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Chronic Meningitis Investigated via Metagenomic Next-Generation Sequencing

Authors :
Vanja C. Douglas
Gary Green
Mark P. Gorman
Eric D. Chow
Ariane Soldatos
Kelsey C. Zorn
Hannah A. Sample
Debarko Banerji
Maulik P. Shah
Michael R. Wilson
Megan B. Richie
Lillian M. Khan
Leonard H. Calabrese
Jeffrey M. Gelfand
Luke Strnad
Chloe Bryson-Cahn
Bruce J. Brew
John P. Betjemann
Sarah B Doernberg
Jairam R Lingappa
Ari J. Green
Joseph L. DeRisi
Felicia C. Chow
S. Andrew Josephson
Whitney E. Harrington
Brian D. O’Donovan
Cheryl A. Jay
John E. Greenlee
Jonathan H Blum
Niraj M. Shanbhag
Chaz Langelier
Rula A. Hajj-Ali
Source :
JAMA Neurology. 75:947
Publication Year :
2018
Publisher :
American Medical Association (AMA), 2018.

Abstract

Importance Identifying infectious causes of subacute or chronic meningitis can be challenging. Enhanced, unbiased diagnostic approaches are needed. Objective To present a case series of patients with diagnostically challenging subacute or chronic meningitis using metagenomic next-generation sequencing (mNGS) of cerebrospinal fluid (CSF) supported by a statistical framework generated from mNGS of control samples from the environment and from patients who were noninfectious. Design, Setting, and Participants In this case series, mNGS data obtained from the CSF of 94 patients with noninfectious neuroinflammatory disorders and from 24 water and reagent control samples were used to develop and implement a weighted scoring metric based onzscores at the species and genus levels for both nucleotide and protein alignments to prioritize and rank the mNGS results. Total RNA was extracted for mNGS from the CSF of 7 participants with subacute or chronic meningitis who were recruited between September 2013 and March 2017 as part of a multicenter study of mNGS pathogen discovery among patients with suspected neuroinflammatory conditions. The neurologic infections identified by mNGS in these 7 participants represented a diverse array of pathogens. The patients were referred from the University of California, San Francisco Medical Center (n = 2), Zuckerberg San Francisco General Hospital and Trauma Center (n = 2), Cleveland Clinic (n = 1), University of Washington (n = 1), and Kaiser Permanente (n = 1). A weightedzscore was used to filter out environmental contaminants and facilitate efficient data triage and analysis. Main Outcomes and Measures Pathogens identified by mNGS and the ability of a statistical model to prioritize, rank, and simplify mNGS results. Results The 7 participants ranged in age from 10 to 55 years, and 3 (43%) were female. A parasitic worm (Taenia solium, in 2 participants), a virus (HIV-1), and 4 fungi (Cryptococcus neoformans,Aspergillus oryzae,Histoplasma capsulatum, andCandida dubliniensis) were identified among the 7 participants by using mNGS. Evaluating mNGS data with a weightedzscore–based scoring algorithm reduced the reported microbial taxa by a mean of 87% (range, 41%-99%) when taxa with a combined score of 0 or less were removed, effectively separating bona fide pathogen sequences from spurious environmental sequences so that, in each case, the causative pathogen was found within the top 2 scoring microbes identified using the algorithm. Conclusions and Relevance Diverse microbial pathogens were identified by mNGS in the CSF of patients with diagnostically challenging subacute or chronic meningitis, including a case of subarachnoid neurocysticercosis that defied diagnosis for 1 year, the first reported case of CNS vasculitis caused byAspergillus oryzae, and the fourth reported case ofC dubliniensismeningitis. Prioritizing metagenomic data with a scoring algorithm greatly clarified data interpretation and highlighted the problem of attributing biological significance to organisms present in control samples used for metagenomic sequencing studies.

Details

ISSN :
21686149
Volume :
75
Database :
OpenAIRE
Journal :
JAMA Neurology
Accession number :
edsair.doi...........49c4e225475c835ba5da7edb2ccb727a
Full Text :
https://doi.org/10.1001/jamaneurol.2018.0463