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Genomic analysis of serologically untypable human enteroviruses in Taiwan
BACKGROUND: Human enteroviruses contain over 100 serotypes. We have routinely conducted enterovirus surveillance in northern Taiwan; but about 10% of isolates could not be serotyped using traditional assays. Next-generation sequencing (NGS) is a powerful tool for genome sequencing. METHODS: In this...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607526/ https://www.ncbi.nlm.nih.gov/pubmed/31266491 http://dx.doi.org/10.1186/s12929-019-0541-x |
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author | Chien, Yeh-Sheng Luo, Shu-Ting Tsao, Kuo-Chien Huang, Yhu-Chering Chung, Wan-Yu Liao, Yu-Chieh Tan, Yi Das, Suman R. Lee, Min-Shi |
author_facet | Chien, Yeh-Sheng Luo, Shu-Ting Tsao, Kuo-Chien Huang, Yhu-Chering Chung, Wan-Yu Liao, Yu-Chieh Tan, Yi Das, Suman R. Lee, Min-Shi |
author_sort | Chien, Yeh-Sheng |
collection | PubMed |
description | BACKGROUND: Human enteroviruses contain over 100 serotypes. We have routinely conducted enterovirus surveillance in northern Taiwan; but about 10% of isolates could not be serotyped using traditional assays. Next-generation sequencing (NGS) is a powerful tool for genome sequencing. METHODS: In this study, we established an NGS platform to conduct genome sequencing for the serologically untypable enterovirus isolates. RESULTS: Among 130 serologically untypable isolates, 121 (93%) of them were classified into 29 serotypes using CODEHOP (COnsensus-DEgenerate Hybrid Oligonucleotide Primer)-based RT-PCR to amplify VP1 genes (VP1-CODEHOP). We further selected 52 samples for NGS and identified 59 genome sequences from 51 samples, including 8 samples containing two virus genomes. We also detected 23 genome variants (nucleotide identity < 90% compared with genome sequences in the public domain) which were potential genetic recombination, including 9 inter-serotype recombinants and 14 strains with unknown sources of recombination. CONCLUSIONS: We successfully integrated VP1-CODEHOP and NGS techniques to conduct genomic analysis of serologically untypable enteroviruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12929-019-0541-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6607526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66075262019-07-12 Genomic analysis of serologically untypable human enteroviruses in Taiwan Chien, Yeh-Sheng Luo, Shu-Ting Tsao, Kuo-Chien Huang, Yhu-Chering Chung, Wan-Yu Liao, Yu-Chieh Tan, Yi Das, Suman R. Lee, Min-Shi J Biomed Sci Research BACKGROUND: Human enteroviruses contain over 100 serotypes. We have routinely conducted enterovirus surveillance in northern Taiwan; but about 10% of isolates could not be serotyped using traditional assays. Next-generation sequencing (NGS) is a powerful tool for genome sequencing. METHODS: In this study, we established an NGS platform to conduct genome sequencing for the serologically untypable enterovirus isolates. RESULTS: Among 130 serologically untypable isolates, 121 (93%) of them were classified into 29 serotypes using CODEHOP (COnsensus-DEgenerate Hybrid Oligonucleotide Primer)-based RT-PCR to amplify VP1 genes (VP1-CODEHOP). We further selected 52 samples for NGS and identified 59 genome sequences from 51 samples, including 8 samples containing two virus genomes. We also detected 23 genome variants (nucleotide identity < 90% compared with genome sequences in the public domain) which were potential genetic recombination, including 9 inter-serotype recombinants and 14 strains with unknown sources of recombination. CONCLUSIONS: We successfully integrated VP1-CODEHOP and NGS techniques to conduct genomic analysis of serologically untypable enteroviruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12929-019-0541-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-03 /pmc/articles/PMC6607526/ /pubmed/31266491 http://dx.doi.org/10.1186/s12929-019-0541-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chien, Yeh-Sheng Luo, Shu-Ting Tsao, Kuo-Chien Huang, Yhu-Chering Chung, Wan-Yu Liao, Yu-Chieh Tan, Yi Das, Suman R. Lee, Min-Shi Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title | Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title_full | Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title_fullStr | Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title_full_unstemmed | Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title_short | Genomic analysis of serologically untypable human enteroviruses in Taiwan |
title_sort | genomic analysis of serologically untypable human enteroviruses in taiwan |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607526/ https://www.ncbi.nlm.nih.gov/pubmed/31266491 http://dx.doi.org/10.1186/s12929-019-0541-x |
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