Literature DB >> 27081130

Complete Genome Characterization of Two Wild-Type Measles Viruses from Vietnamese Infants during the 2014 Outbreak.

Bas B Oude Munnink1, My V T Phan1, Paul Kellam2, Matthew Cotten3.   

Abstract

A large measles virus outbreak occurred across Vietnam in 2014. We identified and obtained complete measles virus genomes in stool samples collected from two diarrheal pediatric patients in Dong Thap Province. These are the first complete genome sequences of circulating measles viruses in Vietnam during the 2014 measles outbreak.
Copyright © 2016 Oude Munnink et al.

Entities:  

Year:  2016        PMID: 27081130      PMCID: PMC4832158          DOI: 10.1128/genomeA.00250-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Measles virus is a member of the family Paramyxoviridae and causes measles, a highly contagious infectious disease. Measles mainly affects children age <5 years and was responsible for the deaths of 114,900 individuals in 2014 (1). Although measles vaccination is implemented in the Extended Programme for Immunization in Vietnam, measles virus infection is still prevalent in Vietnam, as demonstrated by a recent outbreak of measles virus in 2014 (2). During this outbreak, measles virus was estimated to have caused 30,000 infections, with 146 deaths (2). Until now, there has been only one report on the genome of a measles virus from Vietnam during this outbreak (3), with 2 short regions of the genome sequenced. No full measles virus genomes are available from Vietnam or Southeast Asia, leaving a large knowledge gap on the genetics of the circulating virus. As part of a viral surveillance project in the Dong Thap Province (southern Vietnam) (4), a randomly primed deep-sequencing (agnostic sequencing) method (5) was used to document viral infections associated with diarrhea. Briefly, nucleic acid was purified from fecal samples, converted to double-stranded DNA (dsDNA) using random primers (6), and sequenced with Illumina HiSeq to generate 4 million 250-nucleotide (nt) paired-end reads per sample. Reads were trimmed from the 3′ end to a median Phred score of 35, with a minimum length of 175 nt, and de novo assembled using SPAdes version 3.5.0 (7), followed by improve_assembly (8). The work identified two complete wild-type measles virus genomes in stool samples from 2 diarrheal patients enrolled in 2014, during the period when measles was known to be circulating in Vietnam. The complete genomes of the virus isolates are named MVs/DongThap.VNM/06_14 (D8) (accession no. KU728742) and MVs/DongThap.VNM/08_14 (D8) (accession no. KU728743), in agreement with the WHO guidelines for naming measles virus strains (9). The average genome coverage of both viral genomes was 91- and 1,835-fold, respectively, demonstrating sufficient coverage to reliably assemble the complete genomes. Complete genome analysis revealed that the Vietnamese measles viruses share 99% nucleotide identity to the measles strain MVi/Muenchen.DEU/19.13[D8], the closest relative measles virus strain. The genomes have 9- and 19-nucleotide differences, respectively, compared to the measles strain MVi/Muenchen.DEU/19.13 (D8). No nucleotide changes were observed in the 450 nucleotides that encode the carboxy-terminal region of the nucleoprotein, the region used for genotyping. Both patients were admitted to the Provincial Hospital of Dong Thap due to acute diarrhea, and the generation of whole measles virus genomes from these patients suggests that the episodes of diarrhea reported in these patients may be a consequence of measles virus infection, consistent with previous observations (10). In addition, these patients were 7 and 8 months of age, demonstrating that children can be infected with measles virus before reaching the age of vaccination (9 months). In conclusion, we report the first 2 whole genomes of wild-type measles virus genotype D8 during the 2014 outbreak in Vietnam. The viral genomes belonged to measles virus genogroup D8 and will provide a useful reference for measles surveillance in the region.

Nucleotide sequence accession numbers.

