Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK; Tropical and Infectious Disease Unit, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK; Leeds Teaching Hospitals NHS Trust, Leeds, UK; National Institute for Health Research Health Protection Research Unit in Emerging and Zoonotic Infections, University of Liverpool, Liverpool, UK.
Center for Infection and Immunity, Mailman School of Public Health, Columbia University, NY, USA.
J Infect. 2022 Apr;84(4):499-510. doi: 10.1016/j.jinf.2021.12.042. Epub 2022 Jan 3.
Many patients with meningitis have no aetiology identified leading to unnecessary antimicrobials and prolonged hospitalisation. We used viral capture sequencing to identify possible pathogenic viruses in adults with community-acquired meningitis.
Cerebrospinal fluid (CSF) from 73 patients was tested by VirCapSeq-VERT, a probe set designed to capture viral targets using high throughput sequencing. Patients were categorised as suspected viral meningitis - CSF pleocytosis, no pathogen identified (n = 38), proven viral meningitis - CSF pleocytosis with a pathogen identified (n = 15) or not meningitis - no CSF pleocytosis (n = 20).
VirCapSeq-VERT detected virus in the CSF of 16/38 (42%) of those with suspected viral meningitis, including twelve individual viruses. A potentially clinically relevant virus was detected in 9/16 (56%). Unexpectedly Toscana virus, rotavirus and Saffold virus were detected and assessed to be potential causative agents.
VirCapSeq-VERT increases the probability of detecting a virus. Using this agnostic approach we identified Toscana virus and, for the first time in adults, rotavirus and Saffold virus, as potential causative agents in adult meningitis. Further work is needed to determine the prevalence of atypical viral candidates as well as the clinical impact of using sequencing methods in real time. This knowledge can help to reduce antimicrobial use and hospitalisations leading to both patient and health system benefits.
许多脑膜炎患者的病因未明,导致不必要的抗生素使用和住院时间延长。我们使用病毒捕获测序来确定社区获得性脑膜炎成人中可能的致病病毒。
对 73 例患者的脑脊液(CSF)进行 VirCapSeq-VERT 检测,这是一种使用高通量测序捕获病毒靶标设计的探针组。患者被分为疑似病毒性脑膜炎 - CSF 白细胞增多,未确定病原体(n=38)、确诊病毒性脑膜炎 - CSF 白细胞增多且病原体已确定(n=15)或非脑膜炎 - CSF 白细胞不增多(n=20)。
VirCapSeq-VERT 在 38 例疑似病毒性脑膜炎患者中的 16 例(42%)CSF 中检测到病毒,包括 12 种单独的病毒。在 9/16 例(56%)中检测到潜在的临床相关病毒。出乎意料的是,检测到了托斯卡纳病毒、轮状病毒和 Saffold 病毒,并评估为潜在的致病因子。
VirCapSeq-VERT 增加了检测病毒的概率。使用这种无偏方法,我们确定了托斯卡纳病毒,并且首次在成人中确定了轮状病毒和 Saffold 病毒为成人脑膜炎的潜在致病因子。需要进一步研究以确定非典型病毒候选物的流行率以及实时使用测序方法的临床影响。这些知识可以帮助减少抗生素的使用和住院时间,从而使患者和医疗系统受益。