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Artículo

An optimized methodology for whole genome sequencing of RNA respiratory viruses from nasopharyngeal aspirates

Goya, StephanieIcon ; Valinotto, Laura ElenaIcon ; Tittarelli, EstefaníaIcon ; Rojo, Gabriel LihueIcon ; Nabaes Jodar, Mercedes SoledadIcon ; Greninger, Alexander L.; Zaiat, Jonathan JavierIcon ; Marti, Marcelo AdrianIcon ; Mistchenko, Alicia Susana; Viegas, MarianaIcon
Fecha de publicación: 06/2018
Editorial: Public Library of Science
Revista: Plos One
ISSN: 1932-6203
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Virología

Resumen

Over the last decade, the number of viral genome sequences deposited in available databases has grown exponentially. However, sequencing methodology vary widely and many published works have relied on viral enrichment by viral culture or nucleic acid amplification with specific primers rather than through unbiased techniques such as metagenomics. The genome of RNA viruses is highly variable and these enrichment methodologies may be difficult to achieve or may bias the results. In order to obtain genomic sequences of human respiratory syncytial virus (HRSV) from positive nasopharyngeal aspirates diverse methodologies were evaluated and compared. A total of 29 nearly complete and complete viral genomes were obtained. The best performance was achieved with a DNase I treatment to the RNA directly extracted from the nasopharyngeal aspirate (NPA), sequence-independent single-primer amplification (SISPA) and library preparation performed with Nextera XT DNA Library Prep Kit with manual normalization. An average of 633,789 and 1,674,845 filtered reads per library were obtained with MiSeq and NextSeq 500 platforms, respectively. The higher output of NextSeq 500 was accompanied by the increasing of duplicated reads percentage generated during SISPA (from an average of 1.5% duplicated viral reads in MiSeq to an average of 74% in NextSeq 500). HRSV genome recovery was not affected by the presence or absence of duplicated reads but the computational demand during the analysis was increased. Considering that only samples with viral load E+06 copies/ml NPA were tested, no correlation between sample viral loads and number of total filtered reads was observed, nor with the mapped viral reads. The HRSV genomes showed a mean coverage of 98.46% with the best methodology. In addition, genomes of human metapneumovirus (HMPV), human rhinovirus (HRV) and human parainfluenza virus types 1–3 (HPIV1-3) were also obtained with the selected optimal methodology.
Palabras clave: Respiratory viruses , NGS , Respiratory syncytial virus , Viral complete genomes
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution 2.5 Unported (CC BY 2.5)
Identificadores
URI: http://hdl.handle.net/11336/97005
DOI: https://doi.org/10.1371/journal.pone.0199714
URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0199714
Colecciones
Articulos(IQUIBICEN)
Articulos de INSTITUTO DE QUIMICA BIOLOGICA DE LA FACULTAD DE CS. EXACTAS Y NATURALES
Articulos(SEDE CENTRAL)
Articulos de SEDE CENTRAL
Citación
Goya, Stephanie; Valinotto, Laura Elena; Tittarelli, Estefanía; Rojo, Gabriel Lihue; Nabaes Jodar, Mercedes Soledad; et al.; An optimized methodology for whole genome sequencing of RNA respiratory viruses from nasopharyngeal aspirates; Public Library of Science; Plos One; 13; 6; 6-2018; 1-15
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