Beale joined the Boyce Thompson Institute for Plant Research in 1924 where she remained until her retirement in 1952. She originally joined the virology laboratory of
Louis O. Kunkel, whose research focus was on the cause and transmission method of yellows disease in plants. casting suspicion on a bacterial cause. Turning to investigate the leaves of infected plant leaves, Beale developed a bioassay method to track the development of an infection with a 0.5% aqueous solution of iodine green, a revolutionary step in identifying viruses. Beale's landmark contribution to the application of serology in the field of plant virology precipitated as a result of her dissertation work in 1929. She demonstrated that infected leaf sap injected into rabbits could produce polyclonal antibodies in rabbit
antiserum that were not found in the control rabbits (not infected with leaf sap during injections). The antibodies were specific to
Tobacco mosaic virus, thus identifying and characterizing the virus as a pathogenic agent in tobacco mosaic disease. The specificity of the antibody for
Tobacco mosaic virus, being unreactive with other viruses, proved to be a useful tool with which to diagnose a
Tobacco mosaic virus infection. It also allowed for the isolation and characterization of unique strains of
Tobacco mosaic virus, making it possible for her collaborator,
Wendell M. Stanley, to work with a single pure strain. This increased research precision helped facilitate and accelerate Stanley's contributions to the advancement of the
Tobacco mosaic virus field. Furthermore, she demonstrated that
Tobacco mosaic virus in leaf sap could be neutralized, or inactivated, by the antibodies isolated from the antiserum. In conclusion, Beale established the basis of using immunology and serology to define the chemical nature of
Tobacco mosaic virus that could be expanded and applied to the virology field in general. == Legacy ==