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Braz. j. med. biol. res ; 27(3): 601-11, Mar. 1994. ilus, graf
Article in English | LILACS | ID: lil-148932

ABSTRACT

1. After MHV3 infection, only macrophages from resistant A/J mice partially restricted virus growth compared to those from susceptible BALB/c mice (2 logs of difference in virus titer). 2. Cellular ribosomal ribonucleic acid (rRNA) synthesis by MHV3-infected macrophages was decreased only in A/J mouse macrophages as indicated by accumulation of the 28S rRNA fraction. 3. The accumulation of viral messenger ribonucleic acids (mRNAs) in MHV3-infected macrophages was also reduced in A/J mouse macrophages compared to BALB/c mice. 4. In pulse-chase experiments of viral protein synthesis, the appearance, glycosylation and cleavage of glycoprotein S, as well as the metabolism of nucleoprotein N were delayed in A/J mouse macrophages. 5. These data show that MHV3 infection of A/J mouse macrophages induced an imbalanced accumulation of the 28S fraction of rRNA. Furthermore the synthesis of mRNAs correlated with viral protein synthesis in both A/J and BALB/c macrophages, but was delayed in A/J mice. 6. These results suggest that the partial restriction of MHV3 replication in macrophages of resistant A/J mice may take place during or before the mRNA synthesis, although it is correlated with the appearance, glycosylation, cleavage and metabolism of viral proteins


Subject(s)
Humans , Mice , Hepatitis, Viral, Animal/metabolism , Coronavirus Infections/microbiology , Macrophages/microbiology , RNA, Ribosomal/biosynthesis , RNA, Messenger/biosynthesis , RNA, Viral/biosynthesis , Murine hepatitis virus/physiology , Macrophages/metabolism , Mice, Inbred A , Mice, Inbred BALB C , Time Factors , Virus Replication
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