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通过联合多重聚合酶链反应方法对不同环境分离株中的乳酸双歧杆菌进行特异性鉴定和靶向表征。

Specific identification and targeted characterization of Bifidobacterium lactis from different environmental isolates by a combined multiplex-PCR approach.

作者信息

Ventura M, Reniero R, Zink R

机构信息

Nestlé Research Center, Vers-Chez-Les-Blanc, 1000 Lausanne 26, Switzerland.

出版信息

Appl Environ Microbiol. 2001 Jun;67(6):2760-5. doi: 10.1128/AEM.67.6.2760-2765.2001.

Abstract

The species Bifidobacterium lactis, with its main representative strain Bb12 (DSM 10140), is a yoghurt isolate used as a probiotic strain and is commercially applied in different types of yoghurts and infant formulas. In order to ensure the genetic identity and safety of this bacterial isolate, species- and strain-specific molecular tools for genetic fingerprinting must be available to identify isolated bifidobacteria or lactic acid bacteria from, e.g., various clinical environments of relevance in medical microbiology. Two opposing rRNA gene-targeted primers have been developed for specific detection of this microorganism by PCR. The specificity of this approach was evaluated and verified with DNA samples isolated from single and mixed cultures of bifidobacteria and lactobacilli (48 isolates, including the type strains of 29 Bifidobacterium and 9 Lactobacillus species). Furthermore, we performed a Multiplex-PCR using oligonucleotide primers targeting a specific region of the 16S rRNA gene for the genus Bifidobacterium and a conserved eubacterial 16S rDNA sequence. The specificity and sensitivity of this detection with a pure culture of B. lactis were, respectively, 100 bacteria/ml after 25 cycles of PCR and 1 to 10 bacteria/ml after a 50-cycle nested-PCR approach.

摘要

乳酸双歧杆菌及其主要代表性菌株Bb12(DSM 10140)是一种从酸奶中分离得到的益生菌菌株,已被商业化应用于不同类型的酸奶和婴儿配方奶粉中。为确保该分离菌株的基因一致性和安全性,必须具备物种和菌株特异性的基因指纹分析分子工具,以便从例如医学微生物学中各种相关临床环境中鉴定分离出的双歧杆菌或乳酸菌。已经开发了两种针对rRNA基因的反向引物,用于通过PCR特异性检测这种微生物。使用从双歧杆菌和乳酸菌的单一及混合培养物中分离的DNA样本(48个分离株,包括29种双歧杆菌和9种乳酸菌的模式菌株)对该方法的特异性进行了评估和验证。此外,我们使用针对双歧杆菌属16S rRNA基因特定区域的寡核苷酸引物和保守的真细菌16S rDNA序列进行了多重PCR。用乳酸双歧杆菌纯培养物进行该检测的特异性和灵敏度,在PCR 25个循环后分别为每毫升100个细菌,在50个循环的巢式PCR方法后为每毫升1至10个细菌。

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