An efficient method for the selective isolation of feline herpesvirus 1 (FHV-1) in feline calicivirus (FCV) coinfected specimens

Author:

Zheng Huanqin1,Wang Baoyan1,YUE Hong1,Yu Xin2,Liu Yang2,Yu Jiayu2,Zhang Jianlong3,Han Kexue4,Han Yinuo4,Su Hanfeng4,Zhu Hongwei1,Zhang Xingxiao3

Affiliation:

1. School of Life Sciences, Ludong University

2. Collaborative Innovation Center for the Pet Infectious Diseases and Public Health in the Middle and Lower Stream Regions of the Yellow River

3. Provincial Engineering Research Center for Pet Animal Vaccines

4. Jinan Baiming Biopharmaceutical Co., Ltd

Abstract

Abstract Background Feline herpesvirus-1 (FHV-1) and feline calicivirus (FCV) are the most common viral pathogens of feline respiratory disease and are highly prevalent in cats worldwide. Coinfection with these viruses is frequent in cats with feline respiratory disease complex (FRDC). It is difficult to isolate pure FHV-1 by conventional laboratory cell culture methods from specimens with FRDC, which brings great trouble to the epidemiological investigation of FHV-1 virus. Methods FCV polyclonal antibodies were obtained by immunizing rabbits, and the coinfected specimens were neutralized with FCV polyclonal antibodies. Then, virus isolation was performed. After several rounds of neutralization, FHV-1 was finally obtained. Results The FCV polyclonal antibody was successfully obtained with neutralizing activities of 1:128, 1:537, and 1:91. After antibody neutralization, the FHV-1 virus was successfully isolated from the coinfected cell culture suspension and confirmed by immunofluorescence and QRT-PCR. Conclusion In this study, all FHV-1 viruses present in the coinfection samples were isolated, without any cross-contamination. This method is also theoretically suitable for the isolation and purification of other FCV coinfections or contaminating disease substances.

Publisher

Research Square Platform LLC

Reference22 articles.

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