Muir P, Kämmerer U, Korn K, Mulders M N, Pöyry T, Weissbrich B, Kandolf R, Cleator G M, van Loon A M
Department of Virology, United Medical School of Guy's Hospital, London, United Kingdom.
Clin Microbiol Rev. 1998 Jan;11(1):202-27. doi: 10.1128/CMR.11.1.202.
Human enteroviruses have traditionally been typed according to neutralization serotype. This procedure is limited by the difficulty in culturing some enteroviruses, the availability of antisera for serotyping, and the cost and technical complexity of serotyping procedures. Furthermore, the impact of information derived from enterovirus serotyping is generally perceived to be low. Enteroviruses are now increasingly being detected by PCR rather than by culture. Classical typing methods will therefore no longer be possible in most instances. An alternative means of enterovirus typing, employing PCR in conjunction with molecular genetic techniques such as nucleotide sequencing or nucleic acid hybridization, would complement molecular diagnosis, may overcome some of the problems associated with serotyping, and would provide additional information regarding the epidemiology and biological properties of enteroviruses. We argue the case for developing a molecular typing system, discuss the genetic basis of such a system, review the literature describing attempts to identify or classify enteroviruses by molecular methods, and suggest ways in which the goal of molecular typing may be realized.
传统上,人类肠道病毒是根据中和血清型进行分型的。这一过程受到一些限制,如某些肠道病毒培养困难、缺乏用于血清分型的抗血清,以及血清分型程序的成本和技术复杂性。此外,人们普遍认为肠道病毒血清分型所得信息的作用有限。目前,越来越多地通过聚合酶链反应(PCR)而非培养来检测肠道病毒。因此,在大多数情况下,经典的分型方法将不再可行。采用PCR结合核苷酸测序或核酸杂交等分子遗传学技术的肠道病毒分型替代方法,将补充分子诊断,可能克服一些与血清分型相关的问题,并能提供有关肠道病毒流行病学和生物学特性的更多信息。我们阐述了开发分子分型系统的理由,讨论了该系统的遗传基础,回顾了描述通过分子方法鉴定或分类肠道病毒的文献,并提出了实现分子分型目标的方法。