Huemer Hartwig P, Wechselberger Christian, Bennett Alice M, Falke Dietrich, Harrington Lesley
Institute of Molecular Biology, Austrian Academy of Sciences, Salzburg, Austria.
Institute for Hygiene and Social Medicine, University of Innsbruck, Fritz-Pregl-Str. 3, A-6020 Innsbruck, Austria.
J Gen Virol. 2003 May;84(Pt 5):1091-1100. doi: 10.1099/vir.0.18949-0.
Simian herpes B virus (SHBV) is the herpes simplex virus (HSV) homologue for the species MACACA: Unlike in its natural host, and unlike other animal herpesviruses, SHBV causes high mortality in accidentally infected humans. SHBV-infected cells, like those infected with HSV-1 and equine herpesvirus types 1 and 4, express complement C3 receptor activity. To study immunoregulatory functions involved in susceptibility/resistance against interspecies transmission, the SHBV glycoprotein C (gC(SHBV)) gene (encoding 467 aa) was isolated. Sequence analysis revealed amino acid identity with gC proteins from HSV-2 (46.9 %), HSV-1 (44.5 %) and pseudorabies virus (21.2 %). Highly conserved cysteine residues were also noted. Similar to gC(HSV-2), gC(SHBV) is less glycosylated than gC(HSV-1), resulting in a molecular mass of 65 kDa if expressed in replication-deficient vaccinia virus Ankara. Stable transfectants expressing full-length gC(SHBV) on the cell surface induced C3 receptor activity and were substantially protected from complement-mediated lysis; no protection was observed with control constructs. This suggests that expression of the gC homologues on infected cell surfaces might also contribute to the survival of infected cells in addition to decreased virion inactivation. Interestingly, soluble gC(SHBV) isolated from protein-free culture supernatants did not interfere with the binding of the alternative complement pathway activator properdin to C3b, which is similar to our findings with gC(HSV-2) and could be attributed to major differences in the amino-terminal portion of the protein with extended deletions in both gC(SHBV) and gC(HSV-2). Binding of recombinant gC(SHBV) to polysulphates was observed. This, together with the heparin-sensitivity of the gC(SHBV)-C3 interaction on the infected cell surface, suggests a role in adherence to heparan sulphate, similar to the gC proteins of other herpesviruses.
猴疱疹病毒B(SHBV)是猕猴属的单纯疱疹病毒(HSV)同源物:与在其自然宿主中不同,也与其他动物疱疹病毒不同,SHBV在意外感染的人类中会导致高死亡率。被SHBV感染的细胞,就像那些被HSV - 1以及马疱疹病毒1型和4型感染的细胞一样,表达补体C3受体活性。为了研究参与种间传播易感性/抗性的免疫调节功能,分离了SHBV糖蛋白C(gC(SHBV))基因(编码467个氨基酸)。序列分析显示其与HSV - 2的gC蛋白有46.9%的氨基酸同一性,与HSV - 1的gC蛋白有44.5%的同一性,与伪狂犬病病毒的gC蛋白有21.2%的同一性。还注意到高度保守的半胱氨酸残基。与gC(HSV - 2)相似,gC(SHBV)的糖基化程度低于gC(HSV - 1),如果在复制缺陷型痘苗病毒安卡拉中表达,其分子量为65 kDa。在细胞表面表达全长gC(SHBV)的稳定转染子诱导C3受体活性,并能显著免受补体介导的裂解作用;对照构建体未观察到保护作用。这表明感染细胞表面gC同源物的表达除了减少病毒粒子失活外,可能也有助于感染细胞的存活。有趣的是,从无蛋白培养上清液中分离出的可溶性gC(SHBV)不会干扰替代补体途径激活剂备解素与C3b的结合,这与我们对gC(HSV - 2)的研究结果相似,这可能归因于该蛋白氨基末端部分的主要差异,gC(SHBV)和gC(HSV - 2)在这部分都有延伸缺失。观察到重组gC(SHBV)与多硫酸盐的结合。这与感染细胞表面gC(SHBV) - C3相互作用对肝素的敏感性一起,表明其在黏附于硫酸乙酰肝素方面发挥作用,类似于其他疱疹病毒的gC蛋白。