Literature DB >> 31319177

Genomic characterization of mumps viruses from a large-scale mumps outbreak in Arkansas, 2016.

Duah Alkam1, Piroon Jenjaroenpun2, Thidathip Wongsurawat3, Zulema Udaondo4, Preecha Patumcharoenpol5, Michael Robeson6, Dirk Haselow7, William Mason8, Intawat Nookaew9, David Ussery10, Se-Ran Jun11.   

Abstract

In 2016, a year-long large-scale mumps outbreak occurred in Arkansas among a highly-vaccinated population. A total of 2954 mumps cases were identified during this outbreak. The majority of cases (1676 (57%)) were school-aged children (5-17 years), 1536 (92%) of these children had completed the mumps vaccination schedule. To weigh the possibility that the mumps virus evaded vaccine-induced immunity in the affected Arkansas population, we established a pipeline for genomic characterization of the outbreak strains. Our pipeline produces whole-genome sequences along with phylogenetic analysis of the outbreak mumps virus strains. We collected buccal swab samples of patients who tested positive for the mumps virus during the 2016 Arkansas outbreak, and used the portable Oxford Nanopore Technology to sequence the extracted strains. Our pipeline identified the genotype of the Arkansas mumps strains as genotype G and presented a genome-based phylogenetic tree with superior resolution to a standard small hydrophobic (SH) gene-based tree. We phylogenetically compared the Arkansas whole-genome sequences to all publicly available mumps strains. While these analyses show that the Arkansas mumps strains are evolutionarily distinct from the vaccine strains, we observed no correlation between vaccination history and phylogenetic grouping. Furthermore, we predicted potential B-cell epitopes encoded by the Arkansas mumps strains using a random forest prediction model trained on antibody-antigen protein structures. Over half of the predicted epitopes of the Jeryl-Lynn vaccine strains in the Hemagglutinin-Neuraminidase (HN) surface glycoprotein (a major target of neutralizing antibodies) region are missing in the Arkansas mumps strains. In-silico analyses of potential epitopes may indicate that the Arkansas mumps strains display antigens with reduced immunogenicity, which may contribute to reduced vaccine effectiveness. However, our in-silico findings should be assessed by robust experiments such as cross neutralization assays. Metadata analysis showed that vaccination history had no effect on the evolution of the Arkansas mumps strains during this outbreak. We conclude that the driving force behind the spread of the mumps virus in the 2016 Arkansas outbreak remains undetermined.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Epitope prediction; Mumps outbreak; Vaccination; Virus resurgence

Mesh:

Substances:

Year:  2019        PMID: 31319177      PMCID: PMC6832845          DOI: 10.1016/j.meegid.2019.103965

Source DB:  PubMed          Journal:  Infect Genet Evol        ISSN: 1567-1348            Impact factor:   3.342


  53 in total

1.  Sensitive quantitative predictions of peptide-MHC binding by a 'Query by Committee' artificial neural network approach.

Authors:  S Buus; S L Lauemøller; P Worning; C Kesmir; T Frimurer; S Corbet; A Fomsgaard; J Hilden; A Holm; S Brunak
Journal:  Tissue Antigens       Date:  2003-11

2.  An increase in the number of mumps cases in the Czech Republic, 2005-2006.

Authors:  N Boxall; M Kubinyiova; V Príkazský; C Benes; J Cástková
Journal:  Euro Surveill       Date:  2008-04-17

Review 3.  Mumps resurgences in the United States: A historical perspective on unexpected elements.

Authors:  Albert E Barskey; John W Glasser; Charles W LeBaron
Journal:  Vaccine       Date:  2009-10-19       Impact factor: 3.641

4.  Sera from different age cohorts in Belgium show limited cross-neutralization between the mumps vaccine and outbreak strains.

Authors:  T Vermeire; C Barbezange; A Francart; A Hamouda; A Litzroth; V Hutse; L Martens; E Vandermarliere; S Van Gucht
Journal:  Clin Microbiol Infect       Date:  2018-11-28       Impact factor: 8.067

5.  Vaccine compliance and the 2016 Arkansas mumps outbreak.

Authors:  Maimuna S Majumder; Colleen M Nguyen; Emily L Cohn; Yulin Hswen; Sumiko R Mekaru; John S Brownstein
Journal:  Lancet Infect Dis       Date:  2017-04       Impact factor: 25.071

6.  Emergent lineages of mumps virus suggest the need for a polyvalent vaccine.

Authors:  Meghan May; Courtney A Rieder; Rebecca J Rowe
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7.  Monitoring Viral Genetic Variation as a Tool To Improve Molecular Diagnostics for Mumps Virus.

Authors:  Meik Dilcher; Kevin Barratt; Jennifer Douglas; Andrew Strathdee; Trevor Anderson; Anja Werno
Journal:  J Clin Microbiol       Date:  2018-09-25       Impact factor: 5.948

Review 8.  Genomic diversity of mumps virus and global distribution of the 12 genotypes.

Authors:  Li Jin; Claes Örvell; Richard Myers; Paul A Rota; Tetsuo Nakayama; Dubravko Forcic; Joanne Hiebert; Kevin E Brown
Journal:  Rev Med Virol       Date:  2014-11-26       Impact factor: 6.989

Review 9.  Mumps.

Authors:  Anders Hviid; Steven Rubin; Kathrin Mühlemann
Journal:  Lancet       Date:  2008-03-15       Impact factor: 79.321

10.  Phylogenetic resolution and quantifying the phylogenetic diversity and dispersion of communities.

Authors:  Nathan G Swenson
Journal:  PLoS One       Date:  2009-02-05       Impact factor: 3.240

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2.  Investigating the etiologic agents of aseptic meningitis outbreak in Iranian children.

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3.  Upward Trends of Parotitis and Mumps in Atlanta over a Decade.

Authors:  Lankala M Reddy; Deborah Bloch; Amanda Mallino; Polly Kumari; Janet Figueroa; Lea Kendrick; Ann Chahroudi; Jessica Tuttle; Ebony Thomas; Claudia R Morris
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4.  Molecular epidemiology of mumps viruses in the Netherlands, 2017-2019.

Authors:  Rogier Bodewes; Linda Reijnen; Jeroen Kerkhof; Jeroen Cremer; Dennis Schmitz; Rob van Binnendijk; Irene K Veldhuijzen
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