Virus Progeny of Murine Cytomegalovirus Bacterial Artificial Chromosome pSM3fr Show Reduced Growth in Salivary Glands due to a Fixed Mutation of MCK-2

被引:122
作者
Jordan, Stefan [1 ]
Krause, Johannes [2 ]
Prager, Adrian [1 ]
Mitrovic, Maja [3 ]
Jonjic, Stipan [3 ]
Koszinowski, Ulrich H. [1 ]
Adler, Barbara [1 ]
机构
[1] Univ Munich, Max von Pettenkofer Inst Virol, D-80336 Munich, Germany
[2] Max Planck Inst Evolutionary Anthropol, Dept Evolutionary Genet, D-04103 Leipzig, Germany
[3] Univ Rijeka, Sch Med, Rijeka 5100, Croatia
关键词
CLONED HERPESVIRUS GENOME; IN-VIVO; CHEMOKINE HOMOLOG; ENDOTHELIAL-CELLS; ESCHERICHIA-COLI; VECTOR SEQUENCES; BETA CHEMOKINE; INFECTION; CLONING; REPLICATION;
D O I
10.1128/JVI.00545-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Murine cytomegalovirus (MCMV) Smith strain has been cloned as a bacterial artificial chromosome (BAC) named pSM3fr and used for analysis of virus gene functions in vitro and in vivo. When sequencing the complete BAC genome, we identified a frameshift mutation within the open reading frame (ORF) encoding MCMV chemokine homologue MCK-2. This mutation would result in a truncated MCK-2 protein. When mice were infected with pSM3fr-derived virus, we observed reduced virus production in salivary glands, which could be reverted by repair of the frameshift mutation. When looking for the source of the mutation, we consistently found that virus stocks of cell culture-passaged MCMV Smith strain are mixtures of viruses with or without the MCK-2 mutation. We conclude that the MCK-2 mutation in the pSM3fr BAC is the result of clonal selection during the BAC cloning procedure.
引用
收藏
页码:10346 / 10353
页数:8
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