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

ISRN Microbiology Pub Date : 2013-09-23 eCollection Date: 2013-01-01 DOI:10.1155/2013/342082
S Piwat, R Teanpaisan
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引用次数: 11

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.

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口腔干酪乳杆菌群的16S rRNA pcr -变性梯度凝胶电泳及其表型表现。
本研究旨在建立16S rRNA pcr -变性梯度凝胶电泳(DGGE)技术,鉴定干酪乳杆菌群的菌种水平,并研究其产酸特性和抑酸作用。PCR-DGGE以16S rRNA基因为基础,采用了一套设计在V2-V3区域的HDA-1-GC和HDA-2,以及一套设计在V1区域的CARP-1-GC和CARP-2。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和46株干酪乳杆菌/副干酪乳杆菌/鼠李糖临床菌株。考察了其对变形链球菌的抑制作用和产酸效果。结果表明,CARP1-GC和CARP2引物显示,每种类型菌株和鉴定的临床分离物均具有独特的DGGE模式。HDA1-GC和HDA2引物可以区分副干酪乳杆菌和干酪乳杆菌。结果表明,副干酪乳杆菌的抑菌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。总之,该技术已被证明能够区分干酪乳杆菌群中密切相关的物种,从而为其表型外观提供可靠的信息。
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