Virological self-sampling to monitor influenza antiviral susceptibility in a community cohort

Angie Lackenby*, Alex Elliot, Cassandra Powers, Nicholas Andrews, Joanna Ellis, Alison Bermingham, Catherine Thompson, Monica Galiano, Shirley Large, Hayley Durnall, Douglas Fleming, Gillian Smith, Maria Zambon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

To perform antiviral susceptibility monitoring of treated individuals in the community during the 2009 influenza A(H1N1) pandemic in England. Patients and methods: Between 200 and 400 patients were enrolled daily through the National Pandemic Flu Service (NPFS) and issued with a self-sampling kit. Initially, only persons aged 16 and over were eligible, but from 12 November (week 45), self-sampling was extended to include school-age children (5 years and older). All samples received were screened for influenza A(H1N1)pdm09 as well as seasonal influenza [A(H1N1), A(H3N2) and influenza B] by a combination of RT-PCR and virus isolation methods. Influenza A(H1N1)pdm09 RT-PCR-positive samples were screened for the oseltamivir resistance-inducing H275Y substitution, and a subset of samples also underwent phenotypic antiviral susceptibility testing by enzyme inhibition assay. We were able to detect virus by RT-PCR in self-taken samples and recovered infectious virus enabling further virological characterization. The majority of influenza A(H1N1)pdm09 RT-PCR-positive NPFS samples (n-1273) were taken after oseltamivir treatment had begun. No reduction in phenotypic susceptibility to neuraminidase inhibitors was detected, but five cases with minority quasi-species of oseltamivir-resistant virus (anH275Y amino acid substitution in neuraminidase) were detected. Self-sampling is a useful tool for community surveillance, particularly for the follow-up of drugtreated patients. The virological study of self-taken samples fromthe NPFS provided a unique opportunity to evaluate the emergence of oseltamivir resistance in treated individuals with mild illness in the community, a target population that may not be captured by traditional sentinel surveillance schemes.

Original languageEnglish
Pages (from-to)2324-2331
Number of pages8
JournalJournal of Antimicrobial Chemotherapy
Volume68
Issue number10
DOIs
Publication statusPublished - Oct 2013

Bibliographical note

Funding Information:
This work was supported by the Health Protection Agency (now known as Public Health England), as part of the national influenza surveillance capacity. Virological characterization, including antiviral susceptibility laboratory analyses, was supported by a research grant from the National Institute for Health Research, UK and Health Protection Agency, UK.

Funding Information:
D. M. F. has received funding to attend influenza related meetings and has received consultancy fees from influenza vaccine manufacturers. A. L. and M. Z. participated in studies with the University of Leicester, funded by Roche. A. L. received funding from Roche for assay development and from Toyama to attend a project meeting. All other authors: none to declare.

Keywords

  • Influenza virus
  • Oseltamivir
  • Pandemic
  • Surveillance
  • Zanamivir

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