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Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples

Nanopore sequencing is becoming increasingly commonplace in clinical settings, particularly for diagnostic assessments and outbreak investigations, due to its portability, low cost, and ability to operate in near real-time. Although high sequencing error rates initially hampered the wider implementa...

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Autores principales: Li, Kathy K., Lau, Betty, Suárez, Nicolás M., Camiolo, Salvatore, Gunson, Rory, Davison, Andrew J., Orton, Richard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303703/
https://www.ncbi.nlm.nih.gov/pubmed/37376548
http://dx.doi.org/10.3390/v15061248
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author Li, Kathy K.
Lau, Betty
Suárez, Nicolás M.
Camiolo, Salvatore
Gunson, Rory
Davison, Andrew J.
Orton, Richard J.
author_facet Li, Kathy K.
Lau, Betty
Suárez, Nicolás M.
Camiolo, Salvatore
Gunson, Rory
Davison, Andrew J.
Orton, Richard J.
author_sort Li, Kathy K.
collection PubMed
description Nanopore sequencing is becoming increasingly commonplace in clinical settings, particularly for diagnostic assessments and outbreak investigations, due to its portability, low cost, and ability to operate in near real-time. Although high sequencing error rates initially hampered the wider implementation of this technology, improvements have been made continually with each iteration of the sequencing hardware and base-calling software. Here, we assess the feasibility of using nanopore sequencing to determine the complete genomes of human cytomegalovirus (HCMV) in high-viral-load clinical samples without viral DNA enrichment, PCR amplification, or prior knowledge of the sequences. We utilised a hybrid bioinformatic approach that involved assembling the reads de novo, improving the consensus sequence by aligning reads to the best-matching genome from a collated set of published sequences, and polishing the improved consensus sequence. The final genomes from a urine sample and a lung sample, the former with an HCMV to human DNA load approximately 50 times greater than the latter, achieved 99.97 and 99.93% identity, respectively, to the benchmark genomes obtained independently by Illumina sequencing. Thus, we demonstrated that nanopore sequencing is capable of determining HCMV genomes directly from high-viral-load clinical samples with a high accuracy.
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spelling pubmed-103037032023-06-29 Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples Li, Kathy K. Lau, Betty Suárez, Nicolás M. Camiolo, Salvatore Gunson, Rory Davison, Andrew J. Orton, Richard J. Viruses Article Nanopore sequencing is becoming increasingly commonplace in clinical settings, particularly for diagnostic assessments and outbreak investigations, due to its portability, low cost, and ability to operate in near real-time. Although high sequencing error rates initially hampered the wider implementation of this technology, improvements have been made continually with each iteration of the sequencing hardware and base-calling software. Here, we assess the feasibility of using nanopore sequencing to determine the complete genomes of human cytomegalovirus (HCMV) in high-viral-load clinical samples without viral DNA enrichment, PCR amplification, or prior knowledge of the sequences. We utilised a hybrid bioinformatic approach that involved assembling the reads de novo, improving the consensus sequence by aligning reads to the best-matching genome from a collated set of published sequences, and polishing the improved consensus sequence. The final genomes from a urine sample and a lung sample, the former with an HCMV to human DNA load approximately 50 times greater than the latter, achieved 99.97 and 99.93% identity, respectively, to the benchmark genomes obtained independently by Illumina sequencing. Thus, we demonstrated that nanopore sequencing is capable of determining HCMV genomes directly from high-viral-load clinical samples with a high accuracy. MDPI 2023-05-26 /pmc/articles/PMC10303703/ /pubmed/37376548 http://dx.doi.org/10.3390/v15061248 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Kathy K.
Lau, Betty
Suárez, Nicolás M.
Camiolo, Salvatore
Gunson, Rory
Davison, Andrew J.
Orton, Richard J.
Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title_full Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title_fullStr Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title_full_unstemmed Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title_short Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples
title_sort direct nanopore sequencing of human cytomegalovirus genomes from high-viral-load clinical samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10303703/
https://www.ncbi.nlm.nih.gov/pubmed/37376548
http://dx.doi.org/10.3390/v15061248
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