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Data for Transmission patterns and evolution of respiratory syncytial virus in a community outbreak identified by genomic analysis

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Agoti, Charles N., Munywoki, Patrick K., Cotten, Matthew and Nokes, D. James (2018) Data for Transmission patterns and evolution of respiratory syncytial virus in a community outbreak identified by genomic analysis. [Dataset]

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Official URL: https://doi.org/10.7910/DVN/L9NFPN

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Abstract

Detailed information on the source, spread and evolution of respiratory syncytial virus (RSV) during seasonal community outbreaks remains sparse. Molecular analyses of attachment (G) gene sequences from hospitalized cases suggest that multiple genotypes and variants co-circulate during epidemics and that RSV persistence over successive seasons is characterized by replacement and multiple new introductions of variants. No studies have defined the patterns of introduction, spread and evolution of RSV at the local community and household level. We present a whole genome sequence analysis of 131 RSV group A viruses collected during 6-month household-based RSV infection surveillance in Coastal Kenya, 2010 within an area of 12 km2. RSV infections were identified by regular symptom-independent screening of all household members twice weekly. Phylogenetic analysis revealed that the RSV A viruses in nine households were closely related to genotype GA2 and fell within a single branch of the global phylogeny. Genomic analysis allowed the detection of household-specific variation in seven households. For comparison, using only G gene analysis, household-specific variation was found only in one of the nine households. Nucleotide changes were observed both intra-host (viruses identified from same individual in follow-up sampling) and inter-host (viruses identified from different household members) and these coupled with sampling dates enabled a partial reconstruction of the within household transmission chains. The genomic evolutionary rate for the household dataset was estimated as 2.307 × 10 − 3 (95% highest posterior density: 0.935–4.165× 10 − 3) substitutions/site/year. We conclude that (i) at the household level, most RSV infections arise from the introduction of a single virus variant followed by accumulation of household specific variation and (ii) analysis of complete virus genomes is crucial to better understand viral transmission in the community. A key question arising is whether prevention of RSV introduction or spread within the household by vaccinating key transmitting household members would lead to a reduced onward community-wide transmission.

Item Type: Dataset
Subjects: R Medicine > RC Internal medicine
Divisions: Faculty of Medicine > Warwick Medical School
Type of Data: Experimental data
Library of Congress Subject Headings (LCSH): Respiratory syncytial virus -- Kenya, Genomes -- Analysis, Human gene mapping, Epidemiology -- Mathematical models
Publisher: Harvard Dataverse
Official Date: 16 January 2018
Dates:
DateEvent
16 January 2018Published
Collection date:
Date fromDate to
December 2009June 2010
Status: Not Peer Reviewed
Publication Status: Published
Media of Output: .py
Access rights to Published version: Open Access
Copyright Holders: University of Warwick
Description:

Data record consists of 3 data files in .py format and 3 documents, including a readme for the dataset and a separate readme for the python files.
Python software code/scripts are as follows:
HiLiter_RSVHH.py generates plots of nucleotide changes in RSV genomes occuring across households.
cartman_einfach.py: a simple nucleotide motif counting script using ack, a faster version of grep (http://beyondgrep.com/why-ack/).
csvtofasta_ID26122012.py.
All sequence files are available from the GenBank database (accession numbers KX510136-KX510266)

RIOXX Funder/Project Grant:
Project/Grant IDRIOXX Funder NameFunder ID
077092Wellcome Trusthttp://dx.doi.org/10.13039/100010269
090853Wellcome Trusthttp://dx.doi.org/10.13039/100010269
100542Wellcome Trusthttp://dx.doi.org/10.13039/100010269
102975Wellcome Trusthttp://dx.doi.org/10.13039/100010269
643476H2020 European Research Councilhttp://dx.doi.org/10.13039/100010663
634650H2020 European Research Councilhttp://dx.doi.org/10.13039/100010663
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Contributors:
ContributionNameContributor ID
Contact PersonNokes, D. James35965

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