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Published on: August 29, 2017
Genetic Lineage and Reassortment of Influenza C Viruses Circulating between 1947 and 2014
Yoko Matsuzaki1, Kanetsu Sugawara2, Yuki Furuse3
1Department of Infectious Diseases, Yamagata University Faculty of Medicine, Yamagata, Japan matuzaki@med.id.yamagata-u.ac.jp.
Abstract:
Since influenza C virus was first isolated in 1947, the virus has been only occasionally isolated by cell culture; there are only four strains for which complete genome sequences are registered. Here, we analyzed a total of 106 complete genomes, ranging from the first isolate from 1947 to recent isolates from 2014, to determine the genetic lineages of influenza C virus, the reassortment events, and the rates of nucleotide substitution. The results showed that there are six lineages, named C/Taylor, C/Mississippi, C/Aichi, C/Yamagata, C/Kanagawa, and C/Sao Paulo. They contain both antigenic and genetic lineages of the hemagglutinin-esterase (HE) gene, and the internal genes PB2, PB1, P3, NP, M, and NS are divided into two major lineages, a C/Mississippi/80-related lineage and a C/Yamagata/81-related lineage. Reassortment events were found over the entire period of 68 years. Several outbreaks of influenza C virus between 1990 and 2014 in Japan consisted of reassortant viruses, suggesting that the genomic constellation is related to influenza C virus epidemics. The nucleotide sequences were highly homologous to each other. The minimum percent identity between viruses ranged from 91.1% for the HE gene to 96.1% for the M gene, and the rate of nucleotide substitution for the HE gene was the highest, at 5.20 × 10(-4) substitutions/site/year. These results indicate that reassortment is an important factor that increases the genetic diversity of influenza C virus, resulting in its ability to prevail in humans. IMPORTANCE Influenza C virus is a pathogen that causes acute respiratory illness in children and results in hospitalization of infants. We previously demonstrated (Y. Matsuzaki et al., J Clin Virol 61:87-93, 2014, http://dx.doi.org/10.1016/j.jcv.2014.06.017) that periodic epidemics of this virus occurred in Japan between 1996 and 2014 and that replacement of the dominant antigenic group occurred every several years as a result of selection by herd immunity. However, the antigenicity of the HE glycoprotein is highly stable, and antigenic drift has not occurred for at least 30 years. Here, we analyzed a total of 106 complete genomes spanning 68 years for the first time, and we found that influenza C viruses are circulating worldwide while undergoing reassortment as well as selection by herd immunity, resulting in an increased ability to prevail in humans. The results presented in this study contribute to the understanding of the evolution, including reassortment events, underlying influenza C virus epidemics.
Insights
Influenza C virus genetic diversity is driven by reassortment, leading to six lineages and contributing to its prevalence in humans. This study analyzed 106 genomes over 68 years to understand its evolution.
Area of Science:
- Virology
- Evolutionary Biology
- Genetics
Background:
- Influenza C virus (ICV) causes acute respiratory illness, particularly in children and infants.
- Limited genomic data has historically hindered understanding of ICV evolution.
- Previous work indicated periodic ICV epidemics in Japan and antigenic stability of the HE glycoprotein.
Purpose of the Study:
- To determine the genetic lineages, reassortment events, and nucleotide substitution rates of ICV.
- To analyze the evolutionary dynamics of ICV over a 68-year period.
- To understand the factors contributing to ICV's ability to prevail in humans.
Main Methods:
- Analysis of 106 complete ICV genomes from 1947 to 2014.
- Phylogenetic analysis to identify genetic lineages.
- Calculation of nucleotide substitution rates and identification of reassortment events.
Main Results:
- Identification of six distinct ICV lineages (C/Taylor, C/Mississippi, C/Aichi, C/Yamagata, C/Kanagawa, C/Sao Paulo).
- Detection of reassortment events throughout the 68-year study period, linked to Japanese outbreaks.
- High nucleotide sequence homology (91.1%-96.1%) with the highest substitution rate in the HE gene (5.20 × 10⁻⁴ substitutions/site/year).
Conclusions:
- Reassortment is a key driver of ICV genetic diversity and adaptation.
- Genomic constellation of reassortant viruses correlates with ICV epidemics.
- ICV circulates globally, evolving through reassortment and herd immunity selection, enhancing its human prevalence.
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