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      Pan-viral serology implicates enteroviruses in acute flaccid myelitis

      research-article
      , MD 1 , 2 , , BS 1 , , MBBS 1 , 2 , , PhD 1 , 2 , , PhD 3 , 4 , , PhD 3 , , PhD 3 , , BS 3 , , PhD 5 , , PhD 3 , , BS 3 , , BS 3 , , BA 3 , , BS 6 , , BS 5 , , MHS 5 , , BS 2 , , BS 5 , , MD 1 , 2 , , MD 1 , 2 , , MD, MAS 1 , , MD, PhD 1 , 2 , , MD 1 , , MD 7 , , MD 7 , 8 , , MD 9 , , MD, MSc 9 , , MD, PhD 10 , , MD, PhD 11 , , DVM, MPVM, MD 12 , , MPH 13 , , MD, MPH 13 , , PhD 13 , , MD, PhD 14 , , PhD 15 , , PhD 15 , , MHS 15 , , BS 15 , , MD, MPH 16 , , MD 17 , , MD 17 , , MD 14 , , PhD 15 , , PhD 15 , , PhD 3 , 5 , , MD, MAS 1 , 2 , **
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          Abstract

          Since 2012, the United States has experienced a biennial spike in pediatric acute flaccid myelitis (AFM). 16 Epidemiologic evidence suggests non-polio enteroviruses (EVs) are a potential etiology, yet EV RNA is rarely detected in cerebrospinal fluid (CSF). 2 We interrogated CSF from children with AFM (n=42) and pediatric other neurologic disease controls (n=58) for intrathecal anti-viral antibodies using a phage display library expressing 481,966 overlapping peptides derived from all known vertebrate and arboviruses (VirScan). We also performed metagenomic next-generation sequencing (mNGS) of AFM CSF RNA (n=20 cases), both unbiased and with targeted enrichment for EVs. Using VirScan, the only viral family significantly enriched by the CSF of AFM cases relative to controls was Picornaviridae, with the most enriched Picornaviridae peptides belonging to the genus Enterovirus (n=29/42 cases versus 4/58 controls). EV VP1 ELISA confirmed this finding (n=22/26 cases versus 7/50 controls). mNGS did not detect additional EV RNA. Despite rare detection of EV RNA, pan-viral serology identified frequently high levels of CSF EV-specific antibodies in AFM compared to controls, providing further evidence for a causal role of non-polio EVs in AFM.

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          Most cited references29

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          Viral immunology. Comprehensive serological profiling of human populations using a synthetic human virome.

          The human virome plays important roles in health and immunity. However, current methods for detecting viral infections and antiviral responses have limited throughput and coverage. Here, we present VirScan, a high-throughput method to comprehensively analyze antiviral antibodies using immunoprecipitation and massively parallel DNA sequencing of a bacteriophage library displaying proteome-wide peptides from all human viruses. We assayed over 10(8) antibody-peptide interactions in 569 humans across four continents, nearly doubling the number of previously established viral epitopes. We detected antibodies to an average of 10 viral species per person and 84 species in at least two individuals. Although rates of specific virus exposure were heterogeneous across populations, antibody responses targeted strongly conserved "public epitopes" for each virus, suggesting that they may elicit highly similar antibodies. VirScan is a powerful approach for studying interactions between the virome and the immune system. Copyright © 2015, American Association for the Advancement of Science.
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            Varicella zoster virus vasculopathies: diverse clinical manifestations, laboratory features, pathogenesis, and treatment.

            Vasculopathies caused by varicella zoster virus (VZV) are indicative of a productive virus infection in cerebral arteries after either reactivation of VZV (shingles) or primary infection (chickenpox). VZV vasculopathy can cause ischaemic infarction of the brain and spinal cord, as well as aneurysm, subarachnoid and cerebral haemorrhage, carotid dissection, and, rarely, peripheral arterial disease. VZV vasculopathy in immunocompetent or immunocompromised individuals can be unifocal or multifocal with deep-seated and superficial infarctions. Lesions at the grey-white matter junction on brain imaging are a clue to diagnosis. Involvement of both large and small arteries is more common than that of either alone. Most patients have a mononuclear cerebrospinal fluid pleocytosis, often with red blood cells. Cerebrospinal fluid pleocytosis and rash are absent in about a third of cases. Anti-VZV IgG antibody in the cerebrospinal fluid is found more frequently than VZV DNA. In recent years, the number of recognised VZV vasculopathies has grown, and accurate diagnosis is important for the effective treatment of these disorders.
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              Is Open Access

              FLASH: a next-generation CRISPR diagnostic for multiplexed detection of antimicrobial resistance sequences

