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J Bacteriol. 1961 September; 82(3): 449-457
Copyright ©, 1961, The Williams & Wilkins Company. All Rights Reserved.

GROWTH OF VENEZUELAN EQUINE ENCEPHALOMYELITIS VIRUS IN L CELLS II.

Growth in Submerged Culture

Frank M. Hardy1 and Arthur Brown

a U. S. Army Chemical Corps, Fort Detrick, Frederick, Maryland

ABSTRACT

HARDY, FRANK M. (U. S. Army Chemical Corps, Fort Detrick, Frederick, Maryland), AND ARTHUR BROWN. Growth of Venezuelan equine encephalomyelitis virus in L cells. II. Growth in submerged culture. J. Bacteriol. 82:449–457. 1961.—The detailed kinetics of Venezuelan equine encephalomyelitis virus multiplication and release and the progressive cell death due to the virus infection were studied in a uniformly susceptible L cell population. The adsorption phase was complete in approximately 15 min with multiplicities of 1, 10, and 100 MICLD50. An eclipse phase showing the disappearance of some of the infectious virus activity lasted between 3 and 4 hr. An exponential increase of cell-associated and free virus then occurred until peak titer was reached (16 to 18 hr). Relatively constant titers of cell-associated or free virus were obtained from the time peak titer was attained until the 52nd hour of incubation. At that time the cell-associated titer declined more rapidly than the free virus titer. These constant titers, however, masked a continued production and release of new infectious virus. By viable and nonviable cell counts, it was determined that cell death occurred relatively late in the phase of constant growth and release.


FOOTNOTES

1 Present address: Walter Reed Army Medical Unit, Fort Detrick, Frederick, Md.


J Bacteriol. 1961 September; 82(3): 449-457
Copyright ©, 1961, The Williams & Wilkins Company. All Rights Reserved.







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