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Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing

Acute encephalitis/encephalopathy is a severe neurological syndrome that is occasionally associated with viral infection. Comprehensive virus detection assays are desirable because viral pathogens have not been identified in many cases. We evaluated the utility of next-generation sequencing (NGS) fo...

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Autores principales: Kawada, Jun-ichi, Okuno, Yusuke, Torii, Yuka, Okada, Ryo, Hayano, Satoshi, Ando, Shotaro, Kamiya, Yasuko, Kojima, Seiji, Ito, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022051/
https://www.ncbi.nlm.nih.gov/pubmed/27625312
http://dx.doi.org/10.1038/srep33452
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author Kawada, Jun-ichi
Okuno, Yusuke
Torii, Yuka
Okada, Ryo
Hayano, Satoshi
Ando, Shotaro
Kamiya, Yasuko
Kojima, Seiji
Ito, Yoshinori
author_facet Kawada, Jun-ichi
Okuno, Yusuke
Torii, Yuka
Okada, Ryo
Hayano, Satoshi
Ando, Shotaro
Kamiya, Yasuko
Kojima, Seiji
Ito, Yoshinori
author_sort Kawada, Jun-ichi
collection PubMed
description Acute encephalitis/encephalopathy is a severe neurological syndrome that is occasionally associated with viral infection. Comprehensive virus detection assays are desirable because viral pathogens have not been identified in many cases. We evaluated the utility of next-generation sequencing (NGS) for detecting viruses in clinical samples of encephalitis/encephalopathy patients. We first determined the sensitivity and quantitative performance of NGS by comparing the NGS-determined number of sequences of human herpesvirus-6 (HHV-6) in clinical serum samples with the HHV-6 load measured using real-time PCR. HHV-6 was measured as it occasionally causes neurologic disorders in children. The sensitivity of NGS for detection of HHV-6 sequences was equivalent to that of real-time PCR, and the number of HHV-6 reads was significantly correlated with HHV-6 load. Next, we investigated the ability of NGS to detect viral sequences in 18 pediatric patients with acute encephalitis/encephalopathy of unknown etiology. A large number of Coxsackievirus A9 and mumps viral sequences were detected in the cerebrospinal fluid of 2 and 1 patients, respectively. In addition, Torque teno virus and Pepper mild mottle viral sequences were detected in the sera of one patient each. These data indicate that NGS is useful for detection of causative viruses in patients with pediatric encephalitis/encephalopathy.
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spelling pubmed-50220512016-09-20 Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing Kawada, Jun-ichi Okuno, Yusuke Torii, Yuka Okada, Ryo Hayano, Satoshi Ando, Shotaro Kamiya, Yasuko Kojima, Seiji Ito, Yoshinori Sci Rep Article Acute encephalitis/encephalopathy is a severe neurological syndrome that is occasionally associated with viral infection. Comprehensive virus detection assays are desirable because viral pathogens have not been identified in many cases. We evaluated the utility of next-generation sequencing (NGS) for detecting viruses in clinical samples of encephalitis/encephalopathy patients. We first determined the sensitivity and quantitative performance of NGS by comparing the NGS-determined number of sequences of human herpesvirus-6 (HHV-6) in clinical serum samples with the HHV-6 load measured using real-time PCR. HHV-6 was measured as it occasionally causes neurologic disorders in children. The sensitivity of NGS for detection of HHV-6 sequences was equivalent to that of real-time PCR, and the number of HHV-6 reads was significantly correlated with HHV-6 load. Next, we investigated the ability of NGS to detect viral sequences in 18 pediatric patients with acute encephalitis/encephalopathy of unknown etiology. A large number of Coxsackievirus A9 and mumps viral sequences were detected in the cerebrospinal fluid of 2 and 1 patients, respectively. In addition, Torque teno virus and Pepper mild mottle viral sequences were detected in the sera of one patient each. These data indicate that NGS is useful for detection of causative viruses in patients with pediatric encephalitis/encephalopathy. Nature Publishing Group 2016-09-14 /pmc/articles/PMC5022051/ /pubmed/27625312 http://dx.doi.org/10.1038/srep33452 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kawada, Jun-ichi
Okuno, Yusuke
Torii, Yuka
Okada, Ryo
Hayano, Satoshi
Ando, Shotaro
Kamiya, Yasuko
Kojima, Seiji
Ito, Yoshinori
Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title_full Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title_fullStr Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title_full_unstemmed Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title_short Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing
title_sort identification of viruses in cases of pediatric acute encephalitis and encephalopathy using next-generation sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5022051/
https://www.ncbi.nlm.nih.gov/pubmed/27625312
http://dx.doi.org/10.1038/srep33452
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