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从咽喉拭子中检测酿脓链球菌的种特异性引物的开发。

Development of species-specific primers for detection of Streptococcus pyogenes from throat swabs.

机构信息

Department of Biotechnology, Alagappa University, Karaikudi, Tamil Nadu, India.

出版信息

FEMS Microbiol Lett. 2010 May;306(2):110-6. doi: 10.1111/j.1574-6968.2010.01939.x. Epub 2010 Feb 25.

Abstract

A species-specific molecular marker has been developed to detect the human pathogen Streptococcus pyogenes from throat swabs. Streptococcus pyogenes is an important pathogen among Gram-positive organisms. A rapid and simple diagnostic tool is of utmost importance for the identification of this pathogen. The random amplified polymorphic DNA (RAPD) technique was used to differentiate the S. pyogenes strains. A differentially amplified fragment obtained from RAPD profiles was sequenced and characterized, which was developed into a sequence characterized amplified region (SCAR) marker to evaluate the specificity of S. pyogenes from other species of Streptococcus. The sensitivity of the SCAR primers was studied by qualitative PCR and the detection limit was found to be 10(-1) ng of genomic DNA or one to two cells of S. pyogenes. The specificity of the primers was assayed in 270 clinical throat swabs wherein 23 samples turned to be positive, which was highly significant over culture-based methods. This species-specific primer enables accurate detection of S. pyogenes from clinical samples and will be a useful tool in epidemiological studies.

摘要

已开发出一种针对特定物种的分子标记物,用于从咽喉拭子中检测人类病原体酿脓链球菌。酿脓链球菌是革兰氏阳性菌中的重要病原体。对于鉴定这种病原体,快速而简单的诊断工具至关重要。随机扩增多态性 DNA(RAPD)技术用于区分酿脓链球菌菌株。从 RAPD 图谱中获得的差异扩增片段进行测序和特征分析,开发出序列特征扩增区域(SCAR)标记物,以评估其对其他链球菌物种的特异性。通过定性 PCR 研究了 SCAR 引物的敏感性,检测限为 10(-1)ng 基因组 DNA 或一到两个酿脓链球菌细胞。在 270 份临床咽喉拭子中检测了引物的特异性,其中 23 份呈阳性,与基于培养的方法相比,这具有高度显著性。该种特异性引物可从临床样本中准确检测酿脓链球菌,将成为流行病学研究的有用工具。

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