Article (Scientific journals)
Glycosaminoglycan interactions in murine gammaherpesvirus-68 infection.
Gillet, Laurent; Adler, Heiko; Stevenson, Philip G
2007In PLoS ONE, 2 (4), p. 347
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Abstract :
[en] Glycosaminoglycans (GAGs) commonly participate in herpesvirus entry. They are thought to provide a reversible attachment to cells that promotes subsequent receptor binding. Murine gamma-herpesvirus-68 (MHV-68) infection of fibroblasts and epithelial cells is highly GAG-dependent. This is a function of the viral gp150, in that gp150-deficient mutants are much less GAG-dependent than wild-type. Here we show that the major MHV-68 GAG-binding protein is not gp150 but gp70, a product of ORF4. Surprisingly, ORF4-deficient MHV-68 showed normal cell binding and was more sensitive than wild-type to inhibition by soluble heparin rather than less. Thus, the most obvious viral GAG interaction made little direct contribution to infection. Indeed, a large fraction of the virion gp70 had its GAG-binding domain removed by post-translational cleavage. ORF4 may therefore act mainly to absorb soluble GAGs and prevent them from engaging gp150 prematurely. In contrast to gp70, gp150 bound poorly to GAGs, implying that it provides little in the way of adhesion. We hypothesize that it acts instead as a GAG-sensitive switch that selectively activates MHV-68 entry at cell surfaces.
Disciplines :
Microbiology
Author, co-author :
Gillet, Laurent  ;  Université de Liège - ULiège > Immunologie et vaccinologie
Adler, Heiko
Stevenson, Philip G
Language :
English
Title :
Glycosaminoglycan interactions in murine gammaherpesvirus-68 infection.
Publication date :
2007
Journal title :
PLoS ONE
eISSN :
1932-6203
Publisher :
Public Library of Science, San Franscisco, United States - California
Volume :
2
Issue :
4
Pages :
e347
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 20 November 2010

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