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Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks

BACKGROUND: Measles is a highly infectious disease caused by measles virus (MeV). Despite the availability of a safe and cost-effective vaccine, measles is one of the world-leading causes of death in young children. Within Europe, there is a target for eliminating endemic measles in 2015, with molec...

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Autores principales: Penedos, Ana Raquel, Myers, Richard, Hadef, Besma, Aladin, Farah, Brown, Kevin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646484/
https://www.ncbi.nlm.nih.gov/pubmed/26569100
http://dx.doi.org/10.1371/journal.pone.0143081
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author Penedos, Ana Raquel
Myers, Richard
Hadef, Besma
Aladin, Farah
Brown, Kevin E.
author_facet Penedos, Ana Raquel
Myers, Richard
Hadef, Besma
Aladin, Farah
Brown, Kevin E.
author_sort Penedos, Ana Raquel
collection PubMed
description BACKGROUND: Measles is a highly infectious disease caused by measles virus (MeV). Despite the availability of a safe and cost-effective vaccine, measles is one of the world-leading causes of death in young children. Within Europe, there is a target for eliminating endemic measles in 2015, with molecular epidemiology required on 80% of cases for inclusion/exclusion of outbreak transmission chains. Currently, MeV is genotyped on the basis of a 450 nucleotide region of the nucleoprotein gene (N-450) and the hemagglutinin gene (H). However, this is not sufficiently informative for distinguishing endemic from imported MeV. We have developed an amplicon-based method for obtaining whole genome sequences (WGS) using NGS or Sanger methodologies from cell culture isolates or oral fluid specimens, and have sequenced over 60 samples, including 42 from the 2012 outbreak in the UK. RESULTS: Overall, NGS coverage was over 90% for approximately 71% of the samples tested. Analysis of 32 WGS excluding 3’ and 5’ termini (WGS-t) obtained from the outbreak indicates that the single nucleotide difference found between the two major groups of N-450 sequences detected during the outbreak is most likely a result of stochastic viral mutation during endemic transmission rather than of multiple importation events: earlier strains appear to have evolved into two distinct strain clusters in 2013, one containing strains with both outbreak-associated N-450 sequences. Additionally, phylogenetic analysis of each genomic region of MeV for the strains in this study suggests that the most information is acquired from the non-coding region located between the matrix and fusion protein genes (M/F NCR) and the N-450 genotyping sequence, an observation supported by entropy analysis across genotypes. CONCLUSIONS: We suggest that both M/F NCR and WGS-t could be used to complement the information from classical epidemiology and N-450 sequencing to address specific questions in the context of measles elimination.
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spelling pubmed-46464842015-11-25 Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks Penedos, Ana Raquel Myers, Richard Hadef, Besma Aladin, Farah Brown, Kevin E. PLoS One Research Article BACKGROUND: Measles is a highly infectious disease caused by measles virus (MeV). Despite the availability of a safe and cost-effective vaccine, measles is one of the world-leading causes of death in young children. Within Europe, there is a target for eliminating endemic measles in 2015, with molecular epidemiology required on 80% of cases for inclusion/exclusion of outbreak transmission chains. Currently, MeV is genotyped on the basis of a 450 nucleotide region of the nucleoprotein gene (N-450) and the hemagglutinin gene (H). However, this is not sufficiently informative for distinguishing endemic from imported MeV. We have developed an amplicon-based method for obtaining whole genome sequences (WGS) using NGS or Sanger methodologies from cell culture isolates or oral fluid specimens, and have sequenced over 60 samples, including 42 from the 2012 outbreak in the UK. RESULTS: Overall, NGS coverage was over 90% for approximately 71% of the samples tested. Analysis of 32 WGS excluding 3’ and 5’ termini (WGS-t) obtained from the outbreak indicates that the single nucleotide difference found between the two major groups of N-450 sequences detected during the outbreak is most likely a result of stochastic viral mutation during endemic transmission rather than of multiple importation events: earlier strains appear to have evolved into two distinct strain clusters in 2013, one containing strains with both outbreak-associated N-450 sequences. Additionally, phylogenetic analysis of each genomic region of MeV for the strains in this study suggests that the most information is acquired from the non-coding region located between the matrix and fusion protein genes (M/F NCR) and the N-450 genotyping sequence, an observation supported by entropy analysis across genotypes. CONCLUSIONS: We suggest that both M/F NCR and WGS-t could be used to complement the information from classical epidemiology and N-450 sequencing to address specific questions in the context of measles elimination. Public Library of Science 2015-11-16 /pmc/articles/PMC4646484/ /pubmed/26569100 http://dx.doi.org/10.1371/journal.pone.0143081 Text en © 2015 Penedos et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Penedos, Ana Raquel
Myers, Richard
Hadef, Besma
Aladin, Farah
Brown, Kevin E.
Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title_full Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title_fullStr Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title_full_unstemmed Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title_short Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
title_sort assessment of the utility of whole genome sequencing of measles virus in the characterisation of outbreaks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646484/
https://www.ncbi.nlm.nih.gov/pubmed/26569100
http://dx.doi.org/10.1371/journal.pone.0143081
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