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

被引:62
|
作者
Penedos, Ana Raquel [1 ]
Myers, Richard [1 ]
Hadef, Besma [1 ]
Aladin, Farah [1 ]
Brown, Kevin E. [1 ]
机构
[1] Publ Hlth England, Virus Reference Dept, London NW9 5EQ, England
来源
PLOS ONE | 2015年 / 10卷 / 11期
关键词
REAL-TIME PCR; WILD-TYPE; ANTIBODY; ELIMINATION; ENGLAND; MUMPS; WALES;
D O I
10.1371/journal.pone.0143081
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 out-break-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.
引用
收藏
页数:16
相关论文
共 50 条
  • [31] Clinical Utility of Whole Genome Sequencing for Undiagnosed Rare Genetic Disorders
    Awan, Muhammad Qasim
    JOURNAL OF THE LIAQUAT UNIVERSITY OF MEDICAL AND HEALTH SCIENCES, 2021, 20 (01): : 1 - 2
  • [32] Clinical and public health utility of Mycobacterium tuberculosis whole genome sequencing
    Gordon, Alice Kizny
    Marais, Ben
    Walker, Timothy M.
    Sintchenko, Vitali
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2021, 113 : S40 - S42
  • [33] Clinical utility of whole-genome sequencing in a large ALS cohort
    Grassano, Maurizio
    Calvo, Andrea
    Moglia, Cristina
    Canosa, Antonio
    Vasta, Rosario
    Manera, Umberto
    Brunetti, Maura
    Chia, Ruth
    Ding, Jinhui
    Gibbs, Raphael
    Dalgard, Clifton
    Scholz, Sonja
    Mazzini, Letizia
    De Marchi, Fabiola
    Corrado, Lucia
    D'Alfonso, Sandra
    Traynor, Bryan
    Chio, Adriano
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 429
  • [34] "SOMEDAY IT WILL BE THE NORM": PHYSICIAN PERCEPTIONS OF THE CLINICAL UTILITY: OF WHOLE GENOME SEQUENCING
    Vassy, Jason L.
    Christensen, Kurt D.
    Slashinski, Melody J.
    Lautenbach, Denise
    Robinson, Jill Oliver
    Blumenthal-Barby, Jennifer A.
    Feuerman, Lindsay
    Green, Robert C.
    McGuire, Amy L.
    JOURNAL OF GENERAL INTERNAL MEDICINE, 2014, 29 : S4 - S4
  • [35] Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU*
    Sanford, Erica F.
    Clark, Michelle M.
    Farnaes, Lauge
    Williams, Matthew R.
    Perry, James C.
    Ingulli, Elizabeth G.
    Sweeney, Nathaly M.
    Doshi, Ami
    Gold, Jeffrey J.
    Briggs, Benjamin
    Bainbridge, Matthew N.
    Feddock, Michele
    Watkins, Kelly
    Chowdhury, Shimul
    Nahas, Shareef A.
    Dimmock, David P.
    Kingsmore, Stephen F.
    Coufal, Nicole G.
    Batalov, Sergey
    Caylor, Sara
    Ellsworth, Katarzyna
    Friedman, Jennifer
    Salz, Lisa
    Tokita, Mari
    Wigby, Kristen
    Wong, Terence
    PEDIATRIC CRITICAL CARE MEDICINE, 2019, 20 (11) : 1007 - 1020
  • [36] Whole Genome Sequencing Provides an Added Value to the Investigation of Staphylococcal Food Poisoning Outbreaks
    Nouws, Stephanie
    Bogaerts, Bert
    Verhaegen, Bavo
    Denayer, Sarah
    Laeremans, Lasse
    Marchal, Kathleen
    Roosens, Nancy H. C.
    Vanneste, Kevin
    De Keersmaecker, Sigrid C. J.
    FRONTIERS IN MICROBIOLOGY, 2021, 12
  • [37] Whole-genome sequencing to delineate Mycobacterium tuberculosis outbreaks: a retrospective observational study
    Walker, Timothy M.
    Clp, Camilla L.
    Harrell, Ruth H.
    Evans, Jason T.
    Kapatai, Georgia
    Dedicoat, Martin J.
    Eyre, David W.
    Wilson, Daniel J.
    Hawkey, Peter M.
    Crook, Derrick W.
    Parkhill, Julian
    Harris, David
    Walker, A. Sarah
    Bowden, Rory
    Monk, Philip
    Smith, E. Grace
    Peto, Tim E. A.
    LANCET INFECTIOUS DISEASES, 2013, 13 (02): : 137 - 146
  • [38] Whole-Genome Sequencing as Tool for Investigating International Tuberculosis Outbreaks: A Systematic Review
    van der Werf, Marieke J.
    Kodmon, Csaba
    FRONTIERS IN PUBLIC HEALTH, 2019, 7
  • [39] A custom hepatitis A virus assay for whole-genome sequencing
    Cleary, Nora G.
    Bryant, Patrick W.
    Lamson, Daryl M.
    Newman, Alexandra P.
    George, Kirsten St.
    JOURNAL OF VIROLOGICAL METHODS, 2023, 312
  • [40] A novel isothermal whole genome sequencing approach for Monkeypox Virus
    Licheri, Matthias
    Licheri, Manon Flore
    Probst, Lukas
    Sagesser, Cora
    Bittel, Pascal
    Suter-Riniker, Franziska
    Dijkman, Ronald
    SCIENTIFIC REPORTS, 2024, 14 (01):