A high-throughput, polymerase-targeted RT-PCR for broad detection of mammalian filoviruses.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-07-24 DOI:10.1128/spectrum.01010-24
Na Cui, Yael L Perez, Adam J Hume, B Ethan Nunley, Kevin Kong, Margaret G Mills, Hong Xie, Alexander L Greninger
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Abstract

Filoviruses are some of the most lethal viruses in the modern world, and increasing numbers of filovirus species and genera have been discovered in recent years. Despite the potential severity of filovirus outbreaks in the human population, comparably few sensitive pan-filovirus RT-PCR assays have been described that might facilitate early detection and prevention. Here, we present a new pan-filovirus RT-PCR assay targeting the L polymerase gene for detection of all known mammalian filoviruses. We demonstrate the detection of 10 synthetic filovirus RNA templates with analytical sensitivity ranging from 178 to 3,354 copies/mL, without cross-reactivity on 10 non-filoviral human viral species. We verified assay performance on 10 inactivated filovirus isolates, yielding initial sensitivities of 0.012-44.17 TCID50/mL. We coupled this broadly reactive RT-PCR with a deep sequencing workflow that is amenable to high-throughput pooling to maximize detection and discovery potential. In summary, this pan-filovirus RT-PCR assay targets the most conserved filovirus gene, offers the widest breadth of coverage to date, and may help in the detection and discovery of novel filoviruses.IMPORTANCEFiloviruses remain some of the most mysterious viruses known to the world, with extremely high lethality rates and significant pandemic potential. Yet comparably few filovirus species and genera have been discovered to date and questions surround the definitive host species for zoonotic infections. Here, we describe a novel broadly reactive RT-PCR assay targeting the conserved L polymerase gene for high-throughput screening for filoviruses in a variety of clinical and environmental specimens. We demonstrate the assay can detect all known mammalian filoviruses and determine the sensitivity and specificity of the assay on synthetic RNA sequences, inactivated filovirus isolates, and non-filoviral species.

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用于广泛检测哺乳动物丝状病毒的高通量聚合酶靶向 RT-PCR 技术。
丝状病毒是现代世界中最致命的病毒之一,近年来发现的丝状病毒种类和属越来越多。尽管丝状病毒在人类中爆发的潜在严重性很大,但能帮助早期检测和预防的灵敏的泛丝状病毒 RT-PCR 检测方法却少之又少。在这里,我们介绍了一种新的泛丝状病毒 RT-PCR 检测方法,该方法以 L 聚合酶基因为目标,可检测所有已知的哺乳动物丝状病毒。我们展示了对 10 种合成丝状病毒 RNA 模板的检测,分析灵敏度从 178 到 3,354 拷贝/毫升不等,对 10 种非丝状病毒人类病毒没有交叉反应。我们对 10 种灭活的丝状病毒分离物进行了检测性能验证,初步灵敏度为 0.012-44.17 TCID50/mL。我们将这种反应广泛的 RT-PCR 与适合高通量汇集的深度测序工作流程相结合,以最大限度地提高检测和发现潜力。总之,这种泛丝状病毒 RT-PCR 检测方法以最保守的丝状病毒基因为目标,提供了迄今为止最广泛的覆盖范围,可能有助于新型丝状病毒的检测和发现。 重要意义丝状病毒仍然是世界上已知的最神秘的病毒之一,具有极高的致死率和重大的流行潜力。然而,迄今为止发现的丝状病毒种和属却少得可怜,而且人畜共患感染的确定宿主种类也是个问题。在这里,我们介绍了一种新型的广谱反应RT-PCR检测方法,该方法以保守的L聚合酶基因为目标,用于高通量筛查各种临床和环境标本中的丝状病毒。我们证明该检测方法可以检测所有已知的哺乳动物丝状病毒,并确定了该检测方法对合成 RNA 序列、灭活的丝状病毒分离物和非丝状病毒物种的灵敏度和特异性。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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