COMPARATIVE-ANALYSIS OF ADENOVIRUS FIBER-CELL INTERACTION - ADENOVIRUS TYPE-2 (AD2) AND AD9 UTILIZE THE SAME CELLULAR FIBER RECEPTOR BUT USE DIFFERENT BINDING STRATEGIES FOR ATTACHMENT

Citation
Pw. Roelvink et al., COMPARATIVE-ANALYSIS OF ADENOVIRUS FIBER-CELL INTERACTION - ADENOVIRUS TYPE-2 (AD2) AND AD9 UTILIZE THE SAME CELLULAR FIBER RECEPTOR BUT USE DIFFERENT BINDING STRATEGIES FOR ATTACHMENT, Journal of virology, 70(11), 1996, pp. 7614-7621
Citations number
42
Categorie Soggetti
Virology
Journal title
ISSN journal
0022538X
Volume
70
Issue
11
Year of publication
1996
Pages
7614 - 7621
Database
ISI
SICI code
0022-538X(1996)70:11<7614:COAFI->2.0.ZU;2-8
Abstract
We have analyzed the binding of adenovirus (Ad) serotypes from subgrou ps B, C, and D through fiber-virus and fiber-fiber cross-competition e xperiments. Since viruses in these distinct subgroups display markedly different tropisms, it was unexpected that the subgroup C viruses Ad2 and 5 and the subgroup D virus Ad9 cross-competed for the same cellul ar fiber receptor. The subgroup B serotype Ad3 recognized a receptor d istinct from the Ad2, 5, and 9 fiber receptor. However, despite sharin g the same fiber receptor, Ad2 and Ad9 displayed markedly different bi nding characteristics that appeared to result from direct Ad9 binding to cells via alpha(v)-integrins. Unlike Ad2, Ad9 binding to many cell lines was not abrogated by competition with the fiber 9 knob (F9K). Ad 9 binding to fiber receptor-deficient cells was blocked by a monoclona l antibody to alpha(v)-integrins, In contrast, Ad9 binding to alpha(v) -deficient cells that express fiber receptor was blocked by F9K. Trans fection of an alpha(v)-integrin-deficient cell line with a plasmid tha t expresses alpha(v) beta(d) resulted in Ad9 binding that was not sign ificantly blocked by F9K but was blocked with a combination of F9K and penton base. These results imply that the shorter length of fiber 9 ( 37 nm) relative to fiber 2 (37 nm) permits fiber-independent binding o f Ad9 penton base to alpha(v)-integrins. The difference in fiber lengt h may explain the different binding characteristics and tissue tropism s of each virus despite both utilizing the same fiber and penton base receptors.