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. 2015 May;89(10):5406-18.
doi: 10.1128/JVI.03395-14. Epub 2015 Mar 4.

Origins and Evolutionary Dynamics of H3N2 Canine Influenza Virus

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Origins and Evolutionary Dynamics of H3N2 Canine Influenza Virus

Henan Zhu et al. J Virol. 2015 May.

Abstract

Influenza A viruses (IAVs) are maintained mainly in wild birds, and despite frequent spillover infections of avian IAVs into mammals, only a small number of viruses have become established in mammalian hosts. A new H3N2 canine influenza virus (CIV) of avian origin emerged in Asia in the mid-2000s and is now circulating in dog populations of China and South Korea, and possibly in Thailand. The emergence of CIV provides new opportunities for zoonotic infections and interspecies transmission. We examined 14,764 complete IAV genomes together with all CIV genomes publicly available since its first isolation until 2013. We show that CIV may have originated as early as 1999 as a result of segment reassortment among Eurasian and North American avian IAV lineages. We also identified amino acid changes that might have played a role in CIV emergence, some of which have not been previously identified in other cross-species jumps. CIV evolves at a lower rate than H3N2 human influenza viruses do, and viral phylogenies exhibit geographical structure compatible with high levels of local transmission. We detected multiple intrasubtypic and heterosubtypic reassortment events, including the acquisition of the NS segment of an H5N1 avian influenza virus that had previously been overlooked. In sum, our results provide insight into the adaptive changes required by avian viruses to establish themselves in mammals and also highlight the potential role of dogs to act as intermediate hosts in which viruses with zoonotic and/or pandemic potential could originate, particularly with an estimated dog population of ∼ 700 million.

Importance: Influenza A viruses circulate in humans and animals. This multihost ecology has important implications, as past pandemics were caused by IAVs carrying gene segments of both human and animal origin. Adaptive evolution is central to cross-species jumps, and this is why understanding the evolutionary processes that shape influenza A virus genomes is key to elucidating the mechanisms underpinning viral emergence. An avian-origin canine influenza virus (CIV) has recently emerged in dogs and is spreading in Asia. We reconstructed the evolutionary history of CIV and show that it originated from both Eurasian and North American avian lineages. We also identified the mutations that might have been responsible for the cross-species jump. Finally, we provide evidence of multiple reassortment events between CIV and other influenza viruses (including an H5N1 avian virus). This is a cause for concern, as there is a large global dog population to which humans are highly exposed.

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Figures

FIG 1
FIG 1
Origin of H3N2 CIV. Maximum likelihood trees using an expanded subset derived from a phylogeny comprising 877 IAV sequences representing 14,764 IAV genomes. Colored branches represent distinct lineages as follows. The H3N2 CIV lineage is shown in red, Eurasian avian viruses are shown green, and American avian viruses are shown in blue. Bootstrap values of relevant branches are shown. Arrows indicate gene segments of H3N2 CIV that resulted from heterosubtypic reassortment. The bars are drawn to scale.
FIG 1
FIG 1
Origin of H3N2 CIV. Maximum likelihood trees using an expanded subset derived from a phylogeny comprising 877 IAV sequences representing 14,764 IAV genomes. Colored branches represent distinct lineages as follows. The H3N2 CIV lineage is shown in red, Eurasian avian viruses are shown green, and American avian viruses are shown in blue. Bootstrap values of relevant branches are shown. Arrows indicate gene segments of H3N2 CIV that resulted from heterosubtypic reassortment. The bars are drawn to scale.
FIG 2
FIG 2
Phylogenetic trees of 24 complete genomes of H3N2 CIV collected between 2006 and 2013. The phylogenetic trees for each genomic segment were inferred using MrBayes. The colored boxes indicate the stable clades present among all gene segments with the exception of MP and NS. Clade I is shown by pink, clade II is shown by orange, clade III is shown by yellow, clade IV is shown by green, and clade V is shown by light blue. Circles and squares indicate viruses that underwent homosubtypic and heterosubtypic reassortment, respectively. Posterior probability values are shown for each node.
FIG 2
FIG 2
Phylogenetic trees of 24 complete genomes of H3N2 CIV collected between 2006 and 2013. The phylogenetic trees for each genomic segment were inferred using MrBayes. The colored boxes indicate the stable clades present among all gene segments with the exception of MP and NS. Clade I is shown by pink, clade II is shown by orange, clade III is shown by yellow, clade IV is shown by green, and clade V is shown by light blue. Circles and squares indicate viruses that underwent homosubtypic and heterosubtypic reassortment, respectively. Posterior probability values are shown for each node.
FIG 3
FIG 3
A/canine/Guangdong/2/2007 reassorted with H5N1 avian viruses. (Left) Maximum likelihood phylogenetic tree for 775 NS sequences derived from IAVs of various subtypes. Branches exhibiting H3N2 CIV and H5N1 avian influenza viruses are shown in red and blue, respectively. (Right) Higher magnification of the clade containing H3N2 CIVs and avian H5N1 sequences. The red circle represents the NS sequence of A/canine/Guangdong/2/2007. Bootstrap values are shown for the relevant nodes. The tree was midrooted.
FIG 4
FIG 4
Intrasubtypic reassortment among H3N2 CIVs. The split decomposition network was inferred using Splitstree. Potential reassortment events are shown as reticulation between branches.
FIG 5
FIG 5
Evolutionary rates for avian, canine, human, equine, and swine IAVs. Evolutionary rates for avian (red), canine (green), human (dark blue), equine (light blue) and swine (fuchsia) IAVs are shown. Vertical bars represent 95% HPD of the evolutionary rates estimated by BEAST.

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