Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Gain of Virulence Caused by Loss of a Gene in Murine Cytomegalovirus (CROSBI ID 181172)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Bubić, Ivan ; Wagner, Markus ; Krmpotić, Astrid ; Saulig, Tanja ; Kim, Sungjin ; Yokoyama, Wayne ; Jonjić, Stipan ; Koszinowski, Ulrich Gain of Virulence Caused by Loss of a Gene in Murine Cytomegalovirus // Journal of virology, 78 (2004), 14; 7536-7544. doi: 10.1128/JVI.78.14.7536-7544.2004

Podaci o odgovornosti

Bubić, Ivan ; Wagner, Markus ; Krmpotić, Astrid ; Saulig, Tanja ; Kim, Sungjin ; Yokoyama, Wayne ; Jonjić, Stipan ; Koszinowski, Ulrich

engleski

Gain of Virulence Caused by Loss of a Gene in Murine Cytomegalovirus

Mouse strains are either resistant or susceptible to murine cytomegalovirus (MCMV). Resistance is determined by the Cmv1(r) (Ly49h) gene, which encodes the Ly49H NK cell activation receptor. The protein encoded by the m157 gene of MCMV has been defined as a ligand for Ly49H. To find out whether the m157 protein is the only Ly49H ligand encoded by MCMV, we constructed the m157 deletion mutant and a revertant virus. Viruses were tested for susceptibility to NK cell control in Ly49H+ and Ly49H- mouse strains. Deletion of the m157 gene abolished the viral activation of Ly49H+ NK cells, resulting in higher virus virulence in vivo. Thus, in the absence of m157, Ly49H+ mice react like susceptible strains. 129/SvJ mice lack the Ly49H activation NK cell receptor but express the inhibitory Ly49I NK cell receptor that binds to the m157 protein. The Deltam157 inhibitory phenotype was weak because MCMV encodes a number of proteins that mediate NK inhibition, whose contribution could be shown by another mutant.

cytomegalovirus; innate immunity; NK cells

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

78 (14)

2004.

7536-7544

objavljeno

0022-538X

10.1128/JVI.78.14.7536-7544.2004

Povezanost rada

Temeljne medicinske znanosti

Poveznice
Indeksiranost