TY - JOUR
T1 - Next-generation sequencing in neuropathologic diagnosis of infections of the nervous system
AU - Salzberg, Steven L.
AU - Breitwieser, Florian P.
AU - Kumar, Anupama
AU - Hao, Haiping
AU - Burger, Peter
AU - Rodriguez, Fausto J.
AU - Lim, Michael
AU - Quiñones-Hinojosa, Alfredo
AU - Gallia, Gary L.
AU - Tornheim, Jeffrey A.
AU - Melia, Michael T.
AU - Sears, Cynthia L.
AU - Pardo, Carlos A.
N1 - Funding Information:
S.L. Salzberg is an Associate Editor, Editorial Board member, or Editorial Advisory Board member for the following journals: Genome Biology, PeerJ Computer Science, BMC Biology, Biology Direct, Journal of Computational Biology, BMC Genomics, BMC Bioinformatics, and Evolutionary Bioinformatics; and received research support from NIH. F.P. Breitwieser, A. Kumar, H. Hao, and P. Burger report no disclosures. F.J. Rodriguez receives publishing royalties from Elsevier. M. Lim served on the scientific advisory boards for Novartis-DSMB, BMS, and Stryker; received travel funding and speaker honoraria from Stryker and BMS; holds a patent for the combination of focused radiation and immunotherapy; receives publishing royalties for Handbook of Radiosurgery; performs neurosurgery; and received research support from Stryker, BMS, Aegenus, CellDex, and Arbor. A. Quinones-Hinojosa received travel funding and speaker honoraria from Speak Inc. and American Program Bureau, Inc.; is on the editorial board for Cancer Today; holds patents for Microfluid assay for the determination of tumor cell metastatic propensity, A novel, high-throughput, nanotopo-graphic platform for screening cell migratory behavior, Quantitative tissue property mapping for real time tumor detection and interventional guidance, Nanoparticle modification of human adipose-derived mesenchymal stem cells for brain cancer and other neurological diseases, Hydrogels for local treatment of brain-related diseases, Methods for phenotypic classification of cells based on migratory behavior, Use of AGX/UAP inhibitors to inhibit flux through the hexosamine biosynthetic pathway, Self-assembling verteporfin amphiphiles (SAVA) for local brain cancer therapy, Predicting brain tumor patient prognosis, and NAAG as an indicator of clinical prognosis for glioblastoma; receives publishing royalties from Elsevier, UC Press, LID Espanol, Thieme, Stem Cells International, and Jaypee Brothers Medical Publishers; has consulted for Stryker and Integra; is on the speaker bureau for Speak, Inc., and American Program Bureau, Inc.; and received research support from Stryker, Integra, NIH, Johns Hopkins University, JHU Coulter Foundation, Maryland Stem Cell Research Fund (TEDCO), Maryland Biotechnology Development Award, and Allegheny Health Network-Johns Hopkins Cancer Research Fund. G.L. Gallia received research support from Chordoma. J.A. Tornheim reports no disclosures. M.T. Melia’s institution received research support from Merck, Sharpe & Dohme, Janssen, Gilead, Bristol-Myers Squibb, and AbbVie; and he received research support from NIH, CDC, and Johns Hopkins School of Medicine. C.L. Sears is an associate editor for Clinical Infectious Diseases; holds a patent for biofilms in colon cancer as a diagnostic approach to identify individuals at risk for colon cancer; receives royalties from Up-to-Date; and received research support from NIH, Johns Hopkins, and Institut Merieux. C.A. Pardo received research support from Accorda Pharmaceuticals, NIH/National Institute of Neurological Disorders and Stroke, and Bart McLean Fund for Neuroimmunology Research. Go to Neurology.org/nn for full disclosure forms.
Funding Information:
Supported in part by the NIH under grant R01 HG006677 (S.L.S.) by the US Army Research Office under grant number W911NF-14-1-0490 (S.L.S.) and The Bart McLean Fund for Neuroimmunology Research– Johns Hopkins Project Restore (C.A.P.).
Publisher Copyright:
© 2016 American Academy of Neurology.
PY - 2016
Y1 - 2016
N2 - Objective: To determine the feasibility of next-generation sequencing (NGS) microbiome approaches in the diagnosis of infectious disorders in brain or spinal cord biopsies in patients with suspected CNS infections. Methods: In a prospective pilot study, we applied NGS in combination with a new computational analysis pipeline to detect the presence of pathogenic microbes in brain or spinal cord biopsies from 10 patients with neurologic problems indicating possible infection but for whom conventional clinical and microbiology studies yielded negative or inconclusive results. Results: Direct DNA and RNA sequencing of brain tissue biopsies generated 8.3 million to 29.1 million sequence reads per sample, which successfully identified with high confidence the infectious agent in 3 patients for whom validation techniques confirmed the pathogens identified by NGS. Although NGS was unable to identify with precision infectious agents in the remaining cases, it contributed to the understanding of neuropathologic processes in 5 others, demonstrating the power of large-scale unbiased sequencing as a novel diagnostic tool. Clinical outcomes were consistent with the findings yielded by NGS on the presence or absence of an infectious pathogenic process in 8 of 10 cases, and were noncontributory in the remaining 2. Conclusions: NGS-guided metagenomic studies of brain, spinal cord, or meningeal biopsies offer the possibility for dramatic improvements in our ability to detect (or rule out) a wide range of CNS pathogens, with potential benefits in speed, sensitivity, and cost. NGS-based microbiome approaches present a major new opportunity to investigate the potential role of infectious pathogens in the pathogenesis of neuroinflammatory disorders.
AB - Objective: To determine the feasibility of next-generation sequencing (NGS) microbiome approaches in the diagnosis of infectious disorders in brain or spinal cord biopsies in patients with suspected CNS infections. Methods: In a prospective pilot study, we applied NGS in combination with a new computational analysis pipeline to detect the presence of pathogenic microbes in brain or spinal cord biopsies from 10 patients with neurologic problems indicating possible infection but for whom conventional clinical and microbiology studies yielded negative or inconclusive results. Results: Direct DNA and RNA sequencing of brain tissue biopsies generated 8.3 million to 29.1 million sequence reads per sample, which successfully identified with high confidence the infectious agent in 3 patients for whom validation techniques confirmed the pathogens identified by NGS. Although NGS was unable to identify with precision infectious agents in the remaining cases, it contributed to the understanding of neuropathologic processes in 5 others, demonstrating the power of large-scale unbiased sequencing as a novel diagnostic tool. Clinical outcomes were consistent with the findings yielded by NGS on the presence or absence of an infectious pathogenic process in 8 of 10 cases, and were noncontributory in the remaining 2. Conclusions: NGS-guided metagenomic studies of brain, spinal cord, or meningeal biopsies offer the possibility for dramatic improvements in our ability to detect (or rule out) a wide range of CNS pathogens, with potential benefits in speed, sensitivity, and cost. NGS-based microbiome approaches present a major new opportunity to investigate the potential role of infectious pathogens in the pathogenesis of neuroinflammatory disorders.
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U2 - 10.1212/NXI.0000000000000251
DO - 10.1212/NXI.0000000000000251
M3 - Article
AN - SCOPUS:85010620671
SN - 2332-7812
VL - 3
JO - Neurology: Neuroimmunology and NeuroInflammation
JF - Neurology: Neuroimmunology and NeuroInflammation
IS - 4
M1 - e251
ER -