Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/92478
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Type: Journal article
Title: Sequencing and analysis of globally obtained human respiratory syncytial virus A and B genomes
Author: Bose, M.
He, J.
Shrivastava, S.
Nelson, M.
Bera, J.
Halpin, R.
Town, C.
Lorenzi, H.
Noyola, D.
Falcone, V.
Gerna, G.
De Beenhouwer, H.
Videla, C.
Kok, T.
Venter, M.
Williams, J.
Henrickson, K.
Citation: PLoS One, 2015; 10(3):e0120098-1-e0120098-22
Publisher: Public Library of Science
Issue Date: 2015
ISSN: 1932-6203
1932-6203
Statement of
Responsibility: 
Michael E. Bose, Jie He, Susmita Shrivastava, Martha I. Nelson, Jayati Bera, Rebecca A. Halpin, Christopher D. Town, Hernan A. Lorenzi, Daniel E. Noyola, Valeria Falcone, Giuseppe Gerna, Hans De Beenhouwer, Cristina Videla, Tuckweng Kok, Marietjie Venter, John V. Williams, Kelly J. Henrickson
Abstract: BACKGROUND: Human respiratory syncytial virus (RSV) is the leading cause of respiratory tract infections in children globally, with nearly all children experiencing at least one infection by the age of two. Partial sequencing of the attachment glycoprotein gene is conducted routinely for genotyping, but relatively few whole genome sequences are available for RSV. The goal of our study was to sequence the genomes of RSV strains collected from multiple countries to further understand the global diversity of RSV at a whole-genome level. METHODS: We collected RSV samples and isolates from Mexico, Argentina, Belgium, Italy, Germany, Australia, South Africa, and the USA from the years 1998-2010. Both Sanger and next-generation sequencing with the Illumina and 454 platforms were used to sequence the whole genomes of RSV A and B. Phylogenetic analyses were performed using the Bayesian and maximum likelihood methods of phylogenetic inference. RESULTS: We sequenced the genomes of 34 RSVA and 23 RSVB viruses. Phylogenetic analysis showed that the RSVA genome evolves at an estimated rate of 6.72 × 10(-4) substitutions/site/year (95% HPD 5.61 × 10(-4) to 7.6 × 10(-4)) and for RSVB the evolutionary rate was 7.69 × 10(-4) substitutions/site/year (95% HPD 6.81 × 10(-4) to 8.62 × 10(-4)). We found multiple clades co-circulating globally for both RSV A and B. The predominant clades were GA2 and GA5 for RSVA and BA for RSVB. CONCLUSIONS: Our analyses showed that RSV circulates on a global scale with the same predominant clades of viruses being found in countries around the world. However, the distribution of clades can change rapidly as new strains emerge. We did not observe a strong spatial structure in our trees, with the same three main clades of RSV co-circulating globally, suggesting that the evolution of RSV is not strongly regionalized.
Keywords: Humans; Respiratory Syncytial Virus, Human; Respiratory Syncytial Virus Infections; Evolution, Molecular; Phylogeny; Base Sequence; Polymorphism, Genetic; Genome, Viral; Molecular Sequence Data
Description: Published: March 20, 2015
Rights: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication
RMID: 0030028627
DOI: 10.1371/journal.pone.0120098
Appears in Collections:IPAS publications

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