Haydon D T, Woolhouse M E
Department of Zoology, University of British Columbia, Vancouver, Canada.
J Theor Biol. 1998 Aug 21;193(4):601-12. doi: 10.1006/jtbi.1998.0726.
Highly exposed and protruding amino acid sites on the surface of viral capsids are subject to fewer residue interactions and packing constraints than those buried within protein interiors. Consequently they often experience higher rates of non-synonymous substitution and exhibit greater genetic variability than buried interior sites. However such protrusive surface structures often induce host immune responses and are likely to constitute B cell epitopes. Genetic variation at these surface sites is therefore likely to correspond to antigenic variation. This may be of adaptive value to the virus for two quite different reasons. The first is that antigenic variation arising over the course of a viraemia may result in greater net viral replication, and increased opportunities for viral transmission. The second is that antigenic variation generated rapidly over a single infection or incrementally over several sequential infections may give rise to variants that are sufficiently immunologically distinct that they can reinfect host individuals with previous infection experience of related virus. This would lead to an extension of the susceptible host pool with consequent increase in transmission opportunities. The surface architecture of viral capsid proteins is therefore conceivably subject to two opposing selection pressures: one to minimize the surface area accessible to interaction with elements of the immune system, the other to increase the potential access to antigenic variation by adoption of exposed and unconstrained protein conformations. Therefore, there exists a possible trade-off between the fitness benefits deriving from potential ability to generate antigenic variation, and the increased immunogenicity with which such potential may be associated. We propose that the existence of this trade-off would lead to a continuum of different strategies by which a virus might combat an immune response. We explore this strategy space with simple mathematical models, and show that peak loads of infectious virus particles are proportional to levels of antigenic diversity, and inversely proportional to immunogenicity, thereby creating the potential for a trade-off by which fitness might be maintained with a continuum of strategies. This may remain possible even if the antigenic variants are not transmissible between hosts, so long as immune resources are sufficiently dispersed between antigenic variants. The diversity of possible strategies is discussed with reference to the Picornavirus family.
与埋在蛋白质内部的氨基酸位点相比,病毒衣壳表面高度暴露和突出的氨基酸位点所经历的残基相互作用和堆积限制较少。因此,它们通常经历更高的非同义替换率,并且比埋在内部的位点表现出更大的遗传变异性。然而,这种突出的表面结构常常引发宿主免疫反应,并且很可能构成B细胞表位。因此,这些表面位点的遗传变异很可能与抗原变异相对应。这可能对病毒具有适应性价值,原因有两个截然不同的方面。第一个原因是,在病毒血症过程中出现的抗原变异可能导致病毒净复制增加,以及病毒传播机会增加。第二个原因是,在单次感染过程中迅速产生或在几次连续感染过程中逐渐产生的抗原变异可能产生免疫上足够不同的变体,以至于它们能够再次感染具有相关病毒先前感染经验的宿主个体。这将导致易感宿主库的扩大,从而增加传播机会。因此,可以想象病毒衣壳蛋白的表面结构受到两种相反的选择压力:一种是尽量减少与免疫系统成分相互作用的可及表面积,另一种是通过采用暴露且无限制的蛋白质构象来增加获得抗原变异的可能性。因此,在源自产生抗原变异的潜在能力的适应性益处与这种潜力可能伴随的免疫原性增加之间存在一种可能的权衡。我们提出,这种权衡的存在将导致病毒对抗免疫反应的一系列不同策略。我们用简单的数学模型探索了这个策略空间,并表明感染性病毒颗粒的峰值负荷与抗原多样性水平成正比,与免疫原性成反比,从而创造了一种权衡的可能性,通过一系列策略可以维持适应性。即使抗原变体在宿主之间不可传播,只要免疫资源在抗原变体之间充分分散,这种情况可能仍然存在。本文参照小RNA病毒科讨论了可能策略的多样性。