Evolution of the hemagglutinin gene of H3N8 canine influenza virus in dogs

• Published in: Virus genes 2014-12, Vol.49 (3), p.393-399
• Main Authors: Pecoraro, Heidi L, Bennett, Susi, Spindel, Miranda E, Landolt, Gabriele A
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution; amino acids; Animals; antigenic variation; Biomedical and Life Sciences; Biomedicine; Cluster Analysis; Colorado; Dog Diseases - virology; Dogs; Epitopes - genetics; Evolution, Molecular; genes; Genetic Variation; Hemagglutinin Glycoproteins, Influenza Virus - genetics; hemagglutinins; Influenza A virus; Influenza A Virus, H3N8 Subtype - enzymology; Influenza A Virus, H3N8 Subtype - genetics; Influenza A Virus, H3N8 Subtype - isolation & purification; Influenza virus; Medical Microbiology; Molecular Sequence Data; monitoring; New York; Orthomyxoviridae Infections - veterinary; Orthomyxoviridae Infections - virology; phylogeny; Phylogeography; Plant Sciences; RNA, Viral - genetics; Sequence Analysis, DNA; Sequence Homology; South Carolina; Virology
• ISSN: 0920-8569; 1572-994X
• DOI: 10.1007/s11262-014-1102-8

With the widespread use of a recently developed canine influenza virus (CIV) H3N8 vaccine, continual molecular evaluation of circulating CIVs is necessary for monitoring antigenic drift. The aim of this project was to further describe the genetic evolution of CIV, as well as determine any genetic variation within potential antigenic regions that might result in antigenic drift. To this end, the hemagglutinin gene of 19 CIV isolates from dogs residing in Colorado, New York, and South Carolina humane shelters was sequenced and compared to CIV strains isolated during 2003–2012. Phylogenetic analysis suggests that CIV might be diverging into two geographically distinct lineages. Using a mixed-effects model for evolution and single likelihood ancestor counting methods, several amino acid sites were found to be undergoing selection pressure. Additionally, a total of six amino acid changes were observed in two possible antigenic sites for CIVs isolated from Colorado and New York humane shelters between 2009 and 2011. As CIV isolates might be diverging into geographically distinct lineages, further experiments are warranted to determine the extent of antigenic drift occurring within circulating CIV.