Laboratory of Food Biotechnology, Institute of Food, Nutrition and Health, ETH Zurich, Switzerland.
FEMS Microbiol Lett. 2012 Jan;326(2):144-50. doi: 10.1111/j.1574-6968.2011.02443.x. Epub 2011 Nov 18.
The Streptococcus bovis/Streptococcus equinus complex (SBSEC) comprises pathogenic species associated with different degrees with human infections but also spontaneously fermented dairy products. We aimed therefore at developing a specific identification assay for the SBSEC targeting the 16S rRNA gene comprising a multiplex PCR followed by a differentiating restriction fragment length polymorphisms (RFLP). The multiplex PCR assay was positively applied on 200 SBSEC isolates including reference strains. The assay did not yield false-positive amplifications with strains of closely related bacteria and isolates of non-SBSEC streptococci, lactococci, enterococci, and other genera of dairy origin. The downstream RFLP using MseI and XbaI enabled further discrimination of Streptococcus infantarius/S. bovis (biotype II.1) from Streptococcus gallolyticus (biotype I and II.2)/Streptococcus alactolyticus and S. equinus. Furthermore, the newly developed primers can be used directly for Sanger sequencing. Conclusively, this novel PCR/RFLP assay is applicable in the complex dairy microbial communities and provides an important tool to assess the prevalence of members of the SBSEC in dairy products.
牛链球菌/马肠链球菌复合群(SBSEC)包括与不同程度人类感染相关的致病性物种,但也包括自发发酵的乳制品。因此,我们旨在开发一种针对 SBSEC 的 16S rRNA 基因的特定鉴定检测方法,该方法包括多重 PCR 后进行区分性限制性片段长度多态性(RFLP)。该多重 PCR 检测方法已成功应用于包括参考菌株在内的 200 株 SBSEC 分离株。该检测方法不会与密切相关的细菌菌株以及非 SBSEC 链球菌、乳球菌、肠球菌和其他乳制品来源的属的分离株产生假阳性扩增。使用 MseI 和 XbaI 的下游 RFLP 可进一步区分婴儿链球菌/牛链球菌(生物型 II.1)与结肠链球菌(生物型 I 和 II.2)/无乳链球菌和马肠链球菌。此外,新开发的引物可直接用于 Sanger 测序。总之,这种新的 PCR/RFLP 检测方法适用于复杂的乳制品微生物群落,为评估乳制品中 SBSEC 成员的流行情况提供了重要工具。