              Abstract The growing prevalence of deadly microbes with resistance to previously life-saving drug therapies is a dire threat to human health. Detection of low abundance pathogen sequences remains a challenge for metagenomic Next Generation Sequencing (NGS). We introduce FLASH (Finding Low Abundance Sequences by Hybridization), a next-generation CRISPR/Cas9 diagnostic method that takes advantage of the efficiency, specificity and flexibility of Cas9 to enrich for a programmed set of sequences. FLASH-NGS achieves up to 5 orders of magnitude of enrichment and sub-attomolar gene detection with minimal background. We provide an open-source software tool (FLASHit) for guide RNA design. Here we applied it to detection of antimicrobial resistance genes in respiratory fluid and dried blood spots, but FLASH-NGS is applicable to all areas that rely on multiplex PCR.
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                Author and article information

                Journal
                9502015
                8791
                Nat Med
                Nat. Med.
                Nature medicine
                1078-8956
                1546-170X
                14 September 2019
                21 October 2019
                November 2019
                21 April 2020
                : 25
                : 11
                : 1748-1752
                Affiliations
                [1 ]UCSF Weill Institute for Neurosciences, San Francisco, CA, USA
                [2 ]UCSF Department of Neurology, San Francisco, CA, USA
                [3 ]Chan Zuckerberg Biohub, San Francisco, CA, USA
                [4 ]UCSF Department of Microbiology and Immunology, San Francisco, CA, USA
                [5 ]UCSF Department of Biochemistry & Biophysics, San Francisco, CA, USA
                [6 ]UCSF School of Medicine, San Francisco, CA, USA
                [7 ]Department of Neurology, Massachusetts General Hospital, Boston, MA, USA
                [8 ]Department of Neurology, Brigham and Women’s Hospital, Boston, MA, USA
                [9 ]Division of Neurology, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
                [10 ]Department of Laboratory Medicine and Medicine, Division of Infectious Diseases, University of California, San Francisco, San Francisco, USA
                [11 ]Department of Pediatrics, Division of Infectious Diseases, University of California, San Francisco, San Francisco, USA
                [12 ]Department of Pediatric Infectious Diseases, Kaiser Permanente Oakland Medical Center, Oakland, California, USA
                [13 ]Division of Communicable Disease Control, California Department of Public Health, Richmond, California
                [14 ]Children’s Hospital Colorado and Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
                [15 ]Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
                [16 ]National Institute of Neurological Disorders and Stroke (NINDS), NIH, Bethesda, Maryland, USA.
                [17 ]Department of Neurology, Boston Children’s Hospital, Boston, MA, USA
                Author notes

                Author Contributions

                A.R. computationally designed the VirScan peptide library. R.D.S., I.A.H., and G.A.S. cloned the VirScan library. R.D.S. and I.A.H. performed the VirScan experiments. R.D.S. and B.O. developed the automated IP protocols and analysis pipeline for VirScan. J.E.P., W.W., and C.K.C. cloned and expressed enterovirus VP1 proteins. R.D.S. performed the ELISA experiments. P.S.R., E.D.C., A.L., C.M.T., M.T., and R.D.S. performed metagenomic sequencing and FLASH. P.S.R. and E.D.C. analyzed metagenomic and FLASH data. D.B. and L.M.K. helped prepare samples for sequencing. R.D.S., H.A.S., K.C.Z., R.B., S.L.H., A.A.G., B.J.K., K.N., K.S.K., T.C., J.Z.D., H.J.M., C.Y.C., B.B., C.A.G., C.Y., V.C., D.A.W., S.R.D., R.L.M., A.S.L., W.A.N., A.S., M.P.G., L.B., K.M., J.L.K-A, and M.S.O. identified patients, performed clinical phenotyping and provided patient samples. R.D.S., A.R., T.F.F.N., J.L.D., and M.R.W. analyzed VirScan and ELISA data. R.D.S. and J.L.D. generated the figures. J.L.K-A and M.S.O. provided critical expert guidance on the manuscript. R.D.S., J.L.D., and M.R.W. conceived of and wrote the manuscript. All authors discussed the results and contributed critical review to the manuscript.

                [*]

                Authors contributed equally

                [** ]Corresponding Author Information: Name: Dr. Michael Wilson, Address: UCSF, Department of Neurology, Division of Neuroimmunology and Glial Biology, 675 Nelson Rising Lane, NS212, Campus Box 3206, San Francisco, CA 94158, michael.wilson@ 123456ucsf.edu , Phone: 415-502-7429
                Article
                NIHMS1539954
                10.1038/s41591-019-0613-1
                6858576
                31636453
                3120f733-b4e4-4941-a9dc-f992f3d1f710

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