Identification of a 1.6 kb genome locus of guinea pig cytomegalovirus required for efficient viral growth in animals but not in cell culture

Abstract Guinea pig cytomegalovirus (GPCMV) provides a useful model for studies of congenital CMV infection. During characterization of the GPCMV genome sequence, we identified two types of strains in a virus stock purchased from ATCC. One of them, GPCMV/del, lacks a 1.6 kb locus that positionally c...

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Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 2008-09, Vol.379 (1), p.45-54
Hauptverfasser: Nozawa, Naoki, Yamamoto, Yumiko, Fukui, Yoshiko, Katano, Harutaka, Tsutsui, Yoshihiro, Sato, Yuko, Yamada, Souichi, Inami, Yuhki, Nakamura, Kohnosuke, Yokoi, Masayuki, Kurane, Ichiro, Inoue, Naoki
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Sprache:eng
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Zusammenfassung:Abstract Guinea pig cytomegalovirus (GPCMV) provides a useful model for studies of congenital CMV infection. During characterization of the GPCMV genome sequence, we identified two types of strains in a virus stock purchased from ATCC. One of them, GPCMV/del, lacks a 1.6 kb locus that positionally corresponds to murine CMV (MCMV) M129–M133. Growth of GPCMV/del in cell culture was marginally better than that of the other strain, GPCMV/full, which harbors the 1.6 kb locus. However, in animals infected intraperitoneally with virus stocks containing both strains, GPCMV/full disseminated more efficiently than GPCMV/del, including 200-fold greater viral load in salivary glands. Viral DNA, transcripts of the immediate-early 2 gene homolog, and viral antigens were more abundant in animals infected with GPCMV/full than in those infected with GPCMV/del. Although the observed phenomena have some similarity with the growth properties of MCMV strains defective in mck-1/mck-2 (M129/131) and those defective in sgg (M132), no M129–M132 homologs were found in the 1.6 kb locus. Since one of the ORFs in the locus has a weak sequence similarity with HCMV UL130, which relates to cell tropism, further studies will be required to learn the mechanism for efficient GPCMV growth in animal.
ISSN:0042-6822
1096-0341
DOI:10.1016/j.virol.2008.06.018