Preparation of La Crosse Virus Hemagglutinating Antigen in BHK-21 Suspension Cell Cultures

Author:

Chappell W. Adrian1,Halonen Pekka E.1,Toole Roberta F.1,Calisher Charles H.1,Chester Leo1

Affiliation:

1. Arbovirus Unit, Virology Section, National Communicable Disease Center, Atlanta, Georgia 30333

Abstract

Hemagglutinating and complement-fixing antigens of La Crosse virus (California arbovirus group) were produced in serum-free suspension cultures of BHK-21/13S cells. The appearance and production of these antigens were correlated with the titer of infectious virus. No significant differences in antigen titers were produced by varying virus dose 10-fold. Hemagglutinin appeared 6 to 8 hr after inoculation and reached peak titer in 14 to 22 hr. Both β-propiolactone and Tween 80-ether treatment inactivated infectious virus in the antigens. Unlyophilized antigen was stable at -60, 5 and 24 C for at least 117 days but not for 1 year. Lyophilized antigen was stable for at least a year, however, at -20 and 5 C. Cell culture-produced antigen was more sensitive than brain-produced antigen in detecting hemagglutination inhibition antibody in human sera.

Publisher

American Society for Microbiology

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference17 articles.

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3. Encephalitis Surveillance Report. Annual summaries; 1964 1965 1966 and 1967. Encephalitis Surveillance Unit Epidemiology Program National Communicable Disease Center Atlanta.

4. Hemagglutinin of rabies and some other "Bullet Shaped;Halonen P. E.;viruses. Proc. Soc. Exp. Biol. Med.,1968

5. Rubella complement fixing antigen prepared by alkaline extraction of virus grown in suspension culture of BHK-21 cells;Halonen P. E.;Proc. Soc. Exp. Biol. Med.,1967

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