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J Gen Virol 72 (1991), 2509-2517; DOI 10.1099/0022-1317-72-10-2509
© 1991 Society for General Microbiology

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Role of the gag and pol genes of human immunodeficiency virus in the morphogenesis and maturation of retrovirus-like particles expressed by recombinant vaccinia virus: an ultrastructural study

Nariyoshi Hoshikawa1, Asato Kojima1, Atsushi Yasuda3, Eiko Takayashiki1, Sanae Masuko4, Joe Chiba1, Tetsutaro Sata1,2, and Takeshi Kurata1

1 Department of Pathology
and2 AIDS Research Center, National Institute of Health, 2-10-35, Kamiosaki, Shinagawa-ku, Tokyo 141
3 Biological Science Laboratory, Nippon Zeon Company Ltd, Yako, Kawasaki-ku, Kawasaki-shi, Kanagawa,
and4 Basic Research Laboratories, Toray Industries Inc., Tebiro, Kamakura, Kanagawa, Japan

An ultrastructural study was performed on rabbit epithelial RK-13 cells and CD4+ human T lymphocyte lines infected with various recombinant vaccinia viruses (RVVs) expressing genes of human immunodeficiency virus (HIV): the mature p17 or p24 gag domain alone, the entire or truncated gag gene, the reverse transcriptase domain, or the gag-pol genes with a frameshift mutation. Cells infected with RVVs that produced the gag polyprotein with a predicted Mr of more than 48K showed budding and release of HIV-like particles into the extracellular space. These particles were not observed in cells expressing a truncated gag gene (p17 and p24 regions). Mature HIV-like particles were observed extracellularly when the entire gag gene and the protease region of the pol gene were expressed. In contrast, in cells infected with RVVs that contained the gag-pol gene with a frameshift mutation, neither recognizable budding structures nor extracellular HIV-like particles could be detected. These results suggest that the gag gene, particularly its 3' terminus, is necessary for the assembly of HIV particles. In addition, the protease region of the pol gene seems to be required for morphological maturation of HIV particles, but complete proteolytic cleavage of the gag protein may prevent bud formation.

Received 4 March 1991; accepted 19 June 1991.


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Copyright © 1991 by the Society for General Microbiology.