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用于快速鉴定金黄色葡萄球菌的基于物种特异性和普遍存在DNA的检测方法。

Species-specific and ubiquitous-DNA-based assays for rapid identification of Staphylococcus aureus.

作者信息

Martineau F, Picard F J, Roy P H, Ouellette M, Bergeron M G

机构信息

Centre de Recherche en Infectiologie, Centre Hospitalier Universitaire de Québec, and Université Laval, Ste-Foy, Canada.

出版信息

J Clin Microbiol. 1998 Mar;36(3):618-23. doi: 10.1128/JCM.36.3.618-623.1998.

Abstract

Staphylococcus aureus is the cause of serious infections in humans, including endocarditis, deep-seated abscesses, and bacteremia, which lead to toxic and septic shock syndromes. Rapid and direct identification of this bacterium specifically and ubiquitously directly from clinical specimens would be useful in improving the diagnosis of S. aureus infections in the clinical microbiology laboratory. A wide variety of kits based on biochemical characteristics efficiently identify S. aureus, but the rapidity and the accuracy of each of these methods combined with testing of clinically relevant antibiotic resistance genes need to be improved. On the basis of hybridization assays with randomly selected clones from an S. aureus genomic library, we have identified a chromosomal DNA fragment which is specific for S. aureus and which detected all 82 S. aureus isolates tested. This 442-bp fragment was sequenced and was used to design a set of PCR amplification primers. The PCR assay was also specific and ubiquitous for the identification from bacterial cultures of 195 clinical strains of S. aureus isolated from a variety of anatomical sites and obtained from hospitals throughout the world. The PCR assay that we have developed is simple and can be performed in about 1 h. This DNA-based test provides a novel diagnostic tool for the diagnosis of S. aureus infections.

摘要

金黄色葡萄球菌是人类严重感染的病原体,包括心内膜炎、深部脓肿和菌血症,这些感染会导致中毒性和败血性休克综合征。在临床微生物实验室中,从临床标本中快速、直接且特异性地普遍鉴定这种细菌,将有助于改善金黄色葡萄球菌感染的诊断。基于生化特性的多种试剂盒能有效鉴定金黄色葡萄球菌,但这些方法的速度以及与临床相关抗生素耐药基因检测相结合后的准确性都有待提高。基于与从金黄色葡萄球菌基因组文库中随机挑选的克隆进行杂交分析,我们鉴定出了一个对金黄色葡萄球菌具有特异性的染色体DNA片段,该片段能检测所有82株测试的金黄色葡萄球菌分离株。对这个442碱基对的片段进行了测序,并用于设计一组PCR扩增引物。该PCR检测方法对于从世界各地医院分离的、来自各种解剖部位的195株临床金黄色葡萄球菌菌株的细菌培养物鉴定也具有特异性和普遍性。我们开发的PCR检测方法简单,大约1小时就能完成。这种基于DNA的检测方法为金黄色葡萄球菌感染的诊断提供了一种新型诊断工具。

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