Format

Send to

Choose Destination
Virus Genes. 2020 Feb 27. doi: 10.1007/s11262-020-01748-2. [Epub ahead of print]

Epidemiological survey and genetic evolution of H3N2 subtype influenza viruses from stray dogs in Shanghai, China.

Author information

1
Shanghai Animal Disease Control Center, Shanghai, 201103, People's Republic of China.
2
Shanghai Animal Disease Control Center, Shanghai, 201103, People's Republic of China. Jianwhlj@163.com.
3
Shanghai Animal Disease Control Center, Shanghai, 201103, People's Republic of China. Zhaohongjin945@163.com.

Abstract

An avian-origin canine influenza virus (CIV) has recently emerged in dogs and is spreading in China. Given that humans have frequent contact with dogs, this has prompted an increased emphasis on biosafety. In this study, we collected 693 nasal swab samples and 800 blood samples from stray dogs in animal shelters to survey canine influenza epidemiology and characterize the evolution of CIV H3N2 in Shanghai. We tested samples for canine influenza antibodies and canine influenza RNA in January-May, 2019, and the results showed that the positive rate was 17.62% by ELISA, 15.75% by microneutralization (MN) assay, and 18.51% by real time RT-PCR, respectively. We also performed phylogenetic and genomic analysis on six H3N2 CIV isolates. The H3N2 viruses which prevailed in Shanghai originated from Beijing and Jiangsu isolates. Phylogenetic analysis showed that the sequences of CIV isolates have multiple amino acid antigenic drifts, deletions, and substitutions. The time of the most recent common ancestor (TMRCA) of HA and NA was 2004 and 2005, respectively. Notably, the substitution, 146S, in hemagglutinin and the deletion in the neuraminidase (NA) stalk region we found in this study warrant attention because they have frequently been identified in human influenza viruses. The potential adaptation of this CIV H3N2 clade to mammals and its public health threat should be further evaluated.

KEYWORDS:

CIV; Epidemiology; Evolution; Genomic analysis; Phylogeny

PMID:
32107672
DOI:
10.1007/s11262-020-01748-2

Supplemental Content

Full text links

Icon for Springer
Loading ...
Support Center