The use of molecular techniques for epidemiologic typing of Candida species.

M A Pfaller
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引用次数: 27

Abstract

The availability of an epidemiologic typing system for Candida species that is sensitive, rapid, inexpensive, and easy to perform would clearly be an advantage to the mycologist, microbiologist, and epidemiologist in the ongoing struggle to understand the epidemiology and pathogenesis of candidiasis. This is particularly true given the increasing prominence of organisms such as C. albicans and C. tropicalis which are ubiquitous members of the normal flora yet are also important causes of nosocomial bloodstream infection. Unfortunately, the ideal epidemiologic typing system does not yet exist. Current data suggest that the molecular typing methods of restriction endonuclease digestion of genomic DNA with ethidium bromide staining (DEtBr typing) and electrophoretic karyotyping using pulsed-field electrophoresis offer rapid, simple, and sensitive means of discriminating strains of Candida species. These methods appear at present to be the most practical typing methods for both large- and small-scale epidemiologic studies. Other typing methods using specific DNA probes provide a powerful means of identifying strains and will undoubtedly be applied more broadly in the future. Thus far, studies employing molecular typing methods have documented that (1) most patients are colonized by one strain of Candida species, (2) isolates of Candida species recovered from blood or deep tissue sites are generally identical to those obtained from colonization sites before infection developed, and (3) nosocomial transmission of a single strain of C. albicans may occur, particularly in an intensive care unit setting. Given the limitations of the available typing methods and the complex nature of the patients at risk for candidiasis, both the epidemiologist and laboratory scientist must use these methods with clear epidemiologic objectives in mind. Whenever possible, all organisms to be typed should be typed by the same person on the same day, and typing should always include unrelated as well as epidemiologically related isolates. Additional studies, based upon sound epidemiologic principles, will be necessary to clarify the role of the various molecular typing methods as epidemiologic markers of Candida species and to further our understanding of the epidemiology and pathogenesis of candidiasis.

念珠菌流行病学分型的分子技术应用。
对于真菌学家、微生物学家和流行病学家来说,一种敏感、快速、廉价且易于操作的念珠菌种流行病学分型系统的可用性显然是一种优势,有助于他们不断努力了解念珠菌病的流行病学和发病机制。考虑到诸如白色念珠菌和热带念珠菌等生物日益突出,这一点尤其正确,这些生物是正常菌群中普遍存在的成员,但也是医院血液感染的重要原因。不幸的是,理想的流行病学分型系统尚不存在。目前的数据表明,利用溴化乙啶染色进行基因组DNA限制性内切酶酶切的分子分型(DEtBr分型)和利用脉冲场电泳进行的电泳核型分型是一种快速、简便、敏感的念珠菌种类鉴别方法。这些方法目前看来是大型和小规模流行病学研究中最实用的分型方法。其他使用特定DNA探针的分型方法提供了一种识别菌株的有力手段,毫无疑问,在未来将得到更广泛的应用。到目前为止,采用分子分型方法的研究已经证明:(1)大多数患者被一种念珠菌定植,(2)从血液或深层组织部位分离的念珠菌通常与感染发生前从定植部位获得的念珠菌分离株相同,(3)单一菌株白色念珠菌可能发生院内传播,特别是在重症监护病房环境中。鉴于现有分型方法的局限性和有感染念珠菌病风险的患者的复杂性,流行病学家和实验室科学家在使用这些方法时必须牢记明确的流行病学目标。只要可能,所有待分型的生物应由同一人在同一天分型,分型应始终包括不相关的以及流行病学上相关的分离株。进一步的研究,基于良好的流行病学原理,将有必要澄清各种分子分型方法作为念珠菌种的流行病学标记的作用,并进一步了解念珠菌病的流行病学和发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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