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A novel multiplex PCR/RFLP assay for the identification of Streptococcus bovis/Streptococcus equinus complex members from dairy microbial communities based on the 16S rRNA gene

机译:一种基于16S rRNA基因的新型多重PCR / RFLP检测方法,用于鉴定来自乳品微生物群落的牛链球菌/马链球菌复合物成员

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摘要

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
机译:牛链球菌/马链球菌复合物(SBSEC)包含与人类感染程度不同的致病菌,但也包括自发发酵的乳制品。因此,我们旨在开发针对SBSEC的针对16S rRNA基因的特异性鉴定方法,该方法包括多重PCR,然后进行限制性酶切片段长度多态性分析(RFLP)。多重PCR测定法被积极应用于200 SBSEC分离株,包括参考菌株。该测定法未产生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属的菌株的假阳性扩增。使用MseI和XbaI的下游RFLP能够进一步区分婴儿链球菌/ S。牛溶质链球菌(生物型I和II.2)/解链球菌和马链球菌的牛型(生物型II.1)。此外,新开发的引物可直接用于Sanger测序。最终,这种新颖的PCR / RFLP检测方法适用于复杂的乳制品微生物群落,并提供了一个重要的工具来评估SBSEC成员在乳制品中的流行程度

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