Metagenomic detection of central nervous system infections missed by conventional testing.

IF 6.3 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Noely Evangelista Ferreira, Michael G Berg, Antonio C da Costa, Mary A Rodgers, Esper G Kallas, Cassia G Terrasani Silveira, Mateus Vailant Thomazella, Ana Carolina Soares de Oliveira, Layla Honorato, Heuder Go Paião, Renan Barros Domingues, Carlos Senne, Marina F Côrtes, Tania R Tozetto-Mendoza, Hélio R Gomes, Maria Laura Mariano Matos, Geovani de Oliveria Ribeiro, Steven S Witkin, Gavin A Cloherty, Maria Cassia Mendes-Correa
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引用次数: 0

Abstract

Community-acquired infectious meningoencephalitis is associated with high rates of mortality and morbidity, compounded by limited access to diagnostic resources. The current study assessed acute central nervous system (CNS) infections in patients with meningoencephalitis enrolled in a hospital-based diagnostic surveillance study in São Paulo, Brazil. Cerebrospinal fluid (CSF) was collected from 600 subjects between March 2018 and November 2019 and initially screened for a broad range of pathogens according to a local diagnostic algorithm. Standard microbiological and molecular diagnostic methods were applied. Metagenomic sequencing was used as a complementary approach to investigating etiology in cases where no pathogen was initially identified. Standard testing identified infectious etiologies in 292 cases (48.6%), with 227 (77.7%) confirmed as viral infections, predominantly caused by enteroviruses (n=144) and herpesviruses (n=40). Non-viral agents were identified in 65 cases (22.3%). Metagenomic sequencing (mNGS) of 279 out of 308 undiagnosed cases revealed several additional potential etiologies, including Parvovirus B19, Toxoplasma gondii, Picobirnavirus, other enterovirus species and Vesivirus, the latter being associated with CNS infection for the first time. These findings underscore the complexity of CNS infections and highlight the potential of metagenomics to improve diagnostic accuracy, inform treatment strategies, and support efforts to address future pandemics.

常规检测遗漏的中枢神经系统感染的宏基因组检测。
社区获得性传染性脑膜脑炎与高死亡率和发病率相关,而且诊断资源的获取有限。目前的研究评估了在巴西圣保罗医院诊断监测研究中纳入的脑膜脑炎患者的急性中枢神经系统(CNS)感染。在2018年3月至2019年11月期间,从600名受试者中收集了脑脊液(CSF),并根据当地诊断算法对多种病原体进行了初步筛查。采用标准的微生物学和分子诊断方法。宏基因组测序被用作一种补充方法,在没有病原体最初确定的情况下调查病因。在292例(48.6%)病例中,标准检测确定了感染病因,其中227例(77.7%)确诊为病毒感染,主要由肠病毒(n=144)和疱疹病毒(n=40)引起。65例(22.3%)发现非病毒性药物。308例未确诊病例中279例的元基因组测序(mNGS)显示了几种潜在病因,包括细小病毒B19、刚地弓形虫、小核糖核酸病毒、其他肠道病毒和Vesivirus,后者首次与中枢神经系统感染相关。这些发现强调了中枢神经系统感染的复杂性,并强调了宏基因组学在提高诊断准确性、为治疗策略提供信息和支持应对未来流行病方面的潜力。
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来源期刊
JCI insight
JCI insight Medicine-General Medicine
CiteScore
13.70
自引率
1.20%
发文量
543
审稿时长
6 weeks
期刊介绍: JCI Insight is a Gold Open Access journal with a 2022 Impact Factor of 8.0. It publishes high-quality studies in various biomedical specialties, such as autoimmunity, gastroenterology, immunology, metabolism, nephrology, neuroscience, oncology, pulmonology, and vascular biology. The journal focuses on clinically relevant basic and translational research that contributes to the understanding of disease biology and treatment. JCI Insight is self-published by the American Society for Clinical Investigation (ASCI), a nonprofit honor organization of physician-scientists founded in 1908, and it helps fulfill the ASCI's mission to advance medical science through the publication of clinically relevant research reports.
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