Publication

Duration and Density of Fecal Rotavirus Shedding in Vaccinated Malawian Children With Rotavirus Gastroenteritis

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Persistent URL
Last modified
  • 05/20/2025
Type of Material
Authors
    Aisleen Bennett, University of MalawiLouisa Pollock, University of MalawiKhuzwayo C. Jere, University of MalawiVirginia E. Pitzer, Yale UniversityBenjamin Lopman, Emory UniversityNaor Bar-Zeev, University of MalawiMiren Iturriza-Gomara, University of MalawiNigel A. Cunliffe, University of Malawi
Language
  • English
Date
  • 2020-12-15
Publisher
  • OXFORD UNIV PRESS INC
Publication Version
Copyright Statement
  • © The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 222
Issue
  • 12
Start Page
  • 2035
End Page
  • 2040
Grant/Funding Information
  • This work was supported by Wellcome Trust Clinical PhD Fellowships (grant numbers 102466/Z/13/A to A. B. and 102464/Z/13/A to L. P.); the Wellcome Trust Programme (grant number 091909/Z/10/Z); the Malawi Liverpool Wellcome Trust (MLW) Programme Core Grant Strategic Award (grant number 101113/Z/13/Z); and the US National Institutes of Health (grant number R01-AI112970 to V. E. P.).
Supplemental Material (URL)
Abstract
  • Quantifying rotavirus shedding among vaccinated individuals will aid understanding of vaccine indirect effects. Serial stool samples were collected from 196 children who presented with rotavirus gastroenteritis to health facilities in Blantyre, Malawi, and were tested for rotavirus using a VP6 semi-quantitative, real-time polymerase chain reaction. The median duration of fecal shedding was 28 days (95% CI, 19-28). The median copy numbers for peak shedding were 1.99 × 107 (interquartile range, 3.39 × 106 to 6.37 × 107). The fecal viral load was positively associated with disease severity and negatively associated with serum anti-rotavirus immunoglobin A. High and persistent rotavirus shedding among vaccinated children with breakthrough disease may contribute to ongoing transmission in this setting.
Author Notes
  • Aisleen Bennett, Institute of Infection and Global Health, The Ronald Ross Building, University of Liverpool, 8 West Derby Street, Liverpool L69 7BE, UK abennett@sgul.ac.uk
Keywords
Research Categories
  • Biology, Microbiology
  • Health Sciences, Immunology
  • Biology, Virology

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