Molecular analysis of isolates from influenza B outbreaks in the U.S. and Nepal, 2005

L T Daum1, L C Canas, A I Klimov

  • 1Air Force Institute for Operational Health, Brooks City Base, TX 78235, USA. luke.daum@brooks.af.mil

Insights

Influenza B virus outbreaks in 2005 showed genetic and antigenic divergence from vaccine strains. Monitoring hemagglutinin (HA), neuraminidase (NA), and NB genes is crucial for tracking influenza B evolution.

Area of Science:

  • Virology
  • Molecular Biology
  • Epidemiology

Background:

  • Influenza B viruses circulate in two distinct lineages: B/Yamagata and B/Victoria.
  • Vaccine strains are selected based on prototype strains like B/Yamagata/16/88 and B/Victoria/2/87.
  • Antigenic and genetic drift in influenza viruses necessitate ongoing surveillance.

Purpose of the Study:

  • To analyze the antigenic and genetic characteristics of influenza B virus isolates from 2005 outbreaks.
  • To compare these isolates with contemporary vaccine strains.
  • To assess the potential for future circulation and the need for molecular monitoring.

Main Methods:

  • Antigenic analysis using hemagglutinin inhibition tests.
  • Nucleotide sequence analysis of hemagglutinin (HA1), neuraminidase (NA), and NB genes.
  • Comparison of isolate sequences and reactivity with vaccine strains.

Main Results:

  • 2005 influenza B isolates showed reduced reactivity to both B/Yamagata-like and B/Victoria-like vaccine strains.
  • The majority of isolates were antigenically similar to B/Hawaii/33/2004 (B/Victoria-like).
  • Sequence analysis revealed a mix of B/Victoria-like HA and B/Yamagata-like NA and NB genes in most isolates.
  • Outbreak isolates were genetically similar to the proposed 2006 vaccine strain B/Malaysia/2506/2004.

Conclusions:

  • The 2005 influenza B outbreaks involved viruses antigenically and genetically distinct from current vaccine strains.
  • These viruses possess genetic similarities to the proposed 2006 vaccine strain.
  • Widespread geographical occurrence suggests continued circulation, highlighting the importance of molecular surveillance for HA, NA, and NB gene variations.