. Epub 2016 Jul 11.

Abstract

The most common causes of human infection from the arboviruses that are endemic in Australia are the arthritogenic alphaviruses: Ross River virus (RRV) and Barmah Forest virus (BFV). The most serious infections are caused by the neurotropic flaviviruses, Murray Valley encephalitis virus (MVEV) and the Kunjin subtype of West Nile virus. The greatest individual risk of arbovirus infection occurs in tropical/subtropical northern Australia because of the warm, wet summer conditions from December to June, where conventional arbovirus surveillance is difficult due to a combination of low population density, large distances between population centers, poor roads, and seasonal flooding. Furthermore, virus detection requires samples to be sent to Perth up to 2,000 km away for definitive analysis, causing delays of days to weeks before test results are available and public health interventions can be started. We deployed a portable molecular biology laboratory for remote field detection of endemic arboviruses in northern Queensland, then in tropical Western Australia and detected BFV, MVEV, and RRV RNA by polymerase chain reaction (PCR) assays of extracts from mosquitoes trapped in Queensland. We then used a field-portable compact real-time thermocycler for the samples collected in the Kimberley region of Western Australia. Real-time field PCR assays enabled concurrent endemic arbovirus distribution mapping in outback Queensland and Western Australia. Our deployable laboratory method provides a concept of operations for future remote area arbovirus surveillance.

摘要

在澳大利亚流行的虫媒病毒导致人类感染的最常见原因是致关节炎的甲病毒

罗斯河病毒(RRV)和巴马森林病毒(BFV)。最严重的感染是由嗜神经性黄病毒引起的,如墨累河谷脑炎病毒(MVEV)和西尼罗河病毒的库京亚型。由于12月至6月澳大利亚北部热带/亚热带地区夏季温暖潮湿,虫媒病毒感染的个体风险最高,而该地区传统的虫媒病毒监测工作困难重重,原因包括人口密度低、人口中心之间距离远、道路状况差以及季节性洪水。此外,病毒检测需要将样本送到2000公里外的珀斯进行最终分析,这导致在获得检测结果并启动公共卫生干预措施之前会延迟数天至数周。我们在昆士兰北部,然后在西澳大利亚热带地区部署了一个便携式分子生物学实验室,用于对当地流行的虫媒病毒进行现场检测,并通过聚合酶链反应(PCR)分析昆士兰捕获的蚊子提取物,检测到了BFV、MVEV和RRV RNA。然后,我们对在西澳大利亚金伯利地区采集的样本使用了现场便携式紧凑型实时热循环仪。实时现场PCR分析能够同时绘制昆士兰内陆地区和西澳大利亚地区流行虫媒病毒的分布图。我们这种可部署的实验室方法为未来偏远地区虫媒病毒监测提供了一种操作理念。

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