Characterization of a novel wood mouse virus related to murid herpesvirus 4

Two novel gammaherpesviruses were isolated, one from a field vole (Microtus agrestis) and the other from wood mice (Apodemus sylvaticus). The genome of the latter, designated wood mouse herpesvirus (WMHV), was completely sequenced. WMHV had the same genome structure and predicted gene content as mur...

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Published in:Journal of general virology Vol. 91; no. Pt 4; pp. 867 - 879
Main Authors: HUGHES, David J, KIPAR, Anja, BENNETT, Malcolm, SAMPLE, Jeffery T, BARRELL, Bart, DAVISON, Andrew J, STEWART, James P, MILLIGAN, Steven G, CUNNINGHAM, Charles, SANDERS, Mandy, QUAIL, Michael A, RAJANDREAM, Marie-Adele, EFSTATHIOU, Stacey, BOWDEN, Rory J, CHASTEL, Claude
Format: Journal Article
Language:English
Published: Reading Society for General Microbiology 01-04-2010
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Summary:Two novel gammaherpesviruses were isolated, one from a field vole (Microtus agrestis) and the other from wood mice (Apodemus sylvaticus). The genome of the latter, designated wood mouse herpesvirus (WMHV), was completely sequenced. WMHV had the same genome structure and predicted gene content as murid herpesvirus 4 (MuHV4; murine gammaherpesvirus 68). Overall nucleotide sequence identity between WMHV and MuHV4 was 85 % and most of the 10 kb region at the left end of the unique region was particularly highly conserved, especially the viral tRNA-like sequences and the coding regions of genes M1 and M4. The partial sequence (71 913 bp) of another gammaherpesvirus, Brest herpesvirus (BRHV), which was isolated ostensibly from a white-toothed shrew (Crocidura russula), was also determined. The BRHV sequence was 99.2 % identical to the corresponding portion of the WMHV genome. Thus, WMHV and BRHV appeared to be strains of a new virus species. Biological characterization of WMHV indicated that it grew with similar kinetics to MuHV4 in cell culture. The pathogenesis of WMHV in wood mice was also extremely similar to that of MuHV4, except for the absence of inducible bronchus-associated lymphoid tissue at day 14 post-infection and a higher load of latently infected cells at 21 days post-infection.
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Present address: Department of Microbiology and Immunology, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.
Present address: Oxford Centre for Gene Function, Department of Statistics, 1 South Parks Road, Oxford, OX1 3TG, UK.
Present address: Infection and Immunity Section, Level 9, University of Glasgow Dental School, 378 Sauchiehall Street, Glasgow G2 3JZ, UK.
ISSN:0022-1317
1465-2099
DOI:10.1099/vir.0.017327-0