病毒性脑膜炎
红细胞增多
脑膜炎
病毒学
病毒
医学
轮状病毒
病菌
脑脊液
生物
免疫学
细菌性脑膜炎
儿科
内科学
作者
Fiona McGill,Rafal Tokarz,Emma C. Thomson,Ana da Silva Filipe,Stephen Sameroff,Komal Jain,Nishit Bhuva,Shirin Ashraf,W. Ian Lipkin,Caroline Corless,Chitra Pattabiraman,Barry C. Gibney,Michael Griffiths,Anna María Geretti,Benedict Michael,Nicholas J. Beeching,David McKee,Ian Hart,Ken Mutton,Agam Jung,Alastair Miller,Tom Solomon
标识
DOI:10.1016/j.jinf.2021.12.042
摘要
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.
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