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Genomic analysis of respiratory syncytial virus infections in households and utility in inferring who infects the infant

Abstract:
Infants (under 1-year-old) are at most risk of life threatening respiratory syncytial virus (RSV) disease. RSV epidemiological data alone has been insufficient in defining who acquires infection from whom (WAIFW) within households. We investigated RSV genomic variation within and between infected individuals and assessed its potential utility in tracking transmission in households. Over an entire single RSV season in coastal Kenya, nasal swabs were collected from members of 20 households every 3-4 days regardless of symptom status and screened for RSV nucleic acid. Next generation sequencing was used to generate >90% RSV full-length genomes for 51.1% of positive samples (191/374). Single nucleotide polymorphisms (SNPs) observed during household infection outbreaks ranged from 0-21 (median: 3) while SNPs observed during single-host infection episodes ranged from 0-17 (median: 1). Using the viral genomic data alone there was insufficient resolution to fully reconstruct within-household transmission chains. For households with clear index cases, the most likely source of infant infection was via a toddler (aged 1 to <3 years-old) or school-aged (aged 6 to <12 years-old) co-occupant. However, for best resolution of WAIFW within households, we suggest an integrated analysis of RSV genomic and epidemiological data.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41598-019-46509-w

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Tropical Medicine
Role:
Author
ORCID:
0000-0001-9640-7371
More by this author
Role:
Author
ORCID:
0000-0002-0030-7278


Publisher:
Springer Nature
Journal:
Scientific Reports More from this journal
Volume:
9
Issue:
1
Article number:
10076
Publication date:
2019-07-11
Acceptance date:
2019-06-26
DOI:
EISSN:
2045-2322
ISSN:
2045-2322
Pmid:
31296922

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