Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1969 Sep;18(3):433-7.
doi: 10.1128/am.18.3.433-437.1969.

Preparation of La Crosse virus hemagglutinating antigen in BHK-21 suspension cell cultures

Preparation of La Crosse virus hemagglutinating antigen in BHK-21 suspension cell cultures

W A Chappell et al. Appl Microbiol. 1969 Sep.

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 beta-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.

PubMed Disclaimer

References

    1. Am J Trop Med Hyg. 1966 Mar;15(2):199-204 - PubMed
    1. Am J Trop Med Hyg. 1966 Mar;15(2):219-26 - PubMed
    1. Proc Soc Exp Biol Med. 1967 May;125(1):167-72 - PubMed
    1. J Immunol. 1967 Aug;99(2):276-84 - PubMed
    1. Ann Med Exp Biol Fenn. 1967;45(2):182-5 - PubMed

MeSH terms

LinkOut - more resources