The complete genome sequences of the MVs/DongThap.VNM/06_14 (D8) and the MVs/DongThap.VNM/08_14 (D8) isolates are available at GenBank under the accession numbers KU728742 and KU728743.
  8 in total

1.  SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

Authors:  Anton Bankevich; Sergey Nurk; Dmitry Antipov; Alexey A Gurevich; Mikhail Dvorkin; Alexander S Kulikov; Valery M Lesin; Sergey I Nikolenko; Son Pham; Andrey D Prjibelski; Alexey V Pyshkin; Alexander V Sirotkin; Nikolay Vyahhi; Glenn Tesler; Max A Alekseyev; Pavel A Pevzner
Journal:  J Comput Biol       Date:  2012-04-16       Impact factor: 1.479

2.  Measles virus nomenclature update: 2012.

Authors: 
Journal:  Wkly Epidemiol Rec       Date:  2012-03-02

3.  In Vietnam, an anatomy of a measles outbreak.

Authors:  Leslie Roberts
Journal:  Science       Date:  2015-05-29       Impact factor: 47.728

4.  Etiology of diarrhea in measles.

Authors:  W Varavithya; S Aswasuwana; P Phuapradit; S Louisirirotchanakul; S Supavej; S Nopchinda
Journal:  J Med Assoc Thai       Date:  1989-01

5.  Species-independent detection of RNA virus by representational difference analysis using non-ribosomal hexanucleotides for reverse transcription.

Authors:  Daiji Endoh; Tetsuya Mizutani; Rikio Kirisawa; Yoshiyuki Maki; Hidetoshi Saito; Yasuhiro Kon; Shigeru Morikawa; Masanobu Hayashi
Journal:  Nucleic Acids Res       Date:  2005-04-07       Impact factor: 16.971

6.  Measles Epidemics Among Children in Vietnam: Genomic Characterization of Virus Responsible for Measles Outbreak in Ho Chi Minh City, 2014.

Authors:  Van H Pham; Diem P H Nguyet; Khanh N H Mai; Khanh H Truong; Loc V Huynh; Trang H T Pham; Kenji Abe
Journal:  EBioMedicine       Date:  2014-10-29       Impact factor: 8.143

Review 7.  The Vietnam Initiative on Zoonotic Infections (VIZIONS): A Strategic Approach to Studying Emerging Zoonotic Infectious Diseases.

Authors:  Maia A Rabaa; Ngo Tri Tue; Tran My Phuc; Juan Carrique-Mas; Karen Saylors; Matthew Cotten; Juliet E Bryant; Ho Dang Trung Nghia; Nguyen Van Cuong; Hong Anh Pham; Alessandra Berto; Voong Vinh Phat; Tran Thi Ngoc Dung; Long Hoang Bao; Ngo Thi Hoa; Heiman Wertheim; Behzad Nadjm; Corina Monagin; H Rogier van Doorn; Motiur Rahman; My Phan Vu Tra; James I Campbell; Maciej F Boni; Pham Thi Thanh Tam; Lia van der Hoek; Peter Simmonds; Andrew Rambaut; Tran Khanh Toan; Nguyen Van Vinh Chau; Tran Tinh Hien; Nathan Wolfe; Jeremy J Farrar; Guy Thwaites; Paul Kellam; Mark E J Woolhouse; Stephen Baker
Journal:  Ecohealth       Date:  2015-09-24       Impact factor: 3.184

8.  Full genome virus detection in fecal samples using sensitive nucleic acid preparation, deep sequencing, and a novel iterative sequence classification algorithm.

Authors:  Matthew Cotten; Bas Oude Munnink; Marta Canuti; Martin Deijs; Simon J Watson; Paul Kellam; Lia van der Hoek
Journal:  PLoS One       Date:  2014-04-02       Impact factor: 3.240

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1.  Unbiased whole-genome deep sequencing of human and porcine stool samples reveals circulation of multiple groups of rotaviruses and a putative zoonotic infection.

Authors:  My V T Phan; Pham Hong Anh; Nguyen Van Cuong; Bas B Oude Munnink; Lia van der Hoek; Phuc Tran My; Tue Ngo Tri; Juliet E Bryant; Stephen Baker; Guy Thwaites; Mark Woolhouse; Paul Kellam; Maia A Rabaa; Matthew Cotten
Journal:  Virus Evol       Date:  2016-10-03

2.  Sample descriptors linked to metagenomic sequencing data from human and animal enteric samples from Vietnam.

Authors:  Mark Woolhouse; Jordan Ashworth; Carlijn Bogaardt; Ngo Tri Tue; Steve Baker; Guy Thwaites; Tran My Phuc
Journal:  Sci Data       Date:  2019-10-15       Impact factor: 6.444

  2 in total

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