通过白细胞毒素基因特异性杂交和聚合酶链反应试验鉴定伴放线放线杆菌。

Identification of Actinobacillus actinomycetemcomitans by leukotoxin gene-specific hybridization and polymerase chain reaction assays.

作者信息

Tønjum T, Haas R

机构信息

Kaptein W. Wilhelmsen og Frues Bakteriologiske Institutt, Rikshospitalet, University of Oslo, Norway.

出版信息

J Clin Microbiol. 1993 Jul;31(7):1856-9. doi: 10.1128/jcm.31.7.1856-1859.1993.

Abstract

Eleven strains of Actinobacillus actinomycetemcomitans isolated from cases of systemic infections, local abscesses, and periodontitis were identified by genetic assays using the leukotoxin gene as the target. We have developed a polymerase chain reaction (PCR) assay, based on the leukotoxin structural gene of this pathogen, which clearly identified all tested strains of A. actinomycetemcomitans and separated them from the closely related Haemophilus aphrophilus as well as other bacterial species. Furthermore, DNA-DNA hybridization was performed with the cloned partial leukotoxin structural gene (lktA) as a probe, which again clearly distinguished A. actinomycetemcomitans from H. aphrophilus, parts of the normal oral flora, and species harboring RTX (repeats in toxin) family-related cytotoxins. The PCR fragment amplified from the leukotoxin structural gene gave results similar to those given by the cloned leukotoxin gene when used as a probe in hybridization experiments. The hybridization and PCR assays described here are fundamental improvements for the identification of A. actinomycetemcomitans.

摘要

从全身感染、局部脓肿和牙周炎病例中分离出的11株伴放线放线杆菌,通过以白细胞毒素基因为靶点的基因检测进行鉴定。我们基于该病原体的白细胞毒素结构基因开发了一种聚合酶链反应(PCR)检测方法,该方法能清晰地鉴定所有测试的伴放线放线杆菌菌株,并将它们与密切相关的嗜沫嗜血杆菌以及其他细菌物种区分开来。此外,以克隆的部分白细胞毒素结构基因(lktA)为探针进行DNA-DNA杂交,再次明确地将伴放线放线杆菌与嗜沫嗜血杆菌、部分正常口腔菌群以及携带RTX(毒素重复序列)家族相关细胞毒素的物种区分开来。从白细胞毒素结构基因扩增得到的PCR片段在用作杂交实验探针时,给出的结果与克隆的白细胞毒素基因相似。本文所述的杂交和PCR检测方法是伴放线放线杆菌鉴定方面的重大改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e1/265645/413b1fba521a/jcm00019-0196-a.jpg

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