Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
Department of Microbiology/National Emerging Infectious Diseases Laboratories, Chobanian & Avedisian School of Medicine, Boston University, Boston, Massachusetts, USA.
Microbiol Spectr. 2024 Sep 3;12(9):e0101024. doi: 10.1128/spectrum.01010-24. Epub 2024 Jul 24.
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 TCID/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.
丝状病毒是现代世界中最致命的病毒之一,近年来发现了越来越多的丝状病毒物种和属。尽管丝状病毒在人类中的爆发可能具有潜在的严重性,但相对较少的敏感泛丝状病毒 RT-PCR 检测方法被描述出来,这些方法可能有助于早期发现和预防。在这里,我们提出了一种针对 L 聚合酶基因的新型泛丝状病毒 RT-PCR 检测方法,用于检测所有已知的哺乳动物丝状病毒。我们证明了该方法能够检测到 10 种合成的丝状病毒 RNA 模板,其分析灵敏度范围为 178 到 3,354 拷贝/ml,对 10 种非丝状病毒的人类病毒种没有交叉反应。我们在 10 种灭活的丝状病毒分离物上验证了该检测方法的性能,初始灵敏度为 0.012-44.17 TCID/ml。我们将这种广泛反应性的 RT-PCR 与一种高通量的深度测序工作流程相结合,该流程适用于高容量的池化,以最大限度地提高检测和发现的潜力。总之,这种泛丝状病毒 RT-PCR 检测方法针对最保守的丝状病毒基因,提供了迄今为止最广泛的覆盖范围,可能有助于检测和发现新的丝状病毒。
重要性丝状病毒仍然是世界上最神秘的病毒之一,具有极高的致死率和巨大的大流行潜力。然而,迄今为止发现的丝状病毒物种和属相对较少,关于人畜共患感染的明确宿主物种存在疑问。在这里,我们描述了一种针对保守的 L 聚合酶基因的新型广泛反应性 RT-PCR 检测方法,用于在各种临床和环境标本中高通量筛选丝状病毒。我们证明该检测方法可以检测到所有已知的哺乳动物丝状病毒,并在合成 RNA 序列、灭活的丝状病毒分离物和非丝状病毒种上确定该检测方法的灵敏度和特异性。