Division of Microbiology, Office of Regulatory Science Center for Food Safety and Applied Nutrition, US Food and Drug Administration, College Park, MD 20740, USA.
BMC Microbiol. 2010 Mar 23;10:90. doi: 10.1186/1471-2180-10-90.
The genus Vibrio is a diverse group of Gram-negative bacteria comprised of 74 species. Furthermore, the genus has and is expected to continue expanding with the addition of several new species annually. Consequently, it is of paramount importance to have a method which is able to reliably and efficiently differentiate the numerous Vibrio species.
In this study, a novel and rapid polymerase chain reaction (PCR)-based intergenic spacer (IGS)-typing system for vibrios was developed that is based on the well-known IGS regions located between the 16S and 23S rRNA genes on the bacterial chromosome. The system was optimized to resolve heteroduplex formation as well as to take advantage of capillary gel electrophoresis technology such that reproducible analyses could be achieved in a rapid manner. System validation was achieved through testing of 69 archetypal Vibrio strains, representing 48 Vibrio species, from which an 'IGS-type' profile database was generated. These data, presented here in several cluster analyses, demonstrated successful differentiation of the 69 type strains showing that this PCR-based fingerprinting method easily discriminates bacterial strains at the species level among Vibrio. Furthermore, testing 36 strains each of V. parahaemolyticus and V. vulnificus, important food borne pathogens, isolated from a variety of geographical locations with the IGS-typing method demonstrated distinct IGS-typing patterns indicative of subspecies divergence in both populations making this technique equally useful for intraspecies differentiation, as well.
This rapid, reliable and efficient IGS-typing system, especially in combination with 16S rRNA gene sequencing, has the capacity to not only discern and identify vibrios at the species level but, in some cases, at the sub-species level, as well. This procedure is particularly well-suited for preliminary species identification and, lends itself nicely to epidemiological investigations providing information more quickly than other time-honoured methods traditionally used in these types of analyses.
弧菌属是一组多样化的革兰氏阴性细菌,由 74 种组成。此外,随着每年添加几个新物种,该属预计将继续扩大。因此,拥有一种能够可靠且有效地区分众多弧菌物种的方法至关重要。
在这项研究中,开发了一种新颖且快速的基于聚合酶链反应(PCR)的弧菌种间间隔区(IGS)分型系统,该系统基于细菌染色体上位于 16S 和 23S rRNA 基因之间的知名 IGS 区域。该系统经过优化,可解决异源双链体的形成问题,并利用毛细管凝胶电泳技术,以便快速实现可重复的分析。通过测试 69 种代表性弧菌菌株(代表 48 种弧菌物种)来验证系统,从而生成了 IGS 型档案数据库。这些数据通过几个聚类分析呈现,成功区分了 69 种类型菌株,表明这种基于 PCR 的指纹分析方法很容易区分弧菌属的物种水平上的细菌菌株。此外,使用 IGS 分型方法测试了从不同地理位置分离的 36 株副溶血弧菌和创伤弧菌,这两种都是重要的食源性病原体,结果显示这两种弧菌种群都存在明显的 IGS 分型模式,表明亚种分化。因此,该技术同样可用于种内分化。
这种快速、可靠且高效的 IGS 分型系统,特别是与 16S rRNA 基因测序相结合,不仅能够区分和识别种水平的弧菌,而且在某些情况下还能够识别亚种水平的弧菌。该程序特别适合初步的物种鉴定,并为流行病学研究提供信息,比传统的其他耗时方法更快。