Phylogenetically distinct equine influenza viruses show different tropism for the swine respiratory tract

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Abstract

Influenza A viruses circulate in a wide range of animals. H3N8 equine influenza virus (EIV) is an avian-origin virus that has established in dogs as canine influenza virus (CIV) and has also been isolated from camels and pigs. Previous work suggests that mutations acquired during EIV evolution might have played a role in CIV emergence. Given the potential role of pigs as a source of human infections, we determined the ability of H3N8 EIVs to replicate in pig cell lines and in respiratory explants. We show that phylogenetically distinct EIVs display different infection phenotypes along the pig respiratory tract, but not in cell lines. Our results suggest that EIV displays a dynamic host range along its evolutionary history, supporting the view that evolutionary processes play important roles in host range and tropism and also underscoring the utility of using explant cultures to study influenza pathogenesis.

Figures

  • Fig. 1. Growth kinetics of evolutionary distinct H3N8 EIVs in swine cell lines. (a) Newborn pig trachea cells. (b) Newborn swine kidney cells. Vertical bars show the mean and SD of three independent experiments.
  • Fig. 2. Infection of explants derived from swine nasal mucosa and trachea with evolutionary distinct H3N8 EIVs. (a) Histological features of swine nasal mucosa explants infected with H3N2 SIV (positive control) and various H3N8 EIVs (Uruguay/63, Fontainebleau/79, Argentina/95 and South Africa/2003). Lesions are shown in sections stained with haematoxylin and eosin (H&E). Infected cells were detected by immunohistochemical (IHC) staining of the NP viral protein. Positive cells are stained in brown. Black horizontal bars represent 50 mm. (b) Growth kinetics of the viruses described in (a) in swine tracheal explants. Dots represent values of individual replicates, * P,0.05. (c) Graphical representation of bead clearance assays in infected and control swine tracheal explants. Lines represent the average time to clear the beads in three independent experiments. Error bars represent SEM. (d) Histological features of swine tracheal explants infected with the viruses described in (a). Lesions and infected cells are described as in (a). Bars, 50 mm. Panels (a) and (c) show explants at day two p.i.
  • Fig. 3. Uruguay/63 replicates in swine lung explants at higher levels than other EIVs. (a) Immunohistochemical detection of viral nucleoprotein in lung explants infected with the same viruses as in Figs 1 and 2. Positive cells are stained brown. Bars, 50 mm. (b) Growth kinetics of the viruses in swine lung explants. Dots represent values of individual replicates, ****P,0.0001.

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Patrono, L. V., Bonfante, F., Zanardello, C., Terregino, C., Capua, I., & Murcia, P. R. (2015). Phylogenetically distinct equine influenza viruses show different tropism for the swine respiratory tract. Journal of General Virology, 96(5), 969–974. https://doi.org/10.1099/vir.0.000049

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