Analyses of evolutionary characteristics of the hemagglutinin-esterase gene of influenza C virus during a period of 68 years reveals evolutionary patterns different from influenza A and B viruses

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Abstract

Infections with the influenza C virus causing respiratory symptoms are common, particularly among children. Since isolation and detection of the virus are rarely performed, compared with influenza A and B viruses, the small number of available sequences of the virus makes it difficult to analyze its evolutionary dynamics. Recently, we reported the full genome sequence of 102 strains of the virus. Here, we exploited the data to elucidate the evolutionary characteristics and phylodynamics of the virus compared with influenza A and B viruses. Along with our data, we obtained public sequence data of the hemagglutinin-esterase gene of the virus; the dataset consists of 218 unique sequences of the virus collected from 14 countries between 1947 and 2014. Informatics analyses revealed that (1) multiple lineages have been circulating globally; (2) there have been weak and infrequent selective bottlenecks; (3) the evolutionary rate is low because of weak positive selection and a low capability to induce mutations; and (4) there is no significant positive selection although a few mutations affecting its antigenicity have been induced. The unique evolutionary dynamics of the influenza C virus must be shaped by multiple factors, including virological, immunological, and epidemiological characteristics.

Figures

  • Figure 1. Phylogenetic tree for the hemagglutinin-esterase (HE) gene. The evolutionary history was inferred using the PhyML method for the HE gene (1917 positions) of influenza C viruses. Genetic lineages were defined by our previous study [18]. Approximate likelihood ratio test (aLRT) branch supports at the node to define each lineage are shown. Branches are colored by country.
  • Figure 2. Population dynamics of genetic diversity of each lineage of the influenza C virus. The relative genetic diversity of each lineage of the influenza C virus using the Gaussian Markov random field (GMRF) model. Data are shown after 1985 because few sequences were available before that year. No plots for the C/Aichi lineage and the C/Taylor lineage are presented because of the paucity of sequence data.
  • Table 1. Antigenic groups of the C/Kanagawa lineage.
  • Table 2. Number of isolates for the C/Kanagawa lineage by antigenic group.
  • Figure 3. Time to the most recent common ancestor (tMRCA) of influenza A, B, and C viruses. Temporal trend of tMRCA among contemporaneous (same year) and posterior (at least three years) strains for the HA gene of influenza A and B viruses and the HE gene of the influenza C virus, in panel A, B, and C respectively. We did not plot the tMRCA of all influenza A viruses (A/H3N2, A/H1N1, and A/H1N1pdm together) because they are not monophyly. Additionally, tMRCA of influenza A/H1N1 (before 2009) and influenza A/H1N1pdm (in or after 2009) was calculated separately. Data are shown after 1985, since few sequences were available before that year. Since strains collected over four years are required to calculate tMRCA, sequence data up to 2014 yielded tMRCA up to 2011. No plots for the C/Aichi lineage and the C/Taylor lineage are presented because of the paucity of sequence data.
  • Figure 4. Evolutionary rate and selection pressure of influenza A, B, and C viruses. (A) Evolutionary rate (nucleotide substitution per site per year); (B) selection pressure (relative rate of non-synonymous and synonymous mutation); and (C) relative evolutionary rate of each position in the c don c mpared with the i fluenza A/H3N2 virus. In all thr e panels, results w re calculated using data of the HA gene for influenza A and B viruses and the HE gene fo the influenz C virus. Error b rs show 95% highest posterior density intervals.
  • Figure 5. Site-by-site selection pressure for the HE gene of the influenza C virus. Selection pressure (relative number of non-synonymous substitutions minus synonymous substitutions (dN–dS)) on each codon is shown. Amino acid positions between 1 and 14 encoding signal peptides were excluded for the analysis. Selection pressure on antigenic sites (13 positions in total) is colored in blue. Selection pressure on receptor binding sites (11 positions in total) is colored in red (with statistical significance) and orange (no statistical significance). Black and gray bars indicate significant and non-significant selection pressure on the other positions, respectively. Amino acid positions were depicted with bars for antigenic sites under positive selection and receptor binding sites under negative selection.

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Furuse, Y., Matsuzaki, Y., Nishimura, H., & Oshitani, H. (2016). Analyses of evolutionary characteristics of the hemagglutinin-esterase gene of influenza C virus during a period of 68 years reveals evolutionary patterns different from influenza A and B viruses. Viruses, 8(12). https://doi.org/10.3390/v8120321

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