In the course of investigations concerned with problems relative to the pathogenesis of primary atypical pneumonia, a study was undertaken on the effects of inoculating mice with both a virus and a bacterium. The virus employed in these experiments is known as pneumonia virus of mice, and will hereafter be designated PVM. The bacterium used is a non-hemolytic streptococcus, designated streptococcus MG.When the first experiments were carried out, it was considered that either of two possible results might develop; first, that streptococcus MG would have no discernible influence en the course of an infection induced by PVM; or second, that it might, by contributing to the establishment of a complex infection, cause the results to be more severe than those of infections induced by PVM alone. Surprisingly, neither possibility evolved; instead, the inoculation of streptococcus MG in mice which previously had been inoculated with PVM resulted in a distinctly less severe infection.This unexpected finding was investigated in detail. It is the purpose of this paper to present the results of studies on the modifying effect of certain bacterial species upon the course of infection with PVM. It will be shown that a number of bacterial species are capable of causing such an effect and that this modification, in striking degree, is obtained when suitable bacteria are given either some days before or after inoculation with this virus. Evidence is presented which indicates that this modification phenomenon is the result of inhibition of multiplication of PVM in lung tissue infected with the virus. In addition, data are presented which suggest that the substance responsible for modification with respect to this virus may be polysaccharide in nature.
MethodsVirus.NPneumonia virus of mice (PVM), strain 15 (1), was used exclusively. It was mainmined by occasional lung passage in albino Swiss mice and stored at -70°C. in a manner identical with that described previously (2).Virus Tilration$.NTitrations of PVM were carried out in groups of albino Swiss mice. Serial decimal dilutions were employed; each dilution was tested in a group of six mice and in each titration at least thirty mice were used. The technique of titrations, as well as the method of calculation of the 50 per cent maximum score end point (M.S£0), was identical with 623