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开发和验证一种便携式即时检测犬瘟热病毒 qPCR 检测方法。

Development and validation of a portable, point-of-care canine distemper virus qPCR test.

机构信息

Wildlife Conservation Society, Zoological Health Program, Bronx, New York, United States of America.

Institute of Virology, University of Veterinary Medicine, Vienna, Austria.

出版信息

PLoS One. 2020 Apr 22;15(4):e0232044. doi: 10.1371/journal.pone.0232044. eCollection 2020.

Abstract

Canine distemper virus (CDV) is a multi-host pathogen that can cause significant mortality in domestic, wild terrestrial and marine mammals. It is a major conservation threat in some endangered species. Infection can result in severe respiratory disease and fatal encephalitis. Diagnosis and disease monitoring in wildlife, and differentiation of CDV from rabies (a life-threatening zoonotic disease that can produce similar neurologic signs), would benefit from the availability of a portable, point-of-care (POC) diagnostic test. We therefore developed a quantitative RT-PCR assay for CDV using shelf-stable, lyophilized reagents and target-specific primers and probes for use with the handheld Biomeme two3™ qPCR thermocycler. Biomeme's extraction methodology, lyophilized reagents, and thermocycler were compared to our standard laboratory-based methods to assess sensitivity, efficiency and overall test performance. Results using a positive control plasmid for CDV showed comparable sensitivity (detection of 50 copies) and PCR efficiency between the two platforms, and CDV detection was similar between platforms when tested using a modified live CDV vaccine. Significantly higher Ct values (average Ct = 5.1 cycles) were observed using the Biomeme platform on known CDV positive animal samples. CDV detection using the Biomeme platform was similar in 25 of 26 samples from suspect CDV cases when compared to standard virology laboratory testing. One false positive was observed that was negative upon retest. The Biomeme methodology can be adapted for detection of specific targets, and this portable technology saves time by eliminating the need for local or international sample transport for laboratory-based diagnostics. However, results of our testing suggest that decreased diagnostic sensitivity (higher Ct values) relative to laboratory-based methods was observed using animal samples, so careful validation and optimization are essential. Portable qPCR platforms can empower biologists and wildlife health professionals in remote and low-resource settings, which will greatly improve our understanding of CDV disease ecology and associated conservation threats in wildlife.

摘要

犬瘟热病毒(CDV)是一种多宿主病原体,可导致家养、野生陆地和海洋哺乳动物大量死亡。它是一些濒危物种的主要保护威胁。感染可导致严重的呼吸道疾病和致命的脑炎。在野生动物中进行诊断和疾病监测,以及区分犬瘟热和狂犬病(一种危及生命的人畜共患病,可产生类似的神经症状),将受益于便携式即时诊断测试的可用性。因此,我们使用稳定的冻干试剂和针对 CDV 的靶特异性引物和探针,为手持 Biomeme two3™ qPCR 热循环仪开发了一种定量 RT-PCR 检测方法。我们比较了 Biomeme 的提取方法、冻干试剂和热循环仪与我们的标准实验室方法,以评估敏感性、效率和整体测试性能。使用 CDV 的阳性对照质粒的结果表明,两种平台的敏感性(检测到 50 个拷贝)和 PCR 效率相当,并且当使用改良的活 CDV 疫苗进行测试时,两种平台的 CDV 检测结果相似。在使用 Biomeme 平台对已知 CDV 阳性动物样本进行检测时,观察到显着更高的 Ct 值(平均 Ct = 5.1 个循环)。与标准病毒学实验室检测相比,在 26 个疑似 CDV 病例样本中的 25 个中,使用 Biomeme 平台检测到的 CDV 结果相似。观察到一个假阳性,重新测试为阴性。Biomeme 方法可适用于特定靶标的检测,并且该便携式技术通过消除对基于实验室的诊断的本地或国际样本运输的需求,节省了时间。但是,我们的测试结果表明,与基于实验室的方法相比,使用动物样本观察到诊断敏感性降低(Ct 值更高),因此需要仔细验证和优化。便携式 qPCR 平台可以为偏远和资源匮乏地区的生物学家和野生动物健康专业人员提供支持,这将极大地提高我们对 CDV 疾病生态学和相关野生动物保护威胁的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/988d/7176111/34e7012482d7/pone.0232044.g001.jpg

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