口腔干酪乳杆菌群的16S rRNA聚合酶链反应-变性梯度凝胶电泳及其表型特征

16S rRNA PCR-Denaturing Gradient Gel Electrophoresis of Oral Lactobacillus casei Group and Their Phenotypic Appearances.

作者信息

Piwat S, Teanpaisan R

机构信息

Common Oral Diseases and Epidemiology Research Center, Faculty of Dentistry, Prince of Songkla University, Hat Yai 90112, Thailand ; Department of Preventive Dentistry, Faculty of Dentistry, Prince of Songkla University, Hat Yai 90112, Thailand.

出版信息

ISRN Microbiol. 2013 Sep 23;2013:342082. doi: 10.1155/2013/342082. eCollection 2013.

Abstract

This study aimed to develop a 16S rRNA PCR-denaturing gradient gel electrophoresis (DGGE) to identify the species level of Lactobacillus casei group and to investigate their characteristics of acid production and inhibitory effect. PCR-DGGE has been developed based on the 16S rRNA gene, and a set of HDA-1-GC and HDA-2, designed at V2-V3 region, and another set of CARP-1-GC and CARP-2, designed at V1 region, have been used. The bacterial strains included L. casei ATCC 393, L. paracasei CCUG 32212, L. rhamnosus ATCC 7469, L. zeae CCUG 35515, and 46 clinical strains of L. casei/paracasei/rhamnosus. Inhibitory effect against Streptococcus mutans and acid production were examined. Results revealed that each type species strain and identified clinical isolate showed its own unique DGGE pattern using CARP1-GC and CARP2 primers. HDA1-GC and HDA2 primers could distinguish the strains of L. paracasei from L. casei. It was found that inhibitory effect of L. paracasei was stronger than L. casei and L. rhamnosus. The acid production of L. paracasei was lower than L. casei and L. rhamnosus. In conclusion, the technique has been proven to be able to differentiate between closely related species in L. casei group and thus provide reliable information of their phenotypic appearances.

摘要

本研究旨在开发一种16S rRNA聚合酶链反应-变性梯度凝胶电泳(DGGE)方法,以鉴定干酪乳杆菌组的菌种水平,并研究其产酸特性和抑制作用。基于16S rRNA基因开发了PCR-DGGE方法,并使用了一组在V2-V3区域设计的HDA-1-GC和HDA-2引物,以及另一组在V1区域设计的CARP-1-GC和CARP-2引物。细菌菌株包括干酪乳杆菌ATCC 393、副干酪乳杆菌CCUG 32212、鼠李糖乳杆菌ATCC 7469、玉米乳杆菌CCUG 35515,以及46株干酪乳杆菌/副干酪乳杆菌/鼠李糖乳杆菌临床菌株。检测了对变形链球菌的抑制作用和产酸情况。结果显示,使用CARP1-GC和CARP2引物时,每种类型的菌种菌株和鉴定出的临床分离株都显示出其独特的DGGE图谱。HDA1-GC和HDA2引物可以区分副干酪乳杆菌和干酪乳杆菌菌株。发现副干酪乳杆菌的抑制作用强于干酪乳杆菌和鼠李糖乳杆菌。副干酪乳杆菌的产酸量低于干酪乳杆菌和鼠李糖乳杆菌。总之,该技术已被证明能够区分干酪乳杆菌组中密切相关的菌种,从而提供其表型特征的可靠信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87eb/3794536/9ccbe2be2f35/ISRN.MICROBIOLOGY2013-342082.001.jpg

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