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J Gen Virol 88 (2007), 758-769; DOI 10.1099/vir.0.82623-0

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Extensive sequence variation exists among isolates of murine cytomegalovirus within members of the m02 family of genes

Alexandra J. Corbett1,2, Catherine A. Forbes1,2, Dorian Moro3,{dagger} and Anthony A. Scalzo1,2

1 Immunology and Virology Program, Centre for Ophthalmology and Visual Science, University of Western Australia, Nedlands, WA 6009, Australia
2 Centre for Experimental Immunology, Lions Eye Institute, 2 Verdun Street, Nedlands, WA 6009, Australia
3 School of Natural Sciences, Edith Cowan University, Joondalup, WA 6027, Australia

Correspondence
Anthony A. Scalzo
scals{at}cyllene.uwa.edu.au

Murine cytomegalovirus (MCMV) is a widely used model for human cytomegalovirus (HCMV) and has facilitated many important discoveries about the biology of CMVs. Most of these studies are conducted using the laboratory MCMV strains Smith and K181. However, wild-derived isolates of MCMV, like HCMV clinical isolates, exhibit genetic variation from laboratory strains, particularly at the ends of their genomes in areas containing known or putative immune-evasion and tropism genes. This study analysed the nucleotide sequence of the m02–m05 region, within the m02 gene family, of a number of laboratory and wild-derived MCMV isolates, and found a large degree of variation in both the sequence and arrangement of genes. A new open reading frame (ORF), designated m03.5, was found to be present in a number of wild isolates of MCMV in place of m03. Two distinct isolates, W8 and W8211, were found to possess both m03 and m03.5. Both m03 and m03.5 had early transcription kinetics and the encoded proteins could be detected on the cell surface, consistent with a possible role in immune evasion through binding to host-cell proteins. These data show that gene duplication and sequence variation occur within different isolates of MCMV found in the wild. As this variation among strains may alter the function of genes, these findings should be considered when analysing gene function or host–virus interactions in laboratory models.

The GenBank/EMBL/DDBJ accession numbers for the sequences determined in this study are EF031243–EF031268.

A supplementary table showing primers used for RT-PCR analysis of m03, m03.5 and m04 is available in JGV Online.

{dagger}Present address: Chevron Australia Pty Ltd, QV1 Building, 250 St George's Terrace, Perth, WA 6000, Australia.




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J. Virol.Home page
L. M. Smith, A. R. McWhorter, L. L. Masters, G. R. Shellam, and A. J. Redwood
Laboratory Strains of Murine Cytomegalovirus Are Genetically Similar to but Phenotypically Distinct from Wild Strains of Virus
J. Virol., July 1, 2008; 82(13): 6689 - 6696.
[Abstract] [Full Text] [PDF]




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