Deitsch K W, Moxon E R, Wellems T E
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0425, USA.
Microbiol Mol Biol Rev. 1997 Sep;61(3):281-93. doi: 10.1128/mmbr.61.3.281-293.1997.
Pathogenic microbes have evolved highly sophisticated mechanisms for colonizing host tissues and evading or deflecting assault by the immune response. The ability of these microbes to avoid clearance prolongs infection, thereby promoting their long-term survival within individual hosts and, through transmission, between hosts. Many pathogens are capable of extensive antigenic changes in the face of the multiple constitutive and dynamic components of host immune defenses. As a result, highly diverse populations that have widely different virulence properties can arise from a single infecting organism (clone). In this review, we consider the molecular and genetic features of antigenic variation and corresponding host-parasite interactions of different pathogenic bacterial, fungal, and protozoan microorganisms. The host and microbial molecules involved in these interactions often determine the adhesive, invasive, and antigenic properties of the infecting organisms and can dramatically affect the virulence and pathobiology of individual infections. Pathogens capable of such antigenic variation exhibit mechanisms of rapid mutability in confined chromosomal regions containing specialized genes designated contingency genes. The mechanisms of hypermutability of contingency genes are common to a variety of bacterial and eukaryotic pathogens and include promoter alterations, reading-frame shifts, gene conversion events, genomic rearrangements, and point mutations.
致病微生物已经进化出高度复杂的机制,用于定殖于宿主组织并逃避或抵御免疫反应的攻击。这些微生物避免被清除的能力会延长感染时间,从而促进它们在个体宿主体内的长期存活,并通过传播在宿主之间扩散。面对宿主免疫防御的多种组成性和动态成分,许多病原体能够发生广泛的抗原变化。因此,单一感染生物体(克隆)可能产生具有广泛不同毒力特性的高度多样化群体。在这篇综述中,我们考虑了不同致病细菌、真菌和原生动物微生物的抗原变异的分子和遗传特征以及相应的宿主-寄生虫相互作用。参与这些相互作用的宿主和微生物分子通常决定感染生物体的黏附、侵袭和抗原特性,并可显著影响个体感染的毒力和病理生物学。能够发生这种抗原变异的病原体在含有称为应急基因的特殊基因的受限染色体区域表现出快速突变的机制。应急基因的高突变机制在多种细菌和真核病原体中很常见,包括启动子改变、读码框移位、基因转换事件、基因组重排和点突变。