Affiliations 

  • 1 Department of Pathology, Immunology, and Microbiology, Faculty of Medicine American University of BeirutBeirut, Lebanon; Center for Infectious Disease Research, Faculty of Medicine American University of BeirutBeirut, Lebanon
  • 2 Division of International Health (Public Health), Graduate School of Medical and Dental Sciences, Niigata University Niigata, Japan
  • 3 Influenza and Prion Disease Research Center, National Institute of Animal Health, National Agriculture and Food Research Organization Ibaraki, Japan
  • 4 Department of Traditional Medicine Nay Pyi Taw, Myanmar
  • 5 Sanpya Hospital Yangon, Myanmar
  • 6 National Health Laboratory Yangon, Myanmar
  • 7 Pyinmana Township Hospital Nay Pyi Taw, Myanmar
  • 8 National Institute of Hygiene and Epidemiology Hanoi, Vietnam
  • 9 Division of International Health (Public Health), Graduate School of Medical and Dental Sciences, Niigata UniversityNiigata, Japan; Department of Community Health, Faculty of Medicine, UKM Medical CentreKuala Lumpur, Malaysia
  • 10 Clinical Microbiology, University Hospitals LeicesterLeicester, UK; Department of Infection, Immunity and Inflammation, University of LeicesterLeceister, UK
  • 11 Center for Infectious Disease Research, Faculty of Medicine American University of BeirutBeirut, Lebanon; Division of Pediatric Infectious Diseases, Department of Pediatrics and Adolescent Medicine and the Center for Infectious Diseases Research, American University of Beirut Medical CenterBeirut, Lebanon
Front Microbiol, 2016;7:262.
PMID: 27014195 DOI: 10.3389/fmicb.2016.00262

Abstract

Influenza A viruses evolve at a high rate requiring continuous monitoring to maintain the efficacy of vaccines and antiviral drugs. We performed next generation sequencing analysis of 100 influenza A/H3N2 isolates collected in four Asian countries (Japan, Lebanon, Myanmar, and Vietnam) during 2012-2015. Phylogenetic analysis revealed several reassortment events leading to the circulation of multiple clades within the same season. This was particularly evident during the 2013 and 2013/2014 seasons. Importantly, our data showed that certain lineages appeared to be fitter and were able to persist into the following season. The majority of A/H3N2 viruses continued to harbor the M2-S31N mutation conferring amantadine-resistance. In addition, an S31D mutation in the M2-protein, conferring a similar level of resistance as the S31N mutation, was detected in three isolates obtained in Japan during the 2014/2015 season. None of the isolates possessed the NA-H274Y mutation conferring oseltamivir-resistance, though a few isolates were found to contain mutations at the catalytic residue 151 (D151A/G/N or V) of the NA protein. These variations did not alter the susceptibility to neuraminidase inhibitors and were not detected in the original clinical specimens, suggesting that they had been acquired during their passage in MDCK cells. Novel polymorphisms were detected in the PB1-F2 open-reading frame resulting in truncations in the protein of 24-34 aminoacids in length. Thus, this study has demonstrated the utility of monitoring the full genome of influenza viruses to allow the detection of the potentially fittest lineages. This enhances our ability to predict the strain(s) most likely to persist into the following seasons and predict the potential degree of vaccine match or mismatch with the seasonal influenza season for that year. This will enable the public health and clinical teams to prepare for any related healthcare burden, depending on whether the vaccine match is predicted to be good or poor for that season.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.