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用鉴别培养基和特异性探针鉴定溶蛋白弧菌。

Identification of Vibrio proteolyticus with a differential medium and a specific probe.

作者信息

Muniesa-Pérez M, Jofre J, Blanch A R

机构信息

Department of Microbiology, University of Barcelona, Catalonia, Spain.

出版信息

Appl Environ Microbiol. 1996 Jul;62(7):2673-5. doi: 10.1128/aem.62.7.2673-2675.1996.

Abstract

A differential medium (VP8) and a specific probe, based on the variable region V3 of the 16S rRNA gene, for the detection of Vibrio proteolyticus are defined. The medium contains 8% NaCl, which allows selective growth of moderately halophilic Vibrio strains. D-Sorbitol, as the main carbon source, differentiates the species that can ferment it by the pH indicators cresol red and bromothymol blue. V. proteolyticus and 8 of 418 strains studied grew on the medium and used the D-sorbitol, forming bright yellow colonies. An oligonucleotide, based on the variable region V3 of the 16S rRNA gene (5'CGCTAACGTCAAATAATGCATCTA3'), was used as the specific probe (V3VPR). Only three strains of Vibrio sp. and one strain identified as V. natriegens cross-hybridized with the probe. However, unlike V. proteolyticus, none of the strains grew on VP8. The combined use of VP8 medium and the probe allowed an unequivocal identification of V. proteolyticus.

摘要

定义了一种用于检测溶蛋白弧菌的鉴别培养基(VP8)和一种基于16S rRNA基因可变区V3的特异性探针。该培养基含有8%的氯化钠,可使中度嗜盐弧菌菌株选择性生长。以D - 山梨醇作为主要碳源,通过pH指示剂甲酚红和溴百里酚蓝区分能够发酵它的菌种。溶蛋白弧菌以及所研究的418株菌株中的8株在该培养基上生长,并利用D - 山梨醇,形成亮黄色菌落。基于16S rRNA基因可变区V3(5'CGCTAACGTCAAATAATGCATCTA3')的寡核苷酸用作特异性探针(V3VPR)。只有三株弧菌属菌株和一株鉴定为纳氏弧菌的菌株与该探针发生交叉杂交。然而,与溶蛋白弧菌不同的是,这些菌株在VP8培养基上均不生长。VP8培养基和探针的联合使用能够明确鉴定溶蛋白弧菌。

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