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Volume 20, Number 12—December 2014
Dispatch

Equine Influenza A(H3N8) Virus Infection in Cats

Shuo Su1, Lifang Wang1, Xinliang Fu, Shuyi He, Malin Hong, Pei Zhou, Alexander LaiComments to Author , Gregory C. Gray, and Shoujun LiComments to Author 
Author affiliations: South China Agricultural University, Guangzhou, China (S. Su, L. Wang, X. Fu, S. He, M. Hong, P. Zhou, S. Li); Kentucky State University, Frankfort, Kentucky, USA (A. Lai); University of Florida, Gainesville, Florida, USA (G. Gray); Key Laboratory of Comprehensive Prevention and Control for Severe Clinical Animal Diseases of Guangdong Province, Guangzhou (S. Su, M. Hong, P. Zhou, S. Li)

Main Article

Figure 1

Results of virus titration and hemagglutination-inhibition assay for the cohort of cats inoculated with equine influenza A(H3N8) virus and the contact cohort. Virus shedding was titrated in MDCK cells. Virus titer is shown as log10 median tissue culture infective dose (TCID50) (solid line and circles, inoculated cohort; dashed line and triangles, contact cohort). Hemagglutination-inhibition assay of serum samples was conducted by using 1% horse erythrocytes (black bars, inoculated; white bars, c

Figure 1. Results of virus titration and hemagglutination-inhibition assay for the cohort of cats inoculated with equine influenza A(H3N8) virus and the contact cohort. Virus shedding was titrated in MDCK cells. Virus titer is shown as log10 median tissue culture infective dose (TCID50) (solid line and circles, inoculated cohort; dashed line and triangles, contact cohort). Hemagglutination-inhibition assay of serum samples was conducted by using 1% horse erythrocytes (black bars, inoculated; white bars, contact cohort). Error bars indicate SEM.

Main Article

1These authors contributed equally to this work.

Page created: November 19, 2014
Page updated: November 19, 2014
Page reviewed: November 19, 2014
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