Wohlfart C
Department of Microbiology, University of Lund, Sweden.
J Virol. 1988 Jul;62(7):2321-8. doi: 10.1128/JVI.62.7.2321-2328.1988.
Kinetic curves for neutralization of adenovirus type 2 with anti-hexon serum revealed no lag periods even when the serum was highly diluted or when the temperature was lowered to 4 degrees C, thus indicating a single-hit mechanism. Multiplicity curves determined with anti-hexon serum displayed a linear correlation between the degree of neutralization and dilution of antiserum. Neutralization values experimentally obtained under steady-state conditions fully fitted a single-hit model based on Poisson calculations. Quantitation of the amount of 125I-labeled type-specific anti-hexon antibodies needed for full neutralization of adenovirus showed that 1.4 antibodies were attached per virion under such conditions. Virions already attached to HeLa cells at 4 degrees C were, to a large extent, neutralizable by anti-hexon serum, whereas anti-fiber and anti-penton base antisera were negative. It is suggested that adenovirus may be neutralized by two pathways: aggregation of the virions (extracellular neutralization) as performed by anti-fiber antibodies and blocking of virion entrance from the acidic endosomes into the cytoplasm (intracellular neutralization). The latter effect could be obtained by (i) covering of the penton bases, as performed by anti-penton base antibodies, thereby preventing interaction between the penton bases and the endosomal membrane, which results in trapping of virions within endosomes, and (ii) inhibition of the low-pH-induced conformational change of the viral capsid, which seems to occur in the endosomes and is necessary for proper exposure of the penton bases, as performed by anti-hexon antibodies.
用抗六邻体血清中和2型腺病毒的动力学曲线显示,即使血清被高度稀释或温度降至4℃,也没有延迟期,因此表明是单打击机制。用抗六邻体血清测定的多重复曲线显示中和程度与抗血清稀释度之间呈线性相关。在稳态条件下通过实验获得的中和值完全符合基于泊松计算的单打击模型。对完全中和腺病毒所需的125I标记的型特异性抗六邻体抗体量的定量显示,在这种条件下每个病毒粒子附着1.4个抗体。在4℃时已经附着在HeLa细胞上的病毒粒子在很大程度上可被抗六邻体血清中和,而抗纤维和抗五邻体基底抗血清则呈阴性。有人提出腺病毒可能通过两条途径被中和:病毒粒子的聚集(细胞外中和),如抗纤维抗体所执行的那样;以及阻止病毒粒子从酸性内体进入细胞质(细胞内中和)。后一种效应可以通过以下方式获得:(i)抗五邻体基底抗体覆盖五邻体基底,从而防止五邻体基底与内体膜之间的相互作用,这导致病毒粒子被困在内体中;(ii)抑制病毒衣壳的低pH诱导的构象变化,这种变化似乎发生在内体中,并且是五邻体基底正确暴露所必需的,如抗六邻体抗体所执行的那样。