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一种用于同时鉴定和区分产酸克雷伯菌菌株的新检测方法。

A new assay for the simultaneous identification and differentiation of Klebsiella oxytoca strains.

作者信息

Stojowska-Swędrzyńska Karolina, Krawczyk Beata

机构信息

Department of Molecular Biotechnology and Microbiology, Gdańsk University of Technology, ul. G. Narutowicza 11/12, 80-233, Gdańsk, Poland.

出版信息

Appl Microbiol Biotechnol. 2016 Dec;100(23):10115-10123. doi: 10.1007/s00253-016-7881-1. Epub 2016 Oct 8.

Abstract

Klebsiella oxytoca is the second most frequently identified species of Klebsiella isolated from hospitalized patients. Klebsiella spp. is difficult to identify using conventional methods and is often misclassified in clinical microbiology laboratories. K. oxytoca is responsible for an increasing number of multi-resistant infections in hospitals because of insufficient detection and identification. In this study, we propose a new simple method called pehX-LM PCR/XbaI, which simultaneously indicates K. oxytoca species and genotype by the fingerprint pattern. The pehX-LM PCR/XbaI is a combination of the following two methods: species-specific amplification of pehX gene and non-specific amplification of short restriction fragments by the LM PCR method. The specificity and the discrimination power of the pehX-LM PCR/XbaI method were determined by typing 209 K. oxytoca strains (included 9 reference strains), 28 K. pneumoniae, and other 25 strains belonging to the Enterobacteriaceae. The typing results were confirmed by the PCR melting profile method. Unlike the known fingerprinting methods, the pehX-LM PCR/XbaI leads to a clear pattern (approx. 3-5 bands) with a sufficient, relatively high discriminatory power. As a result, the time and cost of a single analysis are lower. The method can be used both in clinical and environmental research.

摘要

产酸克雷伯菌是从住院患者中分离出的第二常见的克雷伯菌属菌种。克雷伯菌属使用传统方法难以鉴定,在临床微生物实验室中常常被错误分类。由于检测和鉴定不足,产酸克雷伯菌在医院中导致的多重耐药感染数量不断增加。在本研究中,我们提出了一种名为pehX-LM PCR/XbaI的新的简单方法,该方法通过指纹图谱同时显示产酸克雷伯菌的菌种和基因型。pehX-LM PCR/XbaI是以下两种方法的组合:pehX基因的种特异性扩增和通过LM PCR方法对短限制性片段的非特异性扩增。通过对209株产酸克雷伯菌菌株(包括9株参考菌株)、28株肺炎克雷伯菌以及其他25株肠杆菌科菌株进行分型,确定了pehX-LM PCR/XbaI方法的特异性和鉴别能力。分型结果通过PCR熔解曲线法进行确认。与已知的指纹图谱方法不同,pehX-LM PCR/XbaI产生清晰的图谱(约3 - 5条带),具有足够的、相对较高的鉴别能力。因此,单次分析的时间和成本较低。该方法可用于临床和环境研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3173/5102950/d189fe559358/253_2016_7881_Fig1_HTML.jpg

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