Abstract

Past influenza pandemics have been characterized by the signature feature of multiple waves. However, the reasons for multiple waves in a pandemic are not understood. Successive waves in the 2009 influenza pandemic, with a sharp increase in hospitalized and fatal cases, occurred in Taiwan during the winter of 2010. In this study, we sought to discover possible contributors to the multiple waves in this influenza pandemic. We conducted a large-scale analysis of 4703 isolates in an unbiased manner to monitor the emergence, dominance and replacement of various variants. Based on the data from influenza surveillance and epidemic curves of each variant clade, we defined virologically and temporally distinct waves of the 2009 pandemic in Taiwan from May 2009 to April 2011 as waves 1 and 2, an interwave period and wave 3. Except for wave 3, each wave was dominated by one distinct variant. In wave 3, three variants emerged and co-circulated, and formed distinct phylogenetic clades, based on the hemagglutinin (HA) genes and other segments. The severity of influenza was represented as the case fatality ratio (CFR) in the hospitalized cases. The CFRs in waves 1 and 2, the interwave period and wave 3 were 6.4%, 5.1%, 15.2% and 9.8%, respectively. The results highlight the association of virus evolution and variable influenza severity. Further analysis revealed that the major affected groups were shifted in the waves to older individuals, who had higher age-specific CFRs. The successive pandemic waves create challenges for the strategic preparedness of health authorities and make the pandemic uncertain and variable. Our findings indicate that the emergence of new variants and age shift to high fatality groups might contribute potentially to the occurrence of successive severe pandemic waves and offer insights into the adjustment of national responses to mitigate influenza pandemics.

Highlights

  • Since an influenza outbreak caused by swine-origin influenza A (H1N1) viruses was detected initially in Mexico and USA during March and April 2009 [1], the viruses spread rapidly to an increasing number of countries

  • Past influenza pandemics, such as those caused by influenza A (H1N1) from 1918 to 1919, influenza A (H2N2) from 1957 to 1963 and influenza A (H3N2) from 1968 to 1970, have been characterized by several distinct features, including changes in the virus subtype, shifts of the highest death rates to younger populations, multiple waves, higher transmissibility than seasonal influenza, and varying impacts in different geographic regions [16]

  • In the successive wave from December 2010, the new genetic variants of clades 9, 10 and 11 viruses emerged with an increase in case fatality ratio (CFR) from 6.4% and 5.1% to 9.8% (p,0.05), indicating that successive severe waves of the 2009 pandemic occurred in Taiwan

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Summary

Introduction

Since an influenza outbreak caused by swine-origin influenza A (H1N1) viruses was detected initially in Mexico and USA during March and April 2009 [1], the viruses spread rapidly to an increasing number of countries. During the early stage of the 2009 pandemic, data from genetic analyses suggested that the influenza A (H1N1) 2009 viruses (termed ‘‘2009 H1N1 viruses’’ for convenience) had begun to evolve and diversified from April 1 to July 9, 2009 into at least 7 clades (clades 1–7) with spatial and geographic patterns [2], and the viruses in the early stage did not possess genomic signatures associated with high pathogenicity in the PB2, PB1-F2, HA and NS1 proteins [3]. The clade 7 viruses with a signature S220T substitution in the HA protein have spread more widely and become a globally major strain, and this dominated early in New York from April to July 2009 [4]. The severity of the 2009 pandemic in the following years remains uncertain